Gemcitabine plus nab‐paclitaxel for pancreatic cancer and interstitial lung disease: A nationwide longitudinal study

Author:

Saito Kei12,Michihata Nobuaki3,Hamada Tsuyoshi14ORCID,Jo Taisuke35,Matsui Hiroki6,Fushimi Kiyohide7,Nakai Yousuke18,Yasunaga Hideo6,Fujishiro Mitsuhiro1ORCID

Affiliation:

1. Department of Gastroenterology, Graduate School of Medicine The University of Tokyo Tokyo Japan

2. Division of Gastroenterology and Hepatology, Department of Internal Medicine Nihon University School of Medicine Tokyo Japan

3. Department of Health Services Research, Graduate School of Medicine The University of Tokyo Tokyo Japan

4. Department of Hepato‐Biliary‐Pancreatic Medicine The Cancer Institute Hospital of Japanese Foundation for Cancer Research Tokyo Japan

5. Department of Respiratory Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan

6. Department of Clinical Epidemiology and Health Economics, School of Public Health The University of Tokyo Tokyo Japan

7. Department of Health Informatics and Policy, Graduate School of Medicine Tokyo Medical and Dental University Tokyo Japan

8. Department of Endoscopy and Endoscopic Surgery The University of Tokyo Hospital Tokyo Japan

Abstract

AbstractInterstitial lung disease (ILD) is an adverse event associated with gemcitabine administration. Gemcitabine plus nab‐paclitaxel, which is now a first‐line chemotherapy regimen for pancreatic cancer (PC), may increase the risk of ILD; however, large‐scale clinical data on this are limited. Thus, this study aimed to elucidate the incidence and risk factors of ILD in patients with PC receiving gemcitabine plus nab‐paclitaxel. Through the Diagnosis Procedure Combination database, a Japanese nationwide inpatient database with outpatient data, we identified consecutive patients with PC who received gemcitabine‐based chemotherapy between July 2010 and March 2019 at 205 hospitals. Competing‐risk analysis was used to examine the cumulative incidence and risk factors of ILD. Among the 6163 patients who received gemcitabine plus nab‐paclitaxel, we documented 168 patients (2.7%) who developed ILD with cumulative incidence rates (95% confidence intervals [CIs]) of 2.0% (1.6%–2.4%), 2.7% (2.2%–3.1%), and 3.1% (2.6%–3.6%) at 3, 6, and 12 months, respectively. Compared with patients with PC who received gemcitabine monotherapy, those who received gemcitabine plus nab‐paclitaxel had an adjusted subdistribution hazard ratio (SHR) for ILD of 1.93 (95% CI: 1.51–2.47). Older age was associated with a high risk of ILD in patients receiving gemcitabine plus nab‐paclitaxel (adjusted SHR comparing ≥75 to ≤74 years, 1.61; 95% CI: 1.16–2.24). In conclusion, this study demonstrated the clinical course of gemcitabine plus nab‐paclitaxel‐associated ILD in patients with PC. When gemcitabine plus nab‐paclitaxel is administered to elderly patients with PC, symptoms associated with ILD must be monitored.

Funder

Japan Society for the Promotion of Science

Taiho Pharmaceutical

Takeda Science Foundation

Publisher

Wiley

Subject

Cancer Research,Oncology,General Medicine

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