This retrospective cohort study included 196 patients with stage III non-small cell lung cancer treated at 4 hospitals. All patients received induction chemoimmunotherapy before chemoradiotherapy. The study compared outcomes between those who received consolidation immunotherapy versus those who did not receive consolidation immunotherapy.
The primary outcomes were progression-free survival and overall survival. At 2 years, progression-free survival was 52.2% in the induction group versus 47.7% in the induction plus consolidation group, with a P value of 0.472. Overall survival was 78.0% in the induction group versus 83.8% in the induction plus consolidation group, with a P value of 0.578.
After 1:1 propensity score matching, median progression-free survival was 30.2 months in the induction group versus 24.0 months in the induction plus consolidation group (P = 0.261). Median overall survival was 46.0 months in the induction group versus not reached in the induction plus consolidation group (P = 0.960). Safety data, adverse events, and tolerability were not reported.
The authors note that the effect of consolidation immunotherapy on patients with stage III NSCLC who receive induction chemoimmunotherapy before CRT needs to be further studied. Because this was an observational study, causality cannot be inferred. The results indicate no clear clinical benefit from adding consolidation immunotherapy in this population.
View Original Abstract ↓
The purpose of this study was to evaluate the effect of consolidation immunotherapy on patients with stage III non-small cell lung cancer (NSCLC) who received induction chemoimmunotherapy before chemoradiotherapy (CRT).
Patients with stage III NSCLC who received induction chemoimmunotherapy before CRT with or without consolidation immunotherapy at 4 hospitals between February 2018 and December 2022 were retrospectively analyzed. The patients were divided into two groups on the basis of whether they received consolidation immunotherapy (Ind+Con group) or not (Ind group). Progression-free survival (PFS) and overall survival (OS) were assessed from the initiation of treatment and were estimated using the Kaplan–Meier method. One-to-one propensity score matching (PSM) was used to further minimize confounding effects.
A total of 196 eligible patients were enrolled, with 124 (63.3%) in the Ind group and 72 (36.7%) in the Ind+Con group. The median follow-up was 24.6 months, and the median PFS and OS for the whole cohort were 24.8 months and 46.0 months, respectively. The median PFS was 25.5 months in the Ind group vs. 24.0 months in the Ind+Con group, with 2-year PFS rates of 52.2% vs. 47.7% (P = 0.472). The median OS was 46.0 months in the Ind group vs. not reached (NR) in the Ind+Con group, with 2-year OS rates of 78.0% vs. 83.8% (P = 0.578). After 1:1 PSM, the median PFS was 30.2 months vs. 24.0 months, with 2-year PFS rates of 55.4% vs. 47.7% (P = 0.261). The median OS was 46.0 months vs. NR, with 2-year OS rates of 80.8% vs. 83.8% (P = 0.960).
The effect of consolidation immunotherapy on patients with stage III NSCLC who receive induction chemoimmunotherapy before CRT needs to be further studied.