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Toripalimab and Lenvatinib With or Without SBRT Before Surgery for Non-Clear Cell Kidney Cancer (TL-SBRT-nccRCC)

2 de novembro de 2026 atualizado por: ZHOU FANGJIAN, Sun Yat-sen University

A Single-Center, Two-Cohort Phase II Study of Neoadjuvant Toripalimab and Lenvatinib With or Without Stereotactic Body Radiotherapy in Nonmetastatic Locally Advanced Non-Clear Cell Renal Cell Carcinoma

This single-center, nonrandomized, two-cohort Phase II study will evaluate neoadjuvant toripalimab and lenvatinib with or without stereotactic body radiotherapy (SBRT) in patients with resectable, nonmetastatic locally advanced non-clear cell renal cell carcinoma. Approximately 36 participants will be enrolled. Both cohorts will receive six 21-day cycles of toripalimab and lenvatinib; one cohort will also receive SBRT to the primary renal tumor. Surgery is planned after neoadjuvant treatment. The primary outcome is the percentage of necrotic tumor cells in the resected tumor specimen.

Visão geral do estudo

Status

Ainda não está recrutando

Condições

Intervenção / Tratamento

Descrição detalhada

Eligible participants with histologically confirmed, resectable, nonmetastatic locally advanced non-clear cell renal cell carcinoma will be enrolled into two nonrandomized cohorts. Cohort A will receive toripalimab 240 mg intravenously on day 1 of each 21-day cycle plus lenvatinib 12 mg orally once daily for six cycles. Cohort B will receive the same systemic treatment plus SBRT to the primary renal tumor at a total dose of 40 Gy in five fractions, delivered after completion of cycle 2 and before cycle 4. Tumor response will be assessed by imaging during and at the end of neoadjuvant treatment. Surgery will follow neoadjuvant treatment; the operating physician will determine the surgical approach based on imaging. Resected tumor specimens will be assessed for tumor cell necrosis and pathological response. Participants will be followed for recurrence, survival, and adverse events.

Tipo de estudo

Intervencional

Inscrição (Estimado)

36

Estágio

  • Fase 2

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

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

18 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • Voluntary written informed consent.
  • Age 18 years or older.
  • ECOG performance status of 0 or 1 and life expectancy of at least 6 months.
  • Histologically confirmed, resectable, nonmetastatic locally advanced non-clear cell renal cell carcinoma, excluding chromophobe and collecting duct carcinoma. Eligible disease includes T3aNxM0, T3bNxM0 without level III or IV venous tumor thrombus, T4NxM0, or TxN1M0.
  • At least one measurable lesion according to RECIST version 1.1.
  • Adequate organ function: hemoglobin ≥80 g/L; absolute neutrophil count ≥1.5 × 10^9/L; white blood cell count ≥3.5 × 10^9/L; platelets ≥80 × 10^9/L; ALT and AST ≤2.5 × upper limit of normal (ULN); total bilirubin ≤1.5 × ULN; serum creatinine ≤1.5 × ULN or creatinine clearance ≥60 mL/min; APTT, INR, and PT ≤1.5 × ULN.
  • Women of childbearing potential must be confirmed not pregnant before enrollment. All participants must use adequate contraception during treatment and for 4 weeks after treatment completion.
  • Willingness and ability to comply with study procedures.

Exclusion Criteria:

  • Known hypersensitivity to toripalimab, lenvatinib, or their excipients.
  • Chromophobe or collecting duct renal cell carcinoma.
  • Anticancer monoclonal antibody or another investigational drug within 4 weeks before enrollment; prior PD-1/PD-L1-directed treatment for metastatic disease; or prior lenvatinib or another antiangiogenic drug.
  • Distant organ metastasis or inability to undergo surgery.
  • Systemic immunosuppressive treatment, including prednisone >10 mg/day or equivalent, within 2 weeks before enrollment.
  • Active autoimmune disease, a history of autoimmune disease, or congenital or acquired immunodeficiency.
  • Poorly controlled cardiac disease, uncontrolled hypertension, or clinically significant cardiovascular events within 6 months before enrollment.
  • Chemotherapy, targeted therapy, or radiotherapy within 2 weeks before enrollment.
  • Gastrointestinal perforation or major surgery within 4 weeks before enrollment.
  • Arterial or venous thromboembolic event within 6 months before enrollment, except resolved catheter-associated thrombosis as judged by the investigator.
  • Active bleeding or a significant bleeding tendency, including clinically significant hemoptysis of more than 50 mL/day within 3 months before enrollment.
  • Urine dipstick protein ≥2+ or 24-hour urine protein ≥1.0 g.
  • Corrected QT interval >470 ms, subject to the protocol-specified review for pacemaker-related QT prolongation.
  • Suspected additional primary malignancy.
  • Interstitial lung disease, noninfectious pneumonitis, or another uncontrolled systemic disease.
  • Live attenuated vaccine within 28 days before first treatment or planned live attenuated vaccination during the study.
  • Active hepatitis B (HBV DNA ≥500 IU/mL), active hepatitis C (HCV RNA above the assay detection limit), or hepatitis B and C coinfection.
  • Severe infection within 4 weeks before first treatment; CTCAE grade ≥2 active infection requiring systemic antibiotics within 2 weeks before first treatment; unexplained fever >38.5°C during screening or before first treatment unless attributed to the tumor by the investigator; or evidence of active tuberculosis within the preceding year.
  • Prior or planned allogeneic bone marrow or solid-organ transplantation.
  • Peripheral neuropathy of grade ≥2, active brain metastases, leptomeningeal disease, or spinal cord compression.
  • Inability to swallow oral medication, chronic diarrhea, clinically significant intestinal obstruction, or another condition substantially affecting oral-drug absorption.
  • Pregnancy, breastfeeding, or plans to become pregnant during the study.
  • Any other serious physical or psychiatric illness or laboratory abnormality that may increase study risk, interfere with results, or make participation inappropriate in the investigator's judgment.

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: Não randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Toripalimab Plus Lenvatinib

Toripalimab 240 mg intravenously every 3 weeks plus lenvatinib 12 mg orally once daily for six 21-day cycles, followed by surgery.

Toripalimab 240 mg by intravenous infusion on day 1 of each 21-day cycle for six cycles.

Lenvatinib 12 mg orally once daily during six 21-day cycles of neoadjuvant treatment.

Experimental: Toripalimab Plus Lenvatinib and SBRT

Toripalimab 240 mg intravenously every 3 weeks plus lenvatinib 12 mg orally once daily for six 21-day cycles. SBRT at 40 Gy in five fractions is delivered to the primary renal tumor after cycle 2 and before cycle 4, followed by surgery.

Toripalimab 240 mg by intravenous infusion on day 1 of each 21-day cycle for six cycles.

Lenvatinib 12 mg orally once daily during six 21-day cycles of neoadjuvant treatment.

SBRT to the primary renal tumor, 40 Gy in five fractions, after cycle 2 and before cycle 4.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Tumor Cell Necrosis Rate (TCNR)
Prazo: At surgery following neoadjuvant treatment, approximately 5 to 6 months after the first dose.

Percentage of necrotic tumor cells in the resected tumor specimen, calculated from prespecified multisite pathological sampling.

At surgery following neoadjuvant treatment, approximately 5 to 6 months after the first dose.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
R0 Resection Rate
Prazo: At surgery following neoadjuvant treatment, approximately 5 to 6 months after the first dose.

Percentage of enrolled participants who undergo complete tumor resection with microscopically negative margins.

At surgery following neoadjuvant treatment, approximately 5 to 6 months after the first dose.
Objective Response Rate (ORR)
Prazo: From baseline through the final preoperative tumor assessment, approximately 18 weeks.

Percentage of participants with investigator-assessed complete or partial response according to RECIST version 1.1.

From baseline through the final preoperative tumor assessment, approximately 18 weeks.
Disease Control Rate (DCR)
Prazo: From baseline through the final preoperative tumor assessment, approximately 18 weeks.

Percentage of evaluable participants with complete response, partial response, or stable disease according to RECIST version 1.1.

From baseline through the final preoperative tumor assessment, approximately 18 weeks.
Major Pathological Response (MPR) Rate
Prazo: At surgery following neoadjuvant treatment, approximately 5 to 6 months after the first dose.

Percentage of resected participants with no more than 10% residual viable tumor in the tumor bed.

At surgery following neoadjuvant treatment, approximately 5 to 6 months after the first dose.

Colaboradores e Investigadores

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

Patrocinador

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 novembro de 2026

Conclusão Primária (Estimado)

31 de dezembro de 2029

Conclusão do estudo (Estimado)

31 de dezembro de 2030

Datas de inscrição no estudo

Enviado pela primeira vez

2 de novembro de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

2 de novembro de 2026

Primeira postagem (Real)

6 de novembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

6 de novembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

2 de novembro de 2026

Última verificação

1 de novembro de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 2024-FXY-233-Urology
  • 2024-FXY-233-Urology (Outro identificador: Sun Yat-sen University cancer center)

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

Individual participant data will not be shared because this small study collects sensitive clinical, imaging, and molecular data that could increase the risk of participant re-identification. Study results will be reported in aggregate form.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA 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 .