Skip to content

A Prospective Study Evaluating the Clinical Utility of Comprehensive Genomic Testing Before Completion of Standard Treatment in Patients With Advanced or Recurrent Cancer

A Prospective Study Evaluating the Clinical Utility of Comprehensive Genomic Profiling Performed Before Completion of Standard Therapy in Patients With Advanced or Recurrent Solid Tumors - A Prospective Study Evaluating the Clinical Utility of Comprehensive Genomic Profiling Before Exhaustion of Standard Treatment in Patients With Advanced or Recurrent Solid Tumors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000061993
Enrollment
100
Registered
2026-06-22
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with advanced or recurrent solid tumors who are candidates for systemic therapy and are not eligible to undergo comprehensive genomic profiling (CGP) testing under the national insurance system before completion (or anticipated completion) of standard treatment.

Interventions

Japan-approved comprehensive genomic profiling (CGP) tests

Sponsors

Okayama University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with advanced or recurrent solid tumors who are candidates for systemic therapy. 2. No prior comprehensive genomic profiling (CGP) testing reimbursed under the national health insurance system. 3. The treating physician determines that the patient is not currently eligible for insurance-covered CGP testing under the prevailing reimbursement criteria at the time of study enrollment. 4. Availability of specimens suitable for genomic analysis, including archived tumor tissue and/or newly collected peripheral blood samples. 5. Willingness to have clinical and genomic data registered in the Center for Cancer Genomics and Advanced Therapeutics (C-CAT) database and utilized for research purposes. 6. Provision of written informed consent by the patient prior to participation in the study.

Exclusion criteria

Exclusion criteria: Patients who have previously enrolled in this study and undergone CGP testing under the framework of Advanced Medical Care A.

Design outcomes

Primary

MeasureTime frame
Proportion of patients who received molecularly targeted therapy for actionable genomic alterations identified by CGP testing performed in this study.

Countries

Japan

Contacts

Public ContactKiichiro Ninomiya

Okayama University Hospital Center for Comprehensive Genomic Medicine

kiichiro_nino@okayama-u.ac.jp0862357414

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026