Real‐world evidence of efficacy of pembrolizumab plus chemotherapy and nivolumab plus ipilimumab plus chemotherapy as initial treatment for advanced non‐small cell lung cancer

Author:

Kaneko Ayami1,Kobayashi Nobuaki1ORCID,Miura Kenji2,Matsumoto Hiromi1,Somekawa Kohei1,Hirose Tomofumi3,Kajita Yukihito3,Tanaka Anna3,Teranishi Shuhei3ORCID,Sairenji Yu2,Kawashima Hidetoshi4,Yumoto Kentaro5,Tsukahara Toshinori6,Fukuda Nobuhiko7,Nishihira Ryuichi4,Watanabe Keisuke1,Horita Nobuyuki1ORCID,Hara Yu1,Kudo Makoto3,Miyazawa Naoki8,Kaneko Takeshi1

Affiliation:

1. Department of Pulmonology Yokohama City University Graduate School of Medicine Yokohama Japan

2. Department of Respiratory Medicine Yokohama Sakae Kyosai Hospital Yokohama Japan

3. Department of Pulmonology Yokohama City University Medical Center Yokohama Japan

4. Department of Respiratory Medicine Kanto Rosai Hospital Kawasaki Japan

5. Department of Respiratory Medicine Yokohama Minami Kyosai Hospital Ykohama Japan

6. Department of Respiratory Medicine Chigasaki Municipal Hospital Chigasaki Japan

7. Department of Respiratory Medicine Fujisawa Municipal Hospital Fujisawa Japan

8. Department of Respiratory Medicine Yokohama Nanbu Hospital Yokohama Japan

Abstract

AbstractBackgroundFor advanced non‐small cell lung cancer (NSCLC), combination therapies including a PD‐1 inhibitor plus chemotherapy or a PD‐1 inhibitor, CTLA‐4 inhibitor, and chemotherapy are standard first‐line options. However, data directly comparing these regimens are lacking. This study compared the efficacy of pembrolizumab plus chemotherapy (CP) against nivolumab plus ipilimumab and chemotherapy (CNI) in a real‐world setting.MethodsIn this multicenter retrospective study, we compared the efficacy and safety of CP and CNI as first‐line therapies in 182 patients with stage IIIB–IV NSCLC. Primary outcomes were overall survival (OS) and progression‐free survival (PFS), while secondary outcomes included the response rate (RR) and safety profiles. Kaplan–Meier survival curves and Cox proportional hazards models were utilized for data analysis, adjusting for confounding factors such as age, gender, and PD‐L1 expression.ResultsIn this study, 160 patients received CP, while 22 received CNI. The CP group was associated with significantly better PFS than the CNI group (median 11.7 vs. 6.6 months, HR 0.56, p = 0.03). This PFS advantage persisted after propensity score matching to adjust for imbalances. No significant OS differences were observed. Grade 3–4 adverse events occurred comparably, but immune‐related adverse events were numerically more frequent in the CNI group.ConclusionsIn real‐world practice, CP demonstrated superior PFS compared with CNI. These findings can inform treatment selection in advanced NSCLC.

Publisher

Wiley

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