First-line immune checkpoint inhibitors alone or in combination with chemotherapy in real-life elderly patients with advanced non-small cell lung cancer (NEJ057).

Authors

null

Mao Uematsu

Department of Thoracic Oncology and Respiratory Medicine, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan

Mao Uematsu , Yoko Tsukita , Takehiro Tozuka , Kohei Kushiro , Shinobu Hosokawa , Toshiyuki Sumi , Osamu Honjo , Ou Yamaguchi , Tetsuhiko Asao , Jun Sugisaka , Go Saito , Jun Shiihara , Ryo Morita , Seigo Katakura , Takehiro Yasuda , Kakeru Hisakane , Eisaku Miyauchi , Satoshi Morita , Kunihiko Kobayashi , Hajime Asahina

Organizations

Department of Thoracic Oncology and Respiratory Medicine, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan, Department of Respiratory Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan, Department of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan, Department of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan, Department of Respiratory Medicine, Japanese Red Cross Okayama Hospital, Okayama-Shi Kita-Ku, Japan, Department of Respiratory Medicine, Hakodate Goryoukaku Hospital, Hakodate, Japan, Department of Respiratory Medicine, Sapporo Minami-Sanjo Hospital, Sapporo, Japan, Department of Respiratory Medicine, Saiatama Medical University International Medical Center, Hidaka-Shi, Japan, Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan, Department of Pulmonary Medicine, Sendai Kousei Hospital, Sendai, Japan, Department of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan, Department of Respiratory Medicine, Jichi Medical University Saitama Medical Center, Saitama, Japan, Department of Respiratory Medicine, Akita Kousei Medical Center, Akita, Japan, Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan, Department of Respieatory Medicine, Yokosuka Kyosai Hospital, Yokosuka, Japan, Department of Pulmonary Medicine and Medical Oncology, Nippon Medical School Tamanagayama Hospital, Tama, Japan, Department of Biomedical Statistics and Bioinformatics, Kyoto University Graduate School of Medicine, Kyoto, Japan, Department of Pulmonary Medicine, Saitama Medical University International Medical Center, Hidaka, Japan, Department of Respiratory Medicine, Hokkaido University Graduate School of Medicine, Sapporo, Japan

Research Funding

No funding received
None.

Background: Immune checkpoint inhibitor (ICI) plus chemotherapy is now a standard treatment for non-small cell lung cancer (NSCLC) without targetable oncogene alternations. However, the efficacy and safety of ICI plus chemotherapy (ICI-chemo) in 75 years or older patients have not been elucidated. The aim of this study is to reveal the real-world choice of first-line drugs in elderly patients (pts) and evaluate the efficacy and safety of ICI-chemo. Methods: We conducted a multicenter (58 centers in Japan), retrospective cohort study of consecutive 75 years or older pts with clinical stage IIIB, IIIC, IV, postoperative or radiotherapy recurrent NSCLC who started first-line systemic therapy between December 2018 and March 2021. Pts with epidermal growth factor receptor mutations, anaplastic lymphoma kinase rearrangements, or whose first-line systemic therapy was molecular targeted therapy were excluded. Results: A total of 1245 pts were enrolled: median (range) age 78 (75-95) years; 278 (22%) female; 367 (29%) ECOG PS 0, 680 (55%) PS 1 and 171 (14%) PS 2; 678 (54%) adenocarcinoma; PD-L1 tumor proportion score 268 (22%) <1%, 387 (31%) 1-49% and 410 (34%) ≥50%; 354 (28%) ICI-chemo, 425 (34%) ICI alone, 311 (25%) platinum-doublet chemotherapy and 155 (12%) single agent chemotherapy. The median overall survival (OS) was 20.0 months (95%CI, 17.1–23.6) in the ICI-chemo group, 19.8 months (95%CI, 16.5–23.8) in the ICI alone group, 12.8 months (95%CI, 10.7–15.6) in the platinum-doublet chemotherapy group and 9.5 months (95%CI, 7.4–13.4) in the single agent chemotherapy group, respectively. After propensity score matching, there was no difference in OS and progression-free survival (PFS) between ICI-chemo group (n=96) and ICI alone group (n=95) in PD-L1 ≥1% (OS: HR, 0.98; 95% CI, 0.67-1.42, PFS: HR, 0.92; 95% CI, 0.67-1.25). Regardless of PD-L1 subgroups (1-49% or ≥50%), no significant differences in OS and PFS were observed. Concerning safety, Grade 3 or higher immune-related adverse events (irAEs) occurred in 86 pts (24.3%) in the ICI-chemo group and 76 pts (17.9%) in the ICI alone group (p = 0.03). The number of pts who required steroids for irAEs was 115 (32.5%) in the ICI-chemo group and 105 (24.7%) in the ICI alone group (p = 0.02). Pneumonitis was reported in 83 pts (23.4%) in the ICI-chemo group and 66 pts (15.6%) in the ICI alone group (p = 0.006). Conclusions: In real-world data for pts aged 75 years or older, ICI-chemo did not improve survival and increased the incidence of grade 3 or higher irAEs compared to ICI alone. Based on our results, ICI alone is recommended for elderly pts with PD-L1 positive NSCLC. Clinical trial information: UMIN000046700.

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Abstract Details

Meeting

2023 ASCO Annual Meeting

Session Type

Rapid Oral Abstract Session

Session Title

Lung Cancer

Track

Lung Cancer

Sub Track

Metastatic Non–Small Cell Lung Cancer

Clinical Trial Registration Number

UMIN000046700

Citation

J Clin Oncol 41, 2023 (suppl 16; abstr 9012)

DOI

10.1200/JCO.2023.41.16_suppl.9012

Abstract #

9012

Abstract Disclosures

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