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Observational Study to follow up patients enrolled in FIRST-Dx trial.

Observational Study to follow up patients enrolled in "Prospective clinical study of comprehensive genomic profiling for patients with chemotherapy-naive advanced cancer (FIRST-Dx trial)."

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1050220041
Enrollment
180
Registered
2022-06-09
Start date
2022-11-09
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Chemotherapy-naive adult patients with advanced cancer (GI, Lung, Breast, GYN, Melanoma)

Interventions

None listed

Sponsors

Muto Manabu
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Registered in FIRST-Dx trial, and underwent F1CDx. 2. Written informed consent.

Exclusion criteria

Exclusion criteria: 1. Withdrawal of informed consent. 2. Registered in FIRST-Dx trial, but failed in F1CDx. 3. Inappropriate case judged by investigators.

Design outcomes

Primary

MeasureTime frame
Overall Survival

Secondary

MeasureTime frame
1. The ratio of patients who actually receive molecular tumor board recommended therapy (MBRT) 2. Chemotherapy regimens in the subsequent lines of therapy 3. Progression-free survival in each subsequent line of therapy 4. Best Overall Response in each subsequent line of therapy 5. PFS ratio: MBRT/first-line therapy 6. PFS ratio_2: MBRT/prior therapy 7. One year suvival rate

Contacts

Public ContactJunichi Matsubara

Kyoto University Hospital

jmatsuba@kuhp.kyoto-u.ac.jp+81-75-751-3518

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026