Department of Pediatric Oncology, La Timone Children's Hospital, Marseille, France.
Metronomics Global Health Initiative, Marseille, France.
Pediatr Blood Cancer. 2019 Jul;66(7):e27693. doi: 10.1002/pbc.27693. Epub 2019 Mar 28.
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).
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.).
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.
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.
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])。
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。
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。
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。