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.
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
연구 유형
연구 유형
등록 (추정된)
등록
단계
단계
- 2 단계
연락처 및 위치
연구 연락처
연구 연락처
- 이름: Jihui Hao
- 전화번호: 022-2340123-3077
- 이메일: 18622221120@163.com
연구 장소
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Tianjin, 중국
- Tianjin Medical University Cancer Institute & Hospital
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참여기준
자격 기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
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.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위화되지 않음
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
팔의 수
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
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실험적: 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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실험적: 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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실험적: 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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연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
기간 |
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Progression-Free Survival (PFS)
기간: 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)
기간: 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)
기간: 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)
기간: 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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2차 결과 측정
2차 결과 측정
결과 측정 |
기간 |
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Objective Response Rate (ORR)
기간: 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)
기간: 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
기간: 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
기간: 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)
기간: 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)
기간: 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)
기간: 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)
기간: 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
기간: 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
기간: 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)
기간: 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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공동 작업자 및 조사자
스폰서
스폰서
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
연구 시작
기본 완료 (추정된)
기본 완료
연구 완료 (추정된)
연구 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
- 내분비계 질환
- 부위별 신생물
- 신생물
- 소화계 신생물
- 소화기계 질환
- 내분비샘 신생물
- 췌장 질환
- 췌장 신생물
- 아미노산, 펩티드 및 단백질
- 단백질
- 유기 화학 물질
- 이종 사이 클릭 화합물, 1- 링
- 이종 사이 클릭 화합물
- 핵산, 뉴클레오티드 및 뉴 클레오 시드
- 탄화수소
- 사이클로 파라핀
- 탄화수소, alicyclic
- 탄화수소, 순환
- 테르펜
- 무기 화학 물질
- 염소 화합물
- 질소 화합물
- 박습니다
- 사이클로 데카네
- Diterpenes
- 데 옥시 시티 딘
- 시티 딘
- 피리 미딘 뉴 클레오 시드
- 피리 미딘
- 뉴 클레오 시드
- 우라실
- 피리 미디 논
- 백금 화합물
- 데 옥시 리보 뉴 클레오 시드
- Fluorouracil
- 알부민
- 파클리탁셀
- 카페시타빈
- 알부민 결합 파클리탁셀
- 젬시타빈
- 시스플라틴
기타 연구 ID 번호
기타 연구 ID 번호
- CSPC-XBZ-PC-K03
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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