TALAZOPARIB for Malignant pleural mesothelioma | Malignant peritoneal mesothelioma

Inclusion criteria

• {"criterion_text":"- Patients older than 18 years old"}
• {"criterion_text":"- Patients with Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2"}
• {"criterion_text":"- Histologically - or cytologically- confirmed malignant mesotheliomas: epithelioid, sarcomatoid, biphasic -\tDeveloped from pleura (cohort A) or from peritoneum (cohorts B1 and B2) -\tPreviously treated with systemic platinum based-chemotherapy (including minimum one cycle of pemetrexed) for minimum 4 cycles, with no sign of disease progression during chemotherapy"}
• {"criterion_text":"- No previous treatment with bevacizumab and PARP inhibitor"}
• {"criterion_text":"- Minimum 6 weeks and maximum 8 weeks interval between last chemotherapy cycle and talazoparib start OR minimum 6 and maximum 8 weeks after cytoreductive surgery performed after neo-adjuvant treatment (including the necessary number of cycles of platinum-pemetrexed for inclusion) in the absence of adjuvant chemotherapy. -\tFor pleural mesotheliomas (cohort A), primary or interval debulking surgery with or without hyperthermic intrapleural or intrathoracic chemotherapy (HITHOC) will be authorized, in the case of non-complete cytoreductive surgery only -\tFor peritoneal mesotheliomas * In cohort B1, primary or interval debulking surgery ± hyperthermic intraperitoneal chemotherapy (HIPEC) will be authorized in the case of non-complete cytoreductive surgery (CC2 or CC3) only. This cohort will also include patients with non-operated diseases. Intraperitoneal treatments with pressurized intraperitoneal aerosol chemotherapy sessions (PIPAC) are allowed only with systemic chemotherapy for this cohort. * In cohort B2, complete macroscopic (CC0 or CC1) primary or interval debulking surgery ± HIPEC will be required. Intraperitoneal treatments with pressurized intraperitoneal aerosol chemotherapy sessions (PIPAC) are allowed in neoadjuvant chemotherapy treatment prior to surgery. **In all cohorts, HITHOC, HIPEC and PIPAC are NOT considered as systemic platinum-based chemotherapy"}
• {"criterion_text":"- Measurable or non-measurable (but radiologically evaluable) disease as per modified RECIST version 1.1 on computed tomography (CT) scan (within 28 days prior to talazoparib initiation), or for cohort B2, authorization of absence of radiological lesion"}
• {"criterion_text":"- Availability at the study site of a representative Formalin-Fixed Paraffin-Embedded (FFPE) tumor sample in a block if possible or at least 30 unstained slides from biopsy or surgery specimen, aged less than 18 months."}
• {"criterion_text":"- Patients with adequate bone marrow function measured within 28 days prior to administration of study treatment as defined below: o\tAbsolute neutrophil count ≥1.0 x 109 /L o\tPlatelet count ≥50 x 109 /L o\tHaemoglobin ≥8.0 g/dL (may have been blood transfused)"}
• {"criterion_text":"- Patients with adequate hepatic function: o\tTotal bilirubin ≤ 1.5 × upper limit of normal [ULN] o\tASAT/ALAT ≤1.5 × ULN"}
• {"criterion_text":"- Patients with adequate renal function: o\tCalculated Glomerular Filtration Rate ≥30 ml/min/1.73 m2 according to CKD-EPI formula"}
• {"criterion_text":"- Patients must have a life expectancy ≥ 16 weeks."}
• {"criterion_text":"- Confirmation of non-childbearing status (pregnancy test) for women of childbearing potential."}
• {"criterion_text":"- A highly effective method of contraception is required for female patients during treatment of talazoparib, and for at least 7 months after completing therapy. Advise male patients with female partners of reproductive potential and pregnant partners to use a condom, during treatment with talazoparib and for at least 4 months after the final dose"}
• {"criterion_text":"- Patients who gave its written informed consent to participate to the study."}
• {"criterion_text":"- Patients affiliated to a social insurance regime."}
• {"criterion_text":"- Patients are willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up."}

Exclusion criteria

• {"criterion_text":"- Uncontrolled intercurrent illness, including but not limited to, such as congestive heart failure; respiratory distress; liver failure; allergy, or psychiatric illness/social situations that would limit compliance with study requirement according to the investigator, substantially increase risk of incurring AEs or compromise the ability of the patient to give written informed consent."}
• {"criterion_text":"- In cohorts B1 and B2: Patients with tumor recurrence within 9 months of the last cycle of previous platinum-based chemotherapy line"}
• {"criterion_text":"- Patients with second primary cancer, except: adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumours curatively treated with no evidence of disease for ≥ 5 years."}
• {"criterion_text":"- All subjects with brain metastases or meningeal involvement."}
• {"criterion_text":"- Patients receiving any systemic chemotherapy, radiotherapy (except for palliative reasons), within 6 weeks from the last dose prior to study treatment (or a longer period depending on the defined characteristics of the agents used). The patient can receive a stable dose of bisphosphonates for bone metastases, before and during the study as long as these were started at least 4 weeks prior to treatment with study drug."}
• {"criterion_text":"- Persistent toxicities (CTCAE ≥ grade 2) with the exception of alopecia and sensory neuropathy, caused by previous cancer therapy."}
• {"criterion_text":"- Treatment with other investigational agents."}
• {"criterion_text":"- Bowel occlusive syndrome, inflammatory bowel disease, immune colitis, or other gastro-intestinal disorder that does not allow oral medication such as malabsorption."}
• {"criterion_text":"- Known severe hypersensitivity reactions to PARP inhibitors."}
• {"criterion_text":"- Known HIV or AIDS related illness."}
• {"criterion_text":"- Positive test for HBV surface antigen and / or confirmatory HCV RNA (if anti-HCV antibody tested positive)."}
• {"criterion_text":"- Treatment with oral anticoagulant anti-vitamin K such Coumadin®."}
• {"criterion_text":"- Prior organ transplantation, including allogeneic stem cell transplantation (excluding autologous bone marrow transplant)."}
• {"criterion_text":"- Patients under guardianship."}
• {"criterion_text":"- Women who are breastfeeding (during treatment with talazoparib and for at least 1 month after the final dose)."}
• {"criterion_text":"- Participation in other interventional clinical research that may interfere with the experimental drugs efficacy."}

Primary endpoints

• {"endpoint_text":"- Non-progression proportion 6 months after starting talazoparib in TALAMESO trial.","definition_or_measurement_approach":"Assessed by the proportion of patients who are free of progression 6 months after starting talazoparib maintenance treatment (patients having had minimum 4 cycles of systemic platinum-based first line chemotherapy)."}

Secondary endpoints

• {"endpoint_text":"- Related to progression free-survival based on RECIST 1.1 criteria (only for Malignant Peritoneal Mesothelioma)","definition_or_measurement_approach":"Progression-free survival measured based on RECIST 1.1 criteria (applies only to Malignant Peritoneal Mesothelioma cohort)."}
• {"endpoint_text":"- Related to progression free-survival based on mRECIST criteria (For Malignant Peritoneal Mesothelioma and Malignant Pleural Mesothelioma)","definition_or_measurement_approach":"Progression-free survival measured based on modified RECIST (mRECIST) criteria (applies to both peritoneal and pleural mesothelioma cohorts)."}
• {"endpoint_text":"- Related to overall survival","definition_or_measurement_approach":"Overall survival measured as time from study entry (or from start of talazoparib) to death from any cause."}
• {"endpoint_text":"- Related to safety","definition_or_measurement_approach":"Safety assessed by recording adverse events and grading by CTCAE (not further specified in CTIS extract)."}
• {"endpoint_text":"- Translational endpoints : On FFPE (paraffin embedded archival blocks) pretreatment tumor samples : BAP1 and HR genes status","definition_or_measurement_approach":"Molecular characterization of BAP1 and homologous recombination (HR) gene status on pretreatment FFPE tumor samples."}
• {"endpoint_text":"- Translational endpoints : On FFPE (paraffin embedded archival blocks) pretreatment tumor samples : RAD51 foci assay","definition_or_measurement_approach":"RAD51 foci assay performed on pretreatment FFPE tumor samples."}
• {"endpoint_text":"- Translational endpoints : On FFPE (paraffin embedded archival blocks) pretreatment tumor samples : HRD transcriptomic signature","definition_or_measurement_approach":"Assessment of HRD transcriptomic signature on pretreatment FFPE tumor samples."}

France

Earliest CTIS Part Ii Submission Date

18-06-2024

Latest Decision Or Authorization Date

21-08-2024

Processing Time Days

64

Number Of Sites

18

Number Of Participants

40

Primary sponsor

Full Name

Hospices Civils De Lyon

Organisation Type

Hospital/Clinic/Other health care facility

Country Of Registered Address

France

Third parties

• {"country":"","full_name":"PFIZER","duties_or_roles":"Source of monetary support","organisation_type":""}