Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Tislelizumab Combined With Tofacitinib and Docetaxel for NSCLC After Failure of First-Line Immunotherapy

4. november 2026 opdateret af: Junqiang Zhang, Anhui Provincial Hospital

Tislelizumab Combined With Tofacitinib and Docetaxel for Locally Advanced or Metastatic NSCLC After Failure of First-Line Immunotherapy: A Prospective, Single-Arm, Multicenter Phase II Clinical Study

Tofacitinib is a pan-target JAK inhibitor that blocks the activation of immune cells by inhibiting the JAK1/2/3 signaling pathways. When used in combination with immune checkpoint inhibitors, it has the potential to enhance anti-tumor efficacy. This study aims to evaluate the efficacy and safety of Tislelizumab combined with Tofacitinib and Docetaxel in patients with locally advanced or metastatic NSCLC who have failed first-line immunotherapy. Additionally, the study seeks to explore potential genomic and immunological biomarkers of therapeutic response in the second-line treatment setting, providing a basis for subsequent research.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

39

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

    • Anhui
      • Hefei, Anhui, Kina
        • Rekruttering
        • Anhui Provincial Hospital
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 75 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Patients with non-small cell lung cancer (NSCLC) confirmed through pathological histological examination.
  • Adenocarcinoma patients must be verified to lack driver gene mutations such as EGFR, ALK, ROS1, etc.; squamous carcinoma patients are exempt from this requirement.
  • In accordance with the 8th edition of the TNM staging classification of lung cancer by the International Association for the Study of Lung Cancer and the American Joint Committee on Cancer Classification, patients with histologically or cytologically confirmed locally advanced (stage IIIB/C) or metastatic (stage IV) NSCLC who are ineligible for surgical intervention or radical concurrent chemoradiotherapy.
  • Subjects who have previously received one PD-1/L1 inhibitor ± one platinum-based double-drug chemotherapy (either combined or sequential, with the sequence being inconsequential) and have demonstrated clinical benefit (PFS ≥ 84 days) following PD-1/L1 inhibitor treatment (with or without chemotherapy) before experiencing disease progression.
  • According to RECIST1.1 criteria, subjects must possess at least one radiologically measurable lesion. Tumor baseline radiological assessment should be conducted within 28 days prior to the initiation of medication.
  • Age range: 18 to 75 years.
  • ECOG performance status score of 0-1.
  • Normal function of major organs.
  • Women of childbearing potential must employ appropriate contraceptive measures from screening until 3 months post-study treatment cessation and must refrain from breastfeeding.
  • Patients must voluntarily participate in the study, sign informed consent, and demonstrate good compliance.

Exclusion Criteria:

  • Patients with prior exposure to JAK inhibitors.
  • Patients with active interstitial lung disease.
  • Presence of other active malignant tumors requiring concurrent treatment. Previous use of anti-tumor traditional Chinese medicine.
  • Evidence of severe or uncontrolled systemic diseases.
  • Clinically significant active infection.
  • Resting ECG showing clinically significant major abnormalities in rhythm, conduction, or morphology.
  • Myocardial infarction, coronary artery/peripheral artery bypass, or cerebrovascular accident within the past 3 months.
  • Insufficient bone marrow reserve or organ function.
  • Pregnant, breastfeeding, or planning to become pregnant during the study period.
  • Previously or currently suffering from clinically active interstitial lung disease.
  • History of hypersensitivity to any active or inactive components of tislelizumab/tofacitinib or to drugs with similar chemical structure or same category as tislelizumab/tofacitinib.
  • Any severe or uncontrolled eye disease.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Treatment

Participants will receive tislelizumab combined with tofacitinib and docetaxel.

Tofacitinib citrate tablets will be given orally.

Tislelizumab will be administered as an IV infusion, 200mg, Q3W.

Docetaxel will be administered per local SOC.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Overall Response (ORR)
Tidsramme: Up to approximately 1 year
Up to approximately 1 year

Sekundære resultatmål

Resultatmål
Tidsramme
Progression Free Survival (PFS)
Tidsramme: Up to approximately 1 year
Up to approximately 1 year
Disease Control (DCR)
Tidsramme: Up to approximately 1 year
Up to approximately 1 year
Duration of Response (DoR)
Tidsramme: Up to approximately 1 year
Up to approximately 1 year
Overall Survival (OS)
Tidsramme: Up to 1 year
Up to 1 year
Incidence of Treatment-Emergent Adverse Events (TEAE)
Tidsramme: Up to approximately 1 year
Up to approximately 1 year

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

10. juli 2025

Primær færdiggørelse (Anslået)

30. august 2027

Studieafslutning (Anslået)

30. juni 2028

Datoer for studieregistrering

Først indsendt

4. november 2026

Først indsendt, der opfyldte QC-kriterier

4. november 2026

Først opslået (Faktiske)

9. november 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

9. november 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

4. november 2026

Sidst verificeret

1. november 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Abonner