Abstract

Objective: Sodium-glucose cotransporter (SGLT) 2 inhibitors are expected to demonstrate secondary effects against malignancy. However, long-term and large-scale data are required to evaluate the effects of SGLT2 inhibitors on malignancy, which has not been sufficiently studied in clinical practice. This study aimed to evaluate the association between SGLT2 inhibitors and malignancy using the spontaneous adverse reaction database.
Materials and methods: The United States Food and Drug Administration Adverse Event Reporting System database between 1997 (4Q) and 2020 (2Q) was used in this study. Reporting odds ratio (ROR) was selected as the safety-signaling measure. An inverse signal suggesting potential alternative therapeutic opportunities was defined when the upper limit of 95% confidence interval (CI) was < 1. The association between SGLT2 inhibitors and malignancies was evaluated.
Results: The total number of reports in the database during the study period was 13,106,455. SGLT2 inhibitors showed significant associations with pancreatic cancer (ROR: 3.08. 95% CI: 2.68 – 3.55), and kidney cancer (ROR: 1.39. 95% CI: 1.13 – 1.72). SGLT2 inhibitors showed significant inverse associations with breast cancer (ROR: 0.32. 95% CI: 0.27 – 0.39), lung cancer (ROR: 0.47. 95% CI: 0.37 – 0.59), liver cancer (ROR: 0.68. 95% CI: 0.50 – 0.93), and malignant melanoma (ROR: 0.49. 95% CI: 0.34 – 0.70).
Conclusion: SGLT2 inhibitors may increase the incidence of pancreatic cancer and kidney cancer, and decrease the incidence of breast cancer, lung cancer, liver cancer, and malignant melanoma. These associations need to be further examined in other clinical studies and research in the future.

Author Details

Authors

• Ryo Inose
• Yuichi Muraki

Departments

• Laboratory of Clinical Pharmacoepidemiology, Kyoto Pharmaceutical University, Yamashina-ku, Kyoto-shi, Kyoto, Japan

Address

Ryo Inose, PhD
Laboratory of Clinical Pharmacoepidemiology
Kyoto Pharmaceutical University
5 Misasagi-nakauchi-cho, Yamashina-ku,
Kyoto-shi, Kyoto 607-8414, Japan
Email: [email protected]

Citation