Theerin Lanamtieng, Chantana Polprasert, Pimjai Niparuck, Phatsorn Choksomnuk, Thanawat Rattanathammethee, Wasithep Limvorapitak, Kannadit Prayongratana, Rattapan Lamool, Archrob Khuhapinant, Weerapat Owattanapanich, Pisa Phiphitaporn, Kanchana Chansung, Suporn Chuncharunee
Hypomethylating agents (HMAs) are the standard of care for higher-risk myelodysplastic syndromes (MDSs); however, their accessibility remains limited. This retrospective multicenter cohort study aimed to evaluate the real-world overall survival (OS) of HMAs compared to best-available treatments (BATs) in newly diagnosed higher-risk MDS in Thailand. Higher-risk MDS was defined by a Revised International Prognostic Scoring System (IPSS-R) score > 3.5. Data were extracted from the MDS registry of multicenter hospitals in Thailand from 2013 to 2023. Patients who underwent hematopoietic stem cell transplantation were excluded. A total of 155 patients were included, with a median age of 70 years and a male predominance. The median follow-up time was 36 months. Of these, 86 patients (55.5%) received BATs, while 69 patients (44.5%) were treated with HMAs. HMAs were found to significantly improve OS compared to BATs (log-rank test: p = 0.03), with a median OS of 15 months versus 6 months, respectively. Multivariable Cox regression analysis revealed that HMAs were associated with a decreased risk of death (hazard ratio: 0.58, 95% CI, 0.38-0.89, p = 0.01), while age and high- and very high-risk IPSS-R were identified as poor prognostic factors. This study underscores the real-world effectiveness of HMAs for higher-risk MDS in Thailand.