jRCT2031250604招募中不适用
A Phase 3, Randomized, Open-label, Multicenter Study to Evaluate the Efficacy and Safety of Sacituzumab Tirumotecan (MK-2870) in Combination With Pembrolizumab With or Without Bevacizumab Compared With Standard of Care as First-line Maintenance Treatment for Participants With Persistent, Recurrent, or Newly Diagnosed Metastatic Cervical Cancer With PD-L1 CPS Greater Than or Equal to 1 (TroFuse-036/GOG-3123/ENGOT-cx22)
未提供0 个研究点目标入组 68 人开始时间: 待定
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 68
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
入排标准
- 年龄范围
- 18age old over 至 No limit(—)
- 性别
- Female
入选标准
- •Has a histologically confirmed diagnosis of squamous cell carcinoma, adenosquamous carcinoma, or adenocarcinoma of cervix.
- •Has persistent, recurrent, or newly diagnosed metastatic cervical cancer that is not amenable to curative treatment (surgery and/or radiation).
- •If infected with human immunodeficiency virus (HIV), has well controlled HIV on antiretroviral therapy.
- •If positive for hepatitis B surface antigen, has received hepatitis B virus (HBV) antiviral therapy and has undetectable HBV viral load.
- •If has a history of hepatitis C virus (HCV) infection, has undetectable HCV viral load.
- •Has an Eastern Cooperative Oncology Group performance status of 0 or
- •Has tumor programmed cell death ligand 1 expression of combined positive score >=1.
排除标准
- •Has HIV infection with a history of Kaposi's sarcoma and/or Multicentric Castleman's Disease.
- •Has a history of documented severe dry eye syndrome, severe Meibomian gland disease and/or blepharitis, or severe corneal disease that prevents/delays corneal healing.
- •Has active inflammatory bowel disease requiring immunosuppressive medication or previous history of inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis, or chronic diarrhea).
- •Has uncontrolled, significant cardiovascular disease or cerebrovascular disease.
- •Has received prior systemic anticancer therapy other than what is specified in this protocol.
- •Is currently receiving a strong inducer/inhibitor of cytochrome P450 3A4 that cannot be discontinued for the duration of treatment with sac-TMT.
- •Has a diagnosis of immunodeficiency.
- •Has a known additional malignancy that is progressing or has required active treatment within the past 3 years.
- •Has known active central nervous system metastases and/or carcinomatous meningitis.
- •Has active autoimmune disease that has required systemic treatment in the past 2 years; replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid) is allowed.
- •Has a history of (noninfectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease.
- •Has a history of stem cell/solid organ transplant.
- •Has not adequately recovered from major surgery or has ongoing surgical complications.
研究者
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