Benasso M, Sanguineti G, D'Amico M, Corvò R, Ricci I, Numico G, Guarneri D, Vitale V, Pallestrini E, Santelli A, Rosso R
Department of Medical Oncology I, Istituto Nazionale per la Ricerca sul Cancro, Genova.
Br J Cancer. 2000 Dec;83(11):1437-42. doi: 10.1054/bjoc.2000.1485.
In locally advanced undifferentiated nasopharyngeal carcinoma (UNPC), concomitant chemo-radiotherapy is the only strategy that gave better results over radiation alone in a phase III trial. Adding effective chemotherapy to a concomitant chemo-radiotherapy programme may be a way to improve the results further. 30 patients with previously untreated T4 and/or N2-3 undifferentiated nasopharyngeal carcinoma were consecutively enrolled and initially treated with 3 courses of epidoxorubicin, 90 mg/m2, day 1 and cisplatin, 40 mg/m2, days 1 and 2, every 3 weeks. After a radiological and clinical response assessment patients underwent 3 courses of cisplatin, 20 mg/m2/day, days 1-4 and fluorouracil, 200 mg/m2/day, days 1-4, i.v. bolus, (weeks 1, 4, 7) alternated to 3 courses of radiation (week 2-3, 5-6, 8-9-10), with a single daily fractionation, up to 70 Gy. WHO histology was type 2 in 30% and type 3 in 70% of the patients. 57% had T4 and 77% N2-3 disease. All the patients are evaluable for toxicity and response. All but one received 3 courses of induction chemotherapy. Toxicity was mild to moderate in any case. At the end of the induction phase 10% of CRs, 83.3% of PRs and 6.7% of SD were recorded. All the patients but one had the planned number of chemotherapy courses in the alternating phase and all received the planned radiation dose. One patient out of 3 developed grade III-IV mucositis. Haematological toxicity was generally mild to moderate. At the final response evaluation 86.7% of CRs and 13.3% of PRs were observed. At a median follow-up of 31 months, 13.3% of patients had a loco-regional progression and 20% developed distant metastases. The 3-year actuarial progression-free survival and overall survival rates were 64% and 83%. Induction chemotherapy followed by alternating chemo-radiotherapy is feasible and patients' compliance optimal. This approach showed a very promising activity on locally advanced UNPC and merits to be investigated in phase III studies.
在局部晚期未分化鼻咽癌(UNPC)中,同步放化疗是在一项III期试验中唯一比单纯放疗效果更好的策略。在同步放化疗方案中加入有效的化疗可能是进一步改善疗效的一种方法。连续纳入30例先前未接受治疗的T4和/或N2-3期未分化鼻咽癌患者,初始给予3个疗程的表柔比星,90mg/m²,第1天;顺铂,40mg/m²,第1天和第2天,每3周重复一次。在进行放射学和临床反应评估后,患者接受3个疗程的顺铂,20mg/m²/天,第1 - 4天;氟尿嘧啶,200mg/m²/天,第1 - 4天,静脉推注,(第1、4、7周),与3个疗程的放疗(第2 - 3、5 - 6、8 - 9 - 10周)交替进行,每日单次分割,剂量达70Gy。WHO组织学类型2型的患者占30%,3型的患者占70%。57%的患者为T4期,77%的患者为N2 - 3期。所有患者均可进行毒性和反应评估。除1例患者外,所有患者均接受了3个疗程的诱导化疗。无论何种情况,毒性均为轻至中度。在诱导期结束时,记录到完全缓解(CR)的患者占10%,部分缓解(PR)的患者占83.3%,疾病稳定(SD)的患者占6.7%。除1例患者外,所有患者在交替期均接受了计划数量的化疗疗程,且均接受了计划的放疗剂量。3例患者中有1例发生III - IV级黏膜炎。血液学毒性一般为轻至中度。在最终反应评估时,观察到CR患者占86.7%,PR患者占13.3%。在中位随访31个月时,13.3%的患者出现局部区域进展,20%的患者发生远处转移。3年无进展生存率和总生存率分别为64%和83%。诱导化疗后交替进行放化疗是可行的,患者依从性良好。这种方法对局部晚期UNPC显示出非常有前景的活性,值得在III期研究中进一步探索。