- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07680933
Orelabrutinib Combined With Standard Immunochemotherapy With or Without Autologous Hematopoietic Stem Cell Transplantation (Auto-HSCT) for Newly Diagnosed Diffuse Large B-cell Lymphoma (DLBCL)
A Prospective, Phase II Clinical Study Protocol of Orelabrutinib Combined With Standard Immunochemotherapy With or Without Autologous Hematopoietic Stem Cell Transplantation (Auto-HSCT) for Newly Diagnosed Diffuse Large B-cell Lymphoma (DLBCL)
연구 개요
상태
상세 설명
연구 유형
등록 (추정된)
단계
- 2 단계
연락처 및 위치
연구 연락처
- 이름: Feng Zhu
- 전화번호: 0516-85806985
- 이메일: frankfeng_2004@126.com
연구 장소
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Jiangsu
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Xuzhou, Jiangsu, 중국, 221000
- 모병
- The Affiliated Hospital of Xuzhou Medical University
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연락하다:
- Feng Zhu
- 전화번호: 0516-85806985
- 이메일: frankfeng_2004@126.com
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
Signed informed consent;
Age 18-80 years at the time of signing informed consent, and willingness to comply with the study protocol procedures;
Pathologically confirmed CD20-positive DLBCL;
④ IPI score of 2-5;
⑤ ECOG performance status of 0-2;
⑥ Life expectancy ≥12 months;
⑦ Left ventricular ejection fraction (LVEF) ≥50% as assessed by multigated acquisition (MUGA) scan or echocardiography (ECHO);
Adequate hematologic function (unless due to underlying disease, e.g., extensive bone marrow involvement, or hypersplenism secondary to splenic involvement attributed to DLBCL as determined by the investigator; transfusion of blood products is permitted), defined as follows:
- Hemoglobin ≥90 g/L within 7 days prior to enrollment without packed red blood cell transfusion;
- Absolute neutrophil count (ANC) ≥1.0 × 10⁹/L;
Platelet count ≥75 × 10⁹/L.
⑨ Adequate organ function.
Exclusion Criteria:
Presence of uncontrolled cardiovascular or cerebrovascular disease, coagulation disorders, autoimmune diseases, severe infectious diseases, etc.;
Abnormal laboratory values at screening (unless attributable to lymphoma):
- Coagulation function: INR > 1.5× the upper limit of normal (ULN); PT and APTT > 1.5× ULN;
- Liver function: ALT or AST > 2× ULN; ALP and bilirubin > 1.5× ULN;
Renal function: Creatinine > 1.5× ULN; creatinine clearance < 60 mL/min (estimated by the Cockcroft-Gault formula);
③ HIV-infected patients;
④ For HBsAg-positive patients, HBV DNA must be negative prior to enrollment. In addition, if a patient is HBsAg-negative but HBcAb-positive (regardless of HBsAb status), HBV DNA testing is still required. If the result is positive, antiviral therapy is needed, and HBV DNA must be negative prior to enrollment;
⑤ Requiring continuous treatment with strong or moderate CYP3A inhibitors or CYP3A inducers. Patients who have taken strong or moderate CYP3A inhibitors or CYP3A inducers within 7 days prior to the first dose of study drug (or have not completed at least 5 half-lives since the last dose) are not eligible for enrollment;
Inability to swallow capsules or presence of gastrointestinal conditions that significantly affect gastrointestinal function, such as malabsorption syndrome, gastric or small bowel resection, symptomatic inflammatory bowel disease, or partial or complete intestinal obstruction;
- Other concurrent and uncontrolled medical conditions that, in the investigator's opinion, may affect the patient's participation in the study, including patients with psychiatric disorders or other known or suspected inability to fully comply with the study protocol.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Orelabrutinib combined with standard immunochemotherapy with or without auto-HSCT
In the induction phase, patients receive 4 cycles of orelabrutinib combined with standard chemotherapy.
For transplant-eligible patients, based on response assessment after 4 cycles, those achieving PR or CR proceed to auto-HSCT, followed by either 6 cycles of orelabrutinib maintenance or no maintenance based on patient preference.
For transplant-ineligible patients, based on response assessment after 4 cycles, those achieving PR or CR receive an additional 2-4 cycles of orelabrutinib combination therapy.
Depending on the patient's performance status, each cycle lasts 21-28 days.
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1+2.1 or 2.2 ±3 1. Orelabrutinib: 150 mg once daily, orally, Days 1-28 2.1 Pola-R-CHP Regimen: Polatuzumab vedotin: 1.8 mg/kg, intravenous infusion, Day 1 Rituximab: 375 mg/m², intravenous infusion, Day 1 Cyclophosphamide: 750 mg/m², intravenous administration, Day 2 Doxorubicin: 50 mg/m², intravenous administration or per institutional guidelines, Day 2 Prednisone: 100 mg/day, orally, Days 2-6 2.2. R-CHOP Regimen: Rituximab: 375 mg/m², intravenous infusion, Day 0 Cyclophosphamide: 750 mg/m², intravenous administration, Day 1 Doxorubicin: 40-50 mg/m², intravenous administration or per institutional guidelines, Day 1 Vincristine: 1.4 mg/m², intravenous administration, Day 1 (maximum dose 2 mg) OR Vindesine: 4 mg, intravenous administration, Day 1 Prednisone: 100 mg/day, orally, Days 1-5 3. auto-HSCT |
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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1년 무진행 생존율(PFS)
기간: 정보제공동의서 서명일부터 최초로 문서화된 진행일 또는 어떠한 원인으로 인한 사망일 중 먼저 발생한 날짜까지, 최대 1년 동안 평가됨
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PFS는 연구자가 평가한 진행 또는 재발의 첫 발생 시점부터 등록 시점까지의 기간 또는 어떠한 원인으로 인한 사망으로 정의됩니다.
질병 진행, 재발 또는 사망이 없는 환자의 PFS는 마지막 종양 평가 시점에서 중도 절단됩니다.
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정보제공동의서 서명일부터 최초로 문서화된 진행일 또는 어떠한 원인으로 인한 사망일 중 먼저 발생한 날짜까지, 최대 1년 동안 평가됨
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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ORR (Objective Response Rate)
기간: At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days )
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ORR is defined as the proportion of patients with a response of CR or PR
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At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days )
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CRR (Complete Response Rate)
기간: At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days)
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CRR is defined as the proportion of patients with a best response of CR
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At the end of Consolidation therapy (up to 8 cycles, each cycle is 21-28 days)
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2-year Progression free survival (PFS)
기간: From date of signing the informed consent until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 years
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PFS is defined as the time from registration to the first occurrence of progression or relapse as assessed by the investigator, or death from any cause.
PFS for patients without disease progression, relapse, or death will be censored at the time of the last tumor assessment.
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From date of signing the informed consent until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 years
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2-year overall survival (OS)
기간: From date of signing the informed consent until the date of death from any cause, whichever came first, assessed up to 2 years
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Overall survival is defined as the period from the induction registration to death from any cause.
Patients who have not died until the time of the analysis will be censored at their last contact date.
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From date of signing the informed consent until the date of death from any cause, whichever came first, assessed up to 2 years
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The occurrence of adverse events and serious adverse events
기간: At the end of whole theray (through study completion, an average of 1 year)
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At the end of whole theray (through study completion, an average of 1 year)
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
추가 관련 MeSH 약관
기타 연구 ID 번호
- XYFY2026-001-01
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
DLBCL - 미만성 대형 B 세포 림프종에 대한 임상 시험
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Millennium Pharmaceuticals, Inc.완전한GCB(Non-Germinal B-cell-like) 미만성 거대 B-세포 림프종(DLBCL)미국
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SWOG Cancer Research NetworkNational Cancer Institute (NCI); Genentech, Inc.모병미만성 거대 B세포 림프종 | 재발성 미만성 대형 B세포 림프종 | 난치성 미만성 대형 B세포 림프종 | 원발성 종격동(흉선) 대형 B세포 림프종 | 등급 3b 여포성 림프종 | 변형된 여포 림프를 Diff 대형 B-세포 림프종으로 | 변형된 마그 존 림프를 Diff Large B-Cell Lymphoma로미국