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Diabetologia

, Volume 60, Issue 12, pp 2538–2539 | Cite as

Cancer risk in the EMPA-REG OUTCOME trial. Reply to Shaikh AMY [letter] and Kohler S, Lee J, George JT et al [letter]

  • Huilin Tang
  • Jiali Han
  • Yiqing Song
Letter

Keywords

Bladder cancer Empagliflozin SGLT2 inhibitors 

Abbreviations

FDA

Food and Drug Administration

SGLT2

Sodium–glucose cotransporter 2

To the Editor: We strongly but respectfully disagree with the letter by Dr. Shaikh [1] regarding an issue with the reporting of the number of cases of bladder cancer from the EMPA-REG OUTCOME Trial [2] in our meta-analysis of sodium–glucose cotransporter 2 (SGLT2) inhibitors and risk of cancer [3]. Since 2007, Section 801 of the Food and Drug Administration (FDA) Amendments Act (FDAAA) requires the submission of summary results, including adverse events for clinical trials of FDA-regulated drugs, to the ClinicalTrials.gov databank (www.ClinicalTrials.gov) [4]. As stated in our article, ‘If cancer events were not reported in the manuscripts, data from regulatory submissions or the ‘Serious adverse events’ section on ClinicalTrials.gov were extracted’ [3]. Our study included only confirmed cases of bladder cancer, classified as ‘bladder cancer’, ‘bladder cancer transitional cell carcinoma’ and ‘bladder cancer recurrent’, which were identified according to the Medical Dictionary for Regulatory Activities (MedDRA) (such information was also presented in electronic supplementary material (ESM) Table 2 of our article) [3]. Hence, the number of incident cases of bladder cancer in our article was correctly extracted from ClinicalTrials.gov, with the current database for the EMPA-REG OUTCOME Trial (ClinicalTrial.gov registration no. NCT01131676, accessed 9 August 2017) still showing six cases of bladder cancer, two cases of bladder transitional cell carcinoma, and one recurrent case of bladder cancer in the empagliflozin groups, and zero cases in the placebo group (Table 1).
Table 1

Bladder cancer in EMPA-REG OUTCOME Trial

Classification

Placebo

Empagliflozin 10 mg

Empagliflozin 25 mg

Bladder cancer n/N (%)

0/2333 (0.00)

1/2345 (0.04)

5/2342 (0.21)

Bladder cancer recurrent n/N (%)

0/2333 (0.00)

0/2345 (0.00)

1/2342 (0.04)

Bladder transitional cell carcinoma n/N (%)

0/2333 (0.00)

1/2345 (0.04)

1/2342 (0.04)

Data obtained from www.ClinicalTrials.gov (accessed 9 August 2017), which was last updated and verified 7 April 2016

We appreciate the updated data from the US FDA provided by Dr. Shaikh [1], which is also highlighted in a second letter by Kohler et al [5], although the crude comparisons of case numbers made in this second letter could be misleading owing to the small sample size [5]. Even based on the intention-to-treat data or on-treatment data sets provided by Kohler and colleagues [5], we still observed a non-significant trend towards increased risk of bladder cancer in the pooled empagliflozin groups compared with the placebo groups; the relative risks were 1.20 (95% CI 0.42, 3.40) for the intention-to-treat data set and 1.83 (95% CI 0.51, 6.56) for the on-treatment data set. In addition, we feel it is important to note that the actual number of confirmed cancer cases would continue to accumulate during an extended post-trial period of the EMPA-REG OUTCOME Trial. However, given that participants in this trial were no longer receiving randomly assigned treatments, a crude comparison of accrued case numbers on an intention-to-treat basis tends to lead to a biased and incorrect estimate of drug effect owing to potential bias and confounding. Hence, we stand by our statement that ‘there is some evidence suggesting that SGLT2 inhibitors (especially empagliflozin) might increase risk of bladder cancer’, rather than conclusive evidence demonstrating a causal relationship. Given the rapidly increasing use of SGLT2 inhibitors, future large long-term randomised trials, post-trial observational studies and real-world evidence are required to monitor the long-term safety of SGLT2 inhibitors regarding the risk of specific cancer types, especially bladder cancer.

Notes

Acknowledgements

The authors would like to thank Q. Dai from the Department of Medicine, School of Medicine, Vanderbilt University, USA, and W. Shi and S. Zhai from the Department of Pharmacy, Peking University Third Hospital, China, who contributed to the previous study.

Funding

YS was supported by the Indiana University Health–Indiana University School of Medicine Strategic Research Initiative.

Duality of interest

The authors declare that there is no duality of interest associated with this manuscript.

Contribution statement

All authors contributed to data interpretation, drafted the report, and critically reviewed the report. All authors approved the final version of the manuscript.

References

  1. 1.
    Shaikh AMY (2017) SGLT2 inhibitors and cancer: why further evidence is required. Diabetologia  https://doi.org/10.1007/s00125-017-4434-9
  2. 2.
    Zinman B, Wanner C, Lachin JM et al (2015) Empagliflozin, cardiovascular outcomes, and mortality in type 2 diabetes. N Engl J Med 373:2117–2128CrossRefPubMedGoogle Scholar
  3. 3.
    Tang H, Dai Q, Shi W, Zhai S, Song Y, Han J (2017) SGLT2 inhibitors and risk of cancer in type 2 diabetes: a systematic review and meta-analysis of randomised controlled trials. Diabetologia  https://doi.org/10.1007/s00125-017-4370-8
  4. 4.
    US Food and Drug Administration (2007) Food and Drug Administration Amendments Act of 2007. Public Law 110-85. Available from www.gpo.gov/fdsys/pkg/PLAW-110publ85/pdf/PLAW-110publ85.pdf. Accessed 12 August 2017
  5. 5.
    Kohler S, Lee J, George JT, Inzucchi SE, Zinman B (2017) Bladder cancer in the EMPA-REG OUTCOME trial. Diabetologia  https://doi.org/10.1007/s00125-017-4430-0

Copyright information

© Springer-Verlag GmbH Germany 2017

Authors and Affiliations

  1. 1.Department of Epidemiology, Richard M. Fairbanks School of Public HealthIndiana UniversityIndianapolisUSA
  2. 2.Melvin and Bren Simon Cancer CenterIndiana UniversityIndianapolisUSA

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