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DISEASE & TREATMENT SETTING

Endometrial Cancer

Source-derived catalogue. This is not a treatment recommendation or a personalised trial match.

Exact scope

Endometrial Cancer

Source population
Not part of this definition
Disease extent
Not part of this definition
Treatment line
Not part of this definition
Stage
Not part of this definition
Resectability
Not part of this definition
Biomarkers, prior therapy and derivation
molecular
    prior therapy
      derivation status
      unresolved
      derivation note
      Derived from NCI topic(s): Endometrial Cancer. Strongest NCIt resolution: ambiguous. Entity-level scope; stage, biomarker and treatment line are not yet part of this definition.
      source wording
      Source null
      14 more-specific settings

      Study evidence for this setting

      36 linked studies · Applicability is a draft source assessment, not a determination of your eligibility.

      NCT00331760 · Source cited / selected · Scope: narrower

      Intensity-Modulated Radiation Therapy to the Pelvis With or Without Chemotherapy in Treating Patients With Endometrial Cancer or Cervical Cancer That Has Been Removed By Surgery

      6 outcome links · 2 safety-group records · 0 quality-of-life measures

      →

      NCT00381888 · Registry condition search · Scope: narrower

      Fondaparinux in Preventing Blood Clots in Patients Undergoing Surgery for Gynecologic Cancer

      2 outcome links · 1 safety-group records · 0 quality-of-life measures

      →

      NCT00474994 · Registry condition search · Scope: narrower

      Sunitinib in Treating Patients With Metastatic, Locally Advanced, or Locally Recurrent Sarcomas

      1 outcome links · 1 safety-group records · 0 quality-of-life measures

      →

      NCT00542490 · Registry condition search · Scope: narrower

      Vaginal Cuff Brachytherapy Followed by Chemotherapy in Patients With Endometrioid Cancer

      2 outcome links · 1 safety-group records · 0 quality-of-life measures

      →

      NCT00545792 · Registry condition search · Scope: narrower

      Safety Study Of Avastin And Pelvic Radiation In Women With Recurrent Gynecological Cancers

      2 outcome links · 1 safety-group records · 0 quality-of-life measures

      →

      NCT00807768 · Registry condition search · Scope: narrower

      Pelvic Radiation Therapy or Vaginal Implant Radiation Therapy, Paclitaxel, and Carboplatin in Treating Patients With High-Risk Stage I or Stage II Endometrial Cancer

      6 outcome links · 2 safety-group records · 3 quality-of-life measures

      →

      NCT01010126 · Registry condition search · Scope: narrower

      Temsirolimus and Bevacizumab in Treating Patients With Advanced Endometrial, Ovarian, Liver, Carcinoid, or Islet Cell Cancer

      6 outcome links · 6 safety-group records · 0 quality-of-life measures

      →

      NCT01079832 · Registry condition search · Scope: narrower

      Stereotactic Radiosurgery Using CyberKnife in Treating Women With Advanced or Recurrent Gynecological Malignancies

      5 outcome links · 1 safety-group records · 1 quality-of-life measures

      →

      NCT01210222 · Registry condition search · Scope: narrower

      Trebananib in Treating Patients With Persistent or Recurrent Endometrial Cancer

      5 outcome links · 1 safety-group records · 0 quality-of-life measures

      →

      NCT01631552 · Source cited / selected · Scope: narrower

      Study of Sacituzumab Govitecan-hziy (IMMU-132) in Adults With Epithelial Cancer

      6 outcome links · 1 safety-group records · 0 quality-of-life measures

      →

      NCT01797523 · Source cited / selected · Scope: narrower

      A Phase II, Single-Arm Study of RAD001 (Everolimus), Letrozole, and Metformin in Patients With Advanced or Recurrent Endometrial Carcinoma

      4 outcome links · 1 safety-group records · 0 quality-of-life measures

      →

      NCT02001623 · Source cited / selected · Scope: narrower

      Tisotumab Vedotin (HuMax®-TF-ADC) Safety Study in Patients With Solid Tumors

      6 outcome links · 15 safety-group records · 0 quality-of-life measures

      →

      NCT02065687 · Source cited / selected · Scope: narrower

      Paclitaxel and Carboplatin With or Without Metformin Hydrochloride in Treating Patients With Stage III, IV, or Recurrent Endometrial Cancer

      6 outcome links · 2 safety-group records · 1 quality-of-life measures

      →

      NCT02142803 · Registry condition search · Scope: narrower

      TORC1/2 Inhibitor MLN0128 and Bevacizumab in Treating Patients With Recurrent Glioblastoma or Advanced Solid Tumors

      6 outcome links · 3 safety-group records · 1 quality-of-life measures

      →

      NCT02178722 · Registry condition search · Scope: narrower

      Study to Explore the Safety, Tolerability and Efficacy of MK-3475 in Combination With INCB024360 in Participants With Selected Cancers

      6 outcome links · 6 safety-group records · 0 quality-of-life measures

      →

      NCT02228681 · Source cited / selected · Scope: narrower

      Everolimus and Letrozole or Hormonal Therapy to Treat Endometrial Cancer

      6 outcome links · 2 safety-group records · 0 quality-of-life measures

      →

      NCT02393248 · Registry condition search · Scope: narrower

      Open-Label, Dose-Escalation Study of Pemigatinib in Subjects With Advanced Malignancies - (FIGHT-101)

      6 outcome links · 20 safety-group records · 0 quality-of-life measures

      →

      NCT02549989 · Source cited / selected · Scope: narrower

      Study of LY3023414 for the Treatment of Recurrent or Persistent Endometrial Cancer

      5 outcome links · 1 safety-group records · 0 quality-of-life measures

      →

      NCT02552121 · Source cited / selected · Scope: narrower

      Tisotumab Vedotin (HuMax®-TF-ADC) Safety Study in Patients With Solid Tumors

      6 outcome links · 8 safety-group records · 0 quality-of-life measures

      →

      NCT02907073 · Registry condition search · Scope: narrower

      Positron Emission Tomography (PET) Imaging Studies With NIS Reporter

      2 outcome links · 3 safety-group records · 0 quality-of-life measures

      →

      Indication-specific source history

      Dated source events, not confirmation of current approval for every use of a drug.

      2019-09-17 · Keytruda (pembrolizumab) · accelerated approval
      release id
      clinical-indications-draft-1
      disease state id
      ds-endometrial-cancer
      event id
      fda-103a2223bc7cad33
      event date
      2019-09-17
      event kind
      accelerated-approval
      drug or regimen
      Keytruda (pembrolizumab)
      source indication text
      In combination with lenvatinib for advanced endometrial carcinoma not MSI-H or dMMR, with progression following systemic therapy and not candidates for curative surgery or radiation
      match phrase
      endometrial carcinoma
      match status
      candidate
      status category
      verified_clinical_benefit
      has date discrepancy
      0
      source collection
      fda-status-row
      source key
      fda-aa-8e2ca10938accff47498
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/verified-clinical-benefit-cancer-accelerated-approvals
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2019-09-17 · Lenvima (lenvatinib) · accelerated approval
      release id
      clinical-indications-draft-1
      disease state id
      ds-endometrial-cancer
      event id
      fda-e029c5040d387a59
      event date
      2019-09-17
      event kind
      accelerated-approval
      drug or regimen
      Lenvima (lenvatinib)
      source indication text
      In combination with pembrolizumab for advanced endometrial carcinoma not MSI-H or dMMR, with progression following systemic therapy and not candidates for curative surgery or radiation
      match phrase
      endometrial carcinoma
      match status
      candidate
      status category
      verified_clinical_benefit
      has date discrepancy
      0
      source collection
      fda-status-row
      source key
      fda-aa-c6b6c214b9ba3eaea663
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/verified-clinical-benefit-cancer-accelerated-approvals
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2021-04-22 · Jemperli (dostarlimab-gxly) · accelerated approval
      release id
      clinical-indications-draft-1
      disease state id
      ds-endometrial-cancer
      event id
      fda-fcaaccba3db7dec6
      event date
      2021-04-22
      event kind
      accelerated-approval
      drug or regimen
      Jemperli (dostarlimab-gxly)
      source indication text
      Adult patients with mismatch repair deficient (dMMR) recurrent or advanced endometrial cancer (EC), as determined by an FDA-approved test, that has progressed on or following prior treatment with a platinum-containing regimen.
      match phrase
      endometrial cancer
      match status
      candidate
      status category
      verified_clinical_benefit
      has date discrepancy
      0
      source collection
      fda-status-row
      source key
      fda-aa-f1dd6354fd249eb7e7bd
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/verified-clinical-benefit-cancer-accelerated-approvals
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2021-07-21 · Keytruda (pembrolizumab) · traditional approval
      release id
      clinical-indications-draft-1
      disease state id
      ds-endometrial-cancer
      event id
      fda-30f8c31f47289eb2
      event date
      2021-07-21
      event kind
      traditional-approval
      drug or regimen
      Keytruda (pembrolizumab)
      source indication text
      In combination with lenvatinib for advanced endometrial carcinoma not MSI-H or dMMR, with progression following systemic therapy and not candidates for curative surgery or radiation
      match phrase
      endometrial carcinoma
      match status
      candidate
      status category
      verified_clinical_benefit
      has date discrepancy
      0
      source collection
      fda-status-row
      source key
      fda-aa-8e2ca10938accff47498
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/verified-clinical-benefit-cancer-accelerated-approvals
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2021-07-21 · Lenvima (lenvatinib) · traditional approval
      release id
      clinical-indications-draft-1
      disease state id
      ds-endometrial-cancer
      event id
      fda-ff89219ab64e6419
      event date
      2021-07-21
      event kind
      traditional-approval
      drug or regimen
      Lenvima (lenvatinib)
      source indication text
      In combination with pembrolizumab for advanced endometrial carcinoma not MSI-H or dMMR, with progression following systemic therapy and not candidates for curative surgery or radiation
      match phrase
      endometrial carcinoma
      match status
      candidate
      status category
      verified_clinical_benefit
      has date discrepancy
      0
      source collection
      fda-status-row
      source key
      fda-aa-c6b6c214b9ba3eaea663
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/verified-clinical-benefit-cancer-accelerated-approvals
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2023-02-09 · Jemperli (dostarlimab-gxly) · traditional approval
      release id
      clinical-indications-draft-1
      disease state id
      ds-endometrial-cancer
      event id
      fda-eafead42dcf7ec92
      event date
      2023-02-09
      event kind
      traditional-approval
      drug or regimen
      Jemperli (dostarlimab-gxly)
      source indication text
      Adult patients with mismatch repair deficient (dMMR) recurrent or advanced endometrial cancer (EC), as determined by an FDA-approved test, that has progressed on or following prior treatment with a platinum-containing regimen.
      match phrase
      endometrial cancer
      match status
      candidate
      status category
      verified_clinical_benefit
      has date discrepancy
      0
      source collection
      fda-status-row
      source key
      fda-aa-f1dd6354fd249eb7e7bd
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/verified-clinical-benefit-cancer-accelerated-approvals
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      Source relationships and population-mapping limitations
      bindings
      1. release id
        clinical-indications-draft-1
        disease state id
        ds-endometrial-cancer
        binding id
        ncit-C27815
        source collection
        ncit-concept
        source key
        C27815
        source excerpt
        Source null
        match status
        ambiguous
        match note
        Resolution status: ambiguous.
        recorded at
        2026-09-10T00:00:00Z
      2. release id
        clinical-indications-draft-1
        disease state id
        ds-endometrial-cancer
        binding id
        ncit-C7558
        source collection
        ncit-concept
        source key
        C7558
        source excerpt
        Source null
        match status
        ambiguous
        match note
        Resolution status: ambiguous.
        recorded at
        2026-09-10T00:00:00Z
      mappings

        Download this complete draft source relationship record →

        Preserved source evidence · Not medical advice