TY - JOUR
T1 - Perioperative Nivolumab and Chemotherapy in Stage III Non-Small-Cell Lung Cancer
AU - Provencio, Mariano
AU - Nadal, Ernest
AU - González-Larriba, José L.
AU - Martínez-Martí, Alex
AU - Bernabé, Reyes
AU - Bosch-Barrera, Joaquim
AU - Casal-Rubio, Joaquín
AU - Calvo, Virginia
AU - Insa, Amelia
AU - Ponce, Santiago
AU - Reguart, Noemí
AU - De Castro, Javier
AU - Mosquera, Joaquín
AU - Cobo, Manuel
AU - Aguilar, Andrés
AU - López Vivanco, Guillermo
AU - Camps, Carlos
AU - López-Castro, Rafael
AU - Morán, Teresa
AU - Barneto, Isidoro
AU - Rodríguez-Abreu, Delvys
AU - Serna-Blasco, Roberto
AU - Benítez, Raquel
AU - Aguado De La Rosa, Carlos
AU - Palmero, Ramón
AU - Hernando-Trancho, Florentino
AU - Martín-López, Javier
AU - Cruz-Bermúdez, Alberto
AU - Massuti, Bartomeu
AU - Romero, Atocha
N1 - Publisher Copyright:
© 2023 Massachusetts Medical Society.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Background: Approximately 20% of patients with non-small-cell lung cancer (NSCLC) receive a diagnosis of stage III disease. There is no current consensus regarding the most appropriate treatment for these patients. Methods: In this open-label, phase 2 trial, we randomly assigned patients with resectable stage IIIA or IIIB NSCLC to receive neoadjuvant nivolumab plus platinum-based chemotherapy (experimental group) or chemotherapy alone (control group), followed by surgery. Patients in the experimental group who had R0 resections received adjuvant treatment with nivolumab for 6 months. The primary end point was a pathological complete response (0% viable tumor in resected lung and lymph nodes). Secondary end points included progression-free survival and overall survival at 24 months and safety. Results: A total of 86 patients underwent randomization; 57 were assigned to the experimental group and 29 were assigned to the control group. A pathological complete response occurred in 37% of the patients in the experimental group and in 7% in the control group (relative risk, 5.34; 95% confidence interval [CI], 1.34 to 21.23; P=0.02). Surgery was performed in 93% of the patients in the experimental group and in 69% in the control group (relative risk, 1.35; 95% CI, 1.05 to 1.74). Kaplan-Meier estimates of progression-free survival at 24 months were 67.2% in the experimental group and 40.9% in the control group (hazard ratio for disease progression, disease recurrence, or death, 0.47; 95% CI, 0.25 to 0.88). Kaplan-Meier estimates of overall survival at 24 months were 85.0% in the experimental group and 63.6% in the control group (hazard ratio for death, 0.43; 95% CI, 0.19 to 0.98). Grade 3 or 4 adverse events occurred in 11 patients in the experimental group (19%; some patients had events of both grades) and 3 patients in the control group (10%). Conclusions: In patients with resectable stage IIIA or IIIB NSCLC, perioperative treatment with nivolumab plus chemotherapy resulted in a higher percentage of patients with a pathological complete response and longer survival than chemotherapy alone.
AB - Background: Approximately 20% of patients with non-small-cell lung cancer (NSCLC) receive a diagnosis of stage III disease. There is no current consensus regarding the most appropriate treatment for these patients. Methods: In this open-label, phase 2 trial, we randomly assigned patients with resectable stage IIIA or IIIB NSCLC to receive neoadjuvant nivolumab plus platinum-based chemotherapy (experimental group) or chemotherapy alone (control group), followed by surgery. Patients in the experimental group who had R0 resections received adjuvant treatment with nivolumab for 6 months. The primary end point was a pathological complete response (0% viable tumor in resected lung and lymph nodes). Secondary end points included progression-free survival and overall survival at 24 months and safety. Results: A total of 86 patients underwent randomization; 57 were assigned to the experimental group and 29 were assigned to the control group. A pathological complete response occurred in 37% of the patients in the experimental group and in 7% in the control group (relative risk, 5.34; 95% confidence interval [CI], 1.34 to 21.23; P=0.02). Surgery was performed in 93% of the patients in the experimental group and in 69% in the control group (relative risk, 1.35; 95% CI, 1.05 to 1.74). Kaplan-Meier estimates of progression-free survival at 24 months were 67.2% in the experimental group and 40.9% in the control group (hazard ratio for disease progression, disease recurrence, or death, 0.47; 95% CI, 0.25 to 0.88). Kaplan-Meier estimates of overall survival at 24 months were 85.0% in the experimental group and 63.6% in the control group (hazard ratio for death, 0.43; 95% CI, 0.19 to 0.98). Grade 3 or 4 adverse events occurred in 11 patients in the experimental group (19%; some patients had events of both grades) and 3 patients in the control group (10%). Conclusions: In patients with resectable stage IIIA or IIIB NSCLC, perioperative treatment with nivolumab plus chemotherapy resulted in a higher percentage of patients with a pathological complete response and longer survival than chemotherapy alone.
KW - Hematology/Oncology
KW - Lung Cancer
KW - Pulmonary/Critical Care
KW - Pulmonary/Critical Care General
KW - Treatments in Oncology
UR - http://www.scopus.com/inward/record.url?scp=85165561075&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa2215530
DO - 10.1056/NEJMoa2215530
M3 - Article
AN - SCOPUS:85165561075
SN - 0028-4793
VL - 389
SP - 504
EP - 513
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 6
ER -