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Outcome of patients with mantle cell lymphoma is not influenced by vascular endothelial growth factor polymorphisms.

机译:套细胞淋巴瘤患者的结局不受血管内皮生长因子多态性的影响。

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摘要

Notwithstanding the most recent and effective therapeutic strategies, in the majority of patients mantle cell lymphoma (MCL) is still aggressive, with median overall survival (OS) ranging from 26 to 57 months, when patients are stratified according to the mantle cell lymphoma international prognostic index (MIPI) [1,2]. Thus, several immunochemotherapy combinations have been explored to improve outcome, such as R-Hyper-CVAD (rituximab plus hyperfractionated cyclophosphamide, vincristine, doxorubicin, dexamethasone, methotrexate, cytarabine) [2], R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, prednisone) [3], maxi-CHOP [4], bortezomib plus R-CHOP [5], and mTOR (mammalian target of rapamycin) inhibitors [6]. Moreover, also autologous transplant still remains a valid therapeutic option for young patients responsive to dose-intensified induction chemotherapy, with 6-year overall survival and progression-free survival of 70% and 66%, respectively [7].
机译:尽管采用了最新有效的治疗策略,但根据患者的预后,对大多数患者而言,套细胞淋巴瘤(MCL)仍具有侵袭性,中位总生存期(OS)为26至57个月不等指数(MIPI)[1,2]。因此,已经探索了几种免疫化学疗法组合以改善预后,例如R-Hyper-CVAD(利妥昔单抗加超分割环磷酰胺,长春新碱,阿霉素,地塞米松,甲氨蝶呤,阿糖胞苷)[2],R-CHOP(利妥昔单抗加环磷酰胺,阿霉素,v ,泼尼松)[3],maxi-CHOP [4],硼替佐米加R-CHOP [5]和mTOR(雷帕霉素的哺乳动物靶标)抑制剂[6]。此外,自体移植仍然是对剂量强化诱导化疗有反应的年轻患者的有效治疗选择,其6年总生存率和无进展生存率分别为70%和66%[7]。

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