Weiss A J, Horowitz S, Lackman R D
Department of Medicine, Allegheny University Hospital and School of Medicine, Philadelphia, Pennsylvania 19107, USA.
Am J Clin Oncol. 1999 Apr;22(2):193-5. doi: 10.1097/00000421-199904000-00020.
In patients with either desmoids or fibromatosis who do not tolerate vinblastine and methotrexate because of neurotoxicity, the combination of vinorelbine and methotrexate can be substituted in most. Patients with the same condition who had not been previously treated with a combination of vinblastine and methotrexate responded well to the combination of vinorelbine and methotrexate, with significantly less neurotoxicity and a similar objective and subjective response rate. Sixty percent of patients had either a substantial partial remission or a complete remission. In no patients did the disease progress while they were receiving this therapy. Symptomatic relief, primarily of pain, occurred in 80% of patients. While minimal neurotoxicity was seen in 16% of these patients, it did not interfere with the completion of therapy. The combination of vinorelbine and methotrexate appears to be active in the treatment of both desmoid tumors and fibromatosis and is associated with significantly less neurotoxicity then that seen with the combination of vinblastine and methotrexate. No long-term toxicity was seen in any patient in this series.
对于因神经毒性而不耐受长春碱和甲氨蝶呤的韧带样瘤或纤维瘤病患者,多数情况下可改用长春瑞滨与甲氨蝶呤联合治疗。既往未接受过长春碱和甲氨蝶呤联合治疗的相同病情患者,对长春瑞滨与甲氨蝶呤联合治疗反应良好,神经毒性显著降低,客观和主观缓解率相似。60%的患者实现了大幅部分缓解或完全缓解。在接受该治疗期间,无患者疾病进展。80%的患者症状得到缓解,主要是疼痛缓解。这些患者中有16%出现轻微神经毒性,但未影响治疗的完成。长春瑞滨与甲氨蝶呤联合治疗似乎对韧带样瘤和纤维瘤病均有治疗活性,且与长春碱和甲氨蝶呤联合治疗相比,神经毒性显著降低。该系列中无患者出现长期毒性。