Recombinant human endostatin in combination with CHOP regimen for peripheral T cell lymphoma

被引:7
作者
Zhang, Qunling [1 ,2 ]
Cao, Junning [1 ,2 ]
Xue, Kai [1 ,2 ]
Liu, Xiaojian [1 ,2 ]
Ji, Dongmei [1 ,2 ]
Guo, Ye [1 ,2 ]
Hong, Xiaonan [1 ,2 ]
机构
[1] Fudan Univ, Shanghai Canc Ctr, Dept Med Oncol, 270 Dongan Rd, Shanghai 200032, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Dept Oncol, Shanghai, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2017年 / 10卷
关键词
peripheral T cell lymphoma; recombinant human endostatin; VEGFR2; safety; efficacy; prognosis; PROGNOSTIC-SIGNIFICANCE; DOUBLE-BLIND; PHASE-II; ANGIOGENESIS; VEGF; VINCRISTINE; PREDNISONE; INHIBITOR; RECEPTORS; EFFICACY;
D O I
10.2147/OTT.S117007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Peripheral T cell lymphoma (PTCL) has a poor prognosis. Overexpression of vascular endothelial growth factor (VEGF) might contribute to the poor prognosis of PTCL and could be the target of novel therapy. The efficacy and safety of recombinant human endostatin (Endostar) in combination with cyclophosphamide, doxorubicin, vincristine and prednisone (ECHOP) have been explored in 15 PTCL patients. The objective response rate was 80%, with 53.3% patients having achieved complete response (CR) rate. The CR rate was 100% (3/3) in angioimmunoblastic T cell lymphoma (AITL) patients compared to only 36.4% (4/11) in PTCL not otherwise specified (PTCL-NOS) patients. With a median follow-up of 69 months, the 5-year progression-free survival and overall survival (OS) were 53% and 60%, respectively. The 5-year OS was 100% in AITL but was only 45% in PTCL-NOS. Seven out of 11 patients showed overexpression of VEGFR2 in their tumor vessels and had a better efficacy than those with low expression of VEGFR2. Grade 3 or 4 neutropenia is the most common toxicity observed. ECHOP was safe and might display potential benefit in AITL patients.
引用
收藏
页码:145 / 151
页数:7
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