RTOG 9410
For unresectable stage III NSCLC, does concurrent chemoradiotherapy improve survival compared with sequential chemoradiotherapy?
Trial design and population
Key results
Median OS was 17.0 months with once-daily concurrent CRT vs 14.6 months with sequential treatment; 5-year OS was 16% vs 10% (P=.046). Concurrent therapy increased acute esophageal toxicity.
Source-reported outcome visualization
5-year overall survival · 5 years
Bars are scaled to the larger reported group value; endpoint, unit and horizon are labelled. Values are source-reported, not estimated from medians.
Absolute Effect
Absolute 5-year OS difference 6 percentage points; NNT 17 based on 5-year OS. Grade 3+ esophagitis was approximately 22% vs 4%, an 18-point excess; NNH 6 based on grade 3+ esophagitis.
NNT: 17 (5-year OS). Use only at the stated endpoint/time horizon; median survival differences are not converted into NNT.
NNH: ≈6 based on grade 3+ esophagitis during treatment. Grade 3+ esophagitis about 22% vs 4%; NNH ≈6 based on grade 3+ esophagitis. Severe pulmonary and hematologic toxicity and treatment-related deaths also matter.
Time-to-event hazard ratios and median survival are not treated as absolute risk differences. Where no defensible fixed-time NNT/NNH is available, the source-reported endpoint is visualized instead.
Safety and treatment burden
Grade 3+ esophagitis about 22% vs 4%; NNH ≈6 based on grade 3+ esophagitis. Severe pulmonary and hematologic toxicity and treatment-related deaths also matter.
Follow-up, maturity and limitations
Follow-up: Mature long-term follow-up.
Older chemotherapy and RT techniques. Contemporary stage III care often includes consolidation immunotherapy after concurrent CRT; RTOG 9410 established concurrent over sequential CRT, not the full modern regimen.
Clinical interpretation
Current-practice context · reviewed 20 October 2026
This page separates the original trial findings from contemporary treatment sequencing. Confirm current guidelines, local regulatory status, biomarker requirements, prior treatment exposure and patient-specific contraindications before applying the evidence. Historical comparators may no longer represent the current standard; subgroup findings and immature endpoints are labelled rather than generalized.