Yalçin S, Güllü I, Barişta I, Tekuzman G, Ozişik Y, Celik I, Kars A
Hacettepe University Institute of Oncology, Ankara, Turkey.
Cancer Invest. 1998;16(5):297-302. doi: 10.3109/07357909809084647.
Chemotherapy options for resistant advanced-stage sarcomas are limited and in most cases disappointing. In a phase II study, we treated 26 consecutive patients with refractory advanced sarcoma with ifosfamide and etoposide combination chemotherapy. All patients had received prior doxorubicin- and/or cyclophosphamide-based chemotherapies. Seventeen patients were male and 9 were female. The patients' median age was 35 years (range: 19-67 years). A total of 24 patients were eligible for evaluation of responses. Seven patients had a complete response (CR) (29.1%), 3 had a partial response (PR) (12.5%), 3 had stable disease (SD) (12.5%), and 11 had progressive disease (PD) (45.9%). An overall 41.6% objective response was achieved. Median time to treatment failure was 13.3 months. A total of 108 cycles of therapy were evaluable for evaluation of toxicity. Myelosuppression, observed in 55.5% of the treatment courses, was the major dose-limiting toxicity. Nausea and vomiting, seen in 64% of the courses, were the most important nonhematological side effects. Alopecia was almost universal. Hemorrhagic cystitis was observed in only 1 patient. We have concluded that the combination of ifosfamide, mesna, and etoposide is effective in advanced refractory sarcomas, and has acceptable toxicity.
对于耐药晚期肉瘤的化疗选择有限,且在大多数情况下效果不佳。在一项II期研究中,我们用异环磷酰胺和依托泊苷联合化疗连续治疗了26例难治性晚期肉瘤患者。所有患者此前均接受过基于阿霉素和/或环磷酰胺的化疗。17例患者为男性,9例为女性。患者的中位年龄为35岁(范围:19 - 67岁)。共有24例患者符合疗效评估条件。7例患者完全缓解(CR)(29.1%),3例部分缓解(PR)(12.5%),3例病情稳定(SD)(12.5%),11例病情进展(PD)(45.9%)。总体客观缓解率为41.6%。治疗失败的中位时间为13.3个月。共有108个治疗周期可用于毒性评估。55.5%的治疗疗程出现骨髓抑制,这是主要的剂量限制性毒性。64%的疗程出现恶心和呕吐,这是最重要的非血液学副作用。脱发几乎普遍存在。仅1例患者出现出血性膀胱炎。我们得出结论,异环磷酰胺、美司钠和依托泊苷联合方案对晚期难治性肉瘤有效,且毒性可接受。