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异环磷酰胺/依托泊苷联合方案治疗儿童复发性恶性实体瘤。一项儿科肿瘤学组II期研究。

Ifosfamide/etoposide combination in the treatment of recurrent malignant solid tumors of childhood. A Pediatric Oncology Group Phase II study.

作者信息

Kung F H, Pratt C B, Vega R A, Jaffe N, Strother D, Schwenn M, Nitschke R, Homans A C, Holbrook C T, Golembe B

机构信息

Department of Pediatrics, University of California, San Diego.

出版信息

Cancer. 1993 Mar 1;71(5):1898-903. doi: 10.1002/1097-0142(19930301)71:5<1898::aid-cncr2820710529>3.0.co;2-q.

Abstract

BACKGROUND

The prognosis for children with recurrent or resistant malignant solid tumors remains dismal. More effective rescue therapy is needed for these children.

METHODS

Between August 1987 and November 1990, 311 children with recurrent or resistant malignant solid tumors were treated by investigators in the Pediatric Oncology Group with intravenous infusions of 2.0 g/m2 of ifosfamide and 100 mg/m2 of etoposide (VP-16) plus mesna as uroprotection three times daily, with courses being repeated every 14-21 days for as long as the patients responded to therapy.

RESULTS

Seventy-four percent of the 294 assessable patients entered in the study had metastatic disease and previously had been treated heavily. The complete response/partial response rate was 30%, and the overall response rate was 39.5%. Toxic effects included nephrotoxicity, mild liver dysfunction, neurotoxicity, and myelosuppression. Sixty-eight percent had an absolute neutrophil count (ANC) of less than 500/microliters. In 1606 courses of therapy administered, only 3.6% of patients developed a bacterial infection. Only two patients died of gram-negative sepsis. Four percent of the patients had gross hematuria (> 50 erythrocytes/high-power field), and 18.5% had microscopic hematuria (< 20 erythrocytes/high-power field). Fanconi syndrome developed in eight children.

CONCLUSIONS

Ifosfamide/VP-16 is an active combination in children with recurrent malignant solid tumors. Although it was myelosuppressive, the incidence of infection was quite low (3.6%). Mesna was very effective in preventing the development of hematuria.

摘要

背景

复发性或难治性恶性实体瘤患儿的预后仍然很差。这些患儿需要更有效的挽救治疗。

方法

1987年8月至1990年11月期间,儿科肿瘤学组的研究人员对311例复发性或难治性恶性实体瘤患儿进行了治疗,静脉输注2.0 g/m²异环磷酰胺和100 mg/m²依托泊苷(VP - 16),并加用美司钠作为尿路保护剂,每日3次,每14 - 21天重复疗程,只要患者对治疗有反应就持续进行。

结果

该研究纳入的294例可评估患者中,74%有转移性疾病,且之前接受过大量治疗。完全缓解/部分缓解率为30%,总缓解率为39.5%。毒性作用包括肾毒性、轻度肝功能障碍、神经毒性和骨髓抑制。68%的患者绝对中性粒细胞计数(ANC)低于500/微升。在1606个疗程的治疗中,只有3.6%的患者发生细菌感染。只有2例患者死于革兰阴性菌败血症。4%的患者出现肉眼血尿(>50个红细胞/高倍视野),18.5%的患者出现镜下血尿(<20个红细胞/高倍视野)。8名儿童发生了范科尼综合征。

结论

异环磷酰胺/VP - 16对复发性恶性实体瘤患儿是一种有效的联合治疗方案。虽然它有骨髓抑制作用,但感染发生率相当低(3.6%)。美司钠在预防血尿发生方面非常有效。

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