Real-world cost-effectiveness of sequential therapy of in-class transition to ixazomib versus daratumumab for transplant-ineligible newly diagnosed multiple myeloma in China
Publication: Journal of Comparative Effectiveness Research
Abstract
Aim: Expanding treatment options for transplant-ineligible newly diagnosed multiple myeloma (ndMM) in China has increased the need to identify treatment strategies that improve patient outcomes while using healthcare resources efficiently. This study evaluated the cost-effectiveness of in-class transition (iCT) to ixazomib, lenalidomide and dexamethasone (IRd) versus daratumumab, lenalidomide and dexamethasone (DRd) for transplant-ineligible ndMM from the perspective of the Chinese healthcare system. Materials & methods: A cost-effectiveness analysis was conducted using a Markov cohort model that simulated lifetime health benefits and medical costs for the two treatment modalities. Model inputs were estimated from best available real-world evidence in the literature and from public data sources. Deterministic, probabilistic and scenario sensitivity analyses were performed to assess uncertainty in model results. Results: In the base-case analysis, iCT IRd was projected to generate 0.580 additional quality-adjusted life years versus DRd (4.724 vs 4.144) and save lifetime medical costs by $7751. One-way sensitivity analysis indicated that cost-effectiveness was driven by uncertainty in model inputs related to treatment discontinuation and subsequent disease progression. Probabilistic sensitivity analysis estimated that iCT IRd had 79.2%, 88.0% and 91.3% probabilities of being cost-effective at willingness-to-pay thresholds of one, two and three-times China’s 2025 gross domestic product per capita per quality-adjusted life year, respectively. Conclusion: Based on best available real-world evidence, the iCT IRd modality could be cost-effective compared with the DRd modality for transplant-ineligible patients with ndMM in China. Future real-world studies are needed to confirm the projected outcomes.
Plain language summary: Comparing the value of an ixazomib-based sequential strategy with antibody-based treatment for newly diagnosed myeloma in China
What is this article about?
Multiple myeloma is an incurable blood cancer. For newly diagnosed patients in China who are not eligible for stem cell transplant, selecting an initial treatment strategy is clinically important and can also affect long-term health outcomes and medical costs. This study used a computer model to simulate lifetime health outcomes and medical costs under the two treatment strategies (started with bortezomib-based induction therapy and followed by maintenance treatment containing oral ixazomib [iCT IRD] versus using daratumumab [DRd] as induction and maintenance treatment) that could be used in real-world clinical practices.
What were the results?
The model projected that iCT IRd could provide more quality-adjusted survival while reducing total medical expenditures over a patient’s lifetime compared with DRd. These projected differences were driven mainly by treatment discontinuation, the risk of disease progression after discontinuation and the later-line treatments.
Why is this important?
This study suggests that for newly diagnosed multiple myeloma patients in China who cannot undergo a stem cell transplant, the iCT IRd strategy could offer a practical alternative to DRd by extending quality-adjusted life expectancy while reducing overall medical costs. These findings provide initial economic evidence that may help health system planners and policymakers evaluate treatment access, though because these conclusions rely on computer modeling and assumptions, future real-world clinical studies will be essential to confirm whether these projected health and cost benefits hold true in actual practice.
Supplementary Material
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References
Papers of special note have been highlighted as: • of interest
1.
Dou X, Duan G, Zhong Y et al. The burden of multiple myeloma in China: trends from 1990 to 2021 and forecasts for 2050. Cancer Lett. 611, 217440 (2025).
2.
Puertas B, Gonzalez-Calle V, Sobejano-Fuertes E et al. Novel agents as main drivers for continued improvement in survival in multiple myeloma. Cancers (Basel) 15(5), 1558 (2023).
3.
Rodriguez-Lobato LG, de Daniel A, Pereira A et al. Attrition rates and treatment outcomes in multiple myeloma: real-world data over a 40-year period. Blood Cancer J. 15(1), 103 (2025).
4.
Maples KT, Scott SA, Lonial S. Novel approaches to the treatment of multiple myeloma. Clin. Adv. Hematol. Oncol. 21(5), 247–256 (2023).
5.
Branch CMDAHP, Branch CMAH. Guidelines for the diagnosis and management of multiple myeloma in China (2024 revision). Zhonghua Nei Ke Za Zhi 63(12), 1186–1195 (2024).
• Provides the most recent Chinese clinical guideline context for multiple myeloma (MM) diagnosis and treatment, including recommended treatment options for transplant-ineligible newly diagnosed MM.
6.
Facon T, Kumar SK, Plesner T et al. Daratumumab, lenalidomide, and dexamethasone versus lenalidomide and dexamethasone alone in newly diagnosed multiple myeloma (MAIA): overall survival results from a randomised, open-label, Phase III trial. Lancet Oncol. 22(11), 1582–1596 (2021).
7.
Tai M-H, Cai Q, Fu AZ, Khare V, Kaila S. Real-world patient characteristics and treatment outcomes among newly diagnosed multiple myeloma patients initiating daratumumab, lenalidomide, and dexamethasone as first-line therapy. Blood 138(Suppl. 1), 1979 (2021).
8.
McCullough KB, Hobbs MA, Abeykoon JP, Kapoor P. Common adverse effects of novel therapies for multiple myeloma (MM) and their management strategies. Curr. Hematol. Malig. Rep. 13(2), 114–124 (2018).
9.
Mikulski D, Kedzior MK, Mirocha G et al. Predictors and profile of severe infectious complications in multiple myeloma patients treated with daratumumab-based regimens: a machine learning model for pneumonia risk. Cancers (Basel) 16(21), 3709 (2024).
10.
Higano CS, Hafron J. Adherence with oral anticancer therapies: clinical trial vs real-world experiences with a focus on prostate cancer. J. Urol. 209(3), 485–493 (2023).
11.
Bullock JM. Barriers to adherence to oral drug regimens in oncology and strategies for improvement. Clin. Adv. Hematol. Oncol. 20(2), 75–77 (2022).
12.
Liu A, Yu H, Hou R et al. Assessment of prolonged proteasome inhibition through ixazomib-based oral regimen on newly diagnosed and first-relapsed multiple myeloma: a real-world Chinese cohort study. Cancer Med. 13(9), e7177 (2024).
• Provides Chinese real-world evidence on ixazomib-based oral therapy following bortezomib-based induction, supporting the clinical relevance of the iCT IRd treatment strategy evaluated in this model.
13.
Facon T, Venner CP, Bahlis NJ et al. Oral ixazomib, lenalidomide, and dexamethasone for transplant-ineligible patients with newly diagnosed multiple myeloma. Blood 137(26), 3616–3628 (2021).
14.
Husereau D, Drummond M, Augustovski F et al. Consolidated Health Economic Evaluation Reporting Standards 2022 (CHEERS 2022) Statement: updated reporting guidance for health economic evaluations. Value Health 25(1), 3–9 (2022).
• Provides the reporting framework used to structure this economic evaluation and ensure transparent presentation of model assumptions, inputs, uncertainty analyses and study findings.
15.
Ball G, Lemieux C, Cameron D, Seftel MD. Cost-effectiveness of brexucabtagene autoleucel versus best supportive care for the treatment of relapsed/refractory mantle cell lymphoma following treatment with a Bruton's tyrosine kinase inhibitor in Canada. Curr. Oncol. 29(3), 2021–2045 (2022).
16.
van de Wetering G, Ignacio T, Dhanda D et al. Modification of treatment-sequence model with a customizable number of treatments to better reflect contemporary and future clinical practice in moderate to severe psoriasis. J. Med. Econ. 25(1), 421–427 (2022).
17.
Briggs A, Claxton K, Sculpher M. Decision Modelling for Health Economic Evaluation. Oxford University Press, UK (2006).
18.
Wu J, Liu GG. China Guidelines for Pharmacoeconomic Evaluations 2025 (Chinese-English Version). China Planning Press, China Market Press, Beijing (2025).
• Provides the China-specific methodological basis for pharmacoeconomic evaluation, including discounting, willingness-to-pay threshold interpretation, and the joint interpretation of base-case and probabilistic sensitivity analyses.
19.
Lu J, Chen W. Cost–effectiveness of lenalidomide plus low-dose dexamethasone for newly diagnosed multiple myeloma patients ineligible for stem cell transplantation in China. J. Comp. Eff. Res. 8(12), 979–992 (2019).
20.
Huang D, Zhu Y, Xiao Y et al. Cost-utility analysis of dexamethasone combined with bortezomib and lenalidomide in the treatment of newly diagnosed multiple myeloma. Chinese Pharmacy 33(16), 2001–2011 (2022).
21.
Xu Y, Xu W, Chen J et al. Quality of life and related factors in patients with multiple myeloma during maintenance treatment. Zhongguo Shi Yan Xue Ye Xue Za Zhi 27(1), 96–103 (2019).
22.
Wu W, Ding S, Mingming Z et al. Cost effectiveness analysis of CAR-T cell therapy for patients with relapsed/refractory multiple myeloma in China. J. Med. Econ. 26(1), 701–709 (2023).
23.
Hu S, Lu J, Feng Y et al. Cost-effectiveness analysis of lenalidomide combined with low-dose dexamethasone for the treatment of relapsed or refractory multiple myeloma. Chinese Medical Insurance (9), 51–57 (2017).
24.
Zeng X, Liu Q, Peng L et al. Cost-effectiveness analysis of adding daratumumab to a regimen of bortezomib, melphalan, and prednisone in newly diagnosed multiple myeloma. Adv. Ther. 38, 2379–2390 (2021).
25.
Suzuki N, Okuyama T, Akechi T et al. Symptoms and health-related quality of life in patients with newly diagnosed multiple myeloma: a multicenter prospective cohort study. Jpn J. Clin. Oncol. 52(2), 163–169 (2022).
26.
Cai H, Zhang L, Li N et al. Cost-effectiveness analysis on binary/triple therapy on the basis of ixazomib or bortezomib for refractory or relapsed multiple myeloma. Leuk. Lymphoma 60(12), 2951–2959 (2019).
27.
Rifkin RM, Girnius SK, Noga SJ et al. In-class transition (iCT) of proteasome inhibitor-based therapy: a community approach to multiple myeloma management. Blood Cancer J. 13(1), 147 (2023).
• Describes the in-class transition concept for proteasome inhibitor-based therapy and provides real-world support for transitioning from injectable to oral proteasome inhibitor-based treatment.
28.
Gordan LN, Tan CR, Vescio R et al. Progression-free survival of daratumumab versus bortezomib triplet combination with lenalidomide and dexamethasone in transplant ineligible patients with newly diagnosed multiple myeloma: TAURUS chart review study. Clin. Lymphoma Myeloma Leuk. 24(1), 55–63 (2024).
29.
Hansen DK, Gautam S, Lafeuille MH et al. Comparison of time to next treatment or death between front-line daratumumab, lenalidomide, and dexamethasone (DRd) and bortezomib, lenalidomide, and dexamethasone (VRd) in transplant ineligible patients with multiple myeloma. Blood 142, 543 (2023).
• Provides real-world evidence on treatment persistence and time to next treatment or death for front-line daratumumab, lenalidomide and dexamethasone (DRd), supporting the real-world parameterization of DRd continuous therapy in the model.
30.
Han X, Jiang X, He J et al. Clinical outcomes of pomalidomide-based and daratumumab-based therapies in patients with relapsed/refractory multiple myeloma: a real-world cohort study in China. Cancer Med. 13(9), e7232 (2024).
31.
Suzuki K, Dimopoulos MA, Takezako N et al. Daratumumab, lenalidomide, and dexamethasone in East Asian patients with relapsed or refractory multiple myeloma: subgroup analyses of the Phase III POLLUX study. Blood Cancer J. 8(4), 41 (2018).
32.
Siebert U, Alagoz O, Bayoumi AM et al. State-transition modeling: a report of the ISPOR-SMDM modeling good research practices task force-3. Value Health 15(6), 812–820 (2012).
33.
Szende A, Janssen B, Cabases J. Self-reported population health: an international perspective based on EQ-5D. In: Self-Reported Population Health: An International Perspective based on EQ-5D. Szende A, Janssen B, Cabases J (Eds). Springer, The Netherlands (2014).
34.
Mateos MV, Nahi H, Legiec W et al. Subcutaneous versus intravenous daratumumab in patients with relapsed or refractory multiple myeloma (COLUMBA): a multicentre, open-label, non-inferiority, randomised, Phase III trial. Lancet Haematol. 7(5), e370–e380 (2020).
• Supports the scenario analysis comparing intravenous and subcutaneous daratumumab by providing evidence of comparable clinical outcomes between administration routes.
35.
Chari A, Romanus D, DasMahapatra P et al. Patient-reported factors in treatment satisfaction in patients with relapsed/refractory multiple myeloma (RRMM). Oncologist 24(11), 1479–1487 (2019).
36.
Zhang L, Heng Y, Hu H. Advances in research on factors affecting adherence to oral chemotherapy drugs in cancer patients. J. Nurses Training 34(5), 422–425 (2019).
37.
Nunnelee J, Cottini F, Zhao Q et al. Early versus late discontinuation of maintenance therapy in multiple myeloma. J. Clin. Med. 11(19), 5794 (2022).
38.
Palumbo A, Chanan-Khan A, Weisel K et al. Daratumumab, bortezomib, and dexamethasone for multiple myeloma. N. Engl. J. Med. 375(8), 754–766 (2016).
39.
Mateos MV, Sonneveld P, Hungria V et al. Daratumumab, bortezomib, and dexamethasone versus bortezomib and dexamethasone in patients with previously treated multiple myeloma: three-year follow-up of CASTOR. Clin. Lymphoma Myeloma Leuk. 20(8), 509–518 (2020).
40.
Kumar SK, Callander NS, Alsina M et al. Multiple myeloma, Version 3.2017, NCCN Clinical Practice Guidelines in Oncology. J. Natl Compr. Canc. Netw. 15(2), 230–269 (2017).
41.
Dimopoulos MA, Moreau P, Terpos E et al. Multiple myeloma: EHA-ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 32(3), 309–322 (2021).
42.
Thomas C, Ailawadhi S, Popat R et al. Treatment preferences of patients with relapsed or refractory multiple myeloma in the United States, United Kingdom, Italy, Germany, France, and Spain: results from a discrete choice experiment. Front. Med. (Lausanne) 10, 1271657 (2023).
43.
Hou J, Jin J, Xu Y et al. Randomized, double-blind, placebo-controlled Phase III study of ixazomib plus lenalidomide-dexamethasone in patients with relapsed/refractory multiple myeloma: China Continuation study. J. Hematol. Oncol. 10(1), 137 (2017).
44.
Sonneveld P, Avet-Loiseau H, Lonial S et al. Treatment of multiple myeloma with high-risk cytogenetics: a consensus of the International Myeloma Working Group. Blood 127(24), 2955–2962 (2016).
45.
Fazeli MS, Pushkarna D, Howarth A et al. Indirect costs of oral versus non-oral therapies in hematologic malignancies: a systematic literature review. Blood 136(Suppl. 1), 30–31 (2020).
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Received: 3 July 2026
Accepted: 28 August 2026
Published online: 13 October 2026
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Real-world cost-effectiveness of sequential therapy of in-class transition to ixazomib versus daratumumab for transplant-ineligible newly diagnosed multiple myeloma in China. (2026) Journal of Comparative Effectiveness Research. DOI: 10.57264/cer-2026-0146
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