含利妥昔单抗诱导化疗伴体内清除治疗复发或难治性滤泡性淋巴瘤后,大剂量美法兰和全身照射后自体外周血干细胞移植的良好巩固效果

Harumi Kato , Hirofumi Taji , Michinori Ogura , Yoshitoyo Kagami , Yasuhiro Oki , Akane Tsujimura , Nobukazu Fuwa , Takeshi Kodaira , Masao Seto , Kazuhito Yamamoto , Yasuo Morishima
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引用次数: 5

摘要

目的:在本研究中,我们试图评估在含利妥昔单抗的诱导化疗后,自体外周血干细胞移植(autoPBSCT)对复发或难治性化疗敏感的晚期滤泡性淋巴瘤(FL)的疗效和毒性。患者和方法采用利妥昔单抗方案作为诱导化疗和PBSC收集前的体内清除。获得部分或完全缓解的患者接受由高剂量美法兰和全身照射(TBI)组成的治疗方案。结果共纳入18例患者,中位年龄为45岁。既往化疗次数为2次。主要的非血液学毒性为3级发热性中性粒细胞减少症和腹泻。1例发生肺囊虫性肺炎,2例发生间质性肺炎,1例发生无球蛋白血症,除无球蛋白血症患者外均完全好转。未观察到4级毒性,迄今为止也未出现与治疗相关的死亡率和继发性恶性肿瘤。中位随访4年,4年估计总生存率和无失败生存率分别为100%和88.9%。结论对于复发或难治性化疗敏感性FL,大剂量美法兰联合TBI巩固治疗后进行体内清除的autoPBSCT是可行且有效的,需要更长的随访时间来确认其作用和晚期毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Favorable Consolidative Effect of High-Dose Melphalan and Total-Body Irradiation Followed by Autologous Peripheral Blood Stem Cell Transplantation After Rituximab-Containing Induction Chemotherapy With In Vivo Purging in Relapsed or Refractory Follicular Lymphoma

Purpose

In this study, we sought to evaluate the efficacy and toxicity of high-dose therapy followed by autologous peripheral blood stem cell transplantation (autoPBSCT) after rituximab-containing induction chemotherapy with in vivo purging for relapsed or refractory chemosensitive advanced-stage follicular lymphoma (FL).

Patients and Methods

A rituximab-containing regimen was used as induction chemotherapy and as in vivo purging before PBSC collection. Patients achieving partial or complete response received a regimen consisting of high-dose melphalan and total-body irradiation (TBI).

Results

A total of 18 patients with a median age of 45 years were enrolled. The number of previous chemotherapy regimens was 2. The principal nonhematologic toxicities were grade 3 febrile neutropenia and diarrhea. One patient experienced pneumocystis pneumonia, 2 developed interstitial pneumonitis, and 1 experienced agammaglobulinemia, all of whom had complete improvement except for the patient having agammaglobulinemia. Grade 4 toxicities were not observed, and there have been neither treatment-related mortality nor secondary malignancy to date. At a median follow-up of 4.0 years, the 4-year estimated overall and failure-free survival rates were 100% and 88.9%, respectively.

Conclusion

Consolidation of high-dose melphalan and TBI followed by autoPBSCT with in vivo purging is feasible and effective for relapsed or refractory chemosensitive FL. Longer follow-up is needed to confirm the role and late toxicities.

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