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自体干细胞移植联合体内净化祖细胞治疗复发/难治性滤泡淋巴瘤显示出长期疗效。

Autologous stem cell transplantation with in vivo purged progenitor cells shows long-term efficacy in relapsed/refractory follicular lymphoma.

机构信息

Department of Molecular Medicine, University of Pavia, Pavia, Italy; Department of Hematology and Oncology, Fondazione Istituto Di Ricovero E Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.

出版信息

Am J Hematol. 2015 Mar;90(3):230-4. doi: 10.1002/ajh.23919.

Abstract

High-dose chemotherapy with autologous stem cell transplantation (ASCT) has been shown effective in the control of relapsed/refractory follicular lymphoma. We evaluate the long-term outcome of patients with relapsed or refractory follicular lymphoma treated with ASCT with in vivo purged progenitors cells. We report the long-term results of a prospective multicenter phase 2 trial on 124 relapsed/refractory follicular lymphoma patients treated with a program of anthracycline-based debulking chemotherapy, immunochemotherapy, mobilization of in vivo purged PBSC followed by ASCT. Median age was 52 years; 14% of patients had grade 3A histology. Debulking chemotherapy produced CR in 16% and PR in 71%, while 13% of patients progressed. After rituximab, cyclophosphamide, vincristine, prednisone (R-COP), CR was obtained in 60% and PR in 35%; 118 patients successfully mobilized PBSC and 117 proceeded to ASCT. The harvest in all the 32 molecularly informative patients was bcl-2 negative. TRM was 0%. The 5-year PFS was 54% and the 5-year OS was 83%. After a median f-up of 6.7 years (range 1.5-13.6), 54% are still in CR. These data show that prolonged PFS is achievable in relapsed/refractory patients with high dose autologous transplantation of in vivo purged progenitor cells.

摘要

大剂量化疗联合自体造血干细胞移植(ASCT)已被证明在控制复发性/难治性滤泡性淋巴瘤方面有效。我们评估了采用体内净化祖细胞的 ASCT 治疗复发性或难治性滤泡性淋巴瘤患者的长期结果。我们报告了一项前瞻性多中心 2 期试验的长期结果,该试验纳入了 124 例复发性/难治性滤泡性淋巴瘤患者,他们接受了基于蒽环类药物的减瘤化疗、免疫化疗、体内净化 PBSC 动员,然后进行 ASCT。中位年龄为 52 岁;14%的患者组织学分级为 3A。减瘤化疗后,16%的患者达到完全缓解(CR),71%的患者达到部分缓解(PR),而 13%的患者进展。在利妥昔单抗、环磷酰胺、长春新碱、泼尼松(R-COP)治疗后,60%的患者达到 CR,35%的患者达到 PR;118 例患者成功动员 PBSC,117 例患者进行了 ASCT。在所有 32 例分子信息可供分析的患者中,采集物均为 bcl-2 阴性。治疗相关死亡率(TRM)为 0%。5 年无进展生存率(PFS)为 54%,5 年总生存率(OS)为 83%。中位随访 6.7 年后(范围 1.5-13.6 年),54%的患者仍处于 CR。这些数据表明,在复发性/难治性患者中,采用体内净化祖细胞的大剂量自体移植可实现长期 PFS。

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