Pein F, Tournade M F, Zucker J M, Brunat-Mentigny M, Deville A, Boutard P, Dusol F, Gentet J C, Legall E, Mechinaud F
Department of Pediatric Oncology, Institut Gustave Roussy, Villejuif, France.
J Clin Oncol. 1994 May;12(5):931-6. doi: 10.1200/JCO.1994.12.5.931.
Since we had previously demonstrated encouraging efficacy of etoposide in patients with relapsed or refractory Wilms' tumor (WT), the likely synergism between etoposide and platinum compounds prompted us to conduct a phase II study of a combination with carboplatin.
Twenty-six relapsed or refractory WT patients were included in a phase II study of two courses of combination etoposide 100 mg/m2/d for 5 days and carboplatin 160 mg/m2/d for 5 days, with a 21-day interval between the two courses. Initial stages were I (n = 2), II (n = 8), III (n = 6), IV (n = 6), V (n = 3), and unknown (n = 1). Sites of diseases were lung(s) (11 patients), abdomen-pelvis or liver or primary tumor (six patients), and multiple (eight patients). Histology was unfavorable in three of 26 patients.
Complete response (CR) was documented in eight patients and partial remission (PR) in 11 (overall response rate, 73%). Stable disease (SD) was observed in five patients and progressive disease (PD) in two. Thrombocytopenia (grade IV) was the major toxicity, and platelet transfusions were required in all but two patients. Grade III anemia and grade III to IV neutropenia were seen in 19 and 23, respectively, of 25 assessable first courses. Venoocclusive disease of the liver was fatal in one child who had undergone irradiation to the whole abdomen, 8 weeks before study.
Combination etoposide and carboplatin has impressive activity in refractory or relapsed WT at the cost of high-grade hematologic toxicity, especially thrombocytopenia. It is of great interest in second-line therapy, since eight of 26 patients are still alive in continuous CR (median follow-up duration, 40 months; range, 24 to 56). This combination deserves further investigation as first-line or consolidation treatment.
鉴于我们之前已证明依托泊苷对复发或难治性肾母细胞瘤(WT)患者具有令人鼓舞的疗效,依托泊苷与铂类化合物之间可能存在的协同作用促使我们开展一项与卡铂联合使用的II期研究。
26例复发或难治性WT患者纳入一项II期研究,接受两个疗程的联合治疗,依托泊苷100mg/m²/天,共5天,卡铂160mg/m²/天,共5天,两个疗程之间间隔21天。初始分期为I期(n = 2)、II期(n = 8)、III期(n = 6)、IV期(n = 6)、V期(n = 3),分期不明(n = 1)。疾病部位为肺部(11例患者)、腹盆腔或肝脏或原发肿瘤(6例患者)以及多处(8例患者)。26例患者中有3例组织学类型为不良型。
8例患者获得完全缓解(CR),11例患者获得部分缓解(PR)(总缓解率为73%)。5例患者病情稳定(SD),2例患者病情进展(PD)。血小板减少(IV级)是主要毒性反应,除2例患者外,所有患者均需要输注血小板。在25例可评估的首个疗程中,分别有19例和23例出现III级贫血和III至IV级中性粒细胞减少。1例在研究前8周接受全腹照射的儿童因肝静脉闭塞病死亡。
依托泊苷与卡铂联合使用对难治性或复发性WT具有显著活性,但代价是出现高级别血液学毒性,尤其是血小板减少。由于26例患者中有8例仍处于持续CR状态存活(中位随访时间40个月;范围24至56个月),因此该联合方案在二线治疗中具有重大意义。这种联合方案作为一线或巩固治疗值得进一步研究。