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套细胞淋巴瘤:不适用于干细胞移植患者的一线治疗

Mantle Cell Lymphoma: First-line Therapy in Patients Not Eligible for Stem Cell Transplantation.

作者信息

Nazeef Moniba, Kahl Brad S

机构信息

Department of Medicine, Division of Hematology/Oncology, University of Wisconsin School of Medicine and Public Health, 1111 Highland Ave. 4059 WIMR, Madison, WI, 53705, USA.

出版信息

Curr Treat Options Oncol. 2015 Jun;16(6):29. doi: 10.1007/s11864-015-0343-7.

Abstract

Mantle cell lymphoma is a distinct subtype of non-Hodgkin's lymphoma, which has historically been associated with a poor prognosis. It is now recognized as a heterogeneous disease with variable biologic and clinical behavior. Treatment paradigms have evolved along two lines. Younger, fit mantle cell lymphoma (MCL) patients are generally treated with intensive strategies and older less fit patients with non-intensive strategies. Most of the published literature has focused on intensive strategies, which appear to result in more durable remissions, but with an unclear impact on overall survival. The literature is more sparse for the roughly 50% of patients who are not candidates for intensive strategies, and no "standard" approach has been established for this patient population. However, clues are emerging. Randomized clinical trials have (a) established that bendamustine-rituximab (BR) is more efficacious and less toxic than rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP); (b) established that bortezomib should replace vincristine if using an R-CHOP backbone; and (c) established that maintenance rituximab (MR) is beneficial after an R-CHOP induction. In our opinion, it is reasonable to extrapolate the data supporting MR after R-CHOP and apply MR after a BR induction. In our practice, we recommend BR followed by MR for 2 years to MCL patients not eligible for intensive therapy. An ongoing US intergroup trial is testing the addition of bortezomib to the BR backbone and the addition of lenalidomide to MR. This trial may establish a standard of care in the older MCL population. In addition, exciting options for relapsed MCL have emerged in the last few years, with the introduction of the Bruton tyrosine kinase (BTK) inhibitor ibrutinib and the development of the lenalidomide-rituximab combination. In this article, we will discuss the current available options for these older MCL patients and the evidence supporting those options.

摘要

套细胞淋巴瘤是一种独特的非霍奇金淋巴瘤亚型,历史上一直与预后不良相关。现在它被认为是一种具有可变生物学和临床行为的异质性疾病。治疗模式沿着两条路线发展。年轻、健康的套细胞淋巴瘤(MCL)患者通常采用强化治疗策略,而年长、身体状况较差的患者则采用非强化治疗策略。大多数已发表的文献都集中在强化治疗策略上,这种策略似乎能带来更持久的缓解,但对总生存期的影响尚不清楚。对于大约50%不适合强化治疗策略的患者,相关文献更为稀少,并且尚未为这一患者群体建立“标准”治疗方法。然而,线索正在出现。随机临床试验已经(a)证实苯达莫司汀-利妥昔单抗(BR)比利妥昔单抗、环磷酰胺、多柔比星、长春新碱和泼尼松(R-CHOP)更有效且毒性更小;(b)证实如果使用R-CHOP方案,硼替佐米应取代长春新碱;(c)证实利妥昔单抗维持治疗(MR)在R-CHOP诱导治疗后有益。我们认为,推断支持R-CHOP后MR的数据并将MR应用于BR诱导治疗后是合理的。在我们的实践中,我们建议对不符合强化治疗条件的MCL患者采用BR治疗,随后进行2年的MR治疗。美国正在进行的一项组间试验正在测试在BR方案中添加硼替佐米以及在MR中添加来那度胺。该试验可能会确立老年MCL患者群体的护理标准。此外,在过去几年中,随着布鲁顿酪氨酸激酶(BTK)抑制剂伊布替尼的引入和来那度胺-利妥昔单抗联合疗法的发展,复发MCL出现了令人兴奋的治疗选择。在本文中,我们将讨论这些老年MCL患者当前可用的治疗选择以及支持这些选择的证据。

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