Albumin-bound Paclitaxel (Ⅱ)-Combined Regimens for Pancreatic Cancer
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.
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 2
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Jihui Hao
- Telefonnummer: 022-2340123-3077
- E-mail: 18622221120@163.com
Studiesteder
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Tianjin, Kina
- Tianjin Medical University Cancer Institute & Hospital
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
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Eksperimentel: Chort 1
Cisplatin + Albumin-bound Paclitaxel (Ⅱ) + Capecitabine + Gemcitabine, q2w, Treatment will continue until disease progression or intolerable toxicity.
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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
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Eksperimentel: Chort 2
Cisplatin + Albumin-bound Paclitaxel (Ⅱ) + Capecitabine + Gemcitabine, q2w, with a maximum of 12 treatment cycles.
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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
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Eksperimentel: Chort 3
Albumin-bound Paclitaxel (Ⅱ) + Capecitabine + Gemcitabine, q3w, for a total treatment duration of up to 6 months.
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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
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Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tidsramme |
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Progression-Free Survival (PFS)
Tidsramme: 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.
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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.
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1-Year Event-Free Survival Rate (1y-EFS Rate)
Tidsramme: 12 months after signing informed consent, until first EFS event or loss to follow-up.
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12 months after signing informed consent, until first EFS event or loss to follow-up.
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Recommended Phase 2 Dose (RP2D)
Tidsramme: After all participants in each dose cohort complete the 21-day DLT observation period.
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After all participants in each dose cohort complete the 21-day DLT observation period.
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Disease-Free Survival (DFS)
Tidsramme: From informed consent signature to tumor recurrence or all-cause death (whichever occurs first), assessed up to 20 months.
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From informed consent signature to tumor recurrence or all-cause death (whichever occurs first), assessed up to 20 months.
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Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Objective Response Rate (ORR)
Tidsramme: 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.
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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.
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Maximum Tolerated Dose (MTD)
Tidsramme: After DLT observation completion and RP2D determination for all dose cohorts, assessed up to 1 months.
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After DLT observation completion and RP2D determination for all dose cohorts, assessed up to 1 months.
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R0 Resection Rate
Tidsramme: After neoadjuvant therapy completion, at pathological report of surgical specimen, assessed up to 7 months.
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After neoadjuvant therapy completion, at pathological report of surgical specimen, assessed up to 7 months.
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Incidence of Adverse Events
Tidsramme: From the time of informed consent signature through 30 days after last study drug administration.
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From the time of informed consent signature through 30 days after last study drug administration.
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Disease Control Rate (DCR)
Tidsramme: 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..
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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..
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Overall Survival (OS)
Tidsramme: Time from subject's first study drug administration to death from any cause, assessed up to 40 months.
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Time from subject's first study drug administration to death from any cause, assessed up to 40 months.
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Dose-Limiting Toxicity (DLT)
Tidsramme: After all participants in each dose cohort complete the 21-day DLT observation period.
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After all participants in each dose cohort complete the 21-day DLT observation period.
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Event-Free Survival (EFS)
Tidsramme: 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.
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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.
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Major Pathological Response (MPR) Rate
Tidsramme: Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
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Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
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Pathological Complete Response (pCR) Rate
Tidsramme: Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
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Upon completion of pathological diagnosis of resected surgical specimen, assessed up to 7 months.
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Duration of Response (DOR)
Tidsramme: 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.
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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.
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Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Sygdomme i det endokrine system
- Neoplasmer efter sted
- Neoplasmer
- Neoplasmer i fordøjelsessystemet
- Sygdomme i fordøjelsessystemet
- Neoplasmer i endokrine kirtler
- Pancreassygdomme
- Bugspytkirtel neoplasmer
- Aminosyrer, peptider og proteiner
- Proteiner
- Organiske kemikalier
- Heterocykliske forbindelser, 1-ring
- Heterocykliske forbindelser
- Nukleinsyrer, nukleotider og nukleosider
- Kulbrinter
- Cycloparaffiner
- Kulbrinter, alicyklisk
- Kulbrinter, cyklisk
- Terpenes
- Uorganiske kemikalier
- Klorforbindelser
- Nitrogenforbindelser
- Taxoider
- Cyclodecanes
- Diterpenes
- Deoxycytidin
- Cytidin
- Pyrimidin -nukleosider
- Pyrimidiner
- Nukleosider
- Uracil
- Pyrimidinoner
- Platinforbindelser
- Deoxyribonucleosider
- Fluorouracil
- Albuminer
- Paclitaxel
- Capecitabin
- Albumin-bundet Paclitaxel
- Gemcitabin
- Cisplatin
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- CSPC-XBZ-PC-K03
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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