Cisplatin to Patients With Pancreatic Cancer and Homologous Recombination Deficiency

Phase 2

Recruiting

• Conditions: Homologous Recombination Deficiency; Pancreatic Adenocarcinoma
• Interventions: Drug: Cisplatin

• Registration Number: NCT06095141
• Lead Sponsor: Fudan University

Brief Summary

The purpose of this study is to evaluate the efficacy of cisplatin based regimen to patients with advanced pancreatic cancer and homologous recombination deficiency.

Detailed Description

Pancreatic adenocarcinoma (PDAC) is a highly lethal malignancy with a 5-year survival less than 10%. Approximately 80% of patients with pancreatic cancer are diagnosed at an advanced stage. Chemotherapy is one of the major treatments for advanced pancreatic cancer. In 2011, the PRODIGE trial has shown that oxaliplatin, irinotecan, fluorouracil, and leucovorin (FOLFIRINOX) was associated with a survival advantage but had increased toxicity.

Defects in DNA damage response (DDR) genes causing homologous recombination deficiency (HRD) identify a clinically relevant subgroup of patients with PDAC, with both therapeutic and preventative implications. Accumulating evidence from nonrandomized and randomized clinical trials suggests HRD as a putative biomarker of therapeutic response for platinum-based chemotherapy in patients with advanced PDAC. Within HRD, germline variants in BRCA1 and BRCA2 are associated with improved progression-free survival in patients with platinum-sensitive metastatic PDAC treated with the poly (ADP-ribose) polymerase (PARP) inhibitor (PARPi) olaparib as maintenance therapy. Interestingly, based on preclinical evidence and phase II nonrandomized clinical trials, additional non-BRCA HRD aberrations may predict sensitivity to PARPi with other therapeutic strategies targeting DDR currently under clinical investigation (including immunotherapy, ATM, ATR, and PALB2 inhibitors). However, the efficacy of cisplatin based regimen as a second line treatment for patients with HRD has not been systematically studied.

The purpose of this study is to evaluate the efficacy of cisplatin based regimen on improving the progression-free survival (PFS) of advanced pancreatic cancer patients who harbor germline or somatic homologous recombination deficiency. These patients are resistant to at least one line of systemic chemotherapy. PFS, objective response rate (ORR), overall survival (OS) and disease control rate (DCR) are measured every four weeks.

Study Timeline

• Study First Submitted: 2023-10-18
• Study First Submitted QC: 2023-10-18
• Study First Posted: 2023-10-23
• Status Verified: 2023-12
• Study Start: 2023-12-01
• Last Update Submitted: 2023-12-01
• Last Update Posted: 2023-12-07
• Primary Completion: 2025-10-31
• Study Completion: 2026-10-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Ability to understand and the willingness to sign a written informed consent document.
• Age ≥ 18 years and ≤ 80 years.
• Eastern Cooperative Oncology Group (ECOG) performance status 0-2.
• Histologically or cytologically confirmed advanced pancreas adenocarcinoma.
• Tumor progression after at least one line of chemotherapy.
• Genetic or molecular test confirmed the presence of homologous recombination deficiency.
• Presence of at least of one measurable lesion in agreement to RECIST criteria.
• The expected survival ≥ 3 months.
• Adequate organ performance based on laboratory blood tests.
• Women of childbearing potential and men must agree to use adequate contraception prior to study entry and for the duration of study participation.

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Exclusion Criteria

• Pregnant or nursing women.
• Primary pancreatic cancer.
• Patients who have received platinum or PARPi treatment.
• The diagnosis was confirmed by pathology as non-adenocarcinoma of pancreas.
• Inflammation of the digestive tract, including pancreatitis, cholecystitis, cholangitis, etc.
• Severe and uncontrollable accompanying diseases that may affect protocol compliance or interfere with the interpretation of results.
• Renal insufficiency or dialysis
• Other serious accompanying illnesses, which, in the researcher's opinion, could seriously adversely affect the safety of the treatment.
• Patients who are allergic to cisplatin or other platinum drugs.
• Patients who are unwilling or unable to comply with study procedures.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Cisplatin	Cisplatin	Cisplatin 25 mg/m2, ivgtt, 30 min, D1, 8.

Primary Outcome Measures

Name	Time	Method
progression-free survival, PFS	At the end of Cycle 1 (each cycle is 21 days)	PFS of subjects from recruiting to the time of disease progression

Secondary Outcome Measures

Name	Time	Method
objective response rate (ORR)	At the end of Cycle 1 (each cycle is 21 days)	CR + PR
Overall survival，OS	At the end of Cycle 1 (each cycle is 21 days)	OS of subjects from recruiting to the time of death from any cause
disease control rate (DCR)	At the end of Cycle 1 (each cycle is 21 days)	CR + PR + SD

Trial Locations

Locations (1)

Shanghai Cancer Center; 🇨🇳 Shanghai, China