Jacquillat C, Khayat D, Banzet P, Weil M, Avril M F, Fumoleau P, Namer M, Bonneterre J, Kerbrat P, Bonerandi J J
Oncology Department Hôpital Pitié-Salpêtrière, Paris, France.
Cancer Chemother Pharmacol. 1990;25(4):263-6. doi: 10.1007/BF00684883.
A total of 42 patients with cerebral metastases of malignant melanoma were included in this study of the nitrosourea fotemustine. The treatment plan consisted of a l-h i.v. infusion of 100 mg/m2 fotemustine every week for 3-4 weeks, followed by a 4- to 5-week rest period. Responding or stabilised patients then received 100 mg/m2 fotemustine every 3 weeks. Among the 39 evaluable patients, 2 complete responses and 9 partial responses were documented, leading to an overall response rate of 28.2%. Most of the responses were obtained in previously untreated patients and/or those presenting with a single cerebral metastasis. Toxicity was mild and mainly hematological, especially in patients previously treated by polychemotherapeutic regimen. Our study confirms the activity of fotemustine in cerebral metastases of disseminated malignant melanoma.
本研究纳入了42例恶性黑色素瘤脑转移患者,对亚硝基脲类药物福莫司汀进行研究。治疗方案为每周静脉输注100mg/m²福莫司汀,持续1小时,共3 - 4周,随后休息4 - 5周。缓解或病情稳定的患者随后每3周接受100mg/m²福莫司汀治疗。在39例可评估患者中,记录到2例完全缓解和9例部分缓解,总缓解率为28.2%。大多数缓解出现在既往未接受过治疗的患者和/或仅有单个脑转移灶的患者中。毒性较轻,主要为血液学毒性,尤其是在既往接受过多种化疗方案治疗的患者中。我们的研究证实了福莫司汀对播散性恶性黑色素瘤脑转移的疗效。