Cohen Inbar, Vaxman Iuliana, Gertz Morie A
Institute of Hematology, Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel,
Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel,
Acta Haematol. 2025;148(3):289-299. doi: 10.1159/000539225. Epub 2024 May 6.
High-dose therapy (HDT) followed by autologous stem cell transplantation (ASCT) has become part of standard of care (SOC) in newly diagnosed multiple myeloma. In this review, we provide a historical perspective on ASCT since its introduction in the 1990s.
Overall survival (OS) benefit for HDT followed by ASCT was demonstrated in studies comparing HDT with ASCT to standard-dose therapy (SDT) before the era of novel agents. Conditioning is done with melphalan 200 mg/m2. Lower doses (MEL140, MEL150) for older patients with comorbidities are safe and have comparable results. The addition of busulfan to melphalan improves progression-free survival (PFS) but not OS. HDT with ASCT after induction with novel agents prolongs PFS but not OS compared to SDT alone. The benefit is more evident in patients with high-risk cytogenetics. Mobilization can be achieved with granulocyte colony-stimulating factor alone, but is improved with the addition of chemotherapy. Plerixafor reduces mobilization failure and enables sufficient stem cell collection after induction with novel agents. ASCT is safe with a low rate of mortality (1%), and selected patients can be managed as outpatients.
HDT followed by ASCT remains part of SOC due to its PFS benefit and relatively low toxicity.
大剂量治疗(HDT)后行自体干细胞移植(ASCT)已成为新诊断多发性骨髓瘤标准治疗(SOC)的一部分。在本综述中,我们提供了自20世纪90年代引入ASCT以来的历史视角。
在新型药物时代之前,将HDT联合ASCT与标准剂量治疗(SDT)进行比较的研究表明,HDT联合ASCT可带来总生存期(OS)获益。预处理采用美法仑200mg/m²。对于有合并症的老年患者,较低剂量(MEL140、MEL150)是安全的,且结果相当。在美法仑基础上加用白消安可改善无进展生存期(PFS),但不能改善OS。与单独使用SDT相比,新型药物诱导后行HDT联合ASCT可延长PFS,但不能延长OS。这种获益在高危细胞遗传学患者中更明显。动员可单独使用粒细胞集落刺激因子实现,但加用化疗可改善动员效果。普乐沙福可减少动员失败,并能在新型药物诱导后实现足够的干细胞采集。ASCT是安全的,死亡率较低(1%),部分患者可作为门诊患者管理。
由于其对PFS的获益及相对较低的毒性,HDT联合ASCT仍是SOC的一部分。