ORCID
0000-0002-8163-0527 (Carbone)
Document Type
Article
Publication Date
2026
DOI
10.1016/j.jacadv.2026.102790
Publication Title
JACC: Advances
Volume
5
Issue
6
Pages
102790
Abstract
Background
According to available evidence, sodium-glucose cotransporter-2 inhibitors (SGLT2i) may confer cardioprotection in patients with cancer undergoing chemotherapy.
Objectives
The objective of the study was to evaluate the impact of SGLT2i on all-cause mortality and heart failure (HF) outcomes in this population.
Methods
We searched PubMed, Cochrane CENTRAL, and Embase through August 2025 for studies of SGLT2i in adult patients with cancer. Random-effects models were used to pool effects for all-cause mortality and an HF composite (new-onset HF and/or HF hospitalization) in cancer patients >18 years. Meta-regression tested effect modification by beta-blockers, statins, angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, age, and sex.
Results
Thirteen observational studies were included, for a total of 107,126 patients. The median age was 67.6 years (IQR: 62.5-71.0); median follow-up was 24 months (IQR: 19.2-29.0), nearly all patients had diabetes mellitus. SGLT2i were associated with lower all-cause mortality (risk ratio [RR]: 0.47; 95% CI: 0.38-0.58; I² = 96.30%; P < 0.001), with no effect modification by background therapies, age, or sex (all P > 0.05). The HF composite was also significantly reduced (RR: 0.48; 95% CI: 0.29-0.78; I² = 87.01%), again with no evidence that background therapies modified the effect (all P > 0.05). Risk of atrial fibrillation/atrial flutter was lower with SGLT2i (RR: 0.57; 95% CI: 0.42-0.76; I² = 66.4%; P < 0.001). Safety outcomes were not increased in the SGLT2i arm.
Conclusions
In patients with cancer, SGLT2i appear safe and are associated with fewer deaths and HF events, although substantial heterogeneity was observed across studies. Randomized controlled trials are warranted to confirm these hypothesis-generating findings.
Rights
© 2026 The Authors.
This is an open access article under the Creative Commons Attribution 4.0 International (CC BY 4.0) License.
Original Publication Citation
Spadafora, L., Bernardi, M., Sarto, G., Simeone, B., Rocco, E., Carbone, S., Dalla Vecchia, L. A., Pedretti, R. F. E., Valenti, V., Di Mario, R., Forte, M., Frati, G., Abbate, A., Golino, M., Versaci, F., Peruzzi, M., Sabouret, P., Biondi Zoccai, G., & Sciarretta, S. (2026). SGLT2 inhibitors in cardio-oncology: A systematic review and meta-analysis. JACC: Advances, 5(6), Article 102790. https://doi.org/10.1016/j.jacadv.2026.102790
Repository Citation
Spadafora, L., Bernardi, M., Sarto, G., Simeone, B., Rocco, E., Carbone, S., Dalla Vecchia, L. A., Pedretti, R. F. E., Valenti, V., Di Mario, R., Forte, M., Frati, G., Abbate, A., Golino, M., Versaci, F., Peruzzi, M., Sabouret, P., Biondi Zoccai, G., & Sciarretta, S. (2026). SGLT2 inhibitors in cardio-oncology: A systematic review and meta-analysis. JACC: Advances, 5(6), Article 102790. https://doi.org/10.1016/j.jacadv.2026.102790
Supplementary Material