Haffty B G, Son Y H, Sasaki C T, Papac R, Fischer D, Rockwell S, Sartorelli A, Fischer J J
Dept. of Therapeutic Radiology, Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT 06510.
Int J Radiat Oncol Biol Phys. 1993 Sep 30;27(2):241-50. doi: 10.1016/0360-3016(93)90234-m.
This study was undertaken to assess the benefit of mitomycin C as an adjunct to postoperative radiation therapy in patients with operable squamous cell carcinoma of the head and neck.
Between May 1980 and May 1991, 182 patients have been enrolled in two consecutive randomized clinical trials testing mitomycin C as an adjunct to radiation therapy in squamous cell carcinoma of the head and neck. In both trials, patients were stratified by stage, disease site and intent of therapy. This subset analysis includes 113 patients entered into these two randomized trials treated with surgery and postoperative radiation therapy. In the first trial, patients were randomized to receive standard postoperative radiation therapy alone compared with postoperative radiation therapy with concomitant mitomycin C. In the second trial, patients were randomized to postoperative radiation therapy or postoperative radiation therapy with concomitant mitomycin C plus dicoumarol.
As of November 1991, the 113 patients treated with surgery and postoperative radiation therapy in both trials had a median follow-up of 93 months. There have been a total of 12 local recurrences in the radiation therapy alone arm compared to 0 local recurrences in the radiation therapy/mitomycin C arm. There were eight regional recurrences in the radiation therapy alone arm compared with five regional recurrences in the mitomycin C arm. Patients in the mitomycin C arm experienced a superior 5-year actuarial local regional control rate (87% vs. 67%, p < .015) and a statistically significant disease-free survival benefit (67% vs. 44%, p < .03). Overall survival difference between the two arms (56% vs. 41%) has not reached statistical significance.
We conclude from these prospectively designed randomized clinical trials that in patients with operable head and neck cancer treated with surgery and postoperative radiation therapy, concomitant administration of mitomycin C with radiation therapy will result in a statistically significant disease-free survival and local regional control benefit. We are currently investigating the value of other bioreductive alkylating agents as adjuncts to radiation therapy in patients with squamous cell carcinoma of the head and neck.
本研究旨在评估丝裂霉素C作为可手术的头颈部鳞状细胞癌患者术后放疗辅助治疗的益处。
1980年5月至1991年5月期间,182例患者参加了两项连续的随机临床试验,测试丝裂霉素C作为头颈部鳞状细胞癌放疗辅助治疗的效果。在两项试验中,患者均按分期、疾病部位和治疗意图进行分层。该亚组分析包括113例进入这两项随机试验并接受手术和术后放疗的患者。在第一项试验中,患者被随机分为单独接受标准术后放疗与术后放疗联合丝裂霉素C。在第二项试验中,患者被随机分为术后放疗或术后放疗联合丝裂霉素C加双香豆素。
截至1991年11月,两项试验中接受手术和术后放疗的113例患者的中位随访时间为93个月。单纯放疗组共有12例局部复发,而放疗/丝裂霉素C组无局部复发。单纯放疗组有8例区域复发,丝裂霉素C组有5例区域复发。丝裂霉素C组患者的5年精算局部区域控制率更高(87%对67%,p<.015),且无病生存获益具有统计学意义(67%对44%,p<.03)。两组间的总生存差异(56%对41%)未达到统计学意义。
我们从这些前瞻性设计的随机临床试验中得出结论,对于接受手术和术后放疗的可手术头颈部癌患者,丝裂霉素C与放疗联合使用将带来具有统计学意义的无病生存和局部区域控制益处。我们目前正在研究其他生物还原烷化剂作为头颈部鳞状细胞癌患者放疗辅助治疗的价值。