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利妥昔单抗用于治疗与HIV相关的淋巴瘤:权衡利弊

Rituximab for HIV-associated lymphoma: weighing the benefits and risks.

作者信息

Spina Michele, Tirelli Umberto

机构信息

Division of Medical Oncology A, National Cancer Institute, Via Pedemontana Occidentale 12, 33081 Aviano, PN, Italy.

出版信息

Curr Opin Oncol. 2005 Sep;17(5):462-5. doi: 10.1097/01.cco.0000172824.78318.b9.

DOI:10.1097/01.cco.0000172824.78318.b9
PMID:16093796
Abstract

PURPOSE OF REVIEW

This review discusses the potential benefits and risks of using the anti-CD20 monoclonal antibody rituximab for the treatment of HIV-associated B-cell non-Hodgkin's lymphoma.

RECENT FINDINGS

Studies have consistently demonstrated that rituximab improves response and survival when combined with standard chemotherapy compared with chemotherapy alone in immunocompetent patients with intermediate-grade non-Hodgkin's lymphoma. Several recently reported phase II and III trials have evaluated the use of rituximab plus chemotherapy for HIV-associated B-cell non-Hodgkin's lymphoma. Phase II trials combining rituximab with either standard cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy or infusional chemotherapy have reported encouraging results, suggesting a similar benefit in HIV-positive individuals. A phase III trial comparing CHOP with CHOP-plus rituximab (R-CHOP) demonstrated a lower risk from progression of the lymphoma, but a higher risk of early and late infectious-related death in patients with a low CD4 count (< 50/microL).

SUMMARY

Rituximab should be used cautiously in patients with advanced HIV infection who have a CD4 count of less than 50/microL, as it seems to increase the risk of developing fatal infectious complications. In patients with higher CD4 counts, the benefit of rituximab may outweigh its risk, although this has yet to be confirmed in prospective, randomized trials specifically performed in this population.

摘要

综述目的

本综述探讨使用抗CD20单克隆抗体利妥昔单抗治疗HIV相关B细胞非霍奇金淋巴瘤的潜在益处和风险。

最新发现

研究一致表明,在免疫功能正常的中度非霍奇金淋巴瘤患者中,与单纯化疗相比,利妥昔单抗联合标准化疗可改善缓解率和生存率。最近报道的几项II期和III期试验评估了利妥昔单抗加化疗用于HIV相关B细胞非霍奇金淋巴瘤的情况。将利妥昔单抗与标准环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)化疗或输注化疗联合的II期试验报告了令人鼓舞的结果,表明在HIV阳性个体中有类似益处。一项比较CHOP与CHOP加利妥昔单抗(R-CHOP)的III期试验表明,淋巴瘤进展风险较低,但CD4计数低(<50/μL)的患者早期和晚期感染相关死亡风险较高。

总结

对于CD4计数低于50/μL的晚期HIV感染患者,应谨慎使用利妥昔单抗,因为它似乎会增加发生致命感染并发症的风险。在CD4计数较高的患者中,利妥昔单抗的益处可能超过其风险,尽管这尚未在前瞻性随机试验中得到专门针对该人群的证实。

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