GELAD chemotherapy with sandwiched radiotherapy for patients with newly diagnosed stage IE/IIE natural killer/T-cell lymphoma: a prospective multicentre study

被引:10
作者
Zhu, Yang [1 ]
Tian, Shu [2 ]
Xu, Lan [3 ]
Ma, Yujie [1 ]
Zhang, Wenhao [1 ]
Wang, Lifeng [4 ]
Jin, Lina [5 ]
Liu, Chuanxu [1 ]
Zhu, Chuanying [6 ]
Li, Zhichao [1 ]
Hao, Siguo [1 ]
Zhong, Hua [3 ]
Ding, Hao [2 ]
Tao, Rong [1 ]
机构
[1] Shanghai Jiao Tong Univ, Xinhua Hosp, Dept Hematol, Sch Med, Shanghai, Peoples R China
[2] Fudan Univ, Eye Ear Nose & Throat Hosp, Dept Radiat Oncol, Shanghai, Peoples R China
[3] Shanghai Jiao Tong Univ, Renji Hosp, Dept Hematol, Sch Med, Shanghai, Peoples R China
[4] Shanghai Jiao Tong Univ, Xinhua Hosp, Dept Pathol, Sch Med, Shanghai, Peoples R China
[5] Tongji Univ, Dongfang Hosp, Dept Hematol, Shanghai, Peoples R China
[6] Shanghai Jiao Tong Univ, Xinhua Hosp, Dept Oncol, Sch Med, Shanghai, Peoples R China
关键词
natural Killer; T-cell Lymphoma; pegaspargase-based chemotherapy; radiotherapy; early-stage disease; MODERN RADIATION-THERAPY; NON-HODGKIN-LYMPHOMA; L-ASPARAGINASE; NASAL-TYPE; PHASE-II; COMBINATION CHEMOTHERAPY; DOSE GUIDELINES; T-CELL; DEXAMETHASONE; GEMCITABINE;
D O I
10.1111/bjh.17960
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Early-stage natural killer/T-cell lymphoma (NK/TCL) patients usually receive a combination of chemotherapy and radiotherapy, but the optimal treatment approach has not yet been established. This study aimed to investigate the efficacy and safety profile of a novel chemotherapy regimen and sandwiched radiotherapy in early-stage NK/TCL. Patients with newly diagnosed stage IE/IIE disease were eligible. Patients were initially treated with two courses of the GELAD regimen (gemcitabine 1 center dot 0 g/m(2) day 1, etoposide 60 mg/m(2) days 1-3, pegaspargase 2000 units/m(2) day 4, and dexamethasone 40 mg days 1-4), followed by intensity-modulated radiotherapy (IMRT; 50-56 Gy in 25-28 fractions) and two additional courses of GELAD chemotherapy. A total of 52 patients were enrolled. The overall response rate and complete response rate per Lugano 2014 criteria were 94 center dot 2% and 92 center dot 3% respectively. With a median follow-up of 32 months, the estimated four-year overall survival rate and progression-free survival rate were 94 center dot 2% [95% confidence interval (CI), 83 center dot 2% to 93 center dot 1%] and 90 center dot 4% (95% CI, 78 center dot 4% to 95 center dot 9%) respectively. The most common adverse events were related to pegaspargase. Haematological toxicities were mild, with grade 3/4 neutropenia in 15 center dot 4% of patients. Our study provides a new approach with high activity and improved safety for the treatment of early-stage NK/TCL patients. This study was registered at as NCT02733458.
引用
收藏
页码:939 / 946
页数:8
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