A Phase II Study of Anlotinib and Benmelstobart as Second-line Treatment in Locally Advanced or Metastatic Differentiated Thyroid Cancer
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 入组人数
- 23
- 主要终点
- Objective Response Rate，ORR
研究概览
简要总结
This study is a multicenter, open-label, phase II study to evaluate the efficacy and safety of Benmelstobart in combination with Anlotinib as a second-line treatment for locally advanced or metastatic differentiated thyroid cancer. Patients who meet the inclusion criteria and do not meet the exclusion criteria will receive Benmelstobart (1200mg, d1, q3w) in combination with Anlotinib (12mg, qd, d1-14, q3w). Treatment will continue until disease progression, voluntary withdrawal of informed consent, intolerable toxicity, or until the investigator determines that the patient no longer benefits. For locally advanced patients, if the disease converts from unresectable or borderline unresectable to resectable after treatment, surgical intervention will be performed.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •The patient voluntarily agrees to participate in this study and has signed the informed consent form;
- •Age: ≥18 years, regardless of gender;
- •Histologically confirmed differentiated thyroid cancer;
- •Unresectable or borderline unresectable locally advanced thyroid cancer and/or metastatic thyroid adenocarcinoma;
- •Failure of first-line treatment (failure to achieve partial or complete response) or disease progression after first-line treatment;
- •At least one measurable lesion;
- •ECOG PS: 0-2;
- •Expected survival period ≥12 weeks;
- •Patient agrees to undergo tumor tissue biopsy/surgery at the time of enrollment;
- •Normal function of major organs;
- •Willingness to use reliable contraceptive methods during the trial. Women of childbearing potential must have a negative pregnancy test (serum or urine) within 14 days prior to enrollment.
- •The subject voluntarily agrees to participate in this study, signs the informed consent form, demonstrates good compliance, and cooperates with follow-up.
排除标准
- •Presence of other active malignancies within the past 5 years or concurrently. Patients with cured localized tumors, such as basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, carcinoma in situ of the prostate, carcinoma in situ of the cervix, carcinoma in situ of the breast, etc., may be enrolled.
- •Use of other antitumor therapies (including but not limited to chemotherapy, radiotherapy, etc.) within 28 days prior to the first administration of the study drug. Thyrotropin (TSH) suppressive therapy is excluded.
- •Prior treatment with immune checkpoint inhibitors (including but not limited to nivolumab, pembrolizumab, toripalimab, sintilimab, etc.).
- •Any severe or uncontrolled systemic disease, as determined by the investigator, including poorly controlled hypertension (systolic blood pressure >160 mmHg or diastolic blood pressure >100 mmHg) despite medication, uncontrolled diabetes, poorly managed cardiac disease, and signs of active bleeding.
- •Known history of severe allergy to any monoclonal antibody or anti-angiogenic targeted drug.
- •Presence of uncontrolled infection at the time of screening.
- •Pregnant or lactating women.
- •Refusal to undergo tumor tissue biopsy at the time of enrollment.
- •Other conditions considered by the treating physician as unsuitable for inclusion.
研究组 & 干预措施
Treatment
Benmelstobart+Anlotinib
干预措施: Anlotinib and Benmelstobart (Drug)
结局指标
主要结局
Objective Response Rate，ORR
时间窗: 2 years
Objective Response Rate (ORR) as assessed based on RECIST 1.1 criteria.
次要结局
未报告次要终点
研究者
Yu Wang
Chief of Head and Neck Surgery
Fudan University