Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
Int J Radiat Oncol Biol Phys. 2018 Sep 1;102(1):61-70. doi: 10.1016/j.ijrobp.2018.05.046. Epub 2018 May 29.
To investigate the efficacy and toxicity profile of sequential intensity modulated radiation therapy (IMRT) followed by gemcitabine, dexamethasone, and cisplatin (GDP) on previously untreated high-risk, early stage upper aerodigestive tract natural killer/T-cell lymphoma (UADT-NKTCL).
A phase 2 study was designed, and 40 high-risk patients with stage I(E)/II(E) UADT-NKTCL were enrolled between June 2010 and June 2014. High-risk patients were defined as those with at least 1 predefined risk factor: age >60 years, elevated serum lactate dehydrogenase, regional lymph node involvement, B symptoms, and primary tumor invasion. Patients received extended involved-site IMRT and GDP chemotherapy. The primary endpoint was the 2-year progression-free survival rate. Secondary endpoints were the 2-year overall survival rate, overall response rate, and toxicity.
Median follow-up time was 60.1 months. The overall response rate and complete remission rate were 97.5% and 95.0%, respectively. The 2- and 5-year progression-free survival rates were 84.7% and 79.4%, and the corresponding overall survival rates were 89.9% and 82.1%, respectively. The most frequent radiation-induced toxicities were mild mucositis and skin reaction. Grade 3/4 neutropenia (12 of 40 patients), thrombocytopenia (7 of 40), and anemia (2 of 40) were observed during chemotherapy.
First-line IMRT followed by GDP represents an effective and well-tolerated protocol for high-risk, early stage UADT-NKTCL.
研究序贯调强放疗(IMRT)联合吉西他滨、地塞米松和顺铂(GDP)治疗未经治疗的高危早期头颈部自然杀伤/T 细胞淋巴瘤(UADT-NKTCL)的疗效和毒性。
设计了一项 2 期研究,2010 年 6 月至 2014 年 6 月期间共纳入 40 例 I(E)/II(E)期高危 UADT-NKTCL 患者。高危患者定义为至少有 1 个预设风险因素:年龄>60 岁、血清乳酸脱氢酶升高、区域淋巴结受累、B 症状和原发肿瘤侵犯。患者接受扩展累及部位 IMRT 和 GDP 化疗。主要终点是 2 年无进展生存率。次要终点是 2 年总生存率、总缓解率和毒性。
中位随访时间为 60.1 个月。总缓解率和完全缓解率分别为 97.5%和 95.0%。2 年和 5 年无进展生存率分别为 84.7%和 79.4%,相应的总生存率分别为 89.9%和 82.1%。最常见的放射性毒性为轻度黏膜炎和皮肤反应。化疗期间观察到 12 例(40 例中有 12 例)患者出现 3/4 级中性粒细胞减少、7 例(40 例中有 7 例)血小板减少和 2 例(40 例中有 2 例)贫血。
一线 IMRT 联合 GDP 是高危早期 UADT-NKTCL 的一种有效且耐受良好的方案。