The Efficacy and Safety of Fluzoparib Plus Irinotecan as Second-line Treatment in Patients With Homologous Recombination Deficiency (HRD) Metastatic Colorectal Cancer.
- Conditions
- Homologous Recombination Deficiency Alterations Metastatic Colorectal Cancer
- Interventions
- Registration Number
- NCT05732129
- Lead Sponsor
- Fudan University
- Brief Summary
Preclinical data support the investigation of PARP inhibitors in other neoplasms exhibiting homologous recombination deficiency (HRD) as monotherapy as well as in combination with chemotherapy. However，in colorectal cancer (CRC), the role of HRD alterations is mostly unknown. This study aims to explore the the Efficacy and Safety of Fluzoparib combined with Irinotecan in the Second-line treatment of HRD alterations metastatic colorectal cancer.
- Detailed Description
Study protocol for an open-label, single-arm, phase II study of combination of Fluzoparib and rinotecan as the second-line treatment for patients with HRD alterations metastatic colorectal cancer (mCRC). Patients will receive Fluzoparib combined with Irinotecan treatment protocol, which included irinotecan asintravenous infusion at 180mg/m2 (on day 1) and Fluzoparib 150mg capsules given bid (days 1-7) every 2 weeks.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 29
- 18-75 years；
- Histological or cytological confirmed metastatic colorectal cancer;
- HRD alterations（inclued BRCA1/2、ATM、CDK12、PALB2、Check2、RAD51C、RAD51D etc.）；
- Intolerability toxicity occurs 8 weeks within first-line therapy;
- ECOG PS 0-1;
- Adequate hepatic, renal, heart, and hematologic functions;
- Negative serum pregnancy test at screening for women of childbearing potential;
- Informed consent was signed before the study began.
- Prior treatment with PARPi drugs；
- Symptomatic brain or meningeal metastases；
- Patients have received local radiotherapy within 1 month prior to treatment;
- Patients who had active bleeding or coagulopathy before enrollment, had a tendency to bleed, or were receiving thrombolytic therapy and were considered by the investigator to be ineligible for enrollment;
- Women who are pregnant (with a positive pregnancy test before medication) or breastfeeding;
- Expected survival <3 months;
- Received other investigational drugs within 4 weeks prior to treatment;
- Patients who had active uncontrollable neurological, mental disease or mental disorder, poor compliance, unable to cooperate and describe the treatment response;
- Allergy to the study drug or any of its excipients;
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Fluzoparib plus Irinotecan Fluzoparib Patients will receive Fluzoparib combined with Irinotecan treatment protocol, which included irinotecan asintravenous infusion at 180mg/m2 (on day 1) and Fluzoparib 150mg capsules given bid (days 1-7) every 2 weeks . Fluzoparib plus Irinotecan Irinotecan Patients will receive Fluzoparib combined with Irinotecan treatment protocol, which included irinotecan asintravenous infusion at 180mg/m2 (on day 1) and Fluzoparib 150mg capsules given bid (days 1-7) every 2 weeks .
- Primary Outcome Measures
Name Time Method Objective response rate of Metastatic Colorectal Cancer,inculdthe proportion of patients with complete response or partial response assessed up to 1 year using RECIST v 1.1.
- Secondary Outcome Measures
Name Time Method Overall survival of Metastatic Colorectal Cancer, include time from randomization to death from any cause assessed up to 2 year Responses are according to the Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) as assessed by investigator
The Safety of Fluzoparib Plus Irinotecan as Second-line Treatment in Patients With Homologous Recombination Deficiency (HRD) Metastatic Colorectal Cancer. assessed up to 2 year time from enrollment to the first documented disease progression or death due to any cause, whichever occurs first. Responses are according to the Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) as assessed by investigator
Progression-Free Survival of Metastatic Colorectal Cancer，includ time from enrollment to the first documented disease progression or death due to any cause, whichever occurs first assessed up to 1 year Responses are according to the Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) as assessed by investigator
Trial Locations
- Locations (1)
Department of Colorectal Surgery Fudan University Shanghai Caner Center
🇨🇳Shanghai, Shanghai, China