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Albumin-bound Paclitaxel (Ⅱ)-Combined Regimens for Pancreatic Cancer

15 września 2026 zaktualizowane przez: Tianjin Medical University Cancer Institute and Hospital

A Multi-cohort Exploratory Study to Evaluate the Efficacy and Safety of Albumin-bound Paclitaxel (Ⅱ)-Combined Regimens for Pancreatic Cancer

This is a prospective, multi-center, multi-cohort exploratory study. Cohort 1 enrolls 39 patients with unresectable locally advanced or metastatic pancreatic cancer, who will receive first-line treatment with cisplatin plus nab-paclitaxel (Ⅱ), capecitabine, and gemcitabine (PAXG).

Cohort 2 enrolls 27 patients with borderline-resectable or high-risk resectable pancreatic cancer, who will receive neoadjuvant therapy with the PAXG regimen.

Cohort 3 enrolls patients with pancreatic cancer who have undergone curative resection, who will receive adjuvant therapy with nab-paclitaxel (Ⅱ), capecitabine, and gemcitabine.

Objectives of Study: To evaluate the efficacy and safety of nab-paclitaxel (Ⅱ)-based regimes for pancreatic cancer.

Przegląd badań

Typ studiów

Interwencyjne

Zapisy (Szacowany)

147

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

      • Tianjin, Chiny
        • Tianjin Medical University Cancer Institute & Hospital

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  • Aged 18 to 75 years old.
  • Histopathologically confirmed pancreatic adenocarcinoma meeting any one of the following conditions: (1) Unresectable locally advanced or metastatic pancreatic cancer, with no prior systemic anti-tumor therapy for advanced disease. Prior neoadjuvant/adjuvant chemotherapy is permitted, provided the interval from completion of prior chemotherapy to study drug administration is more than 6 months. (2) High-risk resectable or borderline resectable pancreatic cancer assessed by a multidisciplinary team.(3) Curative resection (R0 or R1 resection) performed without prior neoadjuvant therapy, and adjuvant treatment can be initiated within 12 weeks postoperatively.
  • Presence of at least one measurable lesion per RECIST v1.1 (exclusive to participants in Cohort 3).
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1.
  • Estimated survival time ≥ 3 months.
  • Adequate bone marrow function: absolute neutrophil count (ANC) ≥ 1.5×10⁹/L, platelet count (PLT) ≥ 100×10⁹/L, hemoglobin (Hb) ≥ 90 g/L.
  • Adequate liver function: alanine transaminase (ALT) and aspartate transaminase (AST) ≤ 2.5×ULN (≤5×ULN allowed in patients with liver metastases); total bilirubin ≤ 1.5×ULN.
  • Adequate renal function: serum creatinine (Cr) ≤ 1.5×ULN, or creatinine clearance ≥ 60 mL/min (calculated by Cockroft-Gault formula).
  • Adequate coagulation function: prothrombin time (PT) and activated partial thromboplastin time (APTT) ≤ 1.5×ULN.
  • Women of childbearing potential must have a negative serum/urine pregnancy test within 14 days prior to enrollment, be non-lactating, and agree to use effective contraception throughout the study and for 6 months after the last study treatment. Male participants must agree to effective contraception during the study and for 6 months after study completion.
  • Able to understand the study information; participant or legal representative voluntarily provides written informed consent.

Exclusion Criteria:

  • History of other malignant tumors within the past 5 years
  • Known hypersensitivity or intolerance to any study drug or excipients.
  • Confirmed homozygous or compound heterozygous DPYD variants leading to complete dihydropyrimidine dehydrogenase (DPD) deficiency.
  • Presence of any of the following comorbidities: ① Severe or uncontrolled cardiovascular disease: New York Heart Association (NYHA) Class II or higher chronic heart failure, uncontrolled hypertension (systolic BP >150 mmHg and/or diastolic BP >90 mmHg despite stable medication), etc. ② Severe respiratory disorders: asthma requiring inhaled/systemic glucocorticoids, active chronic obstructive pulmonary disease, etc. ③ Confirmed neurological diseases (epilepsy, dementia, etc.) or Grade ≥2 peripheral sensory/motor neuropathy. ④ Uncontrolled diabetes mellitus (fasting blood glucose ≥10 mmol/L under stable treatment). ⑤ Severe chronic or active infections requiring ≥1 consecutive week of systemic antibacterial, antifungal or antiviral therapy (including tuberculosis). ⑥ Active HIV infection (HIV antibody positive); untreated active HBV (HBsAg/HBcAg positive with HBV-DNA above institutional upper limit of normal) or active HCV infection (HCV antibody positive with HCV-RNA above institutional upper limit of normal).
  • Untreated active brain metastases (including symptomatic brain or leptomeningeal metastases). Participants with brain metastases are eligible only if brain lesions are stable on imaging performed ≥4 weeks prior to first study dose, no new neurological symptoms or baseline symptom relapse, and no systemic steroid administration for ≥14 days before study treatment initiation, with no evidence of new or enlarged metastatic lesions.
  • Medical history as follows: ① Major abdominal/thoracic surgery within 28 days prior to first study dose, or planned major surgery during the study period (diagnostic puncture and infusion port implantation excluded). ② Severe cardiovascular/cerebrovascular events (myocardial infarction, unstable angina, cerebrovascular accident) within 6 months prior to enrollment; clinically silent lacunar infarcts are permitted.
  • History of deep vein thrombosis or pulmonary embolism within 3 months prior to enrollment.
  • Inability to swallow or untreated malabsorption syndrome.
  • Receipt of any investigational product within 1 month prior to enrollment.
  • Any other condition judged by the investigator to render the participant unsuitable for study participation.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nielosowe
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Chort 1
Cisplatin + Albumin-bound Paclitaxel (Ⅱ) + Capecitabine + Gemcitabine, q2w, Treatment will continue until disease progression or intolerable toxicity.
Cisplatin: 30 mg/m² , d1
Albumin-bound Paclitaxel (Ⅱ): 150 mg/m² , d1
Albumin-bound Paclitaxel (Ⅱ): 100/125 mg/m² , d1, d8
Capecitabine 625 mg/m²,po,bid, d1-14
Capecitabine 1660 mg/(m² • d), d1-14
Gemcitabine 800 mg/m², d1
Gemcitabine 1000 mg/m², d1, d8
Eksperymentalny: Chort 2
Cisplatin + Albumin-bound Paclitaxel (Ⅱ) + Capecitabine + Gemcitabine, q2w, with a maximum of 12 treatment cycles.
Cisplatin: 30 mg/m² , d1
Albumin-bound Paclitaxel (Ⅱ): 150 mg/m² , d1
Albumin-bound Paclitaxel (Ⅱ): 100/125 mg/m² , d1, d8
Capecitabine 625 mg/m²,po,bid, d1-14
Capecitabine 1660 mg/(m² • d), d1-14
Gemcitabine 800 mg/m², d1
Gemcitabine 1000 mg/m², d1, d8
Eksperymentalny: Chort 3
Albumin-bound Paclitaxel (Ⅱ) + Capecitabine + Gemcitabine, q3w, for a total treatment duration of up to 6 months.
Albumin-bound Paclitaxel (Ⅱ): 150 mg/m² , d1
Albumin-bound Paclitaxel (Ⅱ): 100/125 mg/m² , d1, d8
Capecitabine 625 mg/m²,po,bid, d1-14
Capecitabine 1660 mg/(m² • d), d1-14
Gemcitabine 800 mg/m², d1
Gemcitabine 1000 mg/m², d1, d8

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Ramy czasowe
Progression-Free Survival (PFS)
Ramy czasowe: Time from subject's first study drug administration to first documented disease progression (per RECIST v1.1) or death from any cause, whichever occurs first, assessed up to 5.5 months.
Time from subject's first study drug administration to first documented disease progression (per RECIST v1.1) or death from any cause, whichever occurs first, assessed up to 5.5 months.
1-Year Event-Free Survival Rate (1y-EFS Rate)
Ramy czasowe: 12 months after signing informed consent, until first EFS event or loss to follow-up.
12 months after signing informed consent, until first EFS event or loss to follow-up.
Recommended Phase 2 Dose (RP2D)
Ramy czasowe: After all participants in each dose cohort complete the 21-day DLT observation period.
After all participants in each dose cohort complete the 21-day DLT observation period.
Disease-Free Survival (DFS)
Ramy czasowe: From informed consent signature to tumor recurrence or all-cause death (whichever occurs first), assessed up to 20 months.
From informed consent signature to tumor recurrence or all-cause death (whichever occurs first), assessed up to 20 months.

Miary wyników drugorzędnych

Miara wyniku
Ramy czasowe
Objective Response Rate (ORR)
Ramy czasowe: Tumor response assessment every 8 weeks (±7 days) after first study drug administration until disease progression, death or end-of-follow-up, assessed up to 5.5 months.
Tumor response assessment every 8 weeks (±7 days) after first study drug administration until disease progression, death or end-of-follow-up, assessed up to 5.5 months.
Maximum Tolerated Dose (MTD)
Ramy czasowe: After DLT observation completion and RP2D determination for all dose cohorts, assessed up to 1 months.
After DLT observation completion and RP2D determination for all dose cohorts, assessed up to 1 months.
R0 Resection Rate
Ramy czasowe: After neoadjuvant therapy completion, at pathological report of surgical specimen, assessed up to 7 months.
After neoadjuvant therapy completion, at pathological report of surgical specimen, assessed up to 7 months.
Incidence of Adverse Events
Ramy czasowe: From the time of informed consent signature through 30 days after last study drug administration.
From the time of informed consent signature through 30 days after last study drug administration.
Disease Control Rate (DCR)
Ramy czasowe: Tumor response assessment every 8 weeks (±7 days) after first study drug administration until disease progression, death or end-of-follow-up, assessed up to 5.5 months..
Tumor response assessment every 8 weeks (±7 days) after first study drug administration until disease progression, death or end-of-follow-up, assessed up to 5.5 months..
Overall Survival (OS)
Ramy czasowe: Time from subject's first study drug administration to death from any cause, assessed up to 40 months.
Time from subject's first study drug administration to death from any cause, assessed up to 40 months.
Dose-Limiting Toxicity (DLT)
Ramy czasowe: After all participants in each dose cohort complete the 21-day DLT observation period.
After all participants in each dose cohort complete the 21-day DLT observation period.
Event-Free Survival (EFS)
Ramy czasowe: From informed consent signature to first local recurrence, distant metastasis, tumor progression, second malignancy or all-cause death (whichever occurs first), assessed up to 16 months.
From informed consent signature to first local recurrence, distant metastasis, tumor progression, second malignancy or all-cause death (whichever occurs first), assessed up to 16 months.
Major Pathological Response (MPR) Rate
Ramy czasowe: Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
Pathological Complete Response (pCR) Rate
Ramy czasowe: Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
Duration of Response (DOR)
Ramy czasowe: Time from first documented CR or PR to subsequent disease progression or death from any cause, whichever occurs first, until end-of-follow-up, assessed up to 6 months.
Time from first documented CR or PR to subsequent disease progression or death from any cause, whichever occurs first, until end-of-follow-up, assessed up to 6 months.

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

30 września 2026

Zakończenie podstawowe (Szacowany)

31 października 2027

Ukończenie studiów (Szacowany)

30 kwietnia 2030

Daty rejestracji na studia

Pierwszy przesłany

19 sierpnia 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

15 września 2026

Pierwszy wysłany (Rzeczywisty)

18 września 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

18 września 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

15 września 2026

Ostatnia weryfikacja

1 września 2026

Więcej informacji

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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