- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07819578
Toripalimab Plus Sacituzumab Tirumotecan as Neoadjuvant Therapy for Resectable NSCLC
13 settembre 2026 aggiornato da: 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.
Panoramica dello studio
Stato
Non ancora reclutamento
Condizioni
Intervento / Trattamento
Descrizione dettagliata
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 di studio
Interventistico
Iscrizione (Stimato)
30
Fase
- Fase 2
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Shaodong Hong Hong, M.D., Ph.D.
- Numero di telefono: +8615920527656
- Email: hongshd@sysucc.org.cn
Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
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.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: 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.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Pathological Complete Response (pCR) Rate
Lasso di tempo: 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
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Major Pathological Response (MPR) Rate
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: Up to 60 months from enrollment
|
Time from enrollment to death from any cause.
|
Up to 60 months from enrollment
|
|
Incidence of Adverse Events
Lasso di tempo: 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
|
Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Stimato)
1 ottobre 2026
Completamento primario (Stimato)
1 dicembre 2028
Completamento dello studio (Stimato)
1 dicembre 2028
Date di iscrizione allo studio
Primo inviato
24 luglio 2026
Primo inviato che soddisfa i criteri di controllo qualità
13 settembre 2026
Primo Inserito (Effettivo)
15 settembre 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
15 settembre 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
13 settembre 2026
Ultimo verificato
1 settembre 2026
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 2026-FXY-019-NEIKE
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Descrizione del piano 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.
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .