Zhang Yu-jing, Hu Wei-han, Liu Hui, Cheng Er-cheng, Ren Zhong-min, Xia Yun-fei, Cui Nian-ji
Department of Radiation Oncology, Cancer Center, State Key Laboratory of Oncology in Southern China, Sun Yat-sen University, Guangzhou 510060, China.
Zhonghua Zhong Liu Za Zhi. 2006 Jan;28(1):50-3.
To investigate the clinical features, treatment modalities and the prognosis of nasal type NK/T cell lymphoma.
The data of 39 such patients treated from June 2000 to December 2003 were retrospectively reviewed. Twenty three patients were treated by combined chemoradiotherapy, basing on anthracycline-containing CHOP or similar regimens (median 5 cycles). Eleven patients by chemotherapy alone, 2 by radiotherapy alone and 2 aged patients by palliative chemotherapy or radiotherapy. Radiotherapy was given by high energy photon ray combined with electron beam with a median curative dose of 56 Gy in conventional fractionation. Bivariate correlations and univariate prognostic factors were analyzed.
Median follow-up time for the 21 patients who were still alive was 22.5 months. The overall remission rate (RR) after initial treatment was 66.7% (21 CR, 3 PR). Chemotherapy alone got a CR rate of only 37.5%. The overall local control rate was 59.4%. Local relapse rate after curative radiotherapy was 25.0%. Radiotherapy was positively correlated with local control (P = 0.000) and time to disease progression (TTP, P = 0.002). Skin and intestine were among the extranodal relapse sites. Fifteen patients had highly aggressive tumors with a median survival time of only 5 months. Univariate analysis showed that significant favorable survival prognostic factors were: radiotherapy (P = 0.001); lower risk International Prognostic Index (IPI, P = 0.001); complete remission after primary treatment (P = 0.000); pre-diagnostic history > 2 months (P = 0.024); and free of skin involvement (P = 0.034).
Most of nasal type NK/T cell lymphoma are in early stage when diagnosed. Radiotherapy remains to be the mainstay of treatment. Combined chemoradiotherapy needs further improvement for the progressive disease type. Some patients may have highly aggressive tumors with poor prognosis. Optimal prognostic factors and individualized treatment regimens need to be investigated.
探讨鼻型NK/T细胞淋巴瘤的临床特征、治疗方式及预后。
回顾性分析2000年6月至2003年12月期间治疗的39例此类患者的数据。23例患者接受了以含蒽环类药物的CHOP或类似方案为基础的放化疗联合治疗(中位5个周期)。11例患者仅接受化疗,2例仅接受放疗,2例老年患者接受姑息性化疗或放疗。放疗采用高能光子线联合电子束,常规分割的中位根治剂量为56 Gy。分析双变量相关性和单变量预后因素。
21例存活患者的中位随访时间为22.5个月。初始治疗后的总缓解率(RR)为66.7%(21例完全缓解,3例部分缓解)。单纯化疗的完全缓解率仅为37.5%。总局部控制率为59.4%。根治性放疗后的局部复发率为25.0%。放疗与局部控制(P = 0.000)和疾病进展时间(TTP,P = 0.002)呈正相关。皮肤和肠道是结外复发部位。15例患者肿瘤侵袭性高,中位生存时间仅5个月。单变量分析显示,显著的有利生存预后因素为:放疗(P = 0.001);低风险国际预后指数(IPI,P = 0.001);初始治疗后完全缓解(P = 0.000);诊断前病史>2个月(P = 0.024);无皮肤受累(P = 0.034)。
大多数鼻型NK/T细胞淋巴瘤确诊时处于早期。放疗仍是主要治疗手段。对于进展期疾病类型,放化疗联合治疗需要进一步改进。部分患者可能肿瘤侵袭性高,预后差。需要研究最佳预后因素和个体化治疗方案。