Buesa J M, López-Pousa A, Martín J, Antón A, García del Muro J, Bellmunt J, Arranz F, Valentí V, Escudero P, Menéndez D, Casado A, Poveda A
Hospital Central de Asturias, Oviedo, Spain.
Ann Oncol. 1998 Aug;9(8):871-6. doi: 10.1023/a:1008474802882.
The agent Ifosfamide (IFOS) is active against soft tissue sarcomas (STS), and patients who progress to IFOS at doses < or = 10 g/m2 show remissions when exposed to high-dose ifosfamide (HDI) (i.e., doses > 10 g/m2), which supports a dose-response relationship for this drug. Because of a lack of first-line studies in adult STS patients, we decided to test the activity and toxicity of HDI in a phase II trial.
Forty-eight patients were enrolled in the study. IFOS was administered at a dose of 14 g/m2 by continuous infusion over six days every four weeks. Granulocyte-macrophage colony-stimulating factor (GM-CSF) at 5 micrograms/kg/day for 10 consecutive days was systematically administered after an episode of neutropenic fever or a delay in hematologic recovery. Patients were treated until progression or the occurrence of severe toxicity, and surgical rescue was attempted when possible.
Six pathology-established complete remissions and 11 partial remissions were observed in 45 assessable patients with a response rate of 37.7% (95% CI: 25.5%-50%). Grade 3-4 toxicity (% of cycles) was noted by hemoglobin (17%), leukocyte (75%), granulocyte (75%) and platelet (13%) counts in 158 evaluable cycles. GM-CSF was administered to 28 patients, and 25 suffered one or more episodes of neutropenic fever. Renal toxicity was mild and reversible with some degree of tubular and glomerular dysfunction detected in up to 60% of patients. Grade 3 CNS toxicity was observed in 32% of patients but only one required interruption of therapy. Sixty-four per cent of the patients had asthenia grade 2-3 and 20% were excluded from the study due to excessive toxicity. There was one treatment-related death.
HDI is an active drug in first-line therapy against adult STS. Different administration schedules should be evaluated in an attempt to improve its therapeutic index.
异环磷酰胺(IFOS)对软组织肉瘤(STS)具有活性,对于接受剂量≤10g/m²异环磷酰胺治疗后病情进展的患者,当给予高剂量异环磷酰胺(HDI,即剂量>10g/m²)时会出现缓解,这支持了该药物的剂量反应关系。由于缺乏针对成人STS患者的一线研究,我们决定在一项II期试验中测试HDI的活性和毒性。
48名患者入组本研究。IFOS以14g/m²的剂量每四周连续输注6天给药。在发生中性粒细胞减少性发热或血液学恢复延迟后,系统性地连续10天给予5μg/kg/天的粒细胞-巨噬细胞集落刺激因子(GM-CSF)。患者接受治疗直至病情进展或出现严重毒性,可能时尝试进行手术挽救。
在45例可评估患者中观察到6例经病理证实的完全缓解和11例部分缓解,缓解率为37.7%(95%CI:25.5%-50%)。在158个可评估周期中,血红蛋白(17%)、白细胞(75%)、粒细胞(75%)和血小板(13%)计数出现3-4级毒性(周期百分比)。28例患者接受了GM-CSF治疗,其中25例发生了一次或多次中性粒细胞减少性发热。肾毒性较轻且可逆,高达60%的患者检测到一定程度的肾小管和肾小球功能障碍。32%的患者观察到3级中枢神经系统毒性,但只有1例需要中断治疗。64%的患者出现2-3级乏力,20%的患者因毒性过大被排除在研究之外。有1例与治疗相关的死亡。
HDI是一线治疗成人STS的活性药物。应评估不同的给药方案以试图提高其治疗指数。