Oxford Molecular Pathology Institute, Sir William Dunn School of Pathology, University of Oxford, South Parks Road, and Oxford University Hospital NHS Trust, Oxford, OX1 3RE, UK.
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences and Centre for Statistics in Medicine (CSM), University of Oxford, Botnar Research Centre, Windmill Road, Oxford, OX3 7LD, UK.
BMC Cancer. 2022 Jun 8;22(1):629. doi: 10.1186/s12885-022-09697-9.
The phase III clinical study of adjuvant liposomal muramyl tripeptide (MTP-PE) in resected high-grade osteosarcoma (OS) documented positive results that have been translated into regulatory approval, supporting initial promise for innate immune therapies in OS. There remains, however, no new approved treatment such as MTP-PE for either metastatic or recurrent OS. Whilst the addition of different agents, including liposomal MTP-PE, to surgery for metastatic or recurrent high-grade osteosarcoma has tried to improve response rates, a mechanistic hiatus exists in terms of a detailed understanding the therapeutic strategies required in advanced disease. Here we report a Bayesian designed multi-arm, multi-centre, open-label phase II study with randomisation in patients with metastatic and/or recurrent OS, designed to investigate how patients with OS might respond to liposomal MTP-PE, either given alone or in combination with ifosfamide. Despite the trial closing because of poor recruitment within the allocated funding period, with no objective responses in eight patients, we report the design and feasibility outcomes for patients registered into the trial. We demonstrate the feasibility of the Bayesian design, European collaboration, tissue collection with genomic analysis and serum cytokine characterisation. Further mechanistic investigation of liposomal MTP-PE alone and in combination with other agents remains warranted in metastatic OS.
III 期临床研究表明,在接受手术切除的高级别骨肉瘤(OS)患者中,使用脂质体粘肽三肽(MTP-PE)进行辅助治疗具有积极的效果,这一结果已转化为监管部门的批准,为 OS 的固有免疫治疗提供了初步的依据。然而,对于转移性或复发性 OS,仍然没有新的批准的治疗方法,如 MTP-PE。虽然在转移性或复发性高级别骨肉瘤的手术中加入不同的药物,包括脂质体 MTP-PE,试图提高缓解率,但在理解晚期疾病所需的治疗策略方面存在机制上的差距。在这里,我们报告了一项贝叶斯设计的多臂、多中心、开放标签的 II 期研究,对转移性和/或复发性 OS 患者进行随机分组,旨在研究 OS 患者对脂质体 MTP-PE 的反应,无论是单独使用还是与异环磷酰胺联合使用。尽管该试验因在规定的资金期内招募人数不足而关闭,8 名患者没有客观缓解,但我们仍报告了该试验中登记患者的设计和可行性结果。我们证明了贝叶斯设计、欧洲合作、组织收集和基因组分析以及血清细胞因子特征的可行性。在转移性 OS 中,进一步研究脂质体 MTP-PE 单独使用和联合其他药物的机制仍然是必要的。