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Clinical Study of Ivonescimab Combined With Concurrent Chemoradiotherapy in the Treatment of Advanced Non-small Cell Lung Cancer

10 novembre 2026 aggiornato da: Guizhou Medical University

A Prospective Exploratory Phase II Clinical Study of Ivonescimab Combined With Concurrent Chemoradiotherapy in the Treatment of Patients With Advanced Non-Small Cell Lung Cancer

This prospective, exploratory study will evaluate the objective response rate (ORR), progression-free survival (PFS), overall survival (OS), and toxicity of ivonescimab plus chemotherapy for 2-4 cycles after concurrent chemoradiotherapy, followed by 2 years of ivonescimab maintenance therapy, in patients with stage IV non-small cell lung cancer (NSCLC). The findings will be compared with those of previous studies and with our institutional data on patients with stage IV NSCLC who received concurrent chemoradiotherapy followed by PD-1 inhibitor plus chemotherapy for 2-4 cycles and then 2 years of PD-1 inhibitor maintenance therapy. This comparison may demonstrate that, after concurrent chemoradiotherapy for stage IV NSCLC, ivonescimab plus chemotherapy for 2-4 cycles followed by 2 years of ivonescimab maintenance therapy achieves superior efficacy compared with PD-1 inhibitor plus chemotherapy for 2-4 cycles followed by 2 years of PD-1 inhibitor maintenance therapy, with a comparable toxicity profile.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

40

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

Luoghi di studio

    • Guizhou
      • Guiyang, Guizhou, Cina, 550008
        • the Affiliated Cancer Hospital of Guizhou Medical University
        • Contatto:
        • Contatto:
        • Investigatore principale:
          • Dongdong Cao, MSc
        • Investigatore principale:
          • Wengang Yang, MSc
        • Investigatore principale:
          • Mei Liu, BSc
        • Investigatore principale:
          • Zu Ma, BSc
        • Investigatore principale:
          • Qingsong Li, MD

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

Da 18 anni a 75 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • Have fully understood this study and voluntarily signed the Informed Consent Form (ICF)

  • Aged 18 to 75 years, regardless of gender

  • Previously untreated, histopathologically or cytologically confirmed unresectable PD-L1 TPS ≥ 1% Stage IV non-small cell lung cancer

  • Have measurable lesions according to Response Evaluation Criteria in Solid Tumors version 1.1

  • Have adequate pulmonary function tests (PFTs)

  • Subjects must be able to provide a prior driver gene report based on tissue or blood testing, and the test results must show that targetable driver genes such as EGFR sensitive mutations, ALK rearrangement or fusion, and ROS1 fusion are all negative; or if a certain type of driver gene is positive but the targeted drug is not available, the subject may be enrolled. If the subject does not have a driver gene test report, tumor samples (archived or fresh, primary or metastatic) or blood samples must be collected before enrollment for driver gene testing to confirm negativity (at a local laboratory or central laboratory)

  • ECOG performance status score of 0-1

  • Adequate organ and bone marrow function

    ① Hematology: Absolute neutrophil count (ANC) ≥ 1500/μL; Platelets ≥ 100,000/μL; Hemoglobin ≥ 9.0 g/dL or ≥ 5.6 mmol/L.

    ② Renal: Serum creatinine ≤ 1.5 × ULN or calculated creatinine clearance (CrCl) ≥ 60 mL/min (using the Cockcroft-Gault formula).

    ③ Hepar: Total bilirubin ≤ 1.5 × ULN, or for subjects with total bilirubin levels > 1.5 × ULN, direct bilirubin within normal limits; AST (SGOT) and ALT (SGPT) ≤ 2.5 × ULN.

    ④ Adequate coagulation function: International Normalized Ratio (INR) and Activated Partial Thromboplastin Time (APTT) ≤ 1.5 × ULN; Known left ventricular ejection fraction (LVEF) ≥ 50%; Urine protein < 1+ or if urine protein is 1+, further 24-hour urine protein quantification < 1.0 g.

  • Endocrine System: Thyroid-stimulating hormone (TSH) within normal limits. Note: If TSH is not within the normal range at baseline, the subject may still meet the inclusion criteria if T3 and free T4 are within the normal range;Coagulation function: International Normalized Ratio (INR) or Prothrombin Time (PT), Activated Partial Thromboplastin Time (APTT) ≤ 1.5 × ULN, except for subjects receiving anticoagulant therapy, as long as PT or aPTT is within the intended therapeutic range of the anticoagulant drug.

  • Willing and able to comply with the study plan's visits, treatment plans, laboratory tests, and other study procedures.

  • Childbearing age women must have a serum pregnancy test within 3 days before the first dose, and the result must be negative. Female subjects of childbearing age and male subjects with partners of childbearing age must agree to use highly effective methods of contraception during the study and for 180 days after the last dose of the study drug.

Exclusion Criteria:

  • Presence of resectable or metastatic disease
  • History of interstitial lung disease, drug-induced interstitial lung disease, or radiation pneumonitis requiring steroid therapy, or currently receiving drug treatment or other clinical interventions, or presence of active pulmonary interstitial lesions or imaging findings of interstitial lung disease.
  • Known history of active tuberculosis
  • Known active infection requiring systemic therapy
  • Any known or suspected autoimmune disease or immunodeficiency, except for: patients with a history of hypothyroidism who do not require hormone therapy or are receiving physiological doses of hormone replacement therapy; patients with stable blood glucose-controlled type 1 diabetes.
  • Uncontrolled active hepatitis B (defined as positive hepatitis B surface antigen [HBsAg] test at screening with HBV-DNA levels above the upper limit of normal of the study center's laboratory; patients with HBV-DNA <500 IU/mL within 28 days before enrollment who have received at least 14 days of standard local antiviral therapy and are willing to continue antiviral therapy during the study may be enrolled); active hepatitis C (defined as positive hepatitis C virus surface antibody [HCsAb] test at screening with positive HCV-RNA).
  • Known human immunodeficiency virus (HIV) infection (known HIV antibody positive)
  • Vaccination with live vaccines within 30 days before the first dose, including but not limited to: mumps, rubella, measles, varicella/zoster (chickenpox), yellow fever, rabies, BCG, and typhoid vaccine (inactivated virus vaccines are allowed).
  • History of severe allergic reactions to other monoclonal antibodies;
  • Known severe or uncontrolled underlying diseases
  • Patients with a history of another malignancy within 5 years before the first dose, other than non-small cell lung cancer, are excluded. This exclusion does not apply to malignancies with a negligible risk of metastasis or death (e.g., expected disease-free survival >5 years) that are expected to achieve a curative outcome after treatment (e.g., adequately treated cervical carcinoma in situ, basal cell or squamous cell skin cancer, or ductal carcinoma in situ treated with curative-intent surgery).
  • Class III-IV congestive heart failure (New York Heart Association classification), poorly controlled and clinically significant arrhythmias.
  • Any arterial thrombosis, embolism, or ischemia within 6 months before enrollment, such as myocardial infarction, unstable angina, cerebrovascular accident, or transient ischemic attack.
  • Female subjects who are pregnant, breastfeeding, or planning to become pregnant during the study.
  • Investigators consider other conditions that may make the patient unsuitable for participation in this clinical trial.

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: ivonescimab combined with chemotherapy for 2-4 cycles followed by ivonescimab maintenance therapy

After concurrent chemoradiotherapy, patients received 2-4 cycles of ivonescimab combined with chemotherapy, with each 3-week period defined as one dosing cycle. On Day 1 of each treatment cycle, ivonescimab was administered first by intravenous infusion; after an interval of at least 30 minutes, pemetrexed or paclitaxel/albumin-bound paclitaxel was administered intravenously. On Day 2, carboplatin or cisplatin was administered intravenously. Patients without disease progression received ivonescimab maintenance therapy for up to 2 years or until discontinuation due to toxicity-related intolerance.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Objective response rate
Lasso di tempo: From the first dose to week 24 (±7 days)

Confirmed ORR assessed by investigators per RECIST 1.1, i.e., the proportion of subjects with CR+PR

From the first dose to week 24 (±7 days)
Median progression-free survival
Lasso di tempo: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months
From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 48 months

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Investigatore principale: Weiwei Ouyang, the affiliated cancer hospital of guizhou medical university

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)

30 ottobre 2026

Completamento primario (Stimato)

30 ottobre 2028

Completamento dello studio (Stimato)

30 ottobre 2029

Date di iscrizione allo studio

Primo inviato

26 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

10 novembre 2026

Primo Inserito (Effettivo)

13 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

13 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

10 novembre 2026

Ultimo verificato

1 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • SL-202608234

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

SÌ

Descrizione del piano IPD

We will share the de-identified IPD that underlie the results reported in the publication, including baseline variables, randomization assignment, primary and secondary outcomes, and adverse events, together with a data dictionary. Data not required to reproduce the published results, such as [imaging data/genomic data/free-text fields], will not be shared.

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA
  • RSI

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

prodotto fabbricato ed esportato dagli 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 .