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Testing the Investigational Medication Pembrolizumab After Kidney Removal for Patients With Non-Clear Cell Renal Cell Carcinoma

7 juli 2026 bijgewerkt door: National Cancer Institute (NCI)

Phase III Study of Adjuvant Pembrolizumab vs Active Surveillance After Nephrectomy in Patients With Non-Clear Cell Renal-Cell Carcinoma

This phase III trial compares the effect of pembrolizumab to active surveillance after a surgical procedure to completely or partially remove a kidney (nephrectomy) in improving time without disease in patients with non-clear cell renal cell cancer. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving pembrolizumab after nephrectomy may be more effective than the usual active surveillance approach for improving time without disease in patients with non-clear cell renal cell cancer.

Studie Overzicht

Gedetailleerde beschrijving

PRIMARY OBJECTIVE:

I. To evaluate whether adjuvant treatment of pembrolizumab will lead to better disease-free survival (DFS) compared to patients receiving no adjuvant treatment in the active surveillance arm.

SECONDARY OBJECTIVES:

I. To compare overall survival (OS) between patients receiving pembrolizumab versus (vs.) active surveillance II. To assess the safety and tolerability in each arm. III. To compare DFS between patients randomized to the pembrolizumab arm vs. the active surveillance arm in patients that are circulating tumor deoxyribonucleic acid (ctDNA) positive at baseline.

IV. To compare OS between patients randomized to the pembrolizumab arm vs. the active surveillance arm in patients that are ctDNA positive at baseline.

V. To compare the percentage of baseline ctDNA positive patients that achieve ctDNA clearance at week 12 between the pembrolizumab arm and active surveillance arm at.

VI. To compare DFS with KIM-1 status (high and low) by treatment arms. VII. To assess whether a decrease in KIM-1 after one cycle of adjuvant therapy is associated with improved DFS among patients receiving pembrolizumab.

VIII. To evaluate whether an increase in KIM 1 at predefined landmark timepoints is associated with an increased risk of subsequent DFS events.

IX. To evaluate whether persistently elevated C-reactive protein (CRP) is associated with recurrence.

EXPLORATORY OBJECTIVE:

I. To assess DFS and OS in each histology subgroups (papillary, chromophobe, unclassified, other).

OUTLINE: Patients are randomized to 1 of 2 arms.

ARM A: Patients undergo active surveillance, including computed tomography (CT) or magnetic resonance imaging (MRI), every 3 months for 1 year. Patients also undergo collection of blood samples on study and CT or MRI during follow up. Patients may undergo echocardiography (ECHO) and/or bone scan and/or positron emission tomography (PET)/CT if clinically indicated.

ARM B: Patients receive pembrolizumab intravenously (IV) over 30 minutes on day 1 of each cycle. Cycles repeat every 6 weeks for up to 9 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo CT or MRI throughout the trial and collection of blood samples on study. Patients may undergo ECHO and/or bone scan and/or PET/CT if clinically indicated.

After completion of study treatment, patients are followed up every 3 months up to year 2, every 6 months in years 2-5, and every 12 months in years 5-10.

Studietype

Ingrijpend

Inschrijving (Geschat)

400

Fase

  • Fase 3

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  • Patient must be ≥ 18 years of age
  • Patient must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
  • Patient must have histologically confirmed non-clear cell renal cell carcinoma (nccRCC) with ≥ pT3Nx or pTanyN+ or pTanyNanyM1 with no evidence of disease (NED) per the American Joint Committee on Cancer (AJCC) 8th edition
  • Patient must not have renal medullary carcinoma
  • Patient must have had a partial or radical nephrectomy. In the case of patients with M1 NED status, a complete resection of the metastatic lesion(s) (metastasectomy) must have been completed at the time of nephrectomy or within 1 year after nephrectomy

    • Positive margins are allowed as long as no gross disease
  • Patient must not have residual thrombus post nephrectomy in the vena renalis or vena cava
  • Patient must be randomized ≤ 16 weeks after nephrectomy and/or < 16 weeks after metastasectomy
  • Patient must have undergone imaging of chest, abdomen and pelvis with a CT or MRI after nephrectomy/metastasectomy and within 42 days prior to randomization documenting there is no evidence of liver, bone, or brain metastases
  • Patient must not have received any prior anti-PD-1/PD-L1 or CTLA-4 agents
  • Patient must not have received any prior radiotherapy for nccRCC
  • Patient must not have received prior systemic treatment for nccRCC (except nephrectomy or metastasectomy). Patient must not have received prior immune checkpoint inhibitor agents for other cancers within 2 years prior to randomization
  • Patient must not have active known or suspected autoimmune disease requiring systemic immunosuppression. The following autoimmune disorders are permitted: patients with vitiligo, type I diabetes mellitus, controlled/stable hypo or hyperthyroidism due to autoimmune or non-autoimmune conditions (hormone replacement is allowed), psoriasis not requiring systemic treatment
  • Patient must not be on any immunosuppressant therapy other than inhaled steroids, intranasal steroids, topical steroids, injection steroids and systemic steroids up to 10mg prednisone equivalent
  • Patient must have recovered adequately from toxicity and/or complications related to any surgery received prior to randomization
  • Patient must not have a history or current evidence of uncontrolled intercurrent illness that would limit compliance with study requirement, substantially increase the risk of incurring adverse events (AEs), or compromise the ability of the patient to give written informed consent
  • Patient must not have had a history of allogeneic organ transplantation
  • Patient must not be pregnant or breast-feeding due to the potential harm to an unborn fetus and possible risk for adverse events in nursing infants with the treatment regimens being used

    • All patients of childbearing potential must have a blood test or urine study within 14 days prior to randomization to rule out pregnancy
    • A patient of childbearing potential is defined as anyone, regardless of whether they have undergone tubal ligation, who meets the following criteria: 1) has achieved menarche at some point, 2) has not undergone a hysterectomy or bilateral oophorectomy; or 3) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months)
  • Patient must not expect to conceive or father children by using accepted and effective method(s) of contraception or by abstaining from sexual intercourse for the duration of their participation in the study. Patients of childbearing potential assigned to Arm B must continue contraception requirements for 4 months following the last dose of pembrolizumab. Patients assigned to Arm B must also not breastfeed while on protocol treatment and for 4 months after the last dose of pembrolizumab
  • Patient must have the ability to understand and the willingness to sign a written informed consent document. Patients with impaired decision-making capacity (IDMC) who have a legally authorized representative (LAR) or caregiver and/or family member available will also be considered eligible
  • Leukocytes ≥ 3,000/ mm^3 (must be obtained ≤ 42 days prior to protocol randomization)
  • Absolute neutrophil count (ANC) ≥ 1,500/mm^3 (must be obtained ≤ 42 days prior to protocol randomization)
  • Platelets ≥ 100,000/ mm^3 (must be obtained ≤ 42 days prior to protocol randomization)
  • Total bilirubin ≤ 2 x institutional upper limit of normal (ULN) (must be obtained ≤ 42 days prior to protocol randomization)

    • NOTE: For patients with known Gilbert's syndrome, total bilirubin < 3 x ULN
  • Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) ≤ 3.0 × institutional ULN (must be obtained ≤ 42 days prior to protocol randomization)
  • Estimated glomerular filtration rate (eGFR) clearance ≥ 30 mL/min/1.73 m^2 (must be obtained ≤ 42 days prior to protocol randomization)
  • Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months of randomization are eligible for this trial
  • For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated
  • Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load
  • Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial
  • Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, patients must be class 2 or better

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Actieve vergelijker: Arm A (active surveillance)
Patients undergo active surveillance, including CT or MRI, every 3 months for 1 year. Patients also undergo collection of blood samples on study and CT or MRI during follow up. Patients may undergo ECHO and/or bone scan and/or PET/CT if clinically indicated.
Onderga het verzamelen van bloedmonsters
Andere namen:
  • Biologische monsterverzameling
  • Biospecimen verzameld
  • Specimenverzameling
  • Monsterverzameling
MRI ondergaan
Andere namen:
  • MRI
  • Magnetische resonantie
  • Magnetic Resonance Imaging-scan
  • Medische beeldvorming, magnetische resonantie / nucleaire magnetische resonantie
  • DHR
  • MR-beeldvorming
  • MRI scan
  • NMR-beeldvorming
  • NMRI
  • Nucleaire magnetische resonantie beeldvorming
  • Magnetische resonantiebeeldvorming (MRI)
  • sMRI
  • Magnetische resonantiebeeldvorming (procedure)
  • MRI's
  • Structurele MRI
Onder actief toezicht
Andere namen:
  • Observatie
  • Actief toezicht
  • uitgestelde therapie
  • afwachtend beheer
  • Waakzaam wachten
PET/CT ondergaan
Andere namen:
  • Medische beeldvorming, positronemissietomografie
  • HUISDIER
  • PET-scan
  • Positron Emissie Tomografie Scan
  • Positron-emissietomografie
  • PT
  • Positronemissietomografie (procedure)
Onderga een botscan
Andere namen:
  • Botscintigrafie
CT en PET/CT ondergaan
Andere namen:
  • CT
  • KAT
  • CT-scan
  • Axiale computertomografie
  • Computergestuurde axiale tomografie
  • Computergestuurde tomografie
  • tomografie
  • Geautomatiseerde axiale tomografie (procedure)
  • Computertomografie (CT)-scan
  • Diagnostische kattencan
  • Diagnostisch CAT -scanservice type
Ondergaan echo
Andere namen:
  • Echocardiografie
  • EG
Experimenteel: Arm B (pembrolizumab)
Patients receive pembrolizumab IV over 30 minutes on day 1 of each cycle. Cycles repeat every 6 weeks for up to 9 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo CT or MRI throughout the trial and collection of blood samples on study. Patients may undergo ECHO and/or bone scan and/or PET/CT if clinically indicated.
Onderga het verzamelen van bloedmonsters
Andere namen:
  • Biologische monsterverzameling
  • Biospecimen verzameld
  • Specimenverzameling
  • Monsterverzameling
MRI ondergaan
Andere namen:
  • MRI
  • Magnetische resonantie
  • Magnetic Resonance Imaging-scan
  • Medische beeldvorming, magnetische resonantie / nucleaire magnetische resonantie
  • DHR
  • MR-beeldvorming
  • MRI scan
  • NMR-beeldvorming
  • NMRI
  • Nucleaire magnetische resonantie beeldvorming
  • Magnetische resonantiebeeldvorming (MRI)
  • sMRI
  • Magnetische resonantiebeeldvorming (procedure)
  • MRI's
  • Structurele MRI
IV gegeven
Andere namen:
  • Keytruda
  • MK-3475
  • Lambrolizumab
  • SCH 900475
  • MK3475
  • SCH-900475
  • BCD-201
  • Pembrolizumab Biosimilar BCD-201
  • Pembrolizumab Biosimilar QL2107
  • QL2107
  • GME 751
  • GME751
  • Pembrolizumab Biosimilar GME751
  • SCH900475
  • Pembrolizumab Biosimilar RPH-075
  • RPH 075
  • RPH-075
  • RPH075
  • Pembrolizumab biosimilar SB27
  • SB 27
  • SB-27
  • SB27
PET/CT ondergaan
Andere namen:
  • Medische beeldvorming, positronemissietomografie
  • HUISDIER
  • PET-scan
  • Positron Emissie Tomografie Scan
  • Positron-emissietomografie
  • PT
  • Positronemissietomografie (procedure)
Onderga een botscan
Andere namen:
  • Botscintigrafie
CT en PET/CT ondergaan
Andere namen:
  • CT
  • KAT
  • CT-scan
  • Axiale computertomografie
  • Computergestuurde axiale tomografie
  • Computergestuurde tomografie
  • tomografie
  • Geautomatiseerde axiale tomografie (procedure)
  • Computertomografie (CT)-scan
  • Diagnostische kattencan
  • Diagnostisch CAT -scanservice type
Ondergaan echo
Andere namen:
  • Echocardiografie
  • EG

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Disease-free survival (DFS)
Tijdsspanne: From randomization to first documented local recurrence, distant metastasis, secondary systemic malignancy, or death due to any cause, whichever occurs first, assessed up to 10 years
A superiority test of DFS for pembrolizumab arm versus (vs.) active surveillance arm will be performed at one-sided 0.025 significance level, using a stratified log-rank test assuming exponential failure.
From randomization to first documented local recurrence, distant metastasis, secondary systemic malignancy, or death due to any cause, whichever occurs first, assessed up to 10 years

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Overall survival (OS)
Tijdsspanne: From randomization to death from any cause, assessed up to 10 years
OS will be assessed among all randomized patients. Kaplan-Meier estimate will characterize OS and OS comparison will be made for pembrolizumab vs. active surveillance arm using stratified log-rank test and assuming exponential failure.
From randomization to death from any cause, assessed up to 10 years
Incidence of adverse events
Tijdsspanne: Up to 1 year
Adverse events will be described separately for patients treated on each arm to evaluate safety and tolerability. Toxicity will be defined using the Common Terminology Criteria for Adverse Events. All patients who receive treatment, regardless of eligibility, will be evaluated for toxicity. The 90% confidence interval for the true probability of observing a toxicity of Grade 4 or higher on a given arm will be no wider than 12.1% for each arm. The probability of observing one or more toxicities on a given arm with a true rate of 1% is 86.6% for each arm.
Up to 1 year
DFS among those that are circulating tumor deoxyribonucleic acid (ctDNA) positive
Tijdsspanne: Up to 10 years
The first ctDNA analysis objective is to compare DFS between patients randomized to pembrolizumab arm vs. active surveillance arm among patients that are ctDNA positive at baseline. Among patients that are ctDNA positive at baseline, DFS will be compared between patients randomized to pembrolizumab arm vs. surveillance arm using a stratified log-rank test at 0.05 two-sided alpha level assuming exponential failure. Hazard ratios (HRs) for recurrence or death will be reported using a univariable cox proportional hazards model.
Up to 10 years
OS among those that are ctDNA positive
Tijdsspanne: Up to 10 years
The second ctDNA analysis objective is to compare OS between patients randomized to pembrolizumab arm vs. active surveillance arm among patients that are ctDNA positive at baseline. Among 72 patients that are predicted to be ctDNA positive at baseline, OS will be compared between patients randomized to Pembrolizumab arm vs. surveillance arm using a stratified log-rank test at 0.05 two-sided alpha level assuming exponential failure. HRs for recurrence or death will be reported using a univariable cox proportional hazards model.
Up to 10 years
ctDNA clearance rate prediction
Tijdsspanne: At week 12
Will compare ctDNA clearance rate at week 12 between pembrolizumab arm and active surveillance arm. Among the 72 patients that are predicted to have ctDNA positivity at baseline, comparison of ctDNA clearance between arms will be assessed using Fisher's exact test at 0.05 two-sided alpha level.
At week 12
DFS by KIM-1 status
Tijdsspanne: Up to 10 years
Will to compare DFS between the two arms among high baseline KIM-1 levels (> 86 pg/mL) and low baseline KIM-1 levels separately. Among patients that consent to biomarker study (n=360), DFS will be compared between pembrolizumab arm patients and active surveillance arm patients in each high KIM-1 level and low KIM-1 level subgroups separately, using a stratified log-rank test assuming exponential failure, at 0.05 two-sided alpha level. HRs will be reported using a univariable cox proportional hazards model.
Up to 10 years
DFS by KIM-1 in pembrolizumab arm
Tijdsspanne: Post-cycle 1 (cycle length = 6 weeks)
Will assess whether a decrease in KIM-1 after one cycle of adjuvant therapy identifies patients who derive benefit from treatment. Among patients that consent to biomarker study and get randomized to pembrolizumab arm (n=180), DFS will be compared between pembrolizumab arm patients with a clinically meaningful drop in KIM-1 level after cycle 1 vs. no clinically meaningful drop in KIM-1 level using log-rank test at 0.05 two-sided alpha level. HRs will be reported using a univariable cox proportional hazards model.
Post-cycle 1 (cycle length = 6 weeks)
DFS in patients with any KIM-1 increase and not
Tijdsspanne: Up to 10 years
Will evaluate whether an increase in KIM-1 at any timepoint is associated with better DFS. Among patients that consent to biomarker study (n=360), DFS will be compared between patients with a clinically meaningful increase in KIM-1 level at any timepoint vs. no clinically meaningful increase in KIM-1 level using log-rank test at 0.05 two-sided alpha level. Hazard ratios will be reported using a univariable cox proportional hazards model.
Up to 10 years
Recurrence rate in C-reactive protein (CRP) groups
Tijdsspanne: Up to 10 years
Will evaluate whether persistently elevated CRP is associated with recurrence. Among the patients that consent to biomarker study (n=360), comparison between those with persistently elevated CRP vs. don't will be compared in recurrence rate, using Fisher's exact test at 0.05 two-sided alpha level. Odds ratio will be reported to summarize the strength of association between elevation of CRP (yes vs. no) and development of recurrence disease (yes vs. no).
Up to 10 years

Andere uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
DFS by sex
Tijdsspanne: Up to 10 years
Estimates of the primary outcome treatment effect and the corresponding 95% confidence interval will be provided by sex.
Up to 10 years
DFS by race
Tijdsspanne: Up to 10 years
Estimates of the primary outcome treatment effect and the corresponding 95% confidence interval will be provided by race.
Up to 10 years
DFS by ethnicity
Tijdsspanne: Up to 10 years
Estimates of the primary outcome treatment effect and the corresponding 95% confidence interval will be provided by ethnicity.
Up to 10 years

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Mehmet A Bilen, ECOG-ACRIN Cancer Research Group

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

10 februari 2027

Primaire voltooiing (Geschat)

1 januari 2032

Studie voltooiing (Geschat)

1 januari 2032

Studieregistratiedata

Eerst ingediend

7 juli 2026

Eerst ingediend dat voldeed aan de QC-criteria

7 juli 2026

Eerst geplaatst (Werkelijk)

8 juli 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

8 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

7 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

JA

Beschrijving IPD-plan

NCI is committed to sharing data in accordance with NIH policy. For more details on how clinical trial data is shared, access the link to the NIH data sharing policy page.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Ja

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

product vervaardigd in en geëxporteerd uit de V.S.

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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