此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

EVERolimus and LenvAtinib Versus Everolimus for Bone Sarcoma

2026年5月26日 更新者:Yonsei University

EVERolimus and LenvAtinib Versus Everolimus for Bone Sarcoma Progressing After Standard Treatmen : a Randomized, Phase 2, Multi-center Trial [EVERLAST]

Those studies demonstrate strong rationale to combine a multikinase inhibitor targeting VEGFR, PDGFR with mTOR inhibitor. Moreover, another multi-targeted TKI, lenvatinib monotherapy showed promising activity in osteosarcoma. Therefore, clinical trial with Lenvatinib in combined with everolimus is ongoing for solid tumors (NCT03245151). Considering lenvatinib and everolimus (18 mg/day and 5 mg/day) already approved as standard treatment for renal cell carcinoma based on the powerful ORR, PFS, and OS14, these noteworthy findings advance the treatment paradigm for bone sarcoma patients.

Because all those trials for sarcoma were done in the absence of a control group, based on such clinical studies, a confirmatory trial comparing mTOR inhibitor and a multi-targeted tyrosine kinase inhibitor (multi-TKI) combination versus monotherapy is essential. Therefore, we planned to conduct the randomized phase II trial of everolimus in combination with lenvatinib for advanced/metastatic bone sarcomas. In addition, we will explore predictive biomarkers by repeated biopsies and blood samplings during the treatment.

研究概览

研究类型

介入性

注册 (估计的)

94

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Hyo Song Kim, Professor
  • 电话号码:+82-2-2228-8123
  • 邮箱:hyosong77@yuhs.ac

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 孩子
  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Histologically confirmed advanced Osteosarcoma, Ewing sarcoma, Chondrosarcoma with 1-2 prior chemotherapy

    : neoadjuvnat or adjuvant chemotherapy is counted as one regimen

  2. Age ≥19 years, <80 years
  3. ECOG performance status of 0-1
  4. Has at least 1 measurable lesion (as defined by Response Evaluation Criteria in Solid Tumors Version 1.1).
  5. Has adequate organ function defined by the following criteria:

    • Hb ≥ 9.0 g/dL
    • Absolute neutrophil count (ANC) ≥ 1000 /µL
    • Platelet ≥ 75,000/ µL
    • Serum Creatinine: ≥ 50 mL/min
    • Total Bilirubin: ≤ 1.5 × UNL (upper normal limit)
    • AST(SGOT)): ≤ 3.0 × UNL or ≤ 5.0 × UNL (in patients with liver metastasis)
    • ALT(SGPT): ≤ 3.0 × UNL or ≤ 5.0 × UNL (in patients with liver metastasis)
  6. Female patient of childbearing potential has a negative serum or urine pregnancy test for β-hCG
  7. Able to provide written informed consent and comply with the protocol requirements

    Exclusion Criteria:

    • Any concurrent chemotherapy, biologic, or hormonal therapy for cancer treatment within 2 weeks prior to entering the study. Concurrent use of hormonal therapy for non-cancer-related conditions (e.g., hormone replacement therapy) is acceptable

      • Any previous treatment to lenvatinib or mTOR inhibitor

        • Any unresolved toxicity NCI CTCAE Grade ≥2 from previous anticancer therapy with the exception of alopecia, vitiligo, and the laboratory values defined in the inclusion criteria

          • Major surgical procedure (as defined by the Investigator) within 14 days prior to the first dose of IP ⑤Active or prior documented autoimmune or inflammatory disorders

            -including inflammatory bowel disease [e.g., colitis or Crohn's disease], diverticulitis [with the exception of diverticulosis], systemic lupus erythematosus, Sarcoidosis syndrome, or Wegener syndrome [granulomatosis with polyangiitis, Graves' disease, rheumatoid arthritis, hypophysitis, uveitis, etc.

            • History of the following conditions within the past 6 months.

              • coronary angioplasty or stent placement, myocardial infarction, unstable angina, coronary artery bypass grafting, peripheral arterial disease (Grade III) or congestive heart failure (Grade IV) according to the New York Heart Association classification, thromboembolism (patients on stable anticoagulation for ≥6 weeks are eligible), hemoptysis, intracranial hemorrhage, or clinically significant gastrointestinal bleeding ⑦Has an active infection requiring parenteral treatment

                • History of another primary malignancy.

    However, enrollment is permitted in the following cases:

    • Basal cell or squamous cell carcinoma of the skin after curative resection
    • Cervical carcinoma in situ after at least 1 year following successful treatment
    • Patients who have been disease-free for at least 3 years after completion of treatment

      ⑨Known or active CNS metastasis and/or carcinomatous meningitis

    • Participants with previously treated brain metastases are eligible if radiologically stable.

      • female patients who are pregnant or breastfeeding or male or female patients of reproductive potential who are not willing to emply effective birth control from screening to 90 days after the last dose

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Combo
Everolimus (5 mg) and Lenvatinib (14 mg)
Everolimus (5 mg) and Lenvatinib (14 mg) will be administered orally once daily (QD) in continuous 28-day cycles. In subjects who maintain toxicity at Grade ≤2 during the initial 4-week period (Cycle 1), the Lenvatinib dose may be escalated to 18 mg QD beginning in Cycle 2, at the discretion of the investigator
有源比较器:Mono
Lenvatinib (24 mg) after Everolimus (10 mg)
Everolimus (10 mg) will be administered orally once daily (QD) as monotherapy in continuous 28-day cycles. Upon radiologic or clinical disease progression, subjects may switch to Lenvatinib (24 mg) monotherapy, administered orally once daily (QD) in 28-day cycles.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Progression free rate (PFR6)
大体时间:up to 3 years
Progression free rate (PFR-6) at 24 weeks will be based on RECIST version 1.1
up to 3 years

次要结果测量

结果测量
措施说明
大体时间
Progression-free survival (PFS)
大体时间:up to 3 years
The earlier of the date of first documented progressive disease or death from the date of enrollment
up to 3 years
Overall survival (OS)
大体时间:up to 3 years
From the date of treatment initiation to the date of death or last follow-up
up to 3 years
Number of participants with treatment-related adverse events
大体时间:up to 3 years
Number of participants with treatment-related adverse events: Adverse events considered related to study treatment will be assessed according to CTCAE version 5.0.
up to 3 years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年7月1日

初级完成 (估计的)

2028年11月30日

研究完成 (估计的)

2028年11月30日

研究注册日期

首次提交

2026年5月11日

首先提交符合 QC 标准的

2026年5月26日

首次发布 (实际的)

2026年6月2日

研究记录更新

最后更新发布 (实际的)

2026年6月2日

上次提交的符合 QC 标准的更新

2026年5月26日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

订阅