Dietz A, Rudat V, Nollert J, Flentje M, Maiei H, Wannenmacher M, Weidauer H
Hals-Nasen-Ohren-Universitätsklinik Heidelberg.
Laryngorhinootologie. 1996 Dec;75(12):745-53. doi: 10.1055/s-2007-997669.
Between 1989 and 1992, 38 patients with advanced squamous cell carcinomas of the head and neck were treated by an accelerated hyperfractionated split-course radiochemotherapy (SCRC). This therapy was carried out at the ENT department and department of radiooncology of the University of Heidelberg. Within 51 days, 70.2 Gy were applied in three courses. In every course, simultaneous chemotherapy with cisplatin (60 mg/m2/week)/5 Fu (bolus: 350 mg/m2/d)/Leucovorin (bolus: 50 mg/m2 + 100 mg/m2/24 h) was carried out. Between 1992 and 1994, 50 patients suffering from advanced head and neck cancer (stage III, V) were also treated with an accelerated hyperfractionated concomitant-boost radiochemotherapy (CBRC) at the same departments. A total dose of 66 Gy, was applied within 33 days. The patients were also treated with simultaneous chemotherapy with carboplatin (70 mg/m2/24 h) in the first and fifth week.
In about 50% of the patients treated with SCRC, the therapy was more than 10 days longer than the scheduled period. The lack of compliance due to toxicity was considered as one of the main reasons for this delay. After the first course of SCRC, eight of 38 patients showed mucositis of the upper aerodigestive tract (WHO grade > 3); after the second course, 11 of 38 patients; and after the third course, 15 of 38 patients. Fifty-two percent of the patients developed emesis, 10% leucopenia < 1 nl, 10% nephrotoxicity, 3% pancreatitis, 3% thrombosis, 3% gastritis, and 3% auditory threshold shifts of about more than 10 dB. In about 7.5% of the patients treated with CBRC, the therapy was more than 10 days longer than the scheduled period. The mucositis of the upper aerodigestive tract (50% of the patients showed WHO-grade > 3) was considered to be the main reason for this. In four patients a neutropenia < 1 nl was detected, in one patient anemia < 7 g/dl and n 33 patients thrombocytopenia < 100/nl.
In conclusion, the concomitant boost radiochemotherapy showed a lower toxicity and higher acceptance than the split-course radiochemotherapy. This is documented in lower protocol delays and better results in the two-years survival time in case of concomitant boost radiotherapy.
1989年至1992年期间,38例晚期头颈部鳞状细胞癌患者接受了加速超分割分段疗程放化疗(SCRC)。该治疗在海德堡大学耳鼻喉科和放射肿瘤学系进行。在51天内分三个疗程给予70.2 Gy的剂量。每个疗程同时进行顺铂(60 mg/m²/周)/5-氟尿嘧啶(推注:350 mg/m²/天)/亚叶酸钙(推注:50 mg/m² + 100 mg/m²/24小时)化疗。1992年至1994年期间,50例晚期头颈癌(III期、V期)患者也在同一科室接受了加速超分割同期增量放化疗(CBRC)。在33天内给予总剂量66 Gy。患者在第一周和第五周还同时接受了卡铂(70 mg/m²/24小时)化疗。
在接受SCRC治疗的患者中,约50%的患者治疗时间比预定时间长10天以上。毒性导致的依从性差被认为是延迟的主要原因之一。在SCRC的第一个疗程后,38例患者中有8例出现上消化道黏膜炎(世界卫生组织分级>3级);第二个疗程后,38例患者中有11例;第三个疗程后,38例患者中有15例。52%的患者出现呕吐,10%的患者白细胞减少<1×10⁹/L,10%的患者出现肾毒性,3%的患者出现胰腺炎,3%的患者出现血栓形成,3%的患者出现胃炎,3%的患者听觉阈值偏移约超过10 dB。在接受CBRC治疗的患者中,约7.5%的患者治疗时间比预定时间长10天以上。上消化道黏膜炎(50%的患者世界卫生组织分级>3级)被认为是主要原因。4例患者检测到中性粒细胞减少<1×10⁹/L,1例患者贫血<7 g/dl,33例患者血小板减少<100×10⁹/L。
总之,同期增量放化疗比分段疗程放化疗毒性更低,接受度更高。这在较低的方案延迟以及同期增量放疗情况下两年生存期的更好结果中得到了证明。