Wendt T G, Hartenstein R C, Wustrow T P, Lissner J
Department of Radiology, University of Munich, FRG.
J Clin Oncol. 1989 Apr;7(4):471-6. doi: 10.1200/JCO.1989.7.4.471.
In a phase II study, patients with locally advanced squamous cell carcinoma of the head and neck were treated with simultaneous chemoradiotherapy. Treatment was divided into three courses. Chemotherapy consisted of cis-diamminedichloroplatinum (II) (cisplatin [cis-DDP]) 60 mg/m2 intravenously (IV), fluorouracil (5-FUra) 350 mg/m2 IV, and folinic acid (leucovorin calcium [FA]) 50 mg/m2 IV on day 2 as bolus, and 5-FUra 350 mg/m2 over 24 hours and FA 100 mg/m2 over 24 hours on days 2 through 5. Radiotherapy consisted of 23.4 Gy over nine days divided into 13 fractions of 1.8 Gy each delivered twice a day from day 3 through day 11. This regimen was repeated on days 22 and 44. Total radiation dose amounted to 70.2 Gy over 51 days. Between August 1984 and October 1986, 62 (modified AJCC stage III, four; IV A, eight; IV B, 50) consecutive patients were entered in the study. Three patients died during treatment due to tumor hemorrhage. Of 59 patients, 48 (81%) achieved a clinically complete response (cCR); 11 (19%) achieved a partial response (cPR). Mean follow-up of the surviving patients was 29+ (24 to 44) months. Actuarial 2-year survival probability is 52%, including three early deaths from tumor bleeding. Tumor and neck nodes control rates at 2 years were 92% for stage III and IV A patients and 65% for stage IV B patients. Patients with cCR had a significantly better 2-year tumor and neck nodes control probability compared with patients who achieved cPR after therapy (P less than .001). Six patients developed distant metastases. Overall toxicity was tolerable, mucositis particularly was not a limiting factor.
在一项II期研究中,局部晚期头颈部鳞状细胞癌患者接受同步放化疗。治疗分为三个疗程。化疗方案为第2天静脉推注顺二氨二氯铂(II)(顺铂[顺-DDP])60mg/m²、氟尿嘧啶(5-氟尿嘧啶[5-FUra])350mg/m²和亚叶酸(亚叶酸钙[FA])50mg/m²,第2至5天5-氟尿嘧啶350mg/m²持续24小时静脉滴注,亚叶酸100mg/m²持续24小时静脉滴注。放疗方案为9天内给予23.4Gy,分13次,每次1.8Gy,从第3天至第11天每天照射2次。该方案在第22天和第44天重复。51天内总辐射剂量达70.2Gy。1984年8月至1986年10月,62例(根据美国癌症联合委员会修订分期标准:III期4例;IVA期8例;IVB期50例)连续患者纳入本研究。3例患者在治疗期间因肿瘤出血死亡。59例患者中,48例(81%)达到临床完全缓解(cCR);11例(19%)达到部分缓解(cPR)。存活患者的平均随访时间为29+(24至44)个月。包括3例因肿瘤出血导致的早期死亡,2年总生存率为52%。III期和IVA期患者2年肿瘤和颈部淋巴结控制率为92%,IVB期患者为65%。与治疗后达到cPR的患者相比,达到cCR的患者2年肿瘤和颈部淋巴结控制概率显著更高(P<0.001)。6例患者发生远处转移。总体毒性可耐受,黏膜炎尤其不是限制因素。