- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07719738
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
19. juli 2026 oppdatert av: YONGKUN SUN, Cancer Institute and Hospital, Chinese Academy of Medical Sciences
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.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
32
Fase
- Fase 2
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
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Beijing, Kina, 100021
- National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital
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-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
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:
- Absolute neutrophil count (ANC) ≥1.5 × 10^9/L, platelet count ≥75 × 10^9/L, and hemoglobin ≥85 g/L;
- Serum total bilirubin ≤1.5 × the upper limit of normal (ULN);
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤3 × ULN;
- Estimated glomerular filtration rate (eGFR) >30 mL/min/1.73 m²;
- International normalized ratio (INR) ≤1.5 or prothrombin time (PT) ≤1.5 × ULN;
- 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
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: N/A
- Intervensjonsmodell: Enkeltgruppeoppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: 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.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
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.
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Every 6 weeks until disease progression, up to 24 months
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Progression-Free Survival According to RECIST Version 1.1
Tidsramme: Up to 24 months
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Time from first dose until disease progression according to RECIST version 1.1 or death.
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Up to 24 months
|
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Disease Control Rate (DCR)
Tidsramme: Every 6 weeks from first dose until disease progression, up to 24 months
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Percentage of participants achieving CR, PR or stable disease according to RECIST version 1.1.
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Every 6 weeks from first dose until disease progression, up to 24 months
|
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Duration of Response (DoR)
Tidsramme: Up to 24 months
|
Time from first documented response until disease progression or death.
|
Up to 24 months
|
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Overall Survival (OS)
Tidsramme: Up to 24 months
|
Time from enrollment to the patient's death for any cause
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Up to 24 months
|
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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
|
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Change From Baseline in EORTC QLQ-C30 Global Health Status Score
Tidsramme: Baseline through 24 months
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Quality of life assessed using the EORTC QLQ-C30 questionnaire.
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Baseline through 24 months
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Andre resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Expression of predefined predictive biomarkers associated with treatment response
Tidsramme: Every 6 weeks until disease progression, up to 24 months
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Assessment of predefined tumor and blood biomarkers associated with treatment response.
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Every 6 weeks until disease progression, up to 24 months
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Studierekorddatoer
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Studer hoveddatoer
Studiestart (Faktiske)
23. februar 2026
Primær fullføring (Faktiske)
23. februar 2026
Studiet fullført (Faktiske)
23. februar 2026
Datoer for studieregistrering
Først innsendt
13. juli 2026
Først innsendt som oppfylte QC-kriteriene
19. juli 2026
Først lagt ut (Faktiske)
22. juli 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
22. juli 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
19. juli 2026
Sist bekreftet
1. juli 2026
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- SH-202521
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
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Nei
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Nei
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