| Unique ID issued by UMIN | UMIN000061889 |
|---|---|
| Receipt number | R000070614 |
| Scientific Title | Evaluation of Circulating Tumor DNA Across Multiple Resectable Solid Tumors to Assess Its Association with Multi-Biomarker Profiles and Recurrence Risk |
| Date of disclosure of the study information | 2026/06/15 |
| Last modified on | 2026/06/12 14:36:39 |
Evaluation of Circulating Tumor DNA Across Multiple Resectable Solid Tumors to Assess Its Association with Multi-Biomarker Profiles and Recurrence Risk
Pan-Latitude Monstar-3
Evaluation of Circulating Tumor DNA Across Multiple Resectable Solid Tumors to Assess Its Association with Multi-Biomarker Profiles and Recurrence Risk
Pan-Latitude Monstar-3
| Japan |
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
| Medicine in general | Gastroenterology | Hepato-biliary-pancreatic medicine |
| Infectious disease | Surgery in general | Gastrointestinal surgery |
| Hepato-biliary-pancreatic surgery | Breast surgery | Obstetrics and Gynecology |
| Dermatology | Oto-rhino-laryngology | Orthopedics |
| Urology |
Malignancy
YES
To evaluate the performance of ctDNA analysis using an assay developed by Natera, Inc. in predicting recurrence and prognosis in patients with various cancer types following curative-intent treatment.
Others
Evaluation of the clinical validity of circulating tumor DNA in resectable solid tumors
Mechanistic assessment via multi-Omics evaluation including circulating tumor DNA in resectable solid tumors
The association between ctDNA MRD status and recurrence (Disease-free survival:DFS)
Association between ctDNA status and the efficacy of adjuvant therapy
Overall survival (OS)
ctDNA positivity
Association between ctDNA status and clinicopathological/molecular characteristics, etc.
Observational
| 18 | years-old | <= |
| Not applicable |
Male and Female
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
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.
800
| 1st name | Takayuki |
| Middle name | |
| Last name | Yoshino |
National Cancer Center Hospital East
Division for the Promotion of Drug and Diagnostic Development
277-8577
6-5-1 Kashiwanoha, Kashiwa, Chiba
04-7133-1111
tyoshino@east.ncc.go.jp
| 1st name | Tadayoshi |
| Middle name | |
| Last name | Hashimoto |
National Cancer Center Hospital East
Division for the Promotion of Drug and Diagnostic Development
277-8577
6-5-1 Kashiwanoha, Kashiwa, Chiba
04-7133-1111
tadhashi@east.ncc.go.jp
National Cancer Center Hospital East
Natera, Inc
Department for the Promotion of Drug and Diagnostic Development,Translational Research Support Office
Outside Japan
USA
National Cancer Center Institutional Review Board
5-1-1,tsukiji,chuo-ku,Tokyo
03-3542-2511
NCC_IRBoffice@ml.res.ncc.go.jp
NO
| 2026 | Year | 06 | Month | 15 | Day |
Unpublished
Preinitiation
| 2025 | Year | 12 | Month | 20 | Day |
| 2026 | Year | 06 | Month | 03 | Day |
| 2026 | Year | 06 | Month | 17 | Day |
| 2030 | Year | 03 | Month | 31 | Day |
Study Design: Observational study
Target population:the patients who meet the selection criteria until March 31 2030 from research permit date
| 2026 | Year | 06 | Month | 12 | Day |
| 2026 | Year | 06 | Month | 12 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000070614