Testing MK-3475 (Pembrolizumab) After Surgery for Localized Muscle-Invasive Bladder Cancer and Locally Advanced Urothelial Cancer
Run by National Cancer Institute (NCI) · NCT03244384 · Data updated 2026-11-12
Fully enrolled, still running. This study is not taking new participants. Its registered completion date is 2027-01-01.
This phase III trial studies how well pembrolizumab works in treating patients with bladder cancer that has spread into the deep muscle of the bladder wall (muscle-invasive) or urothelial cancer that has spread from where it started to nearby tissue or lymph nodes (locally advanced). Monoclonal antibodies recognizing and blocking checkpoint molecules can enhance the patient's immune response and therefore help fight cancer. Pembrolizumab is one of the monoclonal antibodies that block the PD-1 axis and can interfere with the ability of tumor cells to grow.
Quick facts
| Phase | Phase 3 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 739 (estimated) |
| Sponsor | National Cancer Institute (NCI) NIH |
| Drugs / interventions | Biospecimen Collection, Clinical Observation, Computed Tomography, CT Urography, Cystoscopy, Magnetic Resonance Imaging, Pembrolizumab, Pharmacological Study, Quality-of-Life Assessment, Questionnaire Administration |
| Locations | 914 sites (Guam, United States) |
| Trial ID | NCT03244384 on ClinicalTrials.gov |
What this trial studies
DUAL PRIMARY OBJECTIVE: I. To determine disease free survival (DFS) and overall survival (OS) in all patients with muscle-invasive bladder and upper-tract urothelial carcinoma treated with adjuvant pembrolizumab versus (vs.) observation. SECONDARY OBJECTIVES: I. To determine DFS and OS in PD-L1 positive and negative patients with muscle-invasive bladder and upper-tract urothelial carcinoma treated with adjuvant pembrolizumab vs. observation. II. To characterize the safety and tolerability of pembrolizumab when administered in the adjuvant setting in patients with muscle-invasive bladder and upper-tract urothelial carcinoma. CORRELATIVE SCIENCE OBJECTIVES: I. To determine if the 12 immune gene signatures are associated with OS and DFS. II. To determine if tumor molecular subtype is associated with OS and DFS. III. To investigate whether the diversity of T-cell receptor (TCR) clonotypes is associated with OS and DFS. IV. To investigate whether persistence of TCR clonotypes is associated with OS and DFS. V. To determine if tumor burden and neoantigen burden are associated with OS and DFS. VI. To determine if HLA subtypes are associated with OS and DFS. VII. To conduct exploratory analyses regarding the association of plasma HGF and VEGF levels with IL-10 and IL-17 and OS and DFS and between treated and untreated patients. PHARMACOGENOMIC STUDY OBJECTIVES: I. To investigate the effect of PDCD1 single-nucleotide polymorphism (SNP) rs11568821 on severe (grade 3 or highe…
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * PRE-REGISTRATION ELIGIBILITY CRITERIA * Histologically confirmed muscle-invasive urothelial carcinoma of the bladder, urethra, upper tract, or lymph node positive (LN+) disease; variant histology allowed as long as urothelial carcinoma is predominant (any amount of squamous differentiation is allowed); any component of neuroendocrine carcinoma is excluded * Paraffin tissue samples obtained by transurethral resection of muscle-invasive bladder tumor, upper tract resection, or radical cystectomy/nephrectomy/ureterectomy/nephroureterectomy/cystoprostatectomy or urethrectomy must be available; this specimen submission is mandatory prior to registration as results will be used for stratification; specimens from radical/definitive surgery (radical cystectomy/nephrectomy/ureterectomy /nephroureterectomy/cystoprostatectomy and LN dissection) are preferred over transurethral resection, if available * Patient must fit into one of the following three categories: * Patients who received neoadjuvant chemotherapy and pathologic stage at surgical resection is \>= pT2 and/or N+ OR * Patients who are not cisplatin-eligible (according to \>= 1 of the following criteria: Eastern Cooperative Oncology Group \[ECOG\] performance status of 2, creatinine clearance \< 60 mL/min, grade \>= 2 hearing loss, grade \>= 2 neuropathy, or New York Heart Association class III heart failure and pathologic stage at surgical resection is \>= pT3 or pN+) OR * Patients that decline adjuvant cisplatin-based or other systemic chemotherapy based on an informed discussion with the physician and pathologic stage at surgical resection is \>= pT3 or pN+ * The 7th edition of American Joint Committee on Cancer (AJCC) staging will be utilized; patient must have had radical cystectomy (cystoprostatectomy for men) and lymph node dissection (for bladder primary), or nephrectomy, nephroureterectomy or ureterectomy (for uppertract tumors) or urethrectomy (in addition to a radical cystectomy-either simultaneously or in the past) \>= 4 weeks but =\< 16 weeks prior to pre-registration; patients who have had a partial cystectomy as definitive therapy are not eligible * No gross cancer at the surgical margins; microscopic invasive urothelial carcinoma positive margins are allowed; carcinoma in situ (CIS) at margins is considered negative margins * No evidence of residual cancer or metastasis after surgery; patients with upper tract urothelial carcinoma must have a negative cystoscopy within 3 months prior to pre-registration; if the bladder has been removed a cystoscopy is not required * No metastatic disease (or radiologic findings "concerning" for metastatic disease) on cross-sectional imaging (according to Response Evaluation Criteria in Solid Tumors \[RECIST\] version \[v\]1.1 criteria) * No active autoimmune disease or history of autoimmune disease that might recur, which may affect vital organ function or require immune suppressive treatment including systemic corticosteroids; these include but are not limited to patients with a history of immune related neurologic disease, multiple sclerosis, autoimmune (demyelinating) neuropathy, Guillain-Barre syndrome, myasthenia gravis; systemic autoimmune disease such as systemic lupus erythematosus (SLE), connective tissue diseases, scleroderma, inflammatory bowel disease (IBD), Crohn's, ulcerative colitis, hepatitis; and patients with a history of toxic epidermal necrolysis (TEN), Stevens-Johnson syndrome, or phospholipid syndrome because of the risk of recurrence or exacerbation of disease; human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible * No current pneumonitis or prior history of non-infectious pneumonitis that required steroids within the previous 5 years * Patients with vitiligo, endocrine deficiencies including type I diabetes mellitus, thyroiditis managed with replacement hormones including physiologic corticosteroids are eligible * Patients with rheumatoid arthritis and other arthropathies, Sjogren's syndrome and psoriasis controlled with topical medication and patients with positive serology, such as antinuclear antibodies (ANA), anti-thyroid antibodies should be evaluated for the presence of target organ involvement and potential need for systemic treatment but should otherwise be eligible * No known active hepatitis B (e.g., hepatitis B surface antigen \[HBsAg\] reactive) or hepatitis C (e.g., hepatitis C virus \[HCV\] ribonucleic acid \[RNA\] \[qualitative\] is detected) * No live vaccine within 30 days prior to the first dose of study drug; examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette-Guerin (BCG), and typhoid vaccine; seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (e.g., FluMist) are live attenuated vaccines and are not allowed * No postoperative/adjuvant systemic therapy * No prior treatment with any therapy on the PD-1/PD-L1 axis * No treatment with any other type of investigational agent =\< 4 weeks before pre-registration * No major surgery =\< 4 weeks before pre-registration * No radiation therapy =\< 4 weeks before pre-registration * No neoadjuvant chemotherapy =\< 4 weeks before pre-registration * Not currently requiring hemodialysis * Age \>= 18 years * Not pregnant and not nursing, because this study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are unknown * ECOG performance status =\< 2 * Absolute neutrophil count (ANC) \>= 1,200/mm\^3 * Leukocytes \>= 3,000/ mm\^3 * Platelet count \>= 75,000/mm\^3 * Hemoglobin \>= 9 g/dL or \>= 5.6 mmol/L * Total bilirubin =\< 1.5 x upper limit of normal (ULN) * Bilirubin for patients with Gilbert's =\< 3.0 x ULN * Calculated (calc.) creatinine clearance \>= 30 mL/min (using either Chronic Kidney Disease Epidemiology Collaboration \[CKD-EPI\] equation or Cockcroft-Gault formula) * Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) =\< 3.0 x upper limit of normal (ULN) * Serum albumin \>= 2.8 g/dL * For women of childbearing potential only: a negative urine or serum pregnancy test done =\< 7 days prior to pre-registration is required * REGISTRATION ELIGIBILITY CRITERIA: Results of central PD-L1 testing available; Q2 Solutions will forward the PD-L1 results to the statistical center and the statistical center will notify the site that the result is available; since the results with be blinded to the site the notification from the Alliance registration/randomization office will serve as a confirmation of this eligibility criteria; after sites receive the confirmation e-mail from Alliance they can register the patient
Where it's running
-
University of Alabama at Birmingham Cancer Center
Birmingham, Alabama, United States -
Anchorage Associates in Radiation Medicine
Anchorage, Alaska, United States -
Anchorage Radiation Therapy Center
Anchorage, Alaska, United States -
Alaska Breast Care and Surgery LLC
Anchorage, Alaska, United States -
Alaska Oncology and Hematology LLC
Anchorage, Alaska, United States -
Alaska Women's Cancer Care
Anchorage, Alaska, United States
Show 44 more locations
-
Anchorage Oncology Centre
Anchorage, Alaska, United States -
Katmai Oncology Group
Anchorage, Alaska, United States -
Providence Alaska Medical Center
Anchorage, Alaska, United States -
Fairbanks Memorial Hospital
Fairbanks, Alaska, United States -
CTCA at Western Regional Medical Center
Goodyear, Arizona, United States -
Kingman Regional Medical Center
Kingman, Arizona, United States -
Cancer Center at Saint Joseph's
Phoenix, Arizona, United States -
Mayo Clinic Hospital in Arizona
Phoenix, Arizona, United States -
Mayo Clinic in Arizona
Scottsdale, Arizona, United States -
Mercy Hospital Fort Smith
Fort Smith, Arkansas, United States -
CHI Saint Vincent Cancer Center Hot Springs
Hot Springs, Arkansas, United States -
John L McClellan Memorial Veterans Hospital
Little Rock, Arkansas, United States -
Kaiser Permanente-Anaheim
Anaheim, California, United States -
Mission Hope Medical Oncology - Arroyo Grande
Arroyo Grande, California, United States -
PCR Oncology
Arroyo Grande, California, United States -
AIS Cancer Center at San Joaquin Community Hospital
Bakersfield, California, United States -
Kaiser Permanente-Baldwin Park
Baldwin Park, California, United States -
Kaiser Permanente-Bellflower
Bellflower, California, United States -
Providence Saint Joseph Medical Center/Disney Family Cancer Center
Burbank, California, United States -
Epic Care-Dublin
Dublin, California, United States -
Bay Area Breast Surgeons Inc
Emeryville, California, United States -
Epic Care Partners in Cancer Care
Emeryville, California, United States -
Kaiser Permanente-Fontana
Fontana, California, United States -
Kaiser Permanente South Bay
Harbor City, California, United States -
Kaiser Permanente-Irvine
Irvine, California, United States -
UC San Diego Moores Cancer Center
La Jolla, California, United States -
Loma Linda University Medical Center
Loma Linda, California, United States -
Kaiser Permanente Los Angeles Medical Center
Los Angeles, California, United States -
Los Angeles General Medical Center
Los Angeles, California, United States -
USC / Norris Comprehensive Cancer Center
Los Angeles, California, United States -
Kaiser Permanente West Los Angeles
Los Angeles, California, United States -
Contra Costa Regional Medical Center
Martinez, California, United States -
Fremont - Rideout Cancer Center
Marysville, California, United States -
Community Hospital of Monterey Peninsula
Monterey, California, United States -
Pacific Cancer Care-Monterey
Monterey, California, United States -
USC Norris Oncology/Hematology-Newport Beach
Newport Beach, California, United States -
Alta Bates Summit Medical Center - Summit Campus
Oakland, California, United States -
Bay Area Tumor Institute
Oakland, California, United States -
Kaiser Permanente-Ontario
Ontario, California, United States -
Stanford Cancer Institute Palo Alto
Palo Alto, California, United States -
Kaiser Permanente - Panorama City
Panorama City, California, United States -
Keck Medical Center of USC Pasadena
Pasadena, California, United States -
Kaiser Permanente-Riverside
Riverside, California, United States -
University of California Davis Comprehensive Cancer Center
Sacramento, California, United States
+864 more sites. See ClinicalTrials.gov for the full list.
Study contacts
- Principal investigator: Andrea B Apolo — Alliance for Clinical Trials in Oncology
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Lenvatinib and Pembrolizumab With or Without SBRT for Metastatic Kidney Cancer
This study tests whether adding SBRT to standard lenvatinib plus pembrolizumab helps people with metastatic kidney cancer who have stable disease after initial treatment.
-
Bladder cancer: test a biomarker-guided plan after neoadjuvant therapy
This phase 2 study tests a biomarker- and response-guided plan to preserve the bladder in patients with muscle-invasive bladder cancer after neoadjuvant therapy.
-
Peripheral neuropathy during perioperative therapy with enfortumab vedotin and pembrolizumab in muscle-invasive urothelial cancer
This study follows adults with muscle-invasive urothelial cancer to see how nerve-related side effects develop when people receive enfortumab vedotin and pembrolizumab around surgery as part of standard care.
-
Sacituzumab Tirumotecan plus Pembrolizumab in advanced biliary tract cancer
This study tests whether the combination of Sacituzumab Tirumotecan and Pembrolizumab can help people with advanced biliary tract cancer who have already had at least one approved therapy fail.
-
Sac-TMT and pembrolizumab with chemoradiation for bladder muscle invasion
This trial tests whether adding Sac-TMT and pembrolizumab to chemoradiation helps people with muscle-invasive bladder cancer live longer without the cancer growing or returning.
-
Ivonescimab plus enfortumab vedotin vs pembrolizumab plus enfortumab vedotin in untreated locally advanced or metastatic urothelial cancer
This trial tests if adding ivonescimab to enfortumab vedotin works better than pembrolizumab plus enfortumab vedotin for people with untreated locally advanced or metastatic urothelial cancer.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.