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
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Studientyp
Studientyp
Einschreibung (Tatsächlich)
Einschreibung
Phase
Phase
- Phase 2
Kontakte und Standorte
Studienorte
-
-
-
Beijing, China, 100021
- National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital
-
-
Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Beschreibung
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.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
|---|---|
|
Experimental: 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.
|
Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Objective Response Rate (ORR) according to RECIST Version 1.1
Zeitfenster: 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
|
Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Progression-Free Survival According to RECIST Version 1.1
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: Up to 24 months
|
Time from first documented response until disease progression or death.
|
Up to 24 months
|
|
Overall Survival (OS)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: Baseline through 24 months
|
Quality of life assessed using the EORTC QLQ-C30 questionnaire.
|
Baseline through 24 months
|
Andere Ergebnismessungen
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Expression of predefined predictive biomarkers associated with treatment response
Zeitfenster: 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
|
Mitarbeiter und Ermittler
Sponsor
Sponsor
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Studienbeginn
Primärer Abschluss (Tatsächlich)
Primärer Abschluss
Studienabschluss (Tatsächlich)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- SH-202521
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .