Results of a Randomized, Double-Blinded, Placebo-Controlled, Phase 2.5 Study of Saracatinib (AZD0530), in Patients with Recurrent Osteosarcoma Localized to the Lung.

Q2 Medicine
Sarcoma Pub Date : 2020-04-30 eCollection Date: 2020-01-01 DOI:10.1155/2020/7935475
Kristin Baird, John Glod, Seth M Steinberg, Denise Reinke, Joseph G Pressey, Leo Mascarenhas, Noah Federman, Neyssa Marina, Sant Chawla, Joanne P Lagmay, John Goldberg, Mohammed Milhem, David M Loeb, James E Butrynski, Brian Turpin, Arthur Staddon, Sheri L Spunt, Robin L Jones, Eve T Rodler, Scott M Schuetze, Scott H Okuno, Lee Helman
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引用次数: 15

Abstract

Purpose: Osteosarcoma is a rare cancer and a third of patients who have completed primary treatment will develop osteosarcoma recurrence. The Src pathway has been implicated in the metastatic behavior of osteosarcoma; about 95% of samples examined express Src or have evidence of downstream activation of this pathway. Saracatinib (AZD0530) is a potent and selective Src kinase inhibitor that was evaluated in adults in Phase 1 studies. The primary goal of this study was to determine if treatment with saracatinib could increase progression-free survival (PFS) for patients who have undergone complete resection of osteosarcoma lung metastases in a double-blinded, placebo-controlled trial. Patients and Methods. Subjects with recurrent osteosarcoma localized to lung and who had complete surgical removal of all lung nodules were randomized within six weeks after complete surgical resection. Saracatinib, or placebo, was administered at a dose of 175 mg orally, once daily, for up to thirteen 28-day cycles.

Results: Thirty-seven subjects were included in the analyses; 18 subjects were randomized to receive saracatinib and 19 to receive placebo. Intent-to-treat analysis demonstrated a median PFS of 19.4 months in the saracatinib treatment group and 8.6 months in the placebo treatment group (p=0.47). Median OS was not reached in either arm.

Conclusions: Although saracatinib was well tolerated in this patient population, there was no apparent impact of the drug in this double-blinded, placebo-controlled trial on OS, and Src inhibition alone may not be sufficient to suppress metastatic progression in osteosarcoma. There is a suggestion of potential clinical benefit as evidenced by longer PFS in patients randomized to saracatinib based on limited numbers of patients treated.

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一项随机、双盲、安慰剂对照、Saracatinib (AZD0530)治疗复发性肺骨肉瘤患者的2.5期研究结果
目的:骨肉瘤是一种罕见的癌症,完成初级治疗的患者中有三分之一会发生骨肉瘤复发。Src通路与骨肉瘤的转移行为有关;大约95%的样本表达Src或有证据表明该途径下游激活。Saracatinib (AZD0530)是一种有效的选择性Src激酶抑制剂,在成人1期研究中进行了评估。本研究的主要目的是在一项双盲、安慰剂对照试验中确定saracatinib治疗是否可以提高肺转移骨肉瘤完全切除患者的无进展生存期(PFS)。患者和方法。复发性骨肉瘤局限于肺部,并且手术切除了所有肺结节的受试者在完全手术切除后的六周内随机分组。Saracatinib,或安慰剂,以175毫克的剂量口服,每天一次,长达13个28天的周期。结果:37名受试者被纳入分析;18名受试者随机接受萨拉卡替尼治疗,19名接受安慰剂治疗。意向治疗分析显示,萨拉卡替尼治疗组的中位PFS为19.4个月,安慰剂治疗组的中位PFS为8.6个月(p=0.47)。两组的中位OS均未达到。结论:尽管saracatinib在该患者群体中耐受性良好,但在这项双盲、安慰剂对照试验中,该药物对骨肉瘤没有明显的影响,仅抑制Src可能不足以抑制骨肉瘤的转移进展。根据有限的患者数量,随机分配到saracatinib的患者的PFS较长,这表明潜在的临床益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Sarcoma
Sarcoma Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
5.00
自引率
0.00%
发文量
15
审稿时长
14 weeks
期刊介绍: Sarcoma is dedicated to publishing papers covering all aspects of connective tissue oncology research. It brings together work from scientists and clinicians carrying out a broad range of research in this field, including the basic sciences, molecular biology and pathology and the clinical sciences of epidemiology, surgery, radiotherapy and chemotherapy. High-quality papers concerning the entire range of bone and soft tissue sarcomas in both adults and children, including Kaposi"s sarcoma, are published as well as preclinical and animal studies. This journal provides a central forum for the description of advances in diagnosis, assessment and treatment of this rarely seen, but often mismanaged, group of patients.
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