Sonneveld P, Michiels J J
Department of Haematology, University Hospital Rotterdam Dijkzigt, The Netherlands.
Br J Cancer. 1990 Jul;62(1):105-8. doi: 10.1038/bjc.1990.238.
A prospective study was performed to evaluate the feasibility of full dose chemotherapy given on schedule in elderly patients with unfavourable non-Hodgkin's lymphoma, stage IE, III and IV. Using a combination regimen of six courses of cyclophosphamide, mitoxantrone, vincristine and prednisone (CNOP) given every 4 weeks, no serious toxicity was encountered in a group of 30 consecutive patients with a mean age of 70.4 years. A 60% complete response rate was observed and a total response rate of 90%. The disease-free survival of complete responders was 50% at 1 year. The overall survival was also 50% at 1 year. In 148 courses of CNOP only two serious infectious episodes were noted, i.e. one herpes zoster infection and one case of bronchopneumonia. Asymptomatic transient thrombocytopenia and granulocytopenia were commonly observed. Nadirs of white blood cells were WHO grade 1, 2, 3 and 4 in six, five, twelve and two patients respectively and nadirs of thrombocytopenia were WHO grade 0 and 1 (22 patients) or 2 (three patients). Based on low white blood cell counts, a delay of 1 week before administration of the next course of CNOP was necessary in 7% of the courses. No dose reductions were applied. Toxicity other than transient granulocytopenia was minor and consisted of alopecia and nausea. WHO grade 0-2. CNOP related toxicity was never a reason to stop treatment. It is concluded that CNOP chemotherapy without initial dose reduction in elderly patients with intermediate and high grade malignant non-Hodgkin's lymphoma is feasible and that no major toxicity is observed.
开展了一项前瞻性研究,以评估在患有不良型非霍奇金淋巴瘤(IE期、III期和IV期)的老年患者中按时给予全剂量化疗的可行性。采用每4周进行六个疗程的环磷酰胺、米托蒽醌、长春新碱和泼尼松(CNOP)联合方案,在一组平均年龄为70.4岁的30例连续患者中未遇到严重毒性反应。观察到完全缓解率为60%,总缓解率为90%。完全缓解者的无病生存率在1年时为50%。1年时的总生存率也为50%。在148个CNOP疗程中,仅记录到两例严重感染事件,即1例带状疱疹感染和1例支气管肺炎。无症状性短暂血小板减少和粒细胞减少很常见。白细胞最低点分别为WHO 1级、2级、3级和4级的患者有6例、5例、12例和2例,血小板减少最低点为WHO 0级和1级(22例患者)或为2级(3例患者)。基于白细胞计数较低,7%的疗程需要在下一疗程CNOP给药前延迟1周。未进行剂量减少。除短暂性粒细胞减少外的毒性较小,包括脱发和恶心,为WHO 0 - 2级。与CNOP相关的毒性从未成为停止治疗的理由。结论是,在患有中、高级别恶性非霍奇金淋巴瘤的老年患者中,不进行初始剂量减少的CNOP化疗是可行的,且未观察到重大毒性。