- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07828873
A Single-Arm Study of QL1706 Combined With DOS as Neoadjuvant Therapy for Locally Advanced Gastric/GEJ Adenocarcinoma
14 settembre 2026 aggiornato da: Yongxu Jia, The First Affiliated Hospital of Zhengzhou University
A Single-Arm, Prospective, Open-Label Clinical Study of Iparomlimab and Tuvonralimab (QL1706) Combined With DOS as Neoadjuvant Therapy for Locally Advanced Gastric and Gastroesophageal Junction Adenocarcinoma
This is an open-label, prospective, interventional study designed to enroll 34 patients with locally advanced gastric or gastroesophageal junction adenocarcinoma, aiming to evaluate and observe the efficacy and safety of QL1706 in combination with DOS for the treatment of locally advanced gastric or gastroesophageal junction adenocarcinoma.
Enrolled patients will receive iparomlimab and tuvonralimab in combination with the DOS regimen (docetaxel + oxaliplatin + S-1) administered in 21-day treatment cycles.
Subjects who complete 3-4 cycles of treatment and are deemed suitable for surgery will undergo gastrectomy, with the specific interval between neoadjuvant therapy and surgery determined by the investigator based on actual clinical circumstances.
Following surgery, clinicians will administer postoperative treatment according to the postoperative pathological assessment results and the clinical practice treatment principles of the study center.
The primary endpoint is the pathological complete response rate assessed by postoperative pathological evaluation.
Panoramica dello studio
Stato
Non ancora reclutamento
Tipo di studio
Interventistico
Iscrizione (Stimato)
34
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: Yongxu Jia
- Numero di telefono: 66271157
- Email: jiayongxu111@126.com
Luoghi di studio
-
-
Henan
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Zhengzhou, Henan, Cina, 450000
- The First Affiliated Hospital of Zhengzhou University
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Contatto:
- Yongxu Jia
- Numero di telefono: 66271157
- Email: jiayongxu111@126.com
-
-
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:
- Aged 18 to 75 years; male or female.
- Previously untreated, resectable adenocarcinoma of the stomach or gastroesophageal junction (GEJ).
- Clinical stage cT3-4a/N+ M0.
- ECOG performance status 0-1.
- Adequate organ function within 7 days prior to treatment, meeting the following criteria: (1) Complete blood count (CBC) criteria (without blood transfusion within 14 days): Hemoglobin (Hb) ≥ 90 g/L; Absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L; Platelet count (PLT) ≥ 80 × 10⁹/L; (2) Serum chemistry criteria: Total bilirubin (TBIL) ≤ 1.5 × upper limit of normal (ULN); Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5 × ULN; Serum creatinine (Cr) ≤ 1.5 × ULN or creatinine clearance (CCr) ≥ 60 mL/min; (3) Doppler echocardiography: left ventricular ejection fraction (LVEF) ≥ lower limit of normal (50%). (4) Thyroid function: thyroid-stimulating hormone (TSH) ≤ upper limit of normal (ULN).
- Participants of childbearing potential must agree to use effective contraception during the study period and for 6 months after study completion.
- The participant voluntarily agrees to participate in this study and signs the informed consent form.
Exclusion Criteria:
- Known history of hypersensitivity or allergy to QL1706 or its excipients, tegafur/gimeracil/oteracil (S-1), oxaliplatin, docetaxel, or any of their excipients.
- History of another malignancy within 5 years prior to screening or concurrent malignancy, except for curatively treated carcinoma in situ of the cervix, non-melanoma skin cancer, and superficial bladder tumors.
- Patients with distant metastasis and/or unresectable disease;
- Prior treatment with immune checkpoint inhibitors, including anti-PD-1, anti-PD-L1, and anti-CTLA-4 agents.
- Receipt of any antineoplastic agents within 4 weeks prior to the first dose of study drug.
- Patients with gastrointestinal disorders such as intestinal obstruction (including partial obstruction), or those with evidence or risk of gastrointestinal bleeding, perforation, or obstruction.
- Any bleeding event ≥ CTCAE Grade 3 within 4 weeks prior to enrollment, or unhealed wounds, ulcers, or fractures.
- Concurrent enrollment in another clinical study, unless it is an observational (non-interventional) study or the follow-up phase of an interventional study.
- Subjects requiring systemic therapy with corticosteroids (>10 mg/day prednisone or equivalent) or other immunosuppressive agents within 2 weeks prior to the first dose of study drug.
- Receipt of live or live-attenuated vaccine within 4 weeks prior to the first dose of study drug.
- Major surgery or significant trauma within 4 weeks prior to the first dose of study drug.
- Active or history of autoimmune disease, with the exception of vitiligo or resolved childhood asthma/atopy that requires no intervention in adulthood.
- History of immunodeficiency, including HIV infection, or other acquired or congenital immunodeficiency disorders, or history of organ transplantation or allogeneic bone marrow transplantation.
- Subjects with inadequately controlled cardiovascular clinical symptoms or diseases.
- Severe infection (CTCAE Grade > 2) within 4 weeks prior to the first dose of study drug.
- Patients with a history of interstitial lung disease (except for radiation pneumonitis not treated with corticosteroids), non-infectious pneumonitis, or active pulmonary tuberculosis; or a history of active pulmonary tuberculosis within 1 year prior to enrollment, or more than 1 year prior to enrollment if not adequately treated.
- Pregnant or breastfeeding women.
- Other concomitant diseases that, in the opinion of the Investigator, pose a serious risk to the subject's safety or may interfere with the subject's ability to complete the study.
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: Iparomlimab and Tuvonralimab Injection (QL1706) Plus DOS Neoadjuvant Therapy Arm
Enrolled patients receive QL1706 (5 mg/kg, IV, D1) combined with the DOS regimen (docetaxel 40 mg/m², IV, D1 + oxaliplatin 100 mg/m², IV, D1 + S-1 40 mg/m², PO, BID, D1-14), administered every 21 days per cycle for 3-4 cycles.
Subjects who complete neoadjuvant therapy and are deemed suitable for surgery will undergo gastrectomy, followed by subsequent treatment based on postoperative pathological assessment.
|
5 mg/kg, intravenous infusion, administered once every 21 days (D1), for 3-4 cycles.
Altri nomi:
40 mg/m², intravenous infusion, administered once every 21 days (D1), for 3-4 cycles.
100 mg/m², intravenous infusion, administered once every 21 days (D1), for 3-4 cycles.
40 mg/m², oral, twice daily (BID), D1-14, every 21 days per cycle, for 3-4 cycles.
Subjects who complete 3-4 cycles of neoadjuvant therapy and are deemed suitable for surgery will undergo gastrectomy.
The specific interval between neoadjuvant therapy and surgery will be determined by the investigator based on actual clinical circumstances.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Pathological Complete Response Rate (pCR Rate)
Lasso di tempo: Perioperative, upon postoperative pathological evaluation
|
Defined as the proportion of patients with no residual tumor cells in the resected tumor tissue and regional lymph nodes upon pathological evaluation.
|
Perioperative, upon postoperative pathological evaluation
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
R0 Resection Rate
Lasso di tempo: Perioperative, upon postoperative pathological evaluation
|
The proportion of patients with microscopically margin-negative resection, with no residual tumor cells either macroscopically or microscopically, and complete resection of the lesion.
|
Perioperative, upon postoperative pathological evaluation
|
|
Major Pathological Response Rate (MPR Rate)
Lasso di tempo: Perioperative, upon postoperative pathological evaluation
|
Defined as the proportion of patients with ≤10% residual viable tumor cells in the postoperative pathological specimen.
|
Perioperative, upon postoperative pathological evaluation
|
|
Objective Response Rate (ORR)
Lasso di tempo: On Day 1 of every 2 cycles (each cycle is 21 days), prior to surgery
|
The proportion of patients achieving complete response (CR) or partial response (PR) as assessed by RECIST version 1.1 criteria.
|
On Day 1 of every 2 cycles (each cycle is 21 days), prior to surgery
|
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Disease Control Rate (DCR)
Lasso di tempo: On Day 1 of every 2 cycles (each cycle is 21 days), prior to surgery
|
The proportion of patients achieving CR, PR, or stable disease (SD) among evaluable patients as assessed by RECIST version 1.1 criteria.
|
On Day 1 of every 2 cycles (each cycle is 21 days), prior to surgery
|
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Number of Participants with Adverse Events (AEs) and Severity Graded
Lasso di tempo: From signing of ICF through 30 days after the last dose
|
Defined as all adverse events occurring from enrollment (i.e., signing of the informed consent form) through 30 days after the last dose.
AEs will be coded using the MedDRA dictionary, with System Organ Class (SOC) and Preferred Term assigned to each adverse event.
The severity of adverse events will be graded according to NCI CTCAE version 5.0.
|
From signing of ICF through 30 days after the last dose
|
|
3-Year Disease-Free Survival Rate (DFS Rate)
Lasso di tempo: 3 years after treatment
|
Defined as the proportion of patients without recurrence or metastasis within 3 years after treatment.
|
3 years after treatment
|
Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Peripheral blood ctDNA Biomarker
Lasso di tempo: Baseline and on Day 1 of every 2 cycles (each cycle is 21 days, synchronized with imaging evaluation), until prior to surgery
|
Serial peripheral blood samples are collected at baseline and during neoadjuvant treatment.
Circulating tumor DNA (ctDNA) molecular profiles are detected by next-generation sequencing.
The exploratory analysis aims to evaluate the correlation between dynamic ctDNA alterations and treatment efficacy and safety outcomes.
|
Baseline and on Day 1 of every 2 cycles (each cycle is 21 days, synchronized with imaging evaluation), until prior to surgery
|
|
Peripheral blood multi-omics biomarker levels
Lasso di tempo: Baseline and on Day 1 of every 2 cycles (each cycle is 21 days, synchronized with imaging evaluation), until prior to surgery
|
Serial peripheral blood samples are collected at baseline and during neoadjuvant treatment.
Genomic, transcriptomic, and proteomic multi-omics profiles in peripheral blood are detected using a multi-omics sequencing platform.
Exploratory analyses are performed to explore the association between peripheral blood multi-omics molecular features and treatment efficacy and safety.
|
Baseline and on Day 1 of every 2 cycles (each cycle is 21 days, synchronized with imaging evaluation), until prior to surgery
|
|
Tumor tissue multi-omics and tumor microenvironment immune signatures
Lasso di tempo: Baseline (pre-treatment biopsy) and perioperative (immediately after radical gastrectomy)
|
Tumor specimens including fresh tissues and formalin-fixed paraffin-embedded (FFPE) sections are collected at baseline (pre-treatment biopsy) and immediately after radical gastrectomy.
Baseline and post-operative tumor tissues are subjected to genomic, transcriptomic, and proteomic multi-omics sequencing to characterize tumor biomarkers and tumor microenvironment immune molecular features.
All tissue collections do not interfere with routine clinical pathological diagnosis, and are performed with written informed consent.
Exploratory analyses will investigate the associations between tissue molecular signatures and treatment efficacy and safety outcomes.
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Baseline (pre-treatment biopsy) and perioperative (immediately after radical gastrectomy)
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Collaboratori
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 novembre 2026
Completamento primario (Stimato)
1 settembre 2029
Completamento dello studio (Stimato)
1 dicembre 2029
Date di iscrizione allo studio
Primo inviato
9 settembre 2026
Primo inviato che soddisfa i criteri di controllo qualità
14 settembre 2026
Primo Inserito (Effettivo)
18 settembre 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
18 settembre 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
14 settembre 2026
Ultimo verificato
1 settembre 2026
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Prodotti chimici organici
- Procedure chirurgiche, operative
- Idrocarburi
- Cicloparaffins
- Idrocarburi, aliciclici
- Idrocarburi, ciclici
- Terpeni
- Complessi di coordinamento
- Taxoidi
- Ciclodecani
- Diterpenes
- Procedure chirurgiche del sistema digestivo
- Docetaxel
- Oxaliplatino
- Gastrectomia
- tegafur-gimeracil-oteracil
Altri numeri di identificazione dello studio
- HN-QL1706-G/GEJ-002
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
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 .