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- Essai clinique NCT07922928
Toripalimab and Lenvatinib With or Without SBRT Before Surgery for Non-Clear Cell Kidney Cancer (TL-SBRT-nccRCC)
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.
Aperçu de l'étude
Statut
Intervention / Traitement
Description détaillée
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.
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
Contacts et emplacements
Coordonnées de l'étude
- Nom: Yulu Peng
- Numéro de téléphone: 02087342318
- E-mail: pengyl1@sysucc.org.cn
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Comparateur actif: 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. |
|
Expérimental: 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. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Tumor Cell Necrosis Rate (TCNR)
Délai: 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.
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
R0 Resection Rate
Délai: 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)
Délai: 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)
Délai: 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
Délai: 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.
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 2024-FXY-233-Urology
- 2024-FXY-233-Urology (Autre identifiant: Sun Yat-sen University cancer center)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime 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.
Informations sur les médicaments et les dispositifs, documents d'étude
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