Shahzad Moazzam, Iqbal Qamar, Amin Muhammad Kashif, Irfan Sohaib, Warraich Sarmad Zaman, Anwar Iqra, Dave Prashil, Basharat Ahmad, Hebishy Ahmed, Faisal Muhammad Salman, Jaglal Michael, Mushtaq Muhammad Umair
H. Lee Moffitt Cancer Center, Tampa, FL, United States; University of South Florida, Tampa, FL, United States.
TidalHealth Peninsula Regional, Salisbury, MD, United States.
Leuk Res. 2025 Jan;148:107640. doi: 10.1016/j.leukres.2024.107640. Epub 2024 Dec 19.
Hematopoietic stem cell transplantation (HCT) is a pivotal treatment modality for primary plasma cell leukemia (pPCL). We aimed to examine the outcomes of allogeneic (allo) and autologous (auto) HCT in adult pPCL patients.
Following PRISMA guidelines, a comprehensive literature search was performed on PubMed, Cochrane, Embase, and Clinicaltrials.gov using relevant MeSH terms and keywords. Twelve original articles reporting outcomes of auto-HCT or allo-HCT in adult pPCL patients were included. The pooled analysis was performed using the 'meta' package in the R program (version 4.3.0).
Our analysis included 1757 pPCL patients (1535 with auto-HCT, 222 with allo-HCT), and 49 % were males. The pooled 3 years overall survival (OS), progression-free survival/event-free survival (PFS/EFS), and relapse rate (RR) in auto-HCT were 51 % (95 % CI 0.4-0.61, I=92 %, p = <0.01), 36 % (95 % CI 0.24-0.52, I 2 =97 %, p < 0.01), and 68 % (95 % CI, 0.65-0.71, I2=0 %, p = 0.42), respectively. Among allo-HCT recipients, the reported OS varied from 71 % at 2.3 years to 31 % at 4 years and EFS/PFS from 29 % at 2.5 years to 19 % at 4 years. The pooled treatment-related mortality (TRM) was 12 % (95 % CI 0.05-0.25, I =35 %, p = 0.22) at a median of 6 months. The pooled incidence of acute and chronic graft versus host disease was 27 % (0.19-0.36, I= 30 %, p = 0.21) and 36 % (0.27-0.45, I= 24 %, p = 0.26), respectively.
HCT remains pivotal in treating primary plasma cell leukemia. However, higher relapse rates warrant novel agents and clinical trials to improve transplant-related outcomes in this challenging subgroup.
造血干细胞移植(HCT)是原发性浆细胞白血病(pPCL)的关键治疗方式。我们旨在研究成年pPCL患者接受异基因(allo)和自体(auto)HCT的疗效。
按照PRISMA指南,使用相关医学主题词(MeSH)和关键词在PubMed、Cochrane、Embase及Clinicaltrials.gov上进行全面的文献检索。纳入12篇报告成年pPCL患者自体HCT或异基因HCT疗效的原始文章。使用R程序(版本4.3.0)中的“meta”包进行汇总分析。
我们的分析纳入了1757例pPCL患者(1535例接受自体HCT,222例接受异基因HCT),其中49%为男性。自体HCT的3年总生存率(OS)、无进展生存率/无事件生存率(PFS/EFS)及复发率(RR)的汇总结果分别为51%(95%CI 0.4 - 0.61,I² = 92%,p < 0.01)、36%(95%CI 0.24 - 0.52,I² = 97%,p < 0.01)及68%(95%CI 0.65 - 0.71,I² = 0%,p = 0.42)。在接受异基因HCT的患者中,报告的OS在2.3年时为71%至4年时为31%不等,EFS/PFS在2.5年时为29%至4年时为19%不等。中位6个月时,汇总的治疗相关死亡率(TRM)为12%(95%CI 0.05 - 0.25,I² = 35%,p = 0.22)。急性和慢性移植物抗宿主病的汇总发生率分别为27%(0.19 - 0.36,I² = 30%,p = 0.21)和36%(0.27 - 0.45,I² = 24%,p = 0.26)。
HCT在原发性浆细胞白血病的治疗中仍然至关重要。然而,较高的复发率需要新的药物和临床试验来改善这个具有挑战性的亚组的移植相关结局。