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[ACNU与达卡巴嗪联合化疗治疗晚期恶性黑色素瘤]

[A combination chemotherapy of ACNU and DTIC for advanced malignant melanoma].

作者信息

Domyo M, Ogawa M, Inagaki J, Horikoshi N, Ezaki K, Inoue K, Aiba K, Nagata T, Miyamoto H

出版信息

Gan To Kagaku Ryoho. 1982 May;9(5):874-9.

PMID:6964041
Abstract

Fourteen patients with advanced malignant melanoma were treated with a combination chemotherapy consisting of ACNU 100 mg/m2 i.v. on Day 1 in 6 week intervals and DTIC 200 mg/m2 i.v. on Days 1 to 5 at 3 week intervals. Four patients had prior chemotherapy and 2 had prior immunotherapy. Excluding 4 patients received the regimen for adjuvant chemotherapy, 10 of 14 patients were evaluable for response. There were 3 patients of partial responses, 3 minor responses, 1 no change, and 3 progressive diseases. The durations of partial responses were 1, 1, and 8 months, respectively, while the survival times in these patients were 5, 21, and 10 months, respectively. Leukopenia less than 4,000/cmm occurred in 10 of 14 patients (71%) and thrombocytopenia less than 100 X 10(3)/cmm in 9 of 14 patients (64%), moreover, these hematologic toxicities were cumulative. Serum GOT and GPT elevated to 3,460 mu/ml and 1,365 mu/ml, respectively in one patient, but this returned to a normal level one month later. Nausea and vomiting were mild to severe in 12 of 14 patients, being most marked on Day 1 and decreasing intensity during the next several days. Other non-hematologic toxicities including skin rash, fever, and phlebitis were noted in each one patient, respectively. Hematologic toxicity of this regimen was a dose limiting toxicity; therefore, intensive supportive therapy to prevent infection and hemorrhage is essential for the management of the patients during this chemotherapy.

摘要

14例晚期恶性黑色素瘤患者接受了联合化疗,方案为第1天静脉注射ACNU 100 mg/m²,每6周1次,同时第1至5天静脉注射DTIC 200 mg/m²,每3周1次。4例患者曾接受过化疗,2例曾接受过免疫治疗。排除4例接受辅助化疗方案的患者后,14例患者中有10例可评估疗效。有3例部分缓解、3例轻微缓解、1例病情无变化、3例病情进展。部分缓解的持续时间分别为1个月、1个月和8个月,而这些患者的生存时间分别为5个月、21个月和10个月。14例患者中有10例(71%)出现白细胞减少至低于4000/cmm,14例患者中有9例(64%)出现血小板减少至低于100×10³/cmm,而且这些血液学毒性是累积性的。1例患者血清谷草转氨酶(GOT)和谷丙转氨酶(GPT)分别升高至3460 μ/ml和1365 μ/ml,但1个月后恢复正常水平。14例患者中有12例出现轻至重度恶心和呕吐,在第1天最为明显,随后几天强度逐渐降低。分别有1例患者出现其他非血液学毒性,包括皮疹、发热和静脉炎。该方案的血液学毒性是剂量限制性毒性;因此,在这种化疗期间,对患者进行强化支持治疗以预防感染和出血对于管理患者至关重要。

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Gan To Kagaku Ryoho. 1982 May;9(5):874-9.
2
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