TY - JOUR
T1 - Cost-Effectiveness Analysis of Initiating Type 2 Diabetes Therapy with a Sodium–Glucose Cotransporter 2 Inhibitor Versus Conventional Therapy in Japan
AU - Igarashi, Ataru
AU - Maruyama-Sakurai, Keiko
AU - Kubota, Anna
AU - Akiyama, Hiroki
AU - Yajima, Toshitaka
AU - Kohsaka, Shun
AU - Miyata, Hiroaki
N1 - Funding Information:
This study, including the journal’s Rapid Service Fee, was supported by the Japan Science and Technology Agency Program on Open Innovation Platform with Enterprises, Research Institute and Academia (JST-OPERA) (grant number, JPMJOP1842) and by AstraZeneca K.K., Osaka, Japan. All named authors meet the International Committee of Medical Journal Editors criteria for authorship, take responsibility for the integrity of the work as a whole, and approved the version of the manuscript to be published. All authors contributed to the study concept and design. AI developed the simulation model. AI and HA drafted the manuscript and all authors critically revised the manuscript for important intellectual content. The final version of the manuscript was approved by all authors. Nicholas D. Smith (EMC K.K.) provided English language editing, which was funded by AstraZeneca K.K. Hiroki Akiyama and Toshitaka Yajima are full-time employees of AstraZeneca K.K. Ataru Igarashi has received lecture/other fees from AstraZeneca K.K., Novartis Pharma K.K., Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., and Sanofi K.K.; and received donation from Takeda Pharmaceutical Company Limited for the endowed laboratory which AI belonged to. Shun Kohsaka has received grants from Daiichi Sankyo Company Limited. And Novartis Pharma K.K.; and lecture/other fees from AstraZeneca K.K., Bayer Yakuhin, Ltd., and Bristol Myers Squibb K.K. Hiroaki Miyata has received grants from Johnson & Johnson, Nipro Corporation, Takeda Pharmaceutical Company Limited, Mitsubishi Tanabe Pharma Corporation; and lecture/other fees from Boehringer Ingelheim GmbH, GE Healthcare Pharma, Astellas Pharma Inc., AstraZeneca K.K., Johnson & Johnson, Chugai Pharmaceutical Co., Ltd., and ROHTO Pharmaceutical Co., Ltd. This article is based on previously conducted studies and does not contain any new studies with human participants or animals performed by any of the authors. All data and parameters used in the present study are available in this article or in the cited articles.
Funding Information:
Hiroki Akiyama and Toshitaka Yajima are full-time employees of AstraZeneca K.K. Ataru Igarashi has received lecture/other fees from AstraZeneca K.K., Novartis Pharma K.K., Novo Nordisk Pharma Ltd., Ono Pharmaceutical Co., Ltd., and Sanofi K.K.; and received donation from Takeda Pharmaceutical Company Limited for the endowed laboratory which AI belonged to. Shun Kohsaka has received grants from Daiichi Sankyo Company Limited. And Novartis Pharma K.K.; and lecture/other fees from AstraZeneca K.K., Bayer Yakuhin, Ltd., and Bristol Myers Squibb K.K. Hiroaki Miyata has received grants from Johnson & Johnson, Nipro Corporation, Takeda Pharmaceutical Company Limited, Mitsubishi Tanabe Pharma Corporation; and lecture/other fees from Boehringer Ingelheim GmbH, GE Healthcare Pharma, Astellas Pharma Inc., AstraZeneca K.K., Johnson & Johnson, Chugai Pharmaceutical Co., Ltd., and ROHTO Pharmaceutical Co., Ltd.
Funding Information:
This study, including the journal’s Rapid Service Fee, was supported by the Japan Science and Technology Agency Program on Open Innovation Platform with Enterprises, Research Institute and Academia (JST-OPERA) (grant number, JPMJOP1842) and by AstraZeneca K.K., Osaka, Japan.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/7
Y1 - 2022/7
N2 - Introduction: Many patients with type 2 diabetes mellitus (T2DM) suffer from complications that impose substantial burdens on prognosis and medical costs. Accumulating evidence has demonstrated the clinical benefit of sodium–glucose cotransporter 2 inhibitors (SGLT2i) on cardiovascular and renal complications. However, the health economic impact of SGLT2i remains unclear. The aim of this study was to evaluate the cost-effectiveness of initiating antidiabetic therapy with an SGLT2i using Japanese real-world data. Methods: We constructed a natural history model incorporating heart failure (HF), myocardial infarction, stroke, chronic kidney disease, and end-stage renal disease (ESRD) as complications. The target population comprised patients with T2DM who newly initiated their first oral glucose-lowering drugs. By using a population-based microsimulation, we estimated the 10-year medical costs in Japanese yen (JPY) and outcomes (hospitalization for/development of complications and quality-adjusted life years [QALY]) for patients who initiated antidiabetic therapy with an SGLT2i or conventional therapy. Sensitivity analyses included a probabilistic sensitivity analysis (PSA) with 1,000,000 iterations. Results: In the base-case analysis, the total medical cost per person was JPY 1,638,806 versus JPY 1,825,033 and the QALYs were 8.732 versus 8.513 for the SGLT2i strategy versus the conventional strategy, respectively. Thus, initiating treatment with an SGLT2i was dominant, more effective (QALY gain), and lower cost. When treating 10,000 patients, the SGLT2i strategy would reduce all-cause deaths by 410 (552 vs 962), HF events by 201 (897 vs 1098), and ESRD events by 16 (16 vs 32) versus the conventional strategy. The PSA revealed that the probability of dominance for initiating SGLT2i therapy was 90.5%, demonstrating the robustness of the results. Conclusion: Our results suggest that initiating T2DM treatment with SGLT2i, aimed at managing cardiovascular and renal complications from the early stages of diabetes, can improve the clinical outcome and reduce cost burden of T2DM.
AB - Introduction: Many patients with type 2 diabetes mellitus (T2DM) suffer from complications that impose substantial burdens on prognosis and medical costs. Accumulating evidence has demonstrated the clinical benefit of sodium–glucose cotransporter 2 inhibitors (SGLT2i) on cardiovascular and renal complications. However, the health economic impact of SGLT2i remains unclear. The aim of this study was to evaluate the cost-effectiveness of initiating antidiabetic therapy with an SGLT2i using Japanese real-world data. Methods: We constructed a natural history model incorporating heart failure (HF), myocardial infarction, stroke, chronic kidney disease, and end-stage renal disease (ESRD) as complications. The target population comprised patients with T2DM who newly initiated their first oral glucose-lowering drugs. By using a population-based microsimulation, we estimated the 10-year medical costs in Japanese yen (JPY) and outcomes (hospitalization for/development of complications and quality-adjusted life years [QALY]) for patients who initiated antidiabetic therapy with an SGLT2i or conventional therapy. Sensitivity analyses included a probabilistic sensitivity analysis (PSA) with 1,000,000 iterations. Results: In the base-case analysis, the total medical cost per person was JPY 1,638,806 versus JPY 1,825,033 and the QALYs were 8.732 versus 8.513 for the SGLT2i strategy versus the conventional strategy, respectively. Thus, initiating treatment with an SGLT2i was dominant, more effective (QALY gain), and lower cost. When treating 10,000 patients, the SGLT2i strategy would reduce all-cause deaths by 410 (552 vs 962), HF events by 201 (897 vs 1098), and ESRD events by 16 (16 vs 32) versus the conventional strategy. The PSA revealed that the probability of dominance for initiating SGLT2i therapy was 90.5%, demonstrating the robustness of the results. Conclusion: Our results suggest that initiating T2DM treatment with SGLT2i, aimed at managing cardiovascular and renal complications from the early stages of diabetes, can improve the clinical outcome and reduce cost burden of T2DM.
KW - Cost-effectiveness
KW - Diabetic complications
KW - SGLT2 inhibitor
KW - Type 2 diabetes mellitus
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U2 - 10.1007/s13300-022-01270-8
DO - 10.1007/s13300-022-01270-8
M3 - Article
AN - SCOPUS:85132101197
SN - 1869-6953
VL - 13
SP - 1367
EP - 1381
JO - Diabetes Therapy
JF - Diabetes Therapy
IS - 7
ER -