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Cross-sectional study of second-line therapy administration after platinum-based chemotherapy for patients with advanced NSCLC.

Cross-sectional study of second-line therapy administration after platinum-based chemotherapy for patients with advanced NSCLC. - Second-line chemotherapy administration for patients with advanced NSCLC, who completed platinum-based "Hyojun" (standard) doublet, In the follow-up period, and at recurrence.(SAPPHIRE)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000006393
Enrollment
750
Registered
2011-09-22
Start date
2010-10-01
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

Advanced lung cancer

Interventions

None listed

Sponsors

SAPPHIRE Executive committee
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients who were diagnosed as advanced or recurrent NSCLC before this study. 2)Consecutive patients in each institution who had started first-line platinum chemotherapy in combination with third generation agent after April 1, 2010.

Exclusion criteria

Exclusion criteria: 1)Recurrent NSCLC patients who had undergone adjuvant platinum based chemotherapy. 2)Active double cancer.

Design outcomes

Primary

MeasureTime frame
Proportion of the patients administered the second-line chemotherapy

Secondary

MeasureTime frame
1)Proportion of the patients who had PD for first-line chemotherapy 2)Proportion of the patients who were administered second-line chemotherapy 3)Proportion of the patients who were administered third-line chemotherapy after the second-line chemotherapy 4)Proportion of the patients who were administered second-line chemotherapy after having PD for first-line chemotherapy. 5)Proportion of the patients who were administered second-line chemotherapy after taking maintenance chemotherapy.

Countries

Japan

Contacts

Public ContactAkira Yamao

Public Health Research Foundation Comprehensive Support Project for Clinical Research

info@csp.or.jp03-5287-2633

Outcome results

None listed

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