Li Juan, Liu Jun-ru, Huang Bei-hui, Chen Mei, Zheng Dong, Xu Duo-rong, Zou Wai-yi
Department of Hematology, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Zhonghua Nei Ke Za Zhi. 2012 Apr;51(4):279-83.
To investigate the efficacy and safety of bortezomib-based induction regimen followed by autologous hematopoietic stem cell transplantation (ASCT) in patients with multiple myeloma (MM).
A retrospective analysis was performed upon clinical data of 62 MM patients who received bortezomib-based induction regimen followed by ASCT from June 2006 to June 2011. All patients were followed up to September 30, 2011.
Overall response rate [complete remission (CR) + near complete remission (nCR) + partial remission (PR)], ≥ nCR rate (CR/nCR) and CR rate of post-induction with bortezomib-based regimen were 88.7%, 66.1% and 24.2%, respectively. After ASCT, CR rate and CR/nCR rate were increased to 50.0% and 82.3%, respectively, with significant differences (P = 0.003 and P = 0.032). The median time of neutrophil and platelet engraftment was 12.0 (9 - 43) days and 13.5 (0 - 120) days, respectively. Significances were found in neutrophil and platelet engraftment between MM patients with and without prior exposure to alkylating agents. Furthermore, engraftment of neutrophil and platelet in patients receiving peripheral blood stem cell transplantation were faster than those receiving bone marrow transplantation. No unexpected side effects occurred. The median time of follow-up was 26.5 (7-61) months. The median overall survival (OS) was not reached and the median progression-free survival (PFS) was 30 months. There were significant differences in OS and PFS between patients obtaining CR/nCR and those with ≤ PR before ASCT.
Bortezomib-based induction regimen can improve the efficacy of ASCT in MM patients. The side effects are tolerant. Higher response quality before ASCT can translate to high rates of OS and PFS following high-dose therapy and stem cell transplantation.
探讨以硼替佐米为基础的诱导方案序贯自体造血干细胞移植(ASCT)治疗多发性骨髓瘤(MM)患者的疗效及安全性。
对2006年6月至2011年6月期间接受以硼替佐米为基础的诱导方案序贯ASCT的62例MM患者的临床资料进行回顾性分析。所有患者随访至2011年9月30日。
以硼替佐米为基础的诱导方案诱导后总体缓解率[完全缓解(CR)+近乎完全缓解(nCR)+部分缓解(PR)]、≥nCR率(CR/nCR)及CR率分别为88.7%、66.1%和24.2%。ASCT后,CR率及CR/nCR率分别升至50.0%和82.3%,差异有统计学意义(P = 0.003和P = 0.032)。中性粒细胞和血小板植入的中位时间分别为12.0(9 - 43)天和13.5(0 - 120)天。在有或无烷化剂暴露史的MM患者之间,中性粒细胞和血小板植入存在显著差异。此外,接受外周血干细胞移植患者的中性粒细胞和血小板植入比接受骨髓移植的患者更快。未发生意外副作用。中位随访时间为26.5(7 - 61)个月。中位总生存期(OS)未达到,中位无进展生存期(PFS)为30个月。ASCT前获得CR/nCR的患者与≤PR的患者在OS和PFS方面存在显著差异。
以硼替佐米为基础的诱导方案可提高MM患者ASCT的疗效。副作用可耐受。ASCT前较高的缓解质量可转化为大剂量治疗和干细胞移植后较高的OS和PFS率。