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SFCE 美托洛尔-01 四药节拍方案治疗儿科颅外肿瘤的 II 期临床试验。

SFCE METRO-01 four-drug metronomic regimen phase II trial for pediatric extracranial tumor.

机构信息

Department of Pediatric Oncology, La Timone Children's Hospital, Marseille, France.

Metronomics Global Health Initiative, Marseille, France.

出版信息

Pediatr Blood Cancer. 2019 Jul;66(7):e27693. doi: 10.1002/pbc.27693. Epub 2019 Mar 28.

Abstract

OBJECTIVE

To investigate the antitumor activity of a four-drug metronomic chemotherapy (MC) regimen in relapsed/progressing pediatric extracranial solid tumors (EST). The primary objective was clinical benefit (complete response /partial response/stable disease [SD]) after two cycles of therapy (four months).

METHODS

Patients aged ≥4 to 25 years with progressing EST and adequate organ function were eligible. Treatment consisted of an eight-week cycle of oral celecoxib b.i.d., weekly vinblastine, and oral cyclophosphamide for three weeks alternating with oral methotrexate for three weeks, with a two-week rest. The Kepner-Chang two-stage model was used with 10 patients in the first stage. If primary objective was reached in two or more patients, eight additional patients were included according to four groups: neuroblastoma (NBL), soft-tissue sarcoma (STS), bone sarcoma (BS), and miscellaneous (Misc.).

RESULTS

Forty-four patients were evaluable. The NBL cohort could be expanded to 18 patients: 4 of 18 patients stabilized with MC treatment for 6 (n = 1) and 12 (n = 3) months. In STS, two of seven patients (metastatic hemangioendothelioma and angiosarcoma) had SD for > 2 cycles. One of nine Misc. (metastatic myoepithelial carcinoma) had SD for one year. All patients with BS had progressive disease. One-year progression-free survival of the whole cohort was 6.8% and one-year overall survival was 55.3%. Grade 3 toxicity occurred in 18 patients and grade 4 in 15 patients. The most frequent toxicity was hematologic, predominantly neutropenia.

CONCLUSIONS

This MC has no activity in BS and limited though interesting activity in NBL with some patients being stable for > 1 year. It is not possible to conclude activity in STS and Misc.

摘要

目的

研究一种四药节拍化疗(MC)方案在复发性/进展性儿科颅外实体瘤(EST)中的抗肿瘤活性。主要目标是治疗两个周期(四个月)后的临床获益(完全缓解/部分缓解/稳定疾病[SD])。

方法

符合条件的患者为年龄≥4 岁至 25 岁、进展性 EST 和足够的器官功能的患者。治疗包括口服塞来昔布,bid;每周长春碱;和口服环磷酰胺三周,与口服甲氨蝶呤三周交替,两周休息。采用 Kepner-Chang 两阶段模型,第一阶段有 10 名患者。如果两个或两个以上患者达到主要目标,则根据神经母细胞瘤(NBL)、软组织肉瘤(STS)、骨肉瘤(BS)和其他(Misc.)四个组纳入另外 8 名患者。

结果

44 名患者可评估。NBL 队列可扩大至 18 名患者:18 名患者中的 4 名患者接受 MC 治疗后稳定 6(n=1)和 12(n=3)个月。在 STS 中,7 名患者中的 2 名(转移性血管内皮细胞瘤和血管肉瘤)有超过 2 个周期的 SD。9 名 Misc.(转移性肌上皮癌)患者中的 1 名有 1 年的 SD。所有 BS 患者均有进展性疾病。整个队列的 1 年无进展生存率为 6.8%,1 年总生存率为 55.3%。18 名患者出现 3 级毒性,15 名患者出现 4 级毒性。最常见的毒性是血液学毒性,主要是中性粒细胞减少。

结论

这种 MC 在 BS 中没有活性,在 NBL 中有一定的活性,但在一些患者中稳定超过 1 年。在 STS 和 Misc.中是否有活性尚无法得出结论。

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