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DISEASE & TREATMENT SETTING

Bladder Cancer

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

Exact scope

Bladder 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): Bladder 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

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

      NCT00022633 · Registry condition search · Scope: narrower

      S0028, Gemcitabine and Paclitaxel in Treating Patients With Advanced or Recurrent Cancer of the Urinary Tract

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

      →

      NCT00045630 · Registry condition search · Scope: narrower

      S0219, Combination Chemotherapy Followed By Observation or Surgery in Patients With Stage II or Stage III Cancer of the Urothelium

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

      →

      NCT00112905 · Registry condition search · Scope: narrower

      Sorafenib in Treating Patients With Regional or Metastatic Cancer of the Urothelium

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

      →

      NCT00365508 · Registry condition search · Scope: narrower

      Counseling and Nicotine Replacement Therapy in Helping Adult Smokers Quit Smoking

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

      →

      NCT00397488 · Registry condition search · Scope: narrower

      Sunitinib in Treating Patients With Progressive Metastatic Transitional Cell Cancer of the Urothelium

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

      →

      NCT00407485 · Registry condition search · Scope: narrower

      VEGF Trap in Treating Patients With Recurrent, Locally Advanced, or Metastatic Cancer of the Urothelium

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

      →

      NCT00471536 · Registry condition search · Scope: narrower

      Pazopanib in Treating Patients With Metastatic Urothelial Cancer

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

      →

      NCT00478361 · Registry condition search · Scope: narrower

      Gemcitabine, Paclitaxel, Doxorubicin in Metastatic or Unresectable Bladder Cancer With Decreased Kidney Function

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

      →

      NCT00534001 · Registry condition search · Scope: narrower

      Bupropion in Helping Adults Stop Smoking

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

      →

      NCT00587964 · Registry condition search · Scope: narrower

      Phase II Trial of Stereotactic Radiosurgery Boost Following Surgical Resection for Brain Metastases

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

      →

      NCT00661609 · Registry condition search · Scope: narrower

      A Phase II Study of AZD4877 (a Novel Anti-mitotic Agent) in Advanced Bladder Cancer

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

      →

      NCT00666978 · Registry condition search · Scope: narrower

      Health Education Counseling With or Without Bupropion in Helping African Americans Stop Smoking

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

      →

      NCT00749892 · Registry condition search · Scope: narrower

      Erlotinib Hydrochloride in Treating Participants With Muscle Invasive or Recurrent Urothelial Cancer

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

      →

      NCT00753415 · Registry condition search · Scope: narrower

      A Study of V934/V935 Vaccine in Cancer Participants With Selected Solid Tumors (V934-002)

      3 outcome links · 10 safety-group records · 0 quality-of-life measures

      →

      NCT00790569 · Registry condition search · Scope: narrower

      Varenicline or Nicotine Patch and Nicotine Gum in Helping Smokers in a Methadone Treatment Program Stop Smoking

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

      →

      NCT00942331 · Registry condition search · Scope: narrower

      Gemcitabine Hydrochloride and Cisplatin With or Without Bevacizumab in Treating Patients With Advanced Urinary Tract Cancer

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

      →

      NCT00957424 · Registry condition search · Scope: narrower

      Acceptability of Less Harmful Alternatives to Cigarettes

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

      →

      NCT01126749 · Registry condition search · Scope: narrower

      Eribulin Mesylate Administered in Combination With Gemcitabine Plus Cisplatin Versus Gemcitabine Plus Cisplatin Alone as First-Line Therapy for Locally Advanced or Metastatic Bladd

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

      →

      NCT01236053 · Registry condition search · Scope: narrower

      Cancer in Patients With Gabapentin (GPRD)

      6 outcome links · 22 safety-group records · 0 quality-of-life measures

      →

      NCT01459653 · Registry condition search · Scope: narrower

      Multi-level Evaluation of Chemotherapy-induced Febrile Neutropenia Prophylaxis, Outcomes, and Determinants With Granulocyte-colony Stimulating Factor

      6 outcome links · 1 safety-group records · 23 quality-of-life measures

      →

      Indication-specific source history

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

      2025-03-28 · durvalumab · approval notification
      release id
      clinical-indications-draft-1
      disease state id
      ds-bladder-cancer
      event id
      notice-6b4d238ec8fdc872
      event date
      2025-03-28
      event kind
      approval-notification
      drug or regimen
      durvalumab
      source indication text
      FDA approved durvalumab with gemcitabine and cisplatin as neoadjuvant treatment, followed by single agent durvalumab as adjuvant treatment following radical cystectomy, for adults with muscle invasive bladder cancer .
      match phrase
      bladder cancer
      match status
      candidate
      status category
      Source null
      has date discrepancy
      0
      source collection
      fda-approval-notice
      source key
      fda-cdab6bdb583859b8
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-durvalumab-muscle-invasive-bladder-cancer
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2025-06-12 · mitomycin intravesical solution · approval notification
      release id
      clinical-indications-draft-1
      disease state id
      ds-bladder-cancer
      event id
      notice-128cec353e3c27eb
      event date
      2025-06-12
      event kind
      approval-notification
      drug or regimen
      mitomycin intravesical solution
      source indication text
      FDA approved mitomycin intravesical solution for adult patients with recurrent low-grade intermediate-risk non-muscle invasive bladder cancer .
      match phrase
      bladder cancer
      match status
      candidate
      status category
      Source null
      has date discrepancy
      0
      source collection
      fda-approval-notice
      source key
      fda-4ef07a829e92c511
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-mitomycin-intravesical-solution-recurrent-low-grade-intermediate-risk-non-muscle
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2025-09-09 · gemcitabine intravesical system · approval notification
      release id
      clinical-indications-draft-1
      disease state id
      ds-bladder-cancer
      event id
      notice-d5efef1d0a2d53e8
      event date
      2025-09-09
      event kind
      approval-notification
      drug or regimen
      gemcitabine intravesical system
      source indication text
      FDA approved gemcitabine intravesical system for adults with Bacillus Calmette-Guérin -unresponsive non-muscle invasive bladder cancer with carcinoma in situ with or without papillary tumors. Gemcitabine intravesical system is co-packaged with a urinary catheter and stylet used for insertion through the urinary catheter into the bladder.
      match phrase
      bladder cancer
      match status
      candidate
      status category
      Source null
      has date discrepancy
      0
      source collection
      fda-approval-notice
      source key
      fda-a71e076b93797c1c
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-gemcitabine-intravesical-system-non-muscle-invasive-bladder-cancer
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2025-11-21 · pembrolizumab with enfortumab vedotin-ejfv · approval notification
      release id
      clinical-indications-draft-1
      disease state id
      ds-bladder-cancer
      event id
      notice-9b17d3dc0111e232
      event date
      2025-11-21
      event kind
      approval-notification
      drug or regimen
      pembrolizumab with enfortumab vedotin-ejfv
      source indication text
      FDA approved pembrolizumab or pembrolizumab and berahyaluronidase alfa-pmph with enfortumab vedotin-ejfv as neoadjuvant treatment followed by adjuvant treatment after cystectomy for adults with muscle invasive bladder cancer who are ineligible for cisplatin.
      match phrase
      bladder cancer
      match status
      candidate
      status category
      Source null
      has date discrepancy
      0
      source collection
      fda-approval-notice
      source key
      fda-645462b4c10c2fb2
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-pembrolizumab-enfortumab-vedotin-ejfv-muscle-invasive-bladder-cancer
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2026-05-15 · atezolizumab · approval notification
      release id
      clinical-indications-draft-1
      disease state id
      ds-bladder-cancer
      event id
      notice-4a013c9e667ffb00
      event date
      2026-05-15
      event kind
      approval-notification
      drug or regimen
      atezolizumab
      source indication text
      FDA approved atezolizumab and atezolizumab and hyaluronidase-tqjs as adjuvant treatments for adults with muscle invasive bladder cancer after cystectomy who have circulating tumor DNA molecular residual disease as determined by an FDA-authorized test.
      match phrase
      bladder cancer
      match status
      candidate
      status category
      Source null
      has date discrepancy
      0
      source collection
      fda-approval-notice
      source key
      fda-7f6ca1fc3c4ca109
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-atezolizumab-adjuvant-treatment-muscle-invasive-bladder-cancer-patients-molecular
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2026-05-28 · durvalumab in combination with Bacillus Calmette-Guerin · approval notification
      release id
      clinical-indications-draft-1
      disease state id
      ds-bladder-cancer
      event id
      notice-69942f3587f1bbbd
      event date
      2026-05-28
      event kind
      approval-notification
      drug or regimen
      durvalumab in combination with Bacillus Calmette-Guerin
      source indication text
      FDA approved durvalumab in combination with Bacillus Calmette-Guerin for the treatment of adult patients with BCG-naïve, high-risk non-muscle invasive bladder cancer .
      match phrase
      bladder cancer
      match status
      candidate
      status category
      Source null
      has date discrepancy
      0
      source collection
      fda-approval-notice
      source key
      fda-c07ece06c8530681
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-durvalumab-combination-bacillus-calmette-guerin-high-risk-non-muscle-invasive-bladder
      curation status
      draft
      reviewed by
      Source null
      reviewed at
      Source null
      created at
      2026-09-10T00:00:00Z
      Original event source →
      2026-07-10 · pembrolizumab or pembrolizumab and berahyaluronidase alfa-pmph each with enfortumab vedotin-ejfv · approval notification
      release id
      clinical-indications-draft-1
      disease state id
      ds-bladder-cancer
      event id
      notice-860ddef787f42e83
      event date
      2026-07-10
      event kind
      approval-notification
      drug or regimen
      pembrolizumab or pembrolizumab and berahyaluronidase alfa-pmph each with enfortumab vedotin-ejfv
      source indication text
      FDA approved pembrolizumab or pembrolizumab and berahyaluronidase alfa-pmph each in combination with enfortumab vedotin-ejfv as neoadjuvant treatment followed by adjuvant treatment after cystectomy for adults with muscle invasive bladder cancer . This extends the prior approval for the regimen in this setting from patients who are cisplatin-ineligible to all patients with MIBC who are candidates for cystectomy.
      match phrase
      bladder cancer
      match status
      candidate
      status category
      Source null
      has date discrepancy
      0
      source collection
      fda-approval-notice
      source key
      fda-0403089146861ff3
      source url
      https://www.fda.gov/drugs/resources-information-approved-drugs/fda-approves-pembrolizumab-or-pembrolizumab-and-berahyaluronidase-alfa-pmph-each-enfortumab-vedotin
      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-bladder-cancer
        binding id
        ncit-C118816
        source collection
        ncit-concept
        source key
        C118816
        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-bladder-cancer
        binding id
        ncit-C4912
        source collection
        ncit-concept
        source key
        C4912
        source excerpt
        Source null
        match status
        ambiguous
        match note
        Resolution status: ambiguous.
        recorded at
        2026-09-10T00:00:00Z
      3. release id
        clinical-indications-draft-1
        disease state id
        ds-bladder-cancer
        binding id
        ncit-C9334
        source collection
        ncit-concept
        source key
        C9334
        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