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Multicenter, retrospective, observational study of chemotherapy for recurrence after chemoradiation and durvalumab consolidation therapy for unresectable locally advanced non-small cell lung cancer.TORG-TG2402

Multicenter, retrospective, observational study of chemotherapy for recurrence after chemoradiation and durvalumab consolidation therapy for unresectable locally advanced non-small cell lung cancer.TORG-TG2402 - Retrospective, observational study of chemotherapy for recurrence after the PACIFIC regimen for unresectable locally advanced NSCLC, TORG-TG2402

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000056263
Enrollment
200
Registered
2024-11-25
Start date
2024-10-28
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

Patient with unresectable locally advanced non-small cell lung cancer who relapsed after chemoradiotherapy and durvalumab consolidation therapy.

Interventions

None listed

Sponsors

Cancer and Infectious Disease Center Tokyo Metropolitan Komagome Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients with NSCLC diagnosed by cytology or histology. (2) Patients with unresectable local progression or postoperative local recurrence. (3) Patients who have undergone radical CRT and at least one course of durvalumab consolidation therapy. (4) Patients who received platinum plus ICI or platinum combination therapy for recurrence from July 2, 2018 to June 30, 2023.

Exclusion criteria

Exclusion criteria: (1) Patients who had prior irradiation of all recurrent lesions. (2) Patients who were judged to be inappropriate for this study by the physician of information collection at each institution. (3) Patients with driver gene mutation (EGFR, ALK, ROS1, MET exon 14 skipping, RET, BRAF) positive.

Design outcomes

Primary

MeasureTime frame
Progression-free survival (PFS) for initial chemotherapy after relapse: A survival curve will be estimated using the Kaplan-Meier method, and the median PFS and its 95% confidence interval will be calculated. To adjust for background factors, multivariate Cox regression models and propensity score matching will be used to compare groups.

Countries

Japan

Contacts

Public ContactSeigo Katakura

Kanagawa Cancer Center Department of Thoracic Oncology

shetland1015@gmail.com0455202222

Outcome results

None listed

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