Study of Nivolumab Combined With Ipilimumab Versus Pemetrexed and Cisplatin or Carboplatin as First Line Therapy in Unresectable Pleural Mesothelioma Patients
- Conditions
- Mesothelioma
- Interventions
- Registration Number
- NCT02899299
- Lead Sponsor
- Bristol-Myers Squibb
- Brief Summary
The purpose of this study is to test the effectiveness and tolerability of the combination of Nivolumab and Ipilimumab compared to Pemetrexed and Cisplatin or Carboplatin in patients with unresectable pleural mesothelioma.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 605
- Males and Females at least 18 years of age
- Histologically confirmed pleural malignant mesothelioma not eligible for curative surgery
- ECOG Performance status of 0 or 1
- Available tumor sample for testing
- Acceptable blood work
- Primitive peritoneal, pericardial and tunica vaginalis testis mesotheliomas
- Prior chemotherapy for pleural mesothelioma
- Prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2 oranti-CTLA-4 antibody
- History of other malignancy unless the subject has been disease-free for at least 3 years
- Active, untreated central nervous system (CNS) metastasis
Other protocol defined inclusion/exclusion criteria could apply
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Nivolumab and Ipilimumab Nivolumab Specified dose on specified days Nivolumab and Ipilimumab Ipilimumab Specified dose on specified days Pemetrexed and Cisplatin (or Carboplatin) Pemetrexed Specified dose on specified days Pemetrexed and Cisplatin (or Carboplatin) Cisplatin Specified dose on specified days Pemetrexed and Cisplatin (or Carboplatin) Carboplatin Specified dose on specified days
- Primary Outcome Measures
Name Time Method Overall Survival (OS) From randomization to the date of death (Up to 40 Months) Overall Survival was defined as the time from randomization to the date of death due to any cause. A participant who has not died was censored at last known date alive.
- Secondary Outcome Measures
Name Time Method Objective Response Rate (ORR) According to PD-L1 Expression Level From randomization date to the date of objectively documented progression or the date of subsequent anti-cancer therapy, whichever occurs first (Up to 76 months) PD-L1 Expression is defined as the percent of tumor cells membrane staining in a minimum of 100 evaluable tumor cells per validated Dako PD-L1 immunohistochemistry (IHC) assay. This is referred to as quantifiable PD-L1 expression and efficacy is determined by objective response rate (ORR) analysis. ORR is defined as the percentage of participants who achieve a best overall response of complete response (CR) or partial response (PR) per Blinded Independent Central Review (BICR) assessments. Per adapted m-RECIST for pleural mesothelioma, each single tumor measurement must be at least 10 mm in length to qualify as measureable disease and contribute to the sum that defines the pleural uni-variate measure.
per RECIST 1.1 for solid tumors, confirmation of response required: CR=Disappearance of all target lesions; PR=At least a 30% decrease in the sum of the Total Tumor Measurement; Progressive disease (PD)=At least a 20% increase in the sum of the Total Tumor Measurement.Disease Control Rate (DCR) From randomization date to the date of objectively documented progression or the date of subsequent anti-cancer therapy, whichever occurs first (Up to 76 months Disease Control Rate is defined as the percentage of all randomized participants whose Best Overall Response was complete response (CR), partial response (PR), stable disease (SD) or Non-CR/Non-PD as assessed by Blinded Independent Central Review (BICR). Per adapted m-RECIST for pleural mesothelioma, each single tumor measurement must be at least 10 mm in length to qualify as measureable disease and contribute to the sum that defines the pleural uni-variate measure. Per RECIST 1.1 for solid tumors, confirmation of response required:
CR=Disappearance of all target lesions; PR=At least a 30% decrease in the sum of the Total Tumor Measurement; Progressive disease (PD)=At least a 20% increase in the sum of the Total Tumor Measurement; SD=Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD; Non-CR/Non-PD: Persistence of one or more non-target lesion(s).Progression Free Survival (PFS) From randomization date to the date of first documented tumor progression or death due to any cause, whichever occurs first. (up to 76 months) Progression Free Survival is defined as the time between the date of randomization and the date of first documented tumor progression per Blinded Independent Central Review (BICR) assessments (using adapted m-RECIST and RECIST 1.1), or death due to any cause, whichever occurs first. Participants who received subsequent anticancer therapy prior to documented progression were censored at the date of the last evaluable tumor assessment conducted on or prior to the date of initiation of the subsequent anticancer therapy.
Progressive disease (PD)=At least a 20% increase in the sum of the Total Tumor Measurement.Overall Survival (OS) According to PD-L1 Expression Level From randomization date to the date of death (Up to 76 Months) PD-L1 Expression is defined as the percent of tumor cells membrane staining in a minimum of 100 evaluable tumor cells per validated Dako PD-L1 immunohistochemistry (IHC) assay. This is referred to as quantifiable PD-L1 expression and efficacy is determined by overall survival (OS) analysis. OS was defined as the time from randomization to the date of death due to any cause. A participant who has not died was censored at last known date alive.
Progression Free Survival (PFS) According to PD-L1 Expression Level From randomization date to the date of first documented tumor progression or death due to any cause, whichever occurs first. (up to 76 months) PD-L1 Expression is defined as the percent of tumor cells membrane staining in a minimum of 100 evaluable tumor cells per validated Dako PD-L1 immunohistochemistry (IHC) assay. This is referred to as quantifiable PD-L1 expression and efficacy is determined by progression free survival (PFS) analysis. PFS is defined as the time between the date of randomization and the date of first documented tumor progression per Blinded Independent Central Review (BICR) assessments (using adapted m-RECIST and RECIST 1.1), or death due to any cause, whichever occurs first. Participants who received subsequent anticancer therapy prior to documented progression were censored at the date of the last evaluable tumor assessment conducted on or prior to the date of initiation of the subsequent anticancer therapy.
Progressive disease (PD)=At least a 20% increase in the sum of the Total Tumor Measurement.Objective Response Rate (ORR) From randomization date to the date of objectively documented progression or the date of subsequent anti-cancer therapy, whichever occurs first (Up to 76 months) Objective Response Rate is defined as the percentage of randomized participants who achieve a best overall response of complete response (CR) or partial response (PR) per Blinded Independent Central Review (BICR) assessments. Per adapted m-RECIST for pleural mesothelioma, each single tumor measurement must be at least 10 mm in length to qualify as measureable disease and contribute to the sum that defines the pleural uni-variate measure. Per RECIST 1.1 for solid tumors, confirmation of response required:
CR=Disappearance of all target lesions; PR=At least a 30% decrease in the sum of the Total Tumor Measurement; Progressive disease (PD)=At least a 20% increase in the sum of the Total Tumor Measurement.
Trial Locations
- Locations (107)
Local Institution - 0014
🇺🇸New Haven, Connecticut, United States
Local Institution - 0013
🇺🇸Detroit, Michigan, United States
Local Institution - 0004
🇺🇸Rochester, Minnesota, United States
Local Institution - 0079
🇲🇽Df, Distrito Federal, Mexico
Local Institution - 0034
🇦🇺Nedlands, Western Australia, Australia
Local Institution - 0084
🇬🇧Edinburgh, Midlothian, United Kingdom
Local Institution - 0081
🇬🇧Leicester, United Kingdom
Local Institution - 0083
🇬🇧London, United Kingdom
Local Institution - 0090
🇬🇧Southampton, United Kingdom
Local Institution - 0007
🇺🇸Cleveland, Ohio, United States
Local Institution - 0086
🇧🇪Edegem, Belgium
Local Institution - 0088
🇧🇪Sint-Niklaas, Belgium
Local Institution - 0133
🇨🇳Harbin Shi, Heilongjiang, China
Local Institution - 0005
🇺🇸Houston, Texas, United States
Local Institution - 0057
🇫🇷Caen, France
Local Institution - 0073
🇫🇷Creteil, France
Local Institution - 0074
🇫🇷La Tronche, France
Local Institution - 0030
🇦🇺Malvern, Victoria, Australia
Local Institution - 0089
🇧🇪Brussels, Belgium
Local Institution - 0039
🇨🇴Bogota, Colombia
Local Institution - 0124
🇨🇳Kunming, China
Local Institution - 0018
🇨🇱Santiago, Metropolitana, Chile
Local Institution - 0056
🇫🇷Paris, France
Local Institution - 0120
🇨🇳Shanghai, China
Local Institution - 0064
🇧🇷Sao Paulo, Brazil
Local Institution - 0069
🇫🇷Marseille Cedex 20, France
Local Institution - 0054
🇩🇪Coswig, Germany
Local Institution - 0040
🇨🇴Bogota, Colombia
Local Institution - 0093
🇫🇷Strasbourg Cedex, France
Local Institution - 0068
🇫🇷Toulouse Cedex 9, France
Local Institution - 0026
🇩🇪Cologne, Germany
Local Institution - 0023
🇩🇪Gottingen, Germany
Local Institution - 0038
🇩🇪Essen, Germany
Local Institution - 0024
🇩🇪Grosshansdorf, Germany
Local Institution - 0019
🇩🇪Moers, Germany
Local Institution - 0021
🇩🇪Homburg an d. Saar, Germany
Local Institution - 0042
🇮🇹Ravenna, Emilia-Romagna, Italy
Local Institution - 0045
🇮🇹Genova, Italy
Local Institution - 0043
🇮🇹Napoli, Italy
Local Institution - 0097
🇯🇵Chiba-shi, Chiba, Japan
Local Institution - 0048
🇮🇹Rozzano, Italy
Local Institution - 0041
🇮🇹Siena, Italy
Local Institution - 0108
🇯🇵Fukuyama-shi, Hiroshima, Japan
Local Institution - 0114
🇯🇵Hiroshima-Shi, Hiroshima, Japan
Local Institution - 0100
🇯🇵Okayama-shi, Okayama, Japan
Local Institution - 0096
🇯🇵Kitaadachi-gun, Saitama, Japan
Local Institution - 0118
🇲🇽Chihuahua, Mexico
Local Institution - 0092
🇳🇱Amsterdam, Netherlands
Local Institution - 0091
🇳🇱Rotterdam, Netherlands
Local Institution - 0076
🇵🇱Krakow, Poland
Local Institution - 0077
🇵🇱Warszawa, Poland
Local Institution - 0060
🇿🇦Pretoria, Gauteng, South Africa
Local Institution - 0059
🇿🇦Cape Town, Western Cape, South Africa
Local Institution - 0111
🇹🇷Diyarbakır, Turkey
Local Institution - 0029
🇨ðŸ‡Zurich, Switzerland
Local Institution - 0049
🇨ðŸ‡Bern, Switzerland
Local Institution - 0036
🇨ðŸ‡Lausanne, Switzerland
Local Institution - 0112
🇹🇷Istanbul, Turkey
Local Institution - 0116
🇬🇧Manchester, United Kingdom
Local Institution - 0085
🇬🇧Truro, Cornwall, United Kingdom
Local Institution - 0027
🇩🇪Hamburg, Germany
Univ Of Maryland Greenbaum Cancer Center
🇺🇸Baltimore, Maryland, United States
Local Institution - 0002
🇺🇸Chicago, Illinois, United States
Memorial Sloan Kettering Nassau
🇺🇸New York, New York, United States
West Virginia University
🇺🇸Morgantown, West Virginia, United States
Local Institution - 0032
🇦🇺Sydney, New South Wales, Australia
Local Institution - 0031
🇦🇺Birtinya, Queensland, Australia
Local Institution - 0033
🇦🇺Clayton, Victoria, Australia
Local Institution - 0087
🇧🇪Liège, Belgium
Local Institution
🇨🇳Shenyang, Liaoning, China
Local Institution - 0067
🇫🇷Lille Cedex, France
Local Institution - 0080
🇫🇷Saint Herblain, France
Local Institution - 0058
🇫🇷Toulon Cedex, France
Local Institution - 0022
🇩🇪Immenhausen, Germany
Local Institution - 0017
🇬🇷Athens, Greece
Local Institution - 0016
🇬🇷Thessaloniki, Greece
Local Institution - 0044
🇮🇹Bari, Italy
Local Institution - 0046
🇮🇹Catania, Italy
Local Institution - 0105
🇯🇵Nagoya-shi, Aichi, Japan
Local Institution - 0047
🇮🇹Aviano, Italy
Local Institution - 0101
🇯🇵Sapporo-shi, Hokkaido, Japan
Local Institution - 0106
🇯🇵Amagasaki-shi, Hyogo, Japan
Local Institution - 0098
🇯🇵Nishinomiya-shi, Hyogo, Japan
Local Institution - 0104
🇯🇵Natori-shi, Miyagi, Japan
Local Institution - 0095
🇯🇵Yokohama-shi, Kanagawa, Japan
Local Institution - 0094
🇯🇵Chuo-ku, Tokyo, Japan
Local Institution - 0107
🇯🇵Niigata-shi, Niigata, Japan
Local Institution - 0099
🇯🇵Ube-shi, Yamaguchi, Japan
Local Institution - 0113
🇯🇵Osakasayama-city, Japan
Local Institution - 0050
🇲🇽Mexico, Distrito Federal, Mexico
Local Institution - 0078
🇵🇱Bytom, Poland
Local Institution - 0115
🇷🇴Bucharest, Romania
Local Institution - 0109
🇷🇴Bucuresti, Romania
Local Institution - 0055
🇷🇴Romania, Romania
Local Institution - 0150
🇷🇺Moscow, Russian Federation
Local Institution - 0071
🇷🇺Moscow, Russian Federation
Local Institution - 0072
🇷🇺Saint Petersburg, Russian Federation
Local Institution - 0102
🇷🇴Craiova, Romania
Local Institution - 0110
🇹🇷Seyhan, Turkey
Allegheny Cancer Center
🇺🇸Pittsburgh, Pennsylvania, United States
Local Institution - 0037
🇩🇪Heidelberg, Germany
University Of Pennsylvania
🇺🇸Philadelphia, Pennsylvania, United States
Local Institution - 0051
🇲🇽Guadalajara, Jalisco, Mexico
Local Institution - 0053
🇲🇽Mexico, Distrito Federal, Mexico
Ucsf
🇺🇸San Francisco, California, United States
H. Lee Moffitt Cancer Center & Research Inst, Inc
🇺🇸Tampa, Florida, United States
Cancer & Hematology Centers Of Western Michigan
🇺🇸Grand Rapids, Michigan, United States