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

7 de julho de 2026 atualizado por: 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.

Visão geral do estudo

Descrição detalhada

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.

Tipo de estudo

Intervencional

Inscrição (Estimado)

400

Estágio

  • Fase 3

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: 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.
Submeta-se à coleta de amostras de sangue
Outros nomes:
  • Coleta de Amostras Biológicas
  • Bioespécime coletado
  • Coleta de amostras
Submeter-se a ressonância magnética
Outros nomes:
  • Ressonância magnética
  • Varredura de imagem por ressonância magnética
  • Imagem Médica, Ressonância Magnética / Ressonância Magnética Nuclear
  • SENHOR
  • Exame de ressonância magnética
  • Imagem NMR
  • Ressonância Magnética Nuclear
  • Ressonância Magnética (MRI)
  • ressonância magnética
  • Ressonância magnética (procedimento)
  • Ressonâncias magnéticas
  • RM estrutural
Submeta-se a vigilância ativa
Outros nomes:
  • Observação
  • Vigilância Ativa
  • terapia adiada
  • gestão expectante
  • Espera vigilante
Submeta-se a PET/CT
Outros nomes:
  • Imagem Médica, Tomografia por Emissão de Pósitrons
  • BICHO DE ESTIMAÇÃO
  • PET scan
  • Tomografia por emissão de pósitrons
  • PT
  • Tomografia por emissão de pósitrons (procedimento)
Fazer varredura óssea
Outros nomes:
  • Cintilografia Óssea
Submeta-se a TC e PET/CT
Outros nomes:
  • TC
  • GATO
  • Tomografia
  • Tomografia Axial Computadorizada
  • Tomografia computadorizada
  • tomografia
  • Tomografia axial computadorizada (procedimento)
  • Tomografia computadorizada (TC)
  • Diagnóstico Cat Scan
  • Tipo de serviço de varredura de gato diagnóstico
Passar por eco
Outros nomes:
  • Ecocardiografia
  • CE
Experimental: 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.
Submeta-se à coleta de amostras de sangue
Outros nomes:
  • Coleta de Amostras Biológicas
  • Bioespécime coletado
  • Coleta de amostras
Submeter-se a ressonância magnética
Outros nomes:
  • Ressonância magnética
  • Varredura de imagem por ressonância magnética
  • Imagem Médica, Ressonância Magnética / Ressonância Magnética Nuclear
  • SENHOR
  • Exame de ressonância magnética
  • Imagem NMR
  • Ressonância Magnética Nuclear
  • Ressonância Magnética (MRI)
  • ressonância magnética
  • Ressonância magnética (procedimento)
  • Ressonâncias magnéticas
  • RM estrutural
Dado IV
Outros nomes:
  • Keytruda
  • MK-3475
  • Lambrolizumabe
  • SCH 900475
  • MK3475
  • SCH-900475
  • BCD-201
  • Pembrolizumabe Biossimilar BCD-201
  • Pembrolizumabe Biossimilar QL2107
  • QL2107
  • GME 751
  • GME751
  • Pembrolizumabe Biossimilar GME751
  • SCH900475
  • Pembrolizumabe Biossimilar RPH-075
  • RPH 075
  • RPH-075
  • RPH075
  • Pembrolizumab biossimilar SB27
  • SB 27
  • SB-27
  • SB27
Submeta-se a PET/CT
Outros nomes:
  • Imagem Médica, Tomografia por Emissão de Pósitrons
  • BICHO DE ESTIMAÇÃO
  • PET scan
  • Tomografia por emissão de pósitrons
  • PT
  • Tomografia por emissão de pósitrons (procedimento)
Fazer varredura óssea
Outros nomes:
  • Cintilografia Óssea
Submeta-se a TC e PET/CT
Outros nomes:
  • TC
  • GATO
  • Tomografia
  • Tomografia Axial Computadorizada
  • Tomografia computadorizada
  • tomografia
  • Tomografia axial computadorizada (procedimento)
  • Tomografia computadorizada (TC)
  • Diagnóstico Cat Scan
  • Tipo de serviço de varredura de gato diagnóstico
Passar por eco
Outros nomes:
  • Ecocardiografia
  • CE

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Disease-free survival (DFS)
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Overall survival (OS)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
DFS by sex
Prazo: 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
Prazo: 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
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

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

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

10 de fevereiro de 2027

Conclusão Primária (Estimado)

1 de janeiro de 2032

Conclusão do estudo (Estimado)

1 de janeiro de 2032

Datas de inscrição no estudo

Enviado pela primeira vez

7 de julho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

7 de julho de 2026

Primeira postagem (Real)

8 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

8 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

7 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

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.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

produto fabricado e exportado dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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