Pancreatic Cancer Clinical Trial
— MAP-02Official title:
The Value of Molecular Residual Disease Monitoring Based on ctDNA in Resected Pancreatic Cancer
The goal of this clinical trial is to explore the value of molecular residual disease (MRD) monitoring based on ctDNA in resected pancreatic cancer. The main questions it aims to answer are: - prognostic value of baseline MRD; - the role of MRD dynamic changes after treatment in guiding treatment. Peripheral blood derived from participants will be obtained for MRD test before adjuvant chemotherapy initiation and at the first imaging assessment after chemotherapy.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | February 1, 2030 |
Est. primary completion date | February 1, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - patients with pancreatic cancer who had undergone curative-intent surgery (R0 or R1 resection); - both sexes, age =18 years old; - ECOG performance status score =2; - the expected survival time was =3 months. Exclusion Criteria: - a known diagnosis of pancreatic cancer other than ductal adenocarcinoma; - treated with any systemic antitumor treatment before first-line chemotherapy onset; - died or lost to follow-up within one month after the initiation of adjuvant chemotherpay; - combined with other primary malignances. |
Country | Name | City | State |
---|---|---|---|
China | Department of Medical Oncology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College | Beijing |
Lead Sponsor | Collaborator |
---|---|
Peking Union Medical College Hospital |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | The prognostic value of MRD | The prognostic value of baseline MRD and dynamic MRD changes | Baseline until death from any cause (up to approximately 60 months) | |
Other | The prognostic role of targeted therapy selected based on MRD | The prognostic role of targeted therapy selected based on MRD | Baseline until death from any cause (up to approximately 60 months) | |
Primary | Disease-free survival | The date of adjuvant chemotherpay initiation to tumor recurrence, local-regional or distant metastases, or death due to any cause. | Baseline until death from any cause (up to approximately 36 months) | |
Secondary | Overall survival | The date of adjuvant chemotherpay initiation to death due to any cause. | Baseline until death from any cause (up to approximately 60 months) |
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