Clinical Cooperation Unit Molecular and Radiation Oncology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Radiat Oncol. 2013 Jan 24;8:20. doi: 10.1186/1748-717X-8-20.
We report our experience in 49 consecutive patients with nasopharyngeal carcinoma who were treated by Intensity-modulated radiation therapy (IMRT) combined with simultaneous but not adjuvant chemotherapy (CHT).
The medical records of 49 patients with histologically proven primary nasopharygeal carcinoma treated with IMRT and concurrent platin-based CHT (predominantly cisplatin weekly) were retrospectively reviewed. The majority of patients showed advanced clinical stages (stage III/IV:72%) with undifferentiated histology (82%). IMRT was performed in step-and-shoot technique using an integrated boost concept in 84%. In this concept, the boost volume covered the primary tumor and involved nodes with doses of 66-70.4 Gy (single dose 2.2 Gy). Uninvolved regional nodal areas were covered with doses of 54-59.4 Gy (median single dose 1.8 Gy). At least one parotid gland was spared. None of the patients received adjuvant CHT.
The median follow-up for the entire cohort was 48 months. Radiation therapy was completed without interruption in all patients and 76% of the patients received at least 80% of the scheduled CHT. Four local recurrences have been observed, transferring into 1-, 3-, and 5-year Local Control (LC) rates of 98%, 90% and 90%. One patient developed an isolated regional nodal recurrence, resulting in 1-, 3-, and 5-year Regional Control (RC) rates of 98%. All locoregional failures were located inside the radiation fields. Distant metastases were found in six patients, transferring into 1-, 3, and 5-year Distant Control (DC) rates of 92%, 86% and 86%. Progression free survival (PFS) rates after 1, 3 and 5 years were 86%, 70% and 69% and 1-, 3- and 5-year Overall Survival (OS) rates were 96%, 82% and 79%. Acute toxicity ≥ grade III mainly consisted of dysphagia (32%), leukopenia (24%), stomatitis (16%), infection (8%) and nausea (8%). Severe late toxicity (grade III) was documented in 18% of the patients, mainly as xerostomia (10%).
Concurrent chemoradiation without the addition of adjuvant chemotherapy cycles using IMRT with an integrated boost concept yielded good disease control and overall survival in patients suffering from primary nasopharyngeal cancer with acceptable acute side effects and limited rates of late toxicity.
我们报告了 49 例连续接受调强放疗(IMRT)联合同期但不辅助化疗(CHT)治疗的鼻咽癌患者的经验。
回顾性分析 49 例经组织学证实的原发性鼻咽癌患者的病历,这些患者接受了 IMRT 和同期铂类为基础的 CHT(主要为每周顺铂)治疗。大多数患者表现为晚期临床分期(III/IV 期:72%),组织学未分化(82%)。采用分步射击技术进行 IMRT,并采用综合增强概念,该概念中,推量体积覆盖原发肿瘤和受累淋巴结,剂量为 66-70.4Gy(单次剂量 2.2Gy)。未受累的区域淋巴结区域覆盖 54-59.4Gy(中位单次剂量 1.8Gy)。至少保留一个腮腺。没有患者接受辅助 CHT。
整个队列的中位随访时间为 48 个月。所有患者均无中断完成放射治疗,76%的患者接受了至少 80%的计划 CHT。4 例局部复发,1、3、5 年局部控制(LC)率分别为 98%、90%和 90%。1 例患者发生孤立性区域淋巴结复发,1、3、5 年区域控制(RC)率分别为 98%。所有局部区域失败均位于放射野内。6 例患者发生远处转移,1、3、5 年远处控制(DC)率分别为 92%、86%和 86%。1、3、5 年无进展生存率(PFS)分别为 86%、70%和 69%,1、3、5 年总生存率(OS)分别为 96%、82%和 79%。急性毒性≥3 级主要为吞咽困难(32%)、白细胞减少(24%)、口炎(16%)、感染(8%)和恶心(8%)。18%的患者发生严重的晚期毒性(3 级),主要为口干(10%)。
采用调强放疗联合同期不辅助化疗周期的同期放化疗,采用综合增强概念,对原发性鼻咽癌患者的疾病控制和总体生存有良好的效果,急性副作用可接受,晚期毒性发生率有限。