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单倍体相合供者血液或骨髓移植治疗骨髓增生异常/骨髓增殖性重叠肿瘤:一项北美合作的结果

Haploidentical Donor Blood or Marrow Transplantation for Myelodysplastic/Myeloproliferative Overlap Neoplasms: Results from a North American Collaboration.

作者信息

Jain Tania, Tsai Hua-Ling, Elmariah Hany, Vachhani Pankit, Karantanos Theodoros, Wall Sarah, Gondek Lukasz, Bashey Asad, Keyzner Alla, Tamari Roni, Grunwald Michael, Abedin Sameem, Nadiminti Kalyan, Iqbal Madiha, Gerds Aaron, Viswabandya Auro, McCurdy Shannon, Malki Monzr Al, Varadhan Ravi, Ali Haris, Gupta Vikas, Jones Richard John, Otoukesh Salman

机构信息

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University.

The Johns Hopkins University.

出版信息

Res Sq. 2023 Mar 21:rs.3.rs-2691216. doi: 10.21203/rs.3.rs-2691216/v1.

Abstract

Haploidentical donors offer a potentially readily available donor, especially for non-White patients, for blood or marrow transplantation (BMT). In this collaboration across North America, we retrospectively analyzed outcomes of first BMT using haploidentical donor and posttransplantation cyclophosphamide (PTCy) in MDS/MPN-overlap neoplasms (MDS/MPN), an otherwise incurable hematological neoplasm. We included 120 patients, 38% of non-White/Caucasian ethnicity, across 15 centers with median age at BMT 62.5 years. The median follow-up is 2.4 years. Graft failure was reported in 6% patients. At 3-years, nonrelapse mortality (NRM) was 25%, relapse 27%, grade 3-4 acute graft versus host disease (GVHD) 12%, chronic GVHD requiring systemic immunosuppression 14%, progression-free survival (PFS) 48% and overall survival (OS) 56%. On multivariable analysis, statistically significant associations included older age at BMT (per decade increment) with NRM (sdHR 3.28, 95%CI 1.30-8.25), PFS (HR 1.98, 95% 1.13-3.45) and OS (HR 2.01, 95% CI 1.11-3.63), presence of mutation in EZH2/RUNX1/SETBP1 with relapse (sdHR 2.61, 95%CI 1.06-6.44), and splenomegaly at BMT/prior splenectomy with OS (HR 2.20, 95%CI 1.04-4.65). Haploidentical donors are a viable option for BMT in MDS/MPN, especially for those disproportionately represented in the unrelated donor registry. Disease-related factors including splenomegaly and high-risk mutations dominate outcomes following BMT.

摘要

单倍体相合供者为血液或骨髓移植(BMT)提供了一个潜在的随时可用的供者,尤其是对于非白人患者。在北美各地的这项合作中,我们回顾性分析了使用单倍体相合供者和移植后环磷酰胺(PTCy)进行首次BMT治疗骨髓增生异常综合征/骨髓增殖性肿瘤(MDS/MPN)重叠肿瘤(一种无法治愈的血液肿瘤)的结果。我们纳入了120例患者,其中38%为非白人/白种人,分布在15个中心,BMT时的中位年龄为62.5岁。中位随访时间为2.4年。6%的患者报告有移植物失败。3年时,非复发死亡率(NRM)为25%,复发率为27%,3-4级急性移植物抗宿主病(GVHD)为12%,需要全身免疫抑制的慢性GVHD为14%,无进展生存期(PFS)为48%,总生存期(OS)为56%。多变量分析显示,具有统计学意义的关联包括BMT时年龄较大(每增加十岁)与NRM(标准化危险比3.28,95%置信区间1.30-8.25)、PFS(危险比1.98,95% 1.13-3.45)和OS(危险比2.01,95%置信区间1.11-3.63),EZH2/RUNX1/SETBP1存在突变与复发(标准化危险比2.61,95%置信区间1.06-6.44),以及BMT时脾肿大/既往脾切除术与OS(危险比2.20,95%置信区间1.04-4.65)。单倍体相合供者是MDS/MPN患者进行BMT的一个可行选择,特别是对于那些在无关供者登记处占比过高的患者。包括脾肿大和高危突变在内的疾病相关因素在BMT后的预后中起主导作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b44/10055643/0a94b0108a4d/nihpp-rs2691216v1-f0001.jpg

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