IIIrd Medical Department with Hematology and Medical Oncology, Hemostaseology, Rheumatology and Infectious Diseases, Oncologic Center, Paracelsus Medical University Salzburg, Müllner Hauptstrasse 48, 5020, Salzburg, Austria.
Salzburg Cancer Research Institute with Laboratory of Immunological and Molecular Cancer Research and Center for Clinical Cancer and Immunology Trials, Salzburg, Austria.
BMC Cancer. 2018 Nov 6;18(1):1074. doi: 10.1186/s12885-018-4979-0.
Triple-negative breast cancer (TNBC) comprises a heterogeneous group of diseases which are generally associated with poor prognosis. Up to now, no targeted treatment beyond anti-VEGF therapy has been approved for TNBC and cytotoxic agents remain the mainstay of treatment. Ixazomib is a selective and reversible inhibitor of the proteasome, which has been mainly investigated in the treatment of multiple myeloma. In a preclinical study TNBC cells were treated with the first-generation proteasome inhibitor bortezomib in combination with cisplatin and synergistic efficacy was demonstrated. Clinical data are available for carboplatin plus bortezomib in metastatic ovarian and lung cancers showing remarkable antitumor activity and good tolerability (Mol Cancer 11:26 2012, J Thorac Oncol 4:87-92 2009, J Thorac Oncol 7:1032-1040, 2012). Based on this evidence, the phase I/II MBC-10 trial will evaluate the toxicity profile and efficacy of the second-generation proteasome inhibitor ixazomib in combination with carboplatin in patients with advanced TNBC.
Patients with metastatic TNBC pretreated with at least one prior line of chemotherapy for advanced disease with a confirmed disease progression and measurable disease according to RECIST criteria 1.1 are eligible for this study. Patients will receive ixazomib in combination with carboplatin on days 1, 8, and 15 in a 28-day cycle. The phase I part of this study utilizes an alternate dose escalation accelerated titration design. After establishing the maximum tolerated dose (MTD), the efficacy and safety of the combination will be further evaluated (phase II, including 41 evaluable patients). All patients will continue on study drugs until disease progression, unacceptable toxicity or discontinuation for any other reason. Primary endpoint of the phase II is overall response rate, secondary endpoints include progression-free survival, safety, and quality of life. This trial is open for patient enrollment since November 2016 in six Austrian cancer centers. Accrual is planned to be completed within 2 years.
Based on preclinical and clinical findings an ixazomib and carboplatin combination is thought to be effective in metastatic TNBC patients. The MBC-10 trial is accompanied by a broad biomarker program investigating predictive biomarkers for treatment response and potential resistance mechanisms to the investigational drug combination.
EudraCT Number: 2016-001421-13 received on March 31, 2016, ClinicalTrials.gov Identifier: NCT02993094 first posted on December 15, 2016. This trial was registered prospectively.
三阴性乳腺癌(TNBC)由一组异质性疾病组成,通常与预后不良有关。到目前为止,除了抗 VEGF 治疗外,还没有批准用于 TNBC 的靶向治疗,细胞毒性药物仍然是治疗的主要方法。依沙佐米是一种选择性和可逆的蛋白酶体抑制剂,主要用于治疗多发性骨髓瘤。在一项临床前研究中,用第一代蛋白酶体抑制剂硼替佐米联合顺铂治疗 TNBC 细胞,证明具有协同疗效。转移性卵巢癌和肺癌的临床数据显示,卡铂联合硼替佐米具有显著的抗肿瘤活性和良好的耐受性(Mol Cancer 11:26 2012、J Thorac Oncol 4:87-92 2009、J Thorac Oncol 7:1032-1040、2012)。基于这一证据,I 期/II 期 MBC-10 试验将评估第二代蛋白酶体抑制剂依沙佐米联合卡铂在晚期 TNBC 患者中的毒性谱和疗效。
本研究纳入至少接受过一线化疗的转移性 TNBC 患者,化疗用于晚期疾病,根据 RECIST 标准 1.1 确认疾病进展且可测量疾病。患者将在 28 天周期内接受卡铂联合依沙佐米治疗,依沙佐米在第 1、8 和 15 天给药。本研究的 I 期部分采用交替剂量递增加速滴定设计。在确定最大耐受剂量(MTD)后,将进一步评估联合用药的疗效和安全性(II 期,包括 41 例可评估患者)。所有患者将继续接受研究药物治疗,直至疾病进展、不可接受的毒性或因任何其他原因停药。II 期的主要终点是总缓解率,次要终点包括无进展生存期、安全性和生活质量。自 2016 年 11 月以来,该试验在奥地利的六家癌症中心招募患者,预计 2 年内完成入组。
基于临床前和临床发现,依沙佐米和卡铂联合治疗转移性 TNBC 患者可能有效。MBC-10 试验伴随着广泛的生物标志物计划,旨在研究治疗反应的预测性生物标志物和潜在的耐药机制。
EudraCT 编号:2016-001421-13,于 2016 年 3 月 31 日获得,ClinicalTrials.gov 标识符:NCT02993094,于 2016 年 12 月 15 日首次发布。该试验是前瞻性注册的。