Concomitant Proton Pump Inhibitor Use With Pembrolizumab Monotherapy vs Immune Checkpoint Inhibitor Plus Chemotherapy in Patients With Non−Small Cell Lung Cancer

Author:

Kawachi Hayato1,Yamada Tadaaki1,Tamiya Motohiro2,Negi Yoshiki3,Goto Yasuhiro4,Nakao Akira5,Shiotsu Shinsuke6,Tanimura Keiko7,Takeda Takayuki7,Okada Asuka8,Harada Taishi9,Date Koji10,Chihara Yusuke11,Hasegawa Isao12,Tamiya Nobuyo13,Ishida Masaki1,Katayama Yuki1,Morimoto Kenji1,Iwasaku Masahiro1,Tokuda Shinsaku1,Kijima Takashi3,Takayama Koichi1

Affiliation:

1. Department of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan

2. Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan

3. Department of Respiratory Medicine and Hematology, School of Medicine, Hyogo Medical University, Nishinomiya, Hyogo, Japan

4. Department of Respiratory Medicine, Fujita Health University School of Medicine, Toyoake, Aichi, Japan

5. Department of Respiratory Medicine, Fukuoka University Hospital, Nanakuma, Fukuoka, Japan

6. Department of Respiratory Medicine, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, Japan

7. Department of Respiratory Medicine, Japanese Red Cross Kyoto Daini Hospital, Kyoto, Japan

8. Department of Respiratory Medicine, Saiseikai Suita Hospital, Suita, Osaka, Japan

9. Department of Medical Oncology, Fukuchiyama City Hospital, Fukuchiyama, Kyoto, Japan

10. Department of Pulmonary Medicine, Kyoto Chubu Medical Center, Nantan, Kyoto, Japan

11. Department of Respiratory Medicine, Uji-Tokushukai Medical Center, Uji, Kyoto, Japan

12. Department of Respiratory Medicine, Saiseikai Shigaken Hospital, Rittou, Shiga, Japan

13. Department of Respiratory Medicine, Rakuwakai Otowa Hospital, Kyoto, Japan

Abstract

ImportanceImmune checkpoint inhibitor (ICI) monotherapy with pembrolizumab and ICI plus chemotherapy have been approved as first-line treatments for non–small cell lung cancer (NSCLC) for patients with a programmed cell death ligand–1 (PD-L1) tumor proportion score (TPS) of 50% or more, but the choice between these 2 therapeutic options is unclear.ObjectiveTo clarify the association of a history of concurrent medication use with treatment outcomes for ICIs with or without chemotherapy in patients with NSCLC with a high PD-L1 TPS and to determine whether these clinical histories are biomarkers for appropriate treatment selection.Design, Setting, and ParticipantsThis retrospective, multicenter cohort study at 13 hospitals in Japan included patients with advanced NSCLC with a PD-L1 TPS of 50% or more who had received pembrolizumab ICI monotherapy or ICI plus chemotherapy as the initial treatment between March 2017 and December 2020. The median (IQR) follow-up duration was 18.5 (9.2-31.2) months. Data were analyzed from April 2022 through May 2023.ExposureICI monotherapy with pembrolizumab or ICI plus chemotherapy as first-line treatment.Main Outcomes and MeasuresThe primary analysis was the association of treatment outcomes with baseline patient characteristics, including concomitant drug history, after propensity score matching. Cox proportional hazard models were used to determine the associations of patient characteristics with survival outcomes. Logistic regression analysis was used to determine the association of concomitant medication history with treatment outcomes and other patient characteristics.ResultsA total of 425 patients with NSCLC were enrolled in the study including 271 patients (median [range] age, 72 [43-90] years; 215 [79%] men) who were treated with pembrolizumab monotherapy as the first-line treatment and 154 patients (median [range] age, 69 [36-86] years; 121 [79%] men) who were treated with ICI plus chemotherapy as the first-line treatment. In multivariable analysis, a history of proton pump inhibitor (PPI) use was independently associated with shorter progression-free survival (PFS) in the pembrolizumab monotherapy group (hazard ratio [HR], 1.38; 95% CI, 1.00-1.91; P = .048), but not in the ICI plus chemotherapy group. In patients with a PPI history, both the median (IQR) PFS (19.3 [9.0 to not reached] months vs 5.7 [2.4 to 15.2] months; HR, 0.38; 95% CI, 0.20-0.72; P = .002) and the median (IQR) overall survival (not reached [9.0 months to not reached) vs 18.4 [10.5 to 50.0] months; HR, 0.43; 95% CI, 0.20-0.92; P = .03) were significantly longer in the ICI plus chemotherapy group than in the pembrolizumab monotherapy group. In patients without a history of PPI use, both the median (IQR) PFS (18.8 months [6.6 months to not reached] vs 10.6 months [2.7 months to not reached]; HR, 0.81; 95% CI, 0.56-1.17; P = .26) and the median (IQR) overall survival (not reached [12.6 months to not reached] vs 29.9 [13.3 to 54.3] months, HR, 0.75; 95% CI, 0.48-1.18; P = .21) did not differ between groups.Conclusions and RelevanceThis cohort study found that a history of PPI use could be an important clinical factor in treatment decision-making for patients with NSCLC with a PD-L1 TPS of 50% or more.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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