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Bevacizumab Plus Nab-paclitaxel and Tegafur Gimeracil Oteracil Potassium Capsule (S-1) as Second-line Treatment for Advanced Biliary Tract Cancer: a Phase Ⅱ Clinical Trial

Efficacy and Safety of Bevacizumab With Nab-paclitaxel and Tegafur Gimeracil Oteracil Potassium Capsule (S-1) in Advanced Biliary Tract Adenocarcinoma

This prospective, single-center, single-arm phase II clinical trial was designed to evaluate the efficacy and safety of bevacizumab plus nab-paclitaxel and S-1 as second-line treatment for patients with advanced biliary tract adenocarcinoma who experienced disease progression or intolerance after first-line systemic therapy. Participants received bevacizumab in combination with nab-paclitaxel and oral S-1 in 21-day treatment cycles until disease progression, unacceptable toxicity, death, withdrawal of consent, or other protocol-defined discontinuation criteria. The primary outcome was objective response rate assessed according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1). Secondary outcomes included progression-free survival, disease control rate, duration of response, overall survival, quality of life, and safety. Exploratory analyses were conducted to investigate potential predictive biomarkers of treatment efficacy.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

32

Fase

  • Fase 2

Kontakter og lokationer

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

Studiesteder

      • Beijing, Kina, 100021
        • National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital

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

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Aged ≥18 years at the time of signing the informed consent form (ICF).
  • Histologically confirmed or clinically diagnosed biliary tract adenocarcinoma.
  • Unresectable disease and not suitable for locoregional therapy, or disease progression after locoregional therapy.
  • Child-Pugh class A or class B with a score of 7.
  • Eastern Cooperative Oncology Group performance status (ECOG PS) ≤1.
  • Radiographic disease progression or intolerance after first-line treatment.
  • Adequate bone marrow, hepatic, and renal function, as defined by:

    1. Absolute neutrophil count (ANC) ≥1.5 × 10^9/L, platelet count ≥75 × 10^9/L, and hemoglobin ≥85 g/L;
    2. Serum total bilirubin ≤1.5 × the upper limit of normal (ULN);
    3. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤3 × ULN;
    4. Estimated glomerular filtration rate (eGFR) >30 mL/min/1.73 m²;
    5. International normalized ratio (INR) ≤1.5 or prothrombin time (PT) ≤1.5 × ULN;
    6. Activated partial thromboplastin time (aPTT) ≤1.5 × ULN.
  • For patients with hepatitis B virus (HBV) infection, HBV deoxyribonucleic acid (DNA) <500 IU/mL (or <2,500 copies/mL).
  • At least one measurable lesion according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1).
  • Women of childbearing potential must use highly effective contraception during the study and for at least 120 days after the last dose of study treatment and must have a negative urine or serum pregnancy test within 7 days before the first dose of study treatment. Non-sterilized male participants must agree to use highly effective contraception during the study and for at least 120 days after the last dose of study treatment.

Exclusion Criteria:

  • Histologically or cytologically confirmed fibrolamellar, sarcomatoid, or mixed cholangiocarcinoma.
  • Active autoimmune disease or a history of autoimmune disease with the potential for recurrence.
  • Any condition requiring systemic treatment with corticosteroids at a dose of >10 mg/day of prednisone or equivalent, or other immunosuppressive agents, within 14 days before the first dose of study treatment.
  • Inadequately controlled hypertension despite medical therapy, defined as systolic blood pressure >140 mmHg or diastolic blood pressure >90 mmHg.
  • Active gastrointestinal disorders, including active gastric or duodenal ulcer or ulcerative colitis; active bleeding from an unresected tumor; or any other condition considered by the investigator to pose a risk of gastrointestinal bleeding or perforation. Patients with a history of gastrointestinal perforation or gastrointestinal fistula that had not healed after surgical treatment were also excluded.
  • A history of arterial thrombosis or deep vein thrombosis within 6 months before enrollment, or evidence or a history of bleeding tendency within 2 months before enrollment, regardless of severity.
  • Any clinical or laboratory abnormality or compliance issue that, in the investigator's judgment, made the participant unsuitable for participation in the study.

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: Bevacizumab plus nab-paclitaxel and tegafur gimeracil oteracil potassium capsule (S-1)
Patients received intravenous nab-paclitaxel at a dose of 125 mg/m2 on day 1 and 8, intravenous bevacizumab at a dose of 7.5 mg/kg on day 1, and oral S-1, 80 to 120 mg/day on days 1-14 of a 21-day cycle.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Objective Response Rate (ORR) according to RECIST Version 1.1
Tidsramme: Every 6 weeks until disease progression, up to 24 months
Percentage of participants achieving a confirmed complete response (CR) or partial response (PR) according to RECIST version 1.1.
Every 6 weeks until disease progression, up to 24 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Progression-Free Survival According to RECIST Version 1.1
Tidsramme: Up to 24 months
Time from first dose until disease progression according to RECIST version 1.1 or death.
Up to 24 months
Disease Control Rate (DCR)
Tidsramme: Every 6 weeks from first dose until disease progression, up to 24 months
Percentage of participants achieving CR, PR or stable disease according to RECIST version 1.1.
Every 6 weeks from first dose until disease progression, up to 24 months
Duration of Response (DoR)
Tidsramme: Up to 24 months
Time from first documented response until disease progression or death.
Up to 24 months
Overall Survival (OS)
Tidsramme: Up to 24 months
Time from enrollment to the patient's death for any cause
Up to 24 months
Incidence of Treatment-Emergent Adverse Events (TEAEs)
Tidsramme: From first dose through 90 days after last dose
Incidence and severity of treatment-emergent adverse events assessed according to CTCAE version 5.0.
From first dose through 90 days after last dose
Change From Baseline in EORTC QLQ-C30 Global Health Status Score
Tidsramme: Baseline through 24 months
Quality of life assessed using the EORTC QLQ-C30 questionnaire.
Baseline through 24 months

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Expression of predefined predictive biomarkers associated with treatment response
Tidsramme: Every 6 weeks until disease progression, up to 24 months
Assessment of predefined tumor and blood biomarkers associated with treatment response.
Every 6 weeks until disease progression, up to 24 months

Samarbejdspartnere og efterforskere

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

Sponsor

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)

23. februar 2026

Primær færdiggørelse (Faktiske)

23. februar 2026

Studieafslutning (Faktiske)

23. februar 2026

Datoer for studieregistrering

Først indsendt

13. juli 2026

Først indsendt, der opfyldte QC-kriterier

19. juli 2026

Først opslået (Faktiske)

22. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

22. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

19. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • SH-202521

Plan for individuelle deltagerdata (IPD)

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INGEN

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