- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07819578
Toripalimab Plus Sacituzumab Tirumotecan as Neoadjuvant Therapy for Resectable NSCLC
13 de septiembre de 2026 actualizado por: Shaodong Hong
A Phase II Study of Toripalimab Combined With Sacituzumab Tirumotecan as Neoadjuvant Therapy for Resectable Non-Small Cell Lung Cancer
This is a prospective, multicenter, single-arm Phase II investigator-initiated trial evaluating neoadjuvant toripalimab plus sacituzumab tirumotecan (SKB264) in treatment-naive adults with resectable or potentially resectable, driver-negative non-small cell lung cancer (NSCLC).
Eligible participants have stage II-IIIA or selected IIIB disease (T3N2 or T4N2) and will receive sacituzumab tirumotecan 5 mg/kg plus toripalimab 3 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles.
Participants deemed operable after multidisciplinary assessment will undergo definitive surgery.
The primary endpoint is pathologic complete response.
A Simon two-stage minimax design plans to enroll 30 participants.
Descripción general del estudio
Estado
Aún no reclutando
Condiciones
Intervención / Tratamiento
Descripción detallada
This prospective, multicenter, single-arm Phase II investigator-initiated trial evaluates neoadjuvant sacituzumab tirumotecan (SKB264), a TROP2-directed antibody-drug conjugate, plus the PD-1 antibody toripalimab in treatment-naive adults with resectable or potentially resectable, driver-negative NSCLC.
Participants have stage II-IIIA or selected IIIB disease (T3N2 or T4N2).
Sacituzumab tirumotecan 5 mg/kg and toripalimab 3 mg/kg are administered intravenously on Day 1 every 2 weeks for up to 6 cycles.
Surgery is planned 4-6 weeks after the final neoadjuvant dose when the participant remains operable following multidisciplinary assessment.
Tumor response is assessed using RECIST 1.1.
Safety is assessed using NCI CTCAE version 5.0, including adverse events, serious adverse events, perioperative complications, and surgery delays or cancellations.
The primary endpoint is pathologic complete response, defined as no residual viable tumor cells in the resected primary tumor and all resected lymph nodes.
Major pathologic response is defined as residual viable tumor of 10% or less.
Tipo de estudio
Intervencionista
Inscripción (Estimado)
30
Fase
- Fase 2
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Estudio Contacto
- Nombre: Shaodong Hong Hong, M.D., Ph.D.
- Número de teléfono: +8615920527656
- Correo electrónico: hongshd@sysucc.org.cn
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- Signed informed consent obtained before any study procedure.
- Age 18 to 75 years, male or female.
- Histologically/cytologically confirmed, treatment-naive, resectable or potentially resectable NSCLC: stage II-IIIA and selected IIIB (T3N2, T4N2) per IASLC/UICC TNM 9th edition.
- Disease staged as cTNM by PET-CT or by neck/chest/abdominal/pelvic CT plus whole-body bone scan and brain MRI.
- Multidisciplinary team including thoracic surgeon judges lesion resectable or potentially resectable.
- At least one measurable target lesion per RECIST 1.1.
- ECOG performance status 0-1.
- Adequate organ function (baseline, no transfusion, rh-EPO, or G-CSF within 2 weeks before first dose): neutrophils ≥1.5 ×10^9/L; platelets ≥100 ×10^9/L; hemoglobin ≥9 g/dL.
- AST, ALT, ALP ≤2.5 × ULN; TBil ≤1.5 × ULN.
- For liver metastases: AST/ALT ≤5 × ULN; TBil ≤2 × ULN.
- For liver or bone metastases: ALP ≤5 × ULN.
- Creatinine clearance (Cockcroft-Gault) ≥60 mL/min.
- INR, APTT, PT ≤1.5 × ULN.
- TSH within normal range; if TSH abnormal but T3 and free T4 normal, eligible.
- Women of childbearing potential must have a negative pregnancy test within 7 days before first dose and use effective contraception during treatment and until 12 months after last dose; men with partners of childbearing potential must use effective contraception during treatment and until 12 months after last dose.
Exclusion Criteria:
- Neuroendocrine histology component in tumor pathology.
- Known EGFR sensitizing mutation or ALK fusion (for non-squamous NSCLC, EGFR/ALK status must be determined).
- Other malignancy within 5 years, except those with clinically negligible metastatic risk and curative treatment intent (e.g., adequately treated carcinoma in situ as per protocol examples).
- Severe or uncontrolled comorbidities, including symptomatic cerebrovascular events or liver disease at Child-Pugh grade ≥A.
- History of allogeneic stem cell transplantation or solid organ transplantation.
- Severe dry eye syndrome, severe meibomian gland dysfunction, severe blepharitis, or corneal disorders that may delay corneal healing.
- History of interstitial lung disease requiring steroids, or active ILD.
- HIV positive or diagnosed AIDS.
- Active tuberculosis.
- Uncontrolled active HBV infection (HBsAg positive with HBV-DNA above local upper limit of normal). HBV-DNA must be <500 IU/mL within 28 days before randomization/inclusion.
- Active HCV infection (HCV antibody positive and HCV RNA positive).
- Known hypersensitivity to toripalimab or sacituzumab tirumotecan (or excipients).
- Live vaccine within 30 days before first dose (except inactivated vaccines allowed where specified by protocol, including local policy).
- Any systemic or local anticancer treatment before first study treatment.
- Use of traditional Chinese medicines with anticancer indication within 7 days before first dose, or need to continue such drugs during study.
- Other investigational drug not discontinued for at least 5 half-lives or 2 months (whichever is longer) before first dose.
- Any known or suspected autoimmune disease or immunodeficiency, except primary hypothyroidism (stable, not requiring hormones, or stable on physiologic hormone replacement) and stable type 1 diabetes mellitus with controlled blood glucose.
- Medical or psychiatric conditions likely to cause premature discontinuation or compromise safety, sampling, or follow-up, including severe social or compliance risks.
- Pregnancy or breastfeeding; unwillingness to use effective contraception as specified.
- Any other condition considered unsuitable by investigator.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Toripalimab plus sacituzumab tirumotecan
Participants will receive sacituzumab tirumotecan 5 mg/kg intravenously on Day 1 every 2 weeks combined with toripalimab 3 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles as neoadjuvant therapy.
Surgery will be performed after multidisciplinary assessment when appropriate.
Postoperative or adjuvant treatment will be determined according to guidelines and investigator assessment.
|
Toripalimab 3 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles as neoadjuvant therapy, administered in combination with sacituzumab tirumotecan.
Sacituzumab tirumotecan (SKB264) 5 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles as neoadjuvant therapy, administered in combination with toripalimab.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Pathological Complete Response (pCR) Rate
Periodo de tiempo: At definitive surgery, up to 18 weeks after first study treatment
|
Proportion of participants with no residual viable tumor cells in the resected primary tumor and all resected lymph nodes.
Participants without surgery or evaluable surgical pathology will be counted as non-pCR.
|
At definitive surgery, up to 18 weeks after first study treatment
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Major Pathological Response (MPR) Rate
Periodo de tiempo: At definitive surgery, up to 18 weeks after first study treatment
|
Proportion of participants with residual viable tumor of 10% or less in the resected primary tumor and all resected lymph nodes.
|
At definitive surgery, up to 18 weeks after first study treatment
|
|
R0 Resection Rate
Periodo de tiempo: At definitive surgery, up to 18 weeks after first study treatment
|
Proportion of participants who undergo R0 resection, defined as microscopically margin-negative resection, after neoadjuvant therapy.
|
At definitive surgery, up to 18 weeks after first study treatment
|
|
Pathological Downstaging Rate
Periodo de tiempo: At definitive surgery, up to 18 weeks after first study treatment
|
Proportion of participants with pathological stage lower than baseline clinical stage at definitive surgery.
|
At definitive surgery, up to 18 weeks after first study treatment
|
|
Objective Response Rate (ORR)
Periodo de tiempo: Up to 18 weeks after first study treatment
|
Proportion of participants with complete response or partial response according to investigator-assessed RECIST 1.1 after neoadjuvant therapy.
|
Up to 18 weeks after first study treatment
|
|
Event-Free Survival (EFS)
Periodo de tiempo: Up to 60 months from enrollment
|
Time from enrollment to disease progression precluding surgery, disease progression or recurrence after surgery, disease progression in participants who do not undergo surgery, or death from any cause, whichever occurs first.
|
Up to 60 months from enrollment
|
|
Overall Survival (OS)
Periodo de tiempo: Up to 60 months from enrollment
|
Time from enrollment to death from any cause.
|
Up to 60 months from enrollment
|
|
Incidence of Adverse Events
Periodo de tiempo: From first study treatment through 90 days after the last study treatment or surgery, whichever occurs later
|
Incidence of adverse events graded according to NCI CTCAE version 5.0.
|
From first study treatment through 90 days after the last study treatment or surgery, whichever occurs later
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Estimado)
1 de octubre de 2026
Finalización primaria (Estimado)
1 de diciembre de 2028
Finalización del estudio (Estimado)
1 de diciembre de 2028
Fechas de registro del estudio
Enviado por primera vez
24 de julio de 2026
Primero enviado que cumplió con los criterios de control de calidad
13 de septiembre de 2026
Publicado por primera vez (Actual)
15 de septiembre de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
15 de septiembre de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
13 de septiembre de 2026
Última verificación
1 de septiembre de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2026-FXY-019-NEIKE
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Descripción del plan IPD
De-identified individual participant data and data dictionaries from this investigator-initiated Phase II oncology study will not be shared at this time due to current sponsor/institutional policy, data governance requirements, and pending legal/ethics arrangements.
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .