Department of Hematologic Oncology, State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, People's Republic of China.
Int J Hematol. 2012 Nov;96(5):617-23. doi: 10.1007/s12185-012-1174-y. Epub 2012 Sep 16.
We conducted a retrospective study of 135 patients of stage IE/IIE extranodal natural killer/T cell lymphoma, nasal type (ENKTL) treated with CHOP as induction chemotherapy to find some valuable prognostic factors and analyze the usefulness of International Prognostic Index (IPI) and Korean Prognostic Index (KPI) in predicting prognosis. Most of the patients were in the low-risk group (IPI score 0-1). Complete remission (CR) after induction chemotherapy was achieved in 31.8 % of the patients, which increased to 69.6 % after radiotherapy. The 2-, 5-, and 10-year overall survival (OS) rates were 60, 48, and 43 %, respectively. Patients with better performance status (ECOG 0-1), normal serum LDH level, without local invasiveness, low KPI scores, and IPI score of 0 had significantly better overall survival (P < 0.05) in univariate analysis. Using multivariate analysis, we identified serum LDH level, ECOG PS score and local invasiveness to be independent prognostic factors. In conclusion, ENKTL is an aggressive lymphoma that shows heterogeneity. The IPI and KPI score systems should be improved further to classify patients into different groups, and should be validated in larger prospective trials. Due to the multi-drug resistance mechanism of ENKTL, CHOP is no longer the state of art and novel drugs should be incorporated into future treatments.
我们回顾性分析了 135 例采用 CHOP 方案作为诱导化疗的ⅠE/ⅡE 期结外 NK/T 细胞淋巴瘤,鼻型(ENKTL)患者,以寻找一些有价值的预后因素,并分析国际预后指数(IPI)和韩国预后指数(KPI)在预测预后中的作用。大多数患者处于低危组(IPI 评分为 0-1)。诱导化疗后完全缓解(CR)率为 31.8%,放疗后增至 69.6%。2、5、10 年总生存率(OS)分别为 60%、48%和 43%。在单因素分析中,体能状态(ECOG 0-1)更好、血清 LDH 水平正常、无局部侵犯、KPI 评分低和 IPI 评分为 0 的患者 OS 显著更好(P<0.05)。多因素分析显示,血清 LDH 水平、ECOG PS 评分和局部侵犯是独立的预后因素。总之,ENKTL 是一种侵袭性淋巴瘤,具有异质性。IPI 和 KPI 评分系统应进一步改进,以将患者分为不同的组别,并在更大的前瞻性试验中进行验证。由于 ENKTL 的多药耐药机制,CHOP 方案不再是治疗的首选,应将新型药物纳入未来的治疗方案中。