Importance: Patients with borderline resectable or unresectable stage III non-small cell lung cancer (NSCLC) with T4 and/or N2-N3 involvement face limited treatment options and poor outcomes. Neoadjuvant chemoimmunotherapy has shown promise in improving resectability and pathological responses. Objective: To evaluate the efficacy of neoadjuvant programmed cell death 1 protein (PD-1) or programmed cell death 1 ligand 1 (PD-L1) blockade combined with chemotherapy in enhancing surgical outcomes and pathological responses in patients with T4 and/or N2-N3 stage III NSCLC. Design, Setting, and Participants: This multicenter cohort study analyzed data from patients treated between February 2018 and January 2024 with neoadjuvant PD-1/PD-L1 inhibitors plus chemotherapy at academic and tertiary care centers across the US and Italy. Pathological and survival outcomes were assessed. Patients with stage III NSCLC and T4 and/or N2-N3 involvement were included. Data were collected from February 2018 to January 2024. Exposures: Neoadjuvant PD-1/PD-L1 blockade combined with platinum-based chemotherapy. Main Outcomes and Measures: Pathological complete response (pCR), major pathological response, surgical resectability, and event-free survival (EFS). Results: Of 112 patients, 58 (51.8%) were female, and the median (range) age was 66 (41-84) years. A total of 84(75.0%) underwent surgical resection, achieving a pCR rate of 29.0% (24 of 83 with available final pathology) and a major pathological response rate of 42.2% (35 of 83). Patients with both PD-L1 expression of 50% or more and high tumor mutational burden achieved the highest pCR rate (4 of 9 [44.4%]; P =.03). Conversely, covariants in KRAS/STK11 or KRAS/KEAP1 were associated with lack of pCR. Patients with single-station or multistation N2/N3 disease exhibited comparable pathological outcomes. The median EFS for all resected patients was 52.6 months (95% CI, 27.8 to not reached), and this was significantly longer in patients with pCR (not reached vs 27.8 months [95% CI, 19.5 to not reached]; P <.001). Conclusions and Relevance: In this study, neoadjuvant PD-1/PD-L1 blockade combined with chemotherapy resulted in high pathological response rates and surgical resectability in patients with T4 and/or N2-N3 stage III NSCLC. This approach offers a viable treatment option for patients with borderline resectable or unresectable NSCLC but requires further validation through prospective studies..

Neoadjuvant PD-1 and PD-L1 blockade with chemotherapy for borderline resectable and unresectable stage III non-small cell lung cancer / Ricciuti, B., Fusco, F., Cooper, A., Garbo, E., Pecci, F., Aldea, M., Wang, X., Mayoral Penalva, M., Ginsberg, M., Sholl, L.M., Nishino, M., Di Federico, A., Shaverdian, N., Bott, M., Santo, V., Rendina, E., Trisolini, R., Ramella, S., Gallina, F., Melis, E., et al.. - In: JAMA ONCOLOGY. - ISSN 2374-2437. - 11:7(2025), pp. 735-741. [10.1001/jamaoncol.2025.1115]

Neoadjuvant PD-1 and PD-L1 blockade with chemotherapy for borderline resectable and unresectable stage III non-small cell lung cancer

Pecci F.;Santo V.;Rendina E.;Trisolini R.;Gallina F.;
2025

Abstract

Importance: Patients with borderline resectable or unresectable stage III non-small cell lung cancer (NSCLC) with T4 and/or N2-N3 involvement face limited treatment options and poor outcomes. Neoadjuvant chemoimmunotherapy has shown promise in improving resectability and pathological responses. Objective: To evaluate the efficacy of neoadjuvant programmed cell death 1 protein (PD-1) or programmed cell death 1 ligand 1 (PD-L1) blockade combined with chemotherapy in enhancing surgical outcomes and pathological responses in patients with T4 and/or N2-N3 stage III NSCLC. Design, Setting, and Participants: This multicenter cohort study analyzed data from patients treated between February 2018 and January 2024 with neoadjuvant PD-1/PD-L1 inhibitors plus chemotherapy at academic and tertiary care centers across the US and Italy. Pathological and survival outcomes were assessed. Patients with stage III NSCLC and T4 and/or N2-N3 involvement were included. Data were collected from February 2018 to January 2024. Exposures: Neoadjuvant PD-1/PD-L1 blockade combined with platinum-based chemotherapy. Main Outcomes and Measures: Pathological complete response (pCR), major pathological response, surgical resectability, and event-free survival (EFS). Results: Of 112 patients, 58 (51.8%) were female, and the median (range) age was 66 (41-84) years. A total of 84(75.0%) underwent surgical resection, achieving a pCR rate of 29.0% (24 of 83 with available final pathology) and a major pathological response rate of 42.2% (35 of 83). Patients with both PD-L1 expression of 50% or more and high tumor mutational burden achieved the highest pCR rate (4 of 9 [44.4%]; P =.03). Conversely, covariants in KRAS/STK11 or KRAS/KEAP1 were associated with lack of pCR. Patients with single-station or multistation N2/N3 disease exhibited comparable pathological outcomes. The median EFS for all resected patients was 52.6 months (95% CI, 27.8 to not reached), and this was significantly longer in patients with pCR (not reached vs 27.8 months [95% CI, 19.5 to not reached]; P <.001). Conclusions and Relevance: In this study, neoadjuvant PD-1/PD-L1 blockade combined with chemotherapy resulted in high pathological response rates and surgical resectability in patients with T4 and/or N2-N3 stage III NSCLC. This approach offers a viable treatment option for patients with borderline resectable or unresectable NSCLC but requires further validation through prospective studies..
2025
neoadjuvant; NSCLC; locally advanced; chemo-immunotherapy; unresectable
01 Pubblicazione su rivista::01a Articolo in rivista
Neoadjuvant PD-1 and PD-L1 blockade with chemotherapy for borderline resectable and unresectable stage III non-small cell lung cancer / Ricciuti, B., Fusco, F., Cooper, A., Garbo, E., Pecci, F., Aldea, M., Wang, X., Mayoral Penalva, M., Ginsberg, M., Sholl, L.M., Nishino, M., Di Federico, A., Shaverdian, N., Bott, M., Santo, V., Rendina, E., Trisolini, R., Ramella, S., Gallina, F., Melis, E., et al.. - In: JAMA ONCOLOGY. - ISSN 2374-2437. - 11:7(2025), pp. 735-741. [10.1001/jamaoncol.2025.1115]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1753683
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