研究项目库 / NCT06366347

Abemaciclib用于子宫内膜癌的II 期研究

这是一项关于子宫内膜癌的II 期研究,登记的药物或干预包括Abemaciclib;Letrozole;Pembrolizumab,当前状态为招募中。登记地点显示中国Boston、Foxborough、Milford、Weymouth有研究中心记录。是否仍有名额以及是否值得进一步询问,需要向研究中心确认。

一分钟看懂

这是一项关于子宫内膜癌的II 期研究,登记的药物或干预包括Abemaciclib;Letrozole;Pembrolizumab,当前状态为招募中。登记地点显示中国Boston、Foxborough、Milford、Weymouth有研究中心记录。是否仍有名额以及是否值得进一步询问,需要向研究中心确认。

药物或干预

Abemaciclib;Letrozole;Pembrolizumab · II 期

中国哪些地方有记录

以下地点来自登记信息,不代表此刻仍有名额;请向研究中心确认最新情况。

  • Beth Israel Deaconess Medical Center · Boston
  • Brigham and Women's Hospital · Boston
  • Dana-Farber Cancer Institute · Boston
  • Dana-Farber Cancer Institute at Foxborough · Foxborough
  • Dana-Farber Cancer Institute at Milford · Milford
  • Dana-Farber Cancer Institute at South Shore Hospital · Weymouth

公开的入选条件

  • * Participants must have histologically confirmed either i) endometrioid endometrial cancer or ii) endometrial carcinosarcoma with endometrioid epithelial component.
  • * Participants must have ER-positive disease, defined as ≥ 1 percent of tumor cell nuclei being immunoreactive by immunohistochemistry (IHC). If multiple analyses have been performed, judgment should be based on the most recent biopsy or pathology specimen ana
  • * Tumor must be TP53 wild-type as determined by immunohistochemistry (IHC) or via CLIA-certified targeted Next-Generation Sequencing (NGS); IHC assessment of p53 status is included in the NCCN guidelines of uterine neoplasms for the molecular analysis of endom
  • * Participants must have mismatch repair proficient (MMRP) endometrial cancer as determined by immunohistochemistry (IHC) or polymerase chain reaction (PCR) or any CLIA-certified next generation sequencing assay.
  • * No known tumor mutational burden ≥ 10 mutations/megabase (Mb).
  • * No known RB1 mutations or two-copy RB1 deletion.
  • * Participants must have just completed a minimum of 4 cycles and a maximum of 10 cycles of a combination of carboplatin and taxane or a combination of taxane and anti-PD-(L)1 inhibitor therapy (e.g., pembrolizumab, or dostarlimab, or durvalumab).
  • * Participants must have had measurable stage III, measurable stage IVA, stage IVB (with or without measurable disease) or recurrent (with or without measurable disease) endometrial cancer.

联系前需要确认

请继续确认中心是否启动、疾病分型、既往治疗、检查费用和知情同意安排。

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登记号:NCT06366347;登记信息更新于 2026-09-16。

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