California Mesothelioma Fact Sheet
While mesothelioma is a problem in all states, the specific incident rate for California is 1 / 100,000. This is below the average rate of 1.1 / 100,000. Click on the tabs below to find mesothelioma and asbestos research in CA, recent CA mesothelioma-related court cases, mesothelioma specialists in CA and potential asbestos hotspots in California.
California Mesothelioma Info
By clicking on the above tabs, you will find information on mesothelioma specific to the state of California
California Research and Clinical Trials
This is a partial list of scientific or medical grants in your state for research into mesothelioma and related illnesses.
California Doctors and Hospitals
This is a partial list of hospitals and physicians that reportedly treat mesothelioma patients in your state.
California Cases
This is a partial list of relevant court cases on mesothelioma in your state.
Disclaimer: Inclusion on this directory does not constitute endorsement by Cancer Monthly, Inc. All physicians who appear in this section do so based on their own expression of interest in the fields of mesothelioma treatment. Cancer Monthly, Inc. has not verified the competence, professional credentials, business practices or validity of the expressed interests of these physicians. Cancer Monthly makes no recommendation of any physician on this list and makes no suggestion that any such physician will cure or prevent any disease. Those consulting a physician on this list should approach the consultation exactly as they would with any other unknown physician.
This is a partial list of scientific or medical grants in your state for research into mesothelioma and related illnesses.
California Doctors and Hospitals
This is a partial list of hospitals and physicians that reportedly treat mesothelioma patients in your state.
California Cases
This is a partial list of relevant court cases on mesothelioma in your state.
Disclaimer: Inclusion on this directory does not constitute endorsement by Cancer Monthly, Inc. All physicians who appear in this section do so based on their own expression of interest in the fields of mesothelioma treatment. Cancer Monthly, Inc. has not verified the competence, professional credentials, business practices or validity of the expressed interests of these physicians. Cancer Monthly makes no recommendation of any physician on this list and makes no suggestion that any such physician will cure or prevent any disease. Those consulting a physician on this list should approach the consultation exactly as they would with any other unknown physician.
Grisham v. Philip Morris U.S.A., Inc.
S132772 , SUPREME COURT OF CALIFORNIA, February 15, 2007, Filed
S132772 , SUPREME COURT OF CALIFORNIA, February 15, 2007, Filed
Kinsman v. Unocal Corp.
S118561 , SUPREME COURT OF CALIFORNIA, December 19, 2005, Filed
S118561 , SUPREME COURT OF CALIFORNIA, December 19, 2005, Filed
Hamilton v. Asbestos Corp.
No. S069596. , SUPREME COURT OF CALIFORNIA , May 15, 2000, Decided
No. S069596. , SUPREME COURT OF CALIFORNIA , May 15, 2000, Decided
Chevron U.S.A., Inc. v. Workers' Comp. Appeals Bd.
No. S059214. , SUPREME COURT OF CALIFORNIA, January 25, 1999, Decided
No. S059214. , SUPREME COURT OF CALIFORNIA, January 25, 1999, Decided
Oxford v. Foster Wheeler LLC
A121577, COURT OF APPEAL OF CALIFORNIA, FIRST APPELLATE DISTRICT, DIVISION ONE, September 9, 2009, Filed
A121577, COURT OF APPEAL OF CALIFORNIA, FIRST APPELLATE DISTRICT, DIVISION ONE, September 9, 2009, Filed
Taylor v. Elliott Turbomachinery Co., Inc.
A116816, A117648, COURT OF APPEAL OF CALIFORNIA, FIRST APPELLATE DISTRICT, DIVISION FIVE, February 25, 2009, Filed
A116816, A117648, COURT OF APPEAL OF CALIFORNIA, FIRST APPELLATE DISTRICT, DIVISION FIVE, February 25, 2009, Filed
Garza v. Asbestos Corp., Ltd.
A116523, A119262, COURT OF APPEAL OF CALIFORNIA, FIRST APPELLATE DISTRICT, DIVISION THREE, March 28, 2008, Filed
A116523, A119262, COURT OF APPEAL OF CALIFORNIA, FIRST APPELLATE DISTRICT, DIVISION THREE, March 28, 2008, Filed
McCann v. Foster Wheeler
B189898, COURT OF APPEAL OF CALIFORNIA, SECOND APPELLATE DISTRICT, DIVISION EIGHT, February 28, 2008, Filed
B189898, COURT OF APPEAL OF CALIFORNIA, SECOND APPELLATE DISTRICT, DIVISION EIGHT, February 28, 2008, Filed
Whitlock v. Foster Wheeler, LLC
A117221, COURT OF APPEAL OF CALIFORNIA, FIRST APPELLATE DISTRICT, DIVISION THREE, February 15, 2008, Filed
A117221, COURT OF APPEAL OF CALIFORNIA, FIRST APPELLATE DISTRICT, DIVISION THREE, February 15, 2008, Filed
Boeken v. Philip Morris USA, Inc.
B198220, COURT OF APPEAL OF CALIFORNIA, SECOND APPELLATE DISTRICT, DIVISION FIVE, February 11, 2008, Filed
B198220, COURT OF APPEAL OF CALIFORNIA, SECOND APPELLATE DISTRICT, DIVISION FIVE, February 11, 2008, Filed
Hospitals and Cancer Centers
Cedars-Sinai Medical Center
8700 Beverly Blvd.
Los Angeles, CA
310.423.5874
City of Hope Comprehensive Cancer Center
City of Hope Comprehensive Cancer Center
Duarte, CA
626-256-4673
Physicians
Dr. Robert Cameron
P. O. Box 951741
Los Angeles, California 90095-1741
(310) 794.7333
rcameron@mednet.ucla.edu
Dr. David Jablons
UCSF Mt. Zion Medical Center
2330 Post St., Suite 420
San Francisco, CA 94115
(415) 885-3882
Dr. Theirry Jahan
2356 Sutter, 7th FL
San Francisco, CA 94115
(415) 567-5581
Cedars-Sinai Medical Center
8700 Beverly Blvd.
Los Angeles, CA
310.423.5874
City of Hope Comprehensive Cancer Center
City of Hope Comprehensive Cancer Center
Duarte, CA
626-256-4673
Physicians
Dr. Robert Cameron
P. O. Box 951741
Los Angeles, California 90095-1741
(310) 794.7333
rcameron@mednet.ucla.edu
Dr. David Jablons
UCSF Mt. Zion Medical Center
2330 Post St., Suite 420
San Francisco, CA 94115
(415) 885-3882
Dr. Theirry Jahan
2356 Sutter, 7th FL
San Francisco, CA 94115
(415) 567-5581
| City | Site |
|
Alpha Beta Market American Brake Shoe American Pipe and Construction Co American Standard Atlantic Richfield Corp Auto Club of Southern California Bechtel Building Bechman Instruments Braun CF Building Builder's Emporium Bullocks Department Store California Federal Savings and Loan Chapman College Consolidated Lumbar Co Crocker Center Crocker Citizens Bank Hughes Aircraft Kimberly Clark McDonnell Douglas Corp Philco Co Ralph's Stores Sears & Roebuck Slowoa Metals South Bay Chevrolet South Coast Plaza St Judes Hospital Town and Country Hotel Union Bank Building University Ford Wells Fargo Bank Building | |
| 29 Palms |
29 Palms Hospital 29 Palms School District |
| Acusa |
Aerojet Rainbird Sprinkler |
| Alameda |
Airsta Naval Shipyard Arista Shipyard Bethlehem Steel United Engineering |
| Albany |
West Roofing |
| Anaheim |
Anaheim Convention Center Anaheim Stadium Children's Hospital |
| Atwater |
Wood Fruit Cannery |
| Bakersfield |
Superior Tank Company |
| Benica |
Exxon Refinery Tosco Refinery |
| Braswell |
Redstone Shipyards |
| Colton |
Colton Cement Colton School District |
| Coronado |
Boat Support Unit 1 Coronado School District |
| Costa Mesa |
Orange Coast College Pomona Avenue Elementary School |
| El Cerrito |
Stauffer Chemical |
| El Segundo |
Standard Oil |
| El Sobrante |
Pal Roofing |
| Eldridge |
Sonoma Development Center |
| Englewood |
Allied Metal Shop |
| Everette |
Schoot Paper |
| Fontana |
Kaiser Steel Mill |
| Haywood |
Continental Can Co |
| Hibbing |
29 Palms Marine Base Schirmer Mechanical |
| Hunters Point |
PG&E Power Plant |
| Huntington Beach |
Phillips 66 |
| Irvine |
University of California |
| Livingston |
Trinity Dam |
| Long Beach |
Bethlehem Steel Douglas Aircraft Long Beach Naval Shipyard McCloskey Sheet Metal Shell Oil Super Temp Todd Shipyard |
| Long Beach |
US Naval Shipyard |
| Los Alamos |
Southern California Edison |
| Los Angeles |
Astancia High School Bethlehem Steel Bonita Street Elementary Bunker Hill Plant Bushnell Way Elementary School Corona Del Mar High School Crocker Tower Dept of Water and Power Firestone Fluor Corp Goodyear Plant Los Angeles Dry Dock and Shipbuilding Procon Inc Rey Junior High School Rocket Dyne Sonora School Superior Oil The Whittier School Tishman Realty & Construction Co Twin Towers VAMC Victoria Street Elementary School Wilson School |
| Malibu |
Pepperdine University |
| March AFB |
Riverside March Hospital |
| Martinez |
Avon Refinery |
| Marysville |
Perini Corporation |
| Menlo Park |
Ray Chemical |
| Modesto |
Gallo winery Sproutse Reito Variety Store Sproutse Reito Variety Store Crows Landing rd Sproutse Reito Variety Store Paradise rd Sproutse Reito Variety Store Yosemite rd. |
| Morrow Bay |
PGE Powerhouse |
| Newport |
US Naval Station |
| Newport Beach |
Bank of Newport |
| North Island |
North Island Navy |
| Oakland |
Ford Motor Company |
| Orange |
Orange County Jail Orange Pulp and Paper |
| Orville |
Orville Dams |
| Pala Alto |
Stanford Hospital |
| Palo Alto |
Sanford Linear Atomic Accelerator Watkins Johnson Building |
| Pannol |
Rogers Roofing |
| Paramount |
Douglas Oil Refinery |
| Pasadena |
Sinclair Oil Refinery |
| Pittsburgh |
Southern Construction Company |
| Point Hueneme |
CBC |
| Point Mugu |
UAMTC |
| Pomona |
California Poly Univ. |
| Realto |
Realto School District |
| Redding |
Redding Service Station Maintenance |
| Redlands |
Redlands Community Hospital |
| Redondo |
Redondo School District |
| Redondo Beach |
Southern California Edison |
| Richmond |
Garwood Industries Richmond Shipyard |
| Riverside |
American Cement Co. Riverside Community Hospital Riverside County Courthouse Riverside County Municipal Annex Courthouse Riverside General Riverside School District Wycoff Building |
| San Benito |
San Benito Hospital |
| San Bernardino |
San Bernardino School District |
| San Bonita |
The LaPama |
| San Diego |
Asbestos Roofing Co Benton Roofing Campbell Machine Shipyard Fleet Maintenance & Assistance Jandy Camps Shipyards National Steel Shipyard San Diego County building San Diego Shipyard Standard Oil Station |
| San Diego |
US Naval Station |
| San Francisco |
Alameda Naval Base Alameda Shipyard Bethlehem Steel Shipyard Cushin Shipyard Hunters Point Shipyard Ping Yang Chinese Senior Housing Facility San Francisco ISD San Francisco Shipyard San Rafael Shipyard Southern Pacific Railroad Standard Oil Building State of the Art Sewage Plant Treasure Island N. Shipyard University of California SF Hospital |
| San Jose |
General Electric Pacific Telephone Building San Jose State University Santa Clara Fairgrounds Santa Teresa Medical building |
| San Juan |
San Juan Caspatrasas School District |
| San Mateo |
State farm Insurance Building Willis Heating |
| San Pablo |
Jackson Roofing |
| San Pedro |
Roosevelt Base San Pedro Naval Shipyard Todd Shipyard US Coast Guard Union 76 Refinery |
| Santa Ana |
Santa Ana Register |
| Santa Clara |
Owens-Corning Fiberglass |
| Santa Cruz |
University of Santa Cruz |
| Santa Monica |
Douglas Aircraft Santa Monica college Santa Monica Unified School District System Development Corp. |
| Saratoga |
Danza College Paso de Saratoga Shopping Center |
| Segundo |
Standard Oil Company |
| Southgate |
Schultz Steel |
| Sunnydale |
Philco Ford Building |
| Sylmar |
Veterans Hospital |
| Turlock |
Snyder Lumber co Sproutse Reito Variety Store |
| Tustin |
Tustin Hospital |
| Vacaville |
Travis AFB |
| Vallego |
Union Oil |
| Vallejo |
Marc Island Naval Shipyard Mare Island Naval Shipyard |
| Watsonville |
City of Watsonville |
Research
He, Jiang Targeted Liposomal Radiotherapy Of Malignant Mesothelioma
Grant: 1R01CA135358-01
Grant: 1R01CA135358-01
Abstract:
DESCRIPTION (provided by applicant): Mesothelioma, a malignancy associated with occupational exposure to asbestos is a devastating disease without attractive therapies. For decades, asbestos was used heavily in construction, industry, the Navy, even household products and appliances, and is still present in many homes, schools, and office buildings. The disease can arise from small exposures, and even as much as 50 years later. As a result, each year 3,000 Americans and many thousands more worldwide develop mesothelioma, and millions of us are at risk, creating a pressing need for new therapeutic strategies. Since mesothelioma is generally a regional disease within the pleura and peritoneum, aggressive surgery can resect most of solid viable tumor. However, microscopic residues and recurrence, especially in the peritoneal mesothelioma because of the complexity of the space and fragility of the organs, are increasingly recognized as major problems. Highly selective tumor location and targeting are needed. Our long term goal is to develop effective radioimmunotherapy (RIT) for human cancers by marrying radiotherapy with nanotechnology. The objective of this application is to engineer nano liposome as the dose delivery media to carry high payload of radionuclides for specific targeting of the methothelioma tumor cells by intraperitoneal administration. To accomplish, the first Aim is to identify optimal scFv antibodies targeting to malignant mesothelioma from a panel of 15 antibodies we have recently discovered. The native antibodies will be labeled with 99mTc for in vitro and in vivo evaluation of targeting. The remaining best 5 will be conjugated to nanosized liposome for further characterization in vitro and in vivo of the performance of these nanoparticle radioimmunoconjugates. The results will guide changes to the synthesis parameters in order to produce antibody liposome conjugates with promising properties for in vivo application. The second aim will focus on the 177Lu labeling of the nanosized liposome conjugated with optimal antibody (177Lu-LP-scFv) to achieve high specific activity and characterize the targeting capability, stability and radiolysis in vitro. In vivo localization and biodistribution will be evaluated and optimized in animals bearing malignant peritoneal mesothelioma. In Aim 3, the biodistribution and treatment efficacy of the best 177Lu-LP-scFv will then be evaluated in mice with malignant peritoneal mesothelioma xenografts. A variety of dosing schemes will also be tested. Execution of this project will provide effective and safe radioimmunotherapy of this aggressive disease. The novel antibody identified from in vivo screening will also have great potential to translate into specific marker for malignant mesothelioma and targeting vector for other targeted modality therapy. Additionally, the modular approach inherent in the nanoliposome simultalously loaded with targeting vector and high payload of cytotoxic agent holds promise as of potential template for multimodality intracavity locoregional therapies (e.g. photodynamic-radiotherapy) for malignant mesothelioma and other human cancers. PUBLIC HEALTH RELEVANCE: Malignant mesothelioma is a neoplasm of the mesothelial lining of the pleural or peritoneal cavity linked to prior exposure to asbestos. For decades, asbestos was used heavily in construction, industry, the Navy, even household products and appliances, and is still present in many homes, schools, and office buildings. The disease can arise from small exposures, and even as much as 50 years later with reported median survivals of only 18 to 24 months after diagnosis. As a result, each year more than 3,000 Americans and many thousands more worldwide develop mesothelioma, millions of us are at risk and projections suggest that the incidence will continue to rise, creating a pressing need for new therapeutic strategies. This project addresses key challenges of radioimmunotherapy (RIT) for the treatment of malignant mesothelioma. The goal for the study is to use nano liposome as the dose delivery media to carry high payload of radionuclides for specific targeting of the methothelioma tumor cells. If successfully completed, this novel method will create far-reaching applications in RIT, particularly for high-potent treatments of malignant mesothelioma.
Tags: There Are No Thesaurus Terms On File For This Project.
Tags: There Are No Thesaurus Terms On File For This Project.
- Followup Grant: 5R01CA135358-02
Jablons, David M. The Wnt Pathway In Malignant Mesothelioma
Grant: 1R01CA093708-01A3
Grant: 1R01CA093708-01A3
Abstract:
DESCRIPTION (provided by applicant): The long-term objective for this proposal is the elucidation of molecular mechanisms for the wingless-type (Wnt)/beta-catenin signaling pathway in malignant mesothelioma (MM) and the development of molecular therapies for this malignancy. Mesothelioma is a relatively uncommon but inexorably fatal tumor, affecting about 3000 new patients in the United States annually. Despite advances in cancer treatment, the medium survival rate remains low and most patients die within two years after diagnosis. The pathogenesis of mesothelioma remains poorly understood and the molecular mechanism by which mesothelial cells undergo neoplastic transformation is largely unknown. For this proposal, we will test the hypothesis that aberrant activation of Wnt signaling pathway plays important roles in malignant mesothelioma. Preliminary data from our laboratory showed that the Wnt signaling pathway is activated in MM as evidenced by increased cytosolic/nuclear beta-catenin, and c-Myc, the two downstream target genes, downregulation of the potential endogenous inhibitor secreted frizzled related protein (SFRP2), and an increased phosphorylation of the Wnt pathway mediator dishevelled protein (Dvl-3). These observations have not been described previously nor elucidated in MM. The specific Aims for this application are 1) to confirm that Wnt signaling pathway is activated in mesothelioma in a large number of primary tumor samples: 2) to investigate molecular mechanisms of Wnt signaling activation in mesothelioma. initially by examining the role of SFRP2 and Dvl-3; 3) to investigate whether a Wnt-1 signaling is a survival factor, thus inhibits apoptosis, in mesothelioma using an anti-Wnt-1 ligand monoclonal antibody and siRNA; and 4) to develop molecular therapies by targeting the Wnt-1 ligand with monoclonal antibody in vivo. Recent information about the Wnt signaling pathway reveals its vital importance in both embryogenesis and oncogenesis. Our study aims to reveals its role in malignant mesothelioma, and to add significantly to the emerging knowledge about the Wnt pathway in cancer in general.
Tags: Cadherin, Gene Expression, Mesothelioma, Molecular Oncology, Neoplastic Process, Oncoprotein, Protooncogene Dna Methylation, Apoptosis, Monoclonal Antibody, Neoplasm /cancer Genetics, Neoplasm /cancer Immunotherapy, Protein Protein Interaction, Transcription Factor Athymic Mouse, Cell Line, Clinical Research, Human Tissue, Immunocytochemistry, In Situ Hybridization, Neoplasm /cancer Transplantation, Small Interfering Rna, Transfection, Xenotransplantation
Tags: Cadherin, Gene Expression, Mesothelioma, Molecular Oncology, Neoplastic Process, Oncoprotein, Protooncogene Dna Methylation, Apoptosis, Monoclonal Antibody, Neoplasm /cancer Genetics, Neoplasm /cancer Immunotherapy, Protein Protein Interaction, Transcription Factor Athymic Mouse, Cell Line, Clinical Research, Human Tissue, Immunocytochemistry, In Situ Hybridization, Neoplasm /cancer Transplantation, Small Interfering Rna, Transfection, Xenotransplantation
- Followup Grant: 5R01CA093708-02
- Followup Grant: 5R01CA093708-03
- Followup Grant: 5R01CA093708-04
Schenker, Marc B. Environmental Asbestos And Mesothelioma In California
Grant: 1R03CA081615-01
Grant: 1R03CA081615-01
Abstract: This study will examine whether environmental asbestos deposits in California are associated with increased rates of mesothelioma, a rare cancer of the pleura and peritoneum that occurs almost solely as a result of asbestos exposure. The project brings together a multidisciplinary team to address geologic occurrence of asbestos in California, potential human exposure based on population patterns and known occupational exposures, and epidemiologic characteristics of disease in the state. The study will provide the ability to assess age-, race- and sex- adjusted mesothelioma rates in relation to asbestiform type and location as determined by geographic mapping. Previous epidemiological studies of asbestos-induced malignancy have focused primarily on occupation asbestos exposures. Studies in other countries have documented mesotheliomas due to environmental asbestos exposure, but there has been little research on this in the U.S. Information on mesothelioma cases from 1988-96 will be obtained from the California Cancer Registry, which maintains a database of all cancer cases in the state. The analysis will examine the distribution of age-, sex- and race-adjusted county-specific mesothelioma rates to assess whether populations in counties with large concentrations of environmental asbestos have a higher rate of mesothelioma than populations in counties with little or no endogenous asbestos. The location and distribution of amphibole and serpentine asbestos deposits in California will be determined by a review of existing geological surveys and publications, along with case studies of the occurrence of tremolite asbestos. This information will be combined with measures of human interaction with environmental asbestos, such as development, mining, and population density, to determine potential human exposure to environmental asbestos by county. Lastly, this project will plan a case-control study to more rigorously test the hypothesis that mesothelioma in California is independently associated with environmental asbestos exposure. The proposed project will be the first study to test the association of environmental asbestos and adjusted county- specific rates of mesothelioma. It is particularly strengthened by a comprehensive analysis of environmental tremolite and asbestos in California to be conducted by Dr. Howard Day, Department of Geology, UC Davis. This study is particularly important and timely because of the increasing population in the state living in asbestos-containing areas. California represents a unique location for these studies because of the statewide tumor registry, the largest tumor registry in the world.
Tags: Asbestos, Disease /disorder Etiology, Environment Related Neoplasm /cancer, Geographic Site, Mesothelioma, Neoplasm /cancer Epidemiology, Soil Environmental Contamination, Environmental Health, Human Population Density, Human Population Distribution, Human Population Study, Soil Sampling Clinical Research, Human Data
Tags: Asbestos, Disease /disorder Etiology, Environment Related Neoplasm /cancer, Geographic Site, Mesothelioma, Neoplasm /cancer Epidemiology, Soil Environmental Contamination, Environmental Health, Human Population Density, Human Population Distribution, Human Population Study, Soil Sampling Clinical Research, Human Data
- Followup Grant: 5R03CA081615-02
- Followup Grant: 5R03CA081615-03
Broaddus, V Courtney. Amplification Of Trail-induced Apoptosis In Mesothelioma
Grant: 1R01CA095671-01A1
Grant: 1R01CA095671-01A1
Abstract:
DESCRIPTION (provided by applicant): Activation of death receptors offers a possible mechanism of bypassing sites of resistance and engaging the caspase machinery of apoptosis directly Death receptor pathways also cooperate in unknown ways with other signals to amplify apoptosis. For several highly resistant mesothelioma lines, including M28, the TNF-related apoptosis inducing ligand (TRAIL) induces apoptosis, an apoptosis greatly amplified by concurrent treatment either with chemotherapeutic agents, such as etoposide, or with proteasome inhibitors In our proposal, the mechanism(s) by which TRAIL-induced apoptosis can be amplified and the relevance of these findings to in vivo models of mesothelioma will be explored. First, specific pathways by which etoposide amplifies TRAIL-induced apoptosis will be investigated, with particular attention to the role of mitochondria, by blocking mitochondrial pathways with overexpression of Bcl-XL or dominant negative caspase 9, by testing mitochondrial sensitivity to the death receptor signal tBid, and by analysis of mitochondrial BH3-containing proteins. The possible role of the stress activated pathway, JNK/SAPK, will be examined in M28 cells with stable blockade with dominant negative JNK1 and/or JNK2 or with stimulation of JNK by MEKK4 Secondly, the mechanism(s) by which proteasome inhibitors amplify TRAIL-induced apoptosis will be investigated Proteasome inhibitors, unlike chemotherapeutic agents, increase expression of the TRAIL receptor, DR5. This suggests a novel role for the proteasome in the degradation and regulation of expression of a death receptor. The role of the proteasome in DR5 degradation, the specificity for DR5 and the contribution of increased DR5 to the amplified apoptosis will be determined. Finally, the in vitro findings will be tested lot their relevance to in vivo mesothelioma models In nude mice with subcutaneous tumors of M28 cells, systemic TRAIL and either chemotherapy, proteasome inhibitors or both given systemically will be assessed for effects on tumor size, apoptotic index and expression of the DR5 receptor In human mesothelioma tumors from individual patients studied as tumor fragment spheroids, response to TRAIL and/or etoposide, proteasome inhibitors or both will also be determined Understanding the mechanisms of amplification of TRAIL-induced apoptosis can provide insight into the means by which malignant cells evade apoptosis and ways to bypass those sites of resistance and thereby improve treatment strategies
Tags: Apoptosis, Cytokine Receptor, Etoposide, Mesothelioma, Neoplastic Growth, Proteasome, Receptor Expression Bcl2 Gene /protein, Jun Kinase, Antineoplastic, Mitochondria, Neoplasm /cancer Pharmacology, Pharmacokinetics, Protease Inhibitor, Tumor Necrosis Factor Alpha Athymic Mouse, Cell Line, Clinical Research, Human Tissue
Tags: Apoptosis, Cytokine Receptor, Etoposide, Mesothelioma, Neoplastic Growth, Proteasome, Receptor Expression Bcl2 Gene /protein, Jun Kinase, Antineoplastic, Mitochondria, Neoplasm /cancer Pharmacology, Pharmacokinetics, Protease Inhibitor, Tumor Necrosis Factor Alpha Athymic Mouse, Cell Line, Clinical Research, Human Tissue
Broaddus, V Courtney. Amplification Of Trial-indcued Apoptosis In Mesothelioma
Grant: 5R01CA095671-02
Grant: 5R01CA095671-02
Abstract:
DESCRIPTION (provided by applicant): Activation of death receptors offers a possible mechanism of bypassing sites of resistance and engaging the caspase machinery of apoptosis directly Death receptor pathways also cooperate in unknown ways with other signals to amplify apoptosis. For several highly resistant mesothelioma lines, including M28, the TNF-related apoptosis inducing ligand (TRAIL) induces apoptosis, an apoptosis greatly amplified by concurrent treatment either with chemotherapeutic agents, such as etoposide, or with proteasome inhibitors In our proposal, the mechanism(s) by which TRAIL-induced apoptosis can be amplified and the relevance of these findings to in vivo models of mesothelioma will be explored. First, specific pathways by which etoposide amplifies TRAIL-induced apoptosis will be investigated, with particular attention to the role of mitochondria, by blocking mitochondrial pathways with overexpression of Bcl-XL or dominant negative caspase 9, by testing mitochondrial sensitivity to the death receptor signal tBid, and by analysis of mitochondrial BH3-containing proteins. The possible role of the stress activated pathway, JNK/SAPK, will be examined in M28 cells with stable blockade with dominant negative JNK1 and/or JNK2 or with stimulation of JNK by MEKK4 Secondly, the mechanism(s) by which proteasome inhibitors amplify TRAIL-induced apoptosis will be investigated Proteasome inhibitors, unlike chemotherapeutic agents, increase expression of the TRAIL receptor, DR5. This suggests a novel role for the proteasome in the degradation and regulation of expression of a death receptor. The role of the proteasome in DR5 degradation, the specificity for DR5 and the contribution of increased DR5 to the amplified apoptosis will be determined. Finally, the in vitro findings will be tested lot their relevance to in vivo mesothelioma models In nude mice with subcutaneous tumors of M28 cells, systemic TRAIL and either chemotherapy, proteasome inhibitors or both given systemically will be assessed for effects on tumor size, apoptotic index and expression of the DR5 receptor In human mesothelioma tumors from individual patients studied as tumor fragment spheroids, response to TRAIL and/or etoposide, proteasome inhibitors or both will also be determined Understanding the mechanisms of amplification of TRAIL-induced apoptosis can provide insight into the means by which malignant cells evade apoptosis and ways to bypass those sites of resistance and thereby improve treatment strategies
Tags: Apoptosis, Cytokine Receptor, Etoposide, Mesothelioma, Neoplastic Growth, Proteasome, Receptor Expression Bcl2 Gene /protein, Jun Kinase, Antineoplastic, Mitochondria, Neoplasm /cancer Pharmacology, Pharmacokinetics, Protease Inhibitor, Tumor Necrosis Factor Alpha Athymic Mouse, Cell Line, Clinical Research, Human Tissue
Tags: Apoptosis, Cytokine Receptor, Etoposide, Mesothelioma, Neoplastic Growth, Proteasome, Receptor Expression Bcl2 Gene /protein, Jun Kinase, Antineoplastic, Mitochondria, Neoplasm /cancer Pharmacology, Pharmacokinetics, Protease Inhibitor, Tumor Necrosis Factor Alpha Athymic Mouse, Cell Line, Clinical Research, Human Tissue
- Followup Grant: 5R01CA095671-03
- Followup Grant: 5R01CA095671-04
Broaddus, V Courtney. Protective Role Of Apoptosis In Asbestos Pleural Injury
Grant: 1R01ES008985-01
Grant: 1R01ES008985-01
Abstract: DESCRIPTION: Pleural mesothelial cells, the progenitor of the
asbestos-induced tumor mesothelioma, undergo apoptosis when exposed to
asbestos. Important mechanisms may include oxygen radical generation, DNA
damage and fiber internalization. Because an inability to undergo apoptosis
may allow cells with DNA damage to survive, a loss of apoptosis may be a
major step in the multistep process leading to neoplasia. Therefore,
mechanisms promoting or inhibiting apoptosis may play a dynamic process
determining whether the toxic effects of asbestos eventually result in
neoplasia. We propose to investigate the role of apoptosis in the pathology
of asbestos to the mesothelial cells and pleura. Initially, Dr. Broaddus
aims to delineate the major mechanisms inducing asbestos-induced apoptosis
in both rabbit and human pleural mesothelial cells and rabbit pleura. By
measures of DNA damage, oxidant stress and stress-related signaling
(ceramide, jun kinase, MAP kinase) in vitro and in vivo, she propose to show
the pathways essential to mesothelial apoptosis. Then, she will determine
the mechanisms by which certain signals, namely those initiated by
vitronectin receptors, inhibit asbestos-induced apoptosis. Using
vitronectin-coated particles or anti-integrin antibodies to activate the
integrins, she will confirm the role of vitronectin receptors as
anti-apoptotic, and identify whether the integrins are altering the balance
of the apoptotic pathways such as ceramide and JNK with proliferative
pathways such as MAP kinase. In in vivo studies in rabbits after activation
or inhibition of vitronectin receptors or in genetically-engineered mice
without vitronectin or vitronectin receptors, she will learn the importance
of this anti-apoptotic effect in vivo. Finally, she intends to use
inhibitors of asbestos-induced apoptosis (anti-oxidant B-carotene,
inhibition of PARP, vitronectin-coated beads) to determine whether longterm
inhibition of apoptosis will lead to accumulation of DNA damage in
asbestos-exposed mesothelial cells. We will assess chronically
asbestos-exposed cells for the presence of DNA structural damage by the
presence of micronuclei and for changes in gene copy number using
comparative genomic hybridization. From these studies, Dr. Broaddus will
proceed to long term studies in genetically-engineered mice without
vitronectin, the B5 subunit of a major vitronectin receptor, or p53 to
confirm that this inhibition of apoptosis leads to an increased sensitivity
to asbestos-induced abnormalities, including mesothelioma. These studies
should provide important information about the mechanisms by which asbestos
induces apoptosis in mesothelial cells and the role of asbestos-induced
apoptosis in asbestos-induced pathology.
Tags: Asbestos, Biological Signal Transduction, Cell Growth Regulation, Mesothelioma, Pleural Cavity, Programmed Cell Death, Vitronectin Dna Damage, Antioxidant, Ceramide, Chemical Carcinogenesis, Free Radical Oxygen, Mitogen Activated Protein Kinase, Oxidative Stress, Receptor Expression Comparative Genomic Hybridization, Human Tissue, Laboratory Mouse, Laboratory Rabbit, Tissue /cell Culture, Transgenic Animal, Western Blotting
Tags: Asbestos, Biological Signal Transduction, Cell Growth Regulation, Mesothelioma, Pleural Cavity, Programmed Cell Death, Vitronectin Dna Damage, Antioxidant, Ceramide, Chemical Carcinogenesis, Free Radical Oxygen, Mitogen Activated Protein Kinase, Oxidative Stress, Receptor Expression Comparative Genomic Hybridization, Human Tissue, Laboratory Mouse, Laboratory Rabbit, Tissue /cell Culture, Transgenic Animal, Western Blotting
- Followup Grant: 5R01ES008985-02
- Followup Grant: 5R01ES008985-03
- Followup Grant: 5R01ES008985-04
- Followup Grant: 3R01ES008985-04S1
- Followup Grant: 5R01ES008985-05
Markman, Maurice Intracavitary Cisplatin With Thiosulfate For Malignant Mesothelioma
Grant: 5M01RR000827-100237
Grant: 5M01RR000827-100237
Abstract: There is no text on file for this abstract.
Tags: Drugs, Pharmacology, Bioavailability, Metals, Heavy Metals, Platinum (compounds), Cis Platinum Compounds, Neoplasms Of Body Cavities, Mesothelioma, Neoplastic Therapy, Cancer Chemotherapy, Sulfates, Thiosulfates Drugs Screening Human, Clinical
Tags: Drugs, Pharmacology, Bioavailability, Metals, Heavy Metals, Platinum (compounds), Cis Platinum Compounds, Neoplasms Of Body Cavities, Mesothelioma, Neoplastic Therapy, Cancer Chemotherapy, Sulfates, Thiosulfates Drugs Screening Human, Clinical
- Followup Grant: 2M01RR000827-110237
Balmes, John R. Caret--the Carotene And Retinol Efficacy Trial
Grant: 2U01CA047989-06
Grant: 2U01CA047989-06
Abstract: This chemoprevention trial tests the efficacy of retinol and beta-
carotene in preventing lung cancer in two related high-risk
populations: (a) heavy smokers recruited from insurance-based
sources, and (b) current and former workers with heavy occupational
asbestos exposure recruited from workers' compensation and
employment-based sources. The double-blind two-arm randomized
protocol compares placebos with a daily combination of 30 mg beta-
carotene plus 25,000 IU retinol. We will recruit eligible
asbestos-exposed subjects from the San Francisco/Oakland area. We
will participate in implementing a cost-effective, well-integrated,
multi-clinic strategy, with the Seattle-based coordinating center
for project management and data analysis. During the first 3 years
of the new grant period (1988-91) we will recruit and enroll 800
subjects randomized according to the multi center protocol. We
will provide all necessary data to evaluate accrual, coordination,
and costs in geographically-dispersed clinic sites to generate best
estimates of the remaining needs for the full-scale enrollment and
follow-up. Current assumptions and projections indicate that the
full-scale Efficacy Trial will be capable of detecting significant
reductions in lung cancer incidence in the high-risk groups
combined, and in either subgroup alone, with 13,000 smokers and
4000 asbestos-exposed subjects.
Tags: All Trans Retinol, Asbestos, Cancer Risk, Carotene, Chemoprevention, Lung Neoplasm, Nutrition Aspect Of Cancer, Tobacco Abuse Chemical Carcinogenesis, Clinical Trial, Combination Chemotherapy, Cooperative Study, Environment Related Neoplasm /cancer, Health Care Cost /financing, Longitudinal Human Study, Mesothelioma, Occupational Hazard, Prognosis, Work Site Computer Data Analysis, Dosage, Human Middle Age (45-64), Human Subject, Nutrition Related Tag, Spirometry
Tags: All Trans Retinol, Asbestos, Cancer Risk, Carotene, Chemoprevention, Lung Neoplasm, Nutrition Aspect Of Cancer, Tobacco Abuse Chemical Carcinogenesis, Clinical Trial, Combination Chemotherapy, Cooperative Study, Environment Related Neoplasm /cancer, Health Care Cost /financing, Longitudinal Human Study, Mesothelioma, Occupational Hazard, Prognosis, Work Site Computer Data Analysis, Dosage, Human Middle Age (45-64), Human Subject, Nutrition Related Tag, Spirometry
- Followup Grant: 5U01CA047989-07
- Followup Grant: 2U01CA052596-05
Lipsett, James A. Southeastern Cancer Study Group Cooperative Trials
Grant: 5U10CA030247-02
Grant: 5U10CA030247-02
Abstract: The city of Hope will participate in the Southeastern Cancer Study Group
(SEG) clinical investigation trials. Dr. Presant will provide leadership
for the Melanoma-Sarcoma Committee which he chairs. SEG members at City of
Hope will provide input into pilot protocol development, group-wide phase
II and phase III protocol development, pharmacology trials, nursing
protocols, data management committee acitivities. In addition, SEG members
will participate heavily in the areas of chemotherapy, and moderately in
the areas of surgery, immunotherapy, radiation therapy, and pathology. By
participation of City of Hope in SEG activities, the quality of SEG
protocols will be improved, and the rate to completion of better quality
protocols will be increased. Research results will be communicated to the
scientific community by presentations at national meetings and publication
of ideas in peer-reviewed journals.
Tags: Cancer Clinical Investigation Review Committee, Neoplasms Immunization (immunotherapy), Neoplasms Surgery, Neoplastic Therapy, Cancer Chemotherapy, Neoplastic Therapy, Cancer Radiotherapy Neoplasms Of Body Cavities, Mesothelioma, Neoplasms, Sarcoma, Pigment Cell Neoplasms, Melanoma, Therapy Evaluation, Cooperative Study Human, Clinical
Tags: Cancer Clinical Investigation Review Committee, Neoplasms Immunization (immunotherapy), Neoplasms Surgery, Neoplastic Therapy, Cancer Chemotherapy, Neoplastic Therapy, Cancer Radiotherapy Neoplasms Of Body Cavities, Mesothelioma, Neoplasms, Sarcoma, Pigment Cell Neoplasms, Melanoma, Therapy Evaluation, Cooperative Study Human, Clinical
Sikic, Branimir I. Gene Expression Profiling Of Unknown Primary Cancers
Grant: 1R33CA089830-01
Grant: 1R33CA089830-01
Abstract:
DESCRIPTION: (Applicant's Description)
Cancers of unknown primary site are a diagnostic and therapeutic dilemma in
oncology. Information from DNA micro array technologies on the gene expression
profile of cancers has led to the hypothesis that there are diagnostic sets of
genes which can resolve the origin of unknown primary cancers (UPC) with a
high degree of confidence. The purpose of this project is to test this
hypothesis, by both retrospective and prospective analysis of cases of UPC
from Stanford Medical Center and the Sarah Cannon Cancer Center, in the
context of a rapidly evolving database of site-specific clusters of gene
expression. Specific Aims are: (1) Definition of the gene expression profile
of known human cancers. We now have extensive information on the profiles of
lymphomas, leukemia, and carcinomas of the breast, prostate, lung, ovary, and
liver. Additional tumors to be accrued from our tumor bank and ongoing sample
acquisitions include sarcomas, germ cell cancers, melanomas, mesotheliomas,
and carcinomas of the colon, stomach, pancreas, bladder, and kidney. (2)
Determination of the diagnostic cluster of gene expression for each of the
above tumor types. We anticipate that several hundred genes may differentiate
one from the others of these known tumors. (3) Acquisition, gene expression
profiling, and diagnostic classification of unknown primary cancer specimens.
This aim will involve a close collaboration with the world's leading center
for the clinical evaluation of unknown primary cancers, the Sarah Cannon
Cancer Center in Nashville. (4) Evaluation of a panel of histospecific
antisera for diagnostic utility with UPC specimens. This aim will utilize
retrospective archived specimens as well as prospectively acquired samples
from this project. (5) Identification of specific or clustered gene expression
associated with known prognostic factors, response to therapies, and survival
of patients with UPC.
Tags: Diagnosis Design /evaluation, Gene Expression, Neoplasm /cancer, Neoplasm /cancer Diagnosis, Neoplasm /cancer Genetics Antitumor Antibody, Bladder Neoplasm, Colon Neoplasm, Germ Cell Neoplasm, Kidney Neoplasm, Melanoma, Mesothelioma, Neoplasm /cancer Classification /staging, Neoplasm /cancer Immunology, Pancreas Neoplasm, Prognosis, Sarcoma, Stomach Neoplasm Clinical Research, Human Genetic Material Tag, Human Subject, Microarray Technology
Tags: Diagnosis Design /evaluation, Gene Expression, Neoplasm /cancer, Neoplasm /cancer Diagnosis, Neoplasm /cancer Genetics Antitumor Antibody, Bladder Neoplasm, Colon Neoplasm, Germ Cell Neoplasm, Kidney Neoplasm, Melanoma, Mesothelioma, Neoplasm /cancer Classification /staging, Neoplasm /cancer Immunology, Pancreas Neoplasm, Prognosis, Sarcoma, Stomach Neoplasm Clinical Research, Human Genetic Material Tag, Human Subject, Microarray Technology
- Followup Grant: 5R33CA089830-02
- Followup Grant: 5R33CA089830-03
Valanis, Barbara G. Caret--study Center
Grant: 2U01CA048203-06
Grant: 2U01CA048203-06
Abstract: CARET is an ongoing double-blind lung cancer chemoprevention trial of the
efficacy and safety of the combination of 30 mg beta-carotene and 25,000
IU retinyl palmitate daily in two high-risk populations: (a) male and
female current and former smokers recruited primarily from insurance-based
sources, and (b) males with extensive occupational asbestos exposure
recruited primarily from employment-based sources. We have documented
successful recruitment, excellent compliance, and minimal side effects in
over 15,000 participants randomized thus far at six study centers. Through
30 April, 1993, CARET has randomized 4,000 asbestos-exposed workers,
exceeding accrual goals at all five CARET asbestos centers, and 11,105
heavy smokers. Seattle and Portland have exceeded their heavy smoker
goals, and Irvine is on track to achieve its goal in July 1994. During the
final five-year period, CARET will focus on retention, adherence to
protocol, ascertainment of endpoints, monitoring of key design parameters,
closeout of the trial, and analysis and publication. Projections indicate
that with 14,240 smokers and 4,010 asbestos-exposed participants and
114,100 person-years of follow-up through February 1998, CARET will be
capable of detecting a 23% reduction in lung cancer incidence in the two
high-risk populations combined, and 27%, 49%, 32%, and 35% reductions in
the smokers, female smokers, male smokers, and asbestos-exposed subgroups,
respectively.
The Portland Study Center will conduct follow-up activities with 4,200
participants randomized into the heavy smoker cohort, 280 participants
randomized into the asbestos-exposed worker cohort, and 32 Vanguard
transfer participants. High adherence and retention and complete
ascertainment of endpoints and other data will be primary goals. Clinical,
data management, and follow-up activities include annual and semiannual
clinic visits; routine telephone interviews; symptom, adherence, ancillary
variables, and study endpoint documentation and reporting; quality
assurance of data collection; and other tasks according to the established
CARET protocol and procedures. The investigators will collaborate with the
Coordinating Center and other Study Centers on the analyses and
publication of data.
Tags: Asbestos, Cancer Prevention, Carotene, Chemoprevention, Drug Screening /evaluation, Human Therapy Evaluation, Lung Neoplasm, Nutrition Aspect Of Cancer, Tobacco Abuse Cancer Risk, Carcinogenesis Inhibitor, Chemical Carcinogen, Clinical Trial, Cooperative Study, Female, Interview, Longitudinal Human Study, Male, Mesothelioma, Occupational Hazard, Sex Difference, Therapy Compliance Human Subject, Nutrition Related Tag, Spirometry
Tags: Asbestos, Cancer Prevention, Carotene, Chemoprevention, Drug Screening /evaluation, Human Therapy Evaluation, Lung Neoplasm, Nutrition Aspect Of Cancer, Tobacco Abuse Cancer Risk, Carcinogenesis Inhibitor, Chemical Carcinogen, Clinical Trial, Cooperative Study, Female, Interview, Longitudinal Human Study, Male, Mesothelioma, Occupational Hazard, Sex Difference, Therapy Compliance Human Subject, Nutrition Related Tag, Spirometry
- Followup Grant: 5U01CA048203-07
Clinical Trials
Condition: Malignant Mesothelioma
Intervention: Drug: belinostat; Genetic: reverse transcriptase-polymerase chain reaction; Other: laboratory biomarker analysis
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Intervention: Drug: belinostat; Genetic: reverse transcriptase-polymerase chain reaction; Other: laboratory biomarker analysis
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Condition: Malignant Mesothelioma
Intervention: Drug: cediranib maleate; Other: laboratory biomarker analysis
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Intervention: Drug: cediranib maleate; Other: laboratory biomarker analysis
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Condition: Mesothelioma
Intervention: Drug: VEGF-Antisense Oligonucleotide , Pemetrexed, Cisplatin
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Intervention: Drug: VEGF-Antisense Oligonucleotide , Pemetrexed, Cisplatin
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Condition: Malignant Mesothelioma
Intervention: Drug: cisplatin; Drug: gemcitabine hydrochloride
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Intervention: Drug: cisplatin; Drug: gemcitabine hydrochloride
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Condition: Malignant Mesothelioma
Intervention: Biological: bevacizumab; Drug: cisplatin; Drug: gemcitabine hydrochloride
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Intervention: Biological: bevacizumab; Drug: cisplatin; Drug: gemcitabine hydrochloride
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Condition: Malignant Pleural Mesothelioma
Intervention: Drug: MORAb-009 by IV on Days 1 and 8 every 21 days for 6 cycles.
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Intervention: Drug: MORAb-009 by IV on Days 1 and 8 every 21 days for 6 cycles.
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Active, not recruiting Dasatinib in Treating Patients With Previously Treated Malignant Mesothelioma
Condition: Malignant Mesothelioma
Intervention: Drug: dasatinib; Other: immunoenzyme technique; Other: immunohistochemistry staining method; Other: laboratory biomarker analysis
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Intervention: Drug: dasatinib; Other: immunoenzyme technique; Other: immunohistochemistry staining method; Other: laboratory biomarker analysis
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Condition: Lung Cancer; Malignant Mesothelioma; Pancreatic Cancer; Sarcoma
Intervention: Drug: L-alanosine
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Intervention: Drug: L-alanosine
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Condition: Malignant Pleural Mesothelioma; MPM; Solid Tumors
Intervention: Drug: pemetrexed, cisplatin and CBP501; Drug: pemetrexed and cisplatin
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Intervention: Drug: pemetrexed, cisplatin and CBP501; Drug: pemetrexed and cisplatin
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Condition: Breast Cancer; Endometrial Cancer; Malignant Mesothelioma
Intervention: Drug: megestrol acetate
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Intervention: Drug: megestrol acetate
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Condition: Lung Cancer; Mesothelioma; Malignant Airway Obstruction
Intervention: Device: CryoSpray Ablation (TM) System
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Intervention: Device: CryoSpray Ablation (TM) System
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Condition: Breast Cancer; Colorectal Cancer; Kidney Cancer; Lung Cancer; Malignant Mesothelioma; Pancreatic Cancer
Intervention: Biological: allogeneic tumor cell vaccine; Biological: autologous tumor cell vaccine; Biological: recombinant interferon alfa; Biological: recombinant interferon gamma; Biological: sargramostim; Drug: cyclophosphamide
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Intervention: Biological: allogeneic tumor cell vaccine; Biological: autologous tumor cell vaccine; Biological: recombinant interferon alfa; Biological: recombinant interferon gamma; Biological: sargramostim; Drug: cyclophosphamide
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Condition: Lung Cancer; Malignant Mesothelioma; Metastatic Cancer; Thymoma and Thymic Carcinoma
Intervention: Procedure: radiofrequency ablation
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Intervention: Procedure: radiofrequency ablation
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