TY - JOUR
T1 - Neoadjuvant PD-1 and PD-L1 Blockade With Chemotherapy for Borderline Resectable and Unresectable Stage III Non-Small Cell Lung Cancer
AU - Ricciuti, Biagio
AU - Fusco, Francesca
AU - Cooper, Alissa
AU - Garbo, Edoardo
AU - Pecci, Federica
AU - Aldea, Mihaela
AU - Wang, Xinan
AU - Mayoral Penalva, Maria
AU - Ginsberg, Michelle
AU - Sholl, Lynette M.
AU - Nishino, Mizuki
AU - Di Federico, Alessandro
AU - Shaverdian, Narek
AU - Bott, Matthew
AU - Santo, Valentina
AU - Rendina, Erino
AU - Trisolini, Rocco
AU - Ramella, Sara
AU - Gallina, Filippo
AU - Melis, Enrico
AU - Buglioni, Simonetta
AU - Minuti, Gabriele
AU - Landi, Lorenza
AU - Ugalde Figueroa, Paula A.
AU - Shaw, Alice T.
AU - Chaft, Jamie
AU - Awad, Mark M.
AU - Cappuzzo, Federico
N1 - Publisher Copyright:
© 2025 American Medical Association. All rights reserved.
PY - 2025/1/1
Y1 - 2025/1/1
N2 - 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..
AB - 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..
UR - http://www.scopus.com/inward/record.url?scp=105006597714&partnerID=8YFLogxK
U2 - 10.1001/jamaoncol.2025.1115
DO - 10.1001/jamaoncol.2025.1115
M3 - Article
C2 - 40402502
AN - SCOPUS:105006597714
SN - 2374-2437
JO - JAMA Oncology
JF - JAMA Oncology
ER -