Breast cancer, gastric cancer, esophageal cancer, liver cancer, biliary truct cancer, pancreatic cancer, urothelial cancer, kidney cancer, endometrial cancer, cervical cancer, head and neck cancer, skin cancer, bone and soft tissue sarcoma
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with breast cancer, gastric cancer, esophageal cancer, liver cancer, biliary truct cancer, pancreatic cancer, urothelial cancer, kidney cancer, endometrial cancer, cervical cancer, head and neck cancer, skin cancer, bone and soft tissue sarcoma who were enrolled in the MONSTAR-SCREEN-3 trial (Cohort B) and received curative treatment
Exclusion criteria
Exclusion criteria: 1.Cases with missing data required for this study. 2.Cases deemed inappropriate for enrollment in this study by the principal investigator. 3.Cases of withdrawal of consent or refusal of secondary use of specimens and/or data.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The association between ctDNA MRD status and recurrence (Disease-free survival:DFS) | — |
Secondary
| Measure | Time frame |
|---|---|
| Association between ctDNA status and the efficacy of adjuvant therapy Overall survival (OS) ctDNA positivity Association between ctDNA status and clinicopathological/molecular characteristics, etc. | — |
Countries
Japan
Contacts
National Cancer Center Hospital East Division for the Promotion of Drug and Diagnostic Development