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异环磷酰胺和多柔比星作为新诊断的转移性横纹肌肉瘤患儿II期“窗口”治疗的疗效:横纹肌肉瘤研究组的报告

Efficacy of ifosfamide and doxorubicin given as a phase II "window" in children with newly diagnosed metastatic rhabdomyosarcoma: a report from the Intergroup Rhabdomyosarcoma Study Group.

作者信息

Sandler E, Lyden E, Ruymann F, Maurer H, Wharam M, Parham D, Link M, Crist W

机构信息

Intergroup Rhabdomyosarcoma Study Group Operations Office, Children's Oncology Group, Arcadia, CA 91066-6012, USA.

出版信息

Med Pediatr Oncol. 2001 Nov;37(5):442-8. doi: 10.1002/mpo.1227.

DOI:10.1002/mpo.1227
PMID:11745872
Abstract

BACKGROUND

The cure rate for children/adolescents with localized rhabdomyosarcoma (RMS) has tripled over the past 25 years, but patients with metastatic disease at presentation have not benefited similarly, and urgently need new therapy. We evaluated a new drug pair, ifosfamide + doxorubicin, for such patients.

PROCEDURE

We estimated the complete and partial response rates (i.e., CR and PR) of 152 previously untreated children/adolescents with metastatic RMS entered on the IRS-IV pilot from July 1988 to October 1991 who received an "up-front window" of ifosfamide (1.8 gm/m(2)/day for 5 days) and doxorubicin (30 mg/m(2)/day for 2 days) given every 3 weeks for 12 weeks. This was followed by combination chemotherapy with vincristine, actinomycin D, and cyclophosphamide (VAC), given every 3 weeks for an additional 36 weeks.

RESULTS

Of 115 patients evaluable for early response at 12 weeks, 28 (20%) had CR and 66 (43%) had PR. The ultimate CR rate was 52%. Overall, about one-third of patients survived. Prognostic factor analysis revealed that patients < 10 years old (P < 0.001), those with embryonal tumors (P = 0.002), or a GU primary site (P = 0.010), and those who lacked nodal disease (P = 0.041), and those who lacked bone or bone marrow metastasis (P < 0.001) fared better than did others.

CONCLUSIONS

The 63% CR + PR rate achieved at 12 weeks and overall 5-year FFS seen with this drug pair is similar to that achieved with previously evaluated drug combinations. We conclude that ifosfamide/doxorubicin is highly active in advanced RMS, and should be considered for inclusion in frontline therapy for children with intermediate or high-risk RMS.

摘要

背景

在过去25年中,局限性横纹肌肉瘤(RMS)患儿/青少年的治愈率提高了两倍,但初诊时患有转移性疾病的患者并未得到同样的益处,迫切需要新的治疗方法。我们评估了一种新药组合,异环磷酰胺+阿霉素,用于此类患者。

程序

我们评估了1988年7月至1991年10月入组IRS-IV试验的152例先前未接受治疗的转移性RMS患儿/青少年的完全缓解率和部分缓解率(即CR和PR),这些患者接受了“前期窗口”治疗,即每3周给予异环磷酰胺(1.8 g/m²/天,共5天)和阿霉素(30 mg/m²/天,共2天),持续12周。随后每3周给予长春新碱、放线菌素D和环磷酰胺(VAC)联合化疗,持续36周。

结果

在115例可在12周时评估早期缓解情况的患者中,28例(20%)达到CR,66例(43%)达到PR。最终CR率为52%。总体而言,约三分之一的患者存活。预后因素分析显示,年龄<10岁的患者(P<0.001)、患有胚胎性肿瘤的患者(P = 0.002)、原发部位为泌尿生殖系统的患者(P = 0.010)、无淋巴结疾病的患者(P = 0.041)以及无骨或骨髓转移的患者(P<0.001)的预后优于其他患者。

结论

该药物组合在12周时达到的63%的CR+PR率以及总体5年无病生存率与先前评估的药物组合相似。我们得出结论,异环磷酰胺/阿霉素在晚期RMS中具有高度活性,应考虑将其纳入中高危RMS患儿的一线治疗方案。

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