Maraninchi D, Viens P, Legros M, Oberling F, Philip T, Herve P, Plagne R, Dufour P, Bergerat J P, Guastalla J P
Unité de Transplantation médullaire et Centre anticancéreux de: Marseille, France.
Bull Cancer. 1990;77(2):149-57.
Reviewed in this study are 40 patients treated by high-doses of alkylating agents followed by autologous marrow rescue for ovarian cancers. All patients received this therapy after extensive surgery and a median of 6 cycles of CDDP containing regimens (CAP or CHAP). All patients, except 4, who showed evidence of progression, had a second surgical exploration before the high dose chemotherapy. Conditioning regimens consisted of: melphalan at a dosage greater than 140 mg/m2 for all patients; in addition, 2 received Endoxan 120 mg/kg and 1 busulfan 16 mg/kg. Autologous marrow rescue was infused 24 h after the conditioning regimen. Severe, but reversible aplasia and mucositis were the most common toxicities. Three patients died from this procedure, 2 from infection and 1 from secondary leukemia. Twelve out of 15 patients evaluated responded (80%) showing evidence of activity in patients who did not respond to first line chemotherapy. Duration of response was short, especially for patients treated for progressive disease rather than in partial or complete response at the time of high doses chemotherapy. With a median follow up of 23 months (range 8.54) 19 patients survived (15 with non-evolutive disease) leading to a projected survival rate of 39% between 27 months and 5 years. These results are encouraging for poor risk patients who failed to respond to initial chemotherapy. For patients who have small or no residual disease after initial therapy, the place of such intensification should be confirmed prospectively in a larger cohort of patients.
本研究回顾了40例接受高剂量烷化剂治疗并随后进行自体骨髓挽救的卵巢癌患者。所有患者在广泛手术及中位6个周期含顺铂方案(CAP或CHAP)治疗后接受了该疗法。除4例有疾病进展证据的患者外,所有患者在高剂量化疗前均进行了二次手术探查。预处理方案包括:所有患者美法仑剂量大于140mg/m²;此外,2例患者接受环磷酰胺120mg/kg,1例患者接受白消安16mg/kg。预处理方案后24小时输注自体骨髓挽救。严重但可逆的再生障碍和粘膜炎是最常见的毒性反应。3例患者死于该治疗过程,2例死于感染,1例死于继发性白血病。15例接受评估的患者中有12例有反应(80%),表明对一线化疗无反应的患者有活性迹象。反应持续时间较短,尤其是对那些接受高剂量化疗时疾病进展而非部分或完全缓解的患者。中位随访23个月(范围8.5 - 4个月),19例患者存活(15例疾病无进展),预计27个月至5年的生存率为39%。这些结果对于初始化疗无反应的高危患者令人鼓舞。对于初始治疗后残留疾病少或无残留疾病的患者,这种强化治疗的地位应在更大的患者队列中进行前瞻性确认。