Haematologica · 2024
Superior outcomes and high-risk features with carfilzomib, lenalidomide, and dexamethasone combination therapy for patients with relapsed and refractory multiple myeloma: results of the multicenter KMMWP2201 study.
СтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Lee Ji Hyun, Choi Jimin, Min Chang-Ki, Park Sung-Soo, Jo Jae-Cheol, Lee Yoo Jin, Kim Jin Seok, Eom Hyeon-Seok, Jung Jongheon, Moon Joon Ho, Cho Hee Jeong, Lee Myung-Won, Yoon Sung-Soo, Byun Ja Min, Lee Jae Hoon, Lee Je-Jung, Jung Sung-Hoon, Shin Ho-Jin, Kim Do Young, Yi Jun Ho, Lee Seung-Shin, Do Young Rok, Yoon Dok Hyun, Cho Hyungwoo, Lee Won Sik, Lee Ho Sup, Uhm Jieun, Kim Hyo Jung, Jang Hee Ryeong, Kim Sung-Hyun, Kim Kihyun
Аннотация
Carfilzomib, lenalidomide, and dexamethasone (KRd) combination therapy improves the survival of patients with relapsed and/or refractory multiple myeloma (RRMM). Nonetheless, evidence on the use of KRd in Asian populations remains scarce. Accordingly, this study aimed to investigate this regimen's efficacy in a large group of patients. This retrospective study included patients with RRMM who were treated with KRd at 21 centers between February 2018 and October 2020. Overall, 364 patients were included (median age, 63 years). The overall response rate was 90% in response-evaluable patients, including 69% who achieved a very good partial response or deeper responses. With a median follow-up duration of 34.8 months, the median progression-free survival (PFS) was 23.4 months and overall survival (OS) was 59.5 months. Among adverse factors affecting PFS, high-risk cytogenetics, extramedullary disease, and doubling of monoclonal protein within 2-3 months prior to start of KRd treatment significantly decreased PFS and OS in multivariate analyses. Patients who underwent post-KRd stem cell transplantation (i.e., delayed transplant) showed prolonged PFS and OS. Grade 3 or higher adverse events (AE) were observed in 56% of the patients, and non-fatal or fatal AE that resulted in discontinuation of KRd were reported in 7% and 2% of patients, respectively. Cardiovascular toxicity was comparable to that reported in the ASPIRE study. In summary, KRd was effective in a large, real-world cohort of patients with RRMM with long-term follow-up. These findings may further inform treatment choices in the treatment of patients with RRMM.