- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07588698
Epcoritamab in Combination With R-CHOP for Patients With Aggressive Non-Hodgkin Lymphoma
Epcoritamab in Combination With R-CHOP Debulking in Newly Diagnosed Patients With Aggressive Non-Hodgkin Lymphoma
연구 개요
상태
상세 설명
PRIMARY OBJECTIVES:
I. To evaluate the incidence and severity of all grade CRS cytokine release syndrome (CRS) in arm A and arm B.
SECONDARY OBJECTIVES:
I. To determine the safety and tolerability of the combination of epcoritamab and rituximab, cyclophosphamide, hydroxydaunorubicin, oncovin, prednisolone (R-CHOP) in both arms and individually.
II. The anti-tumor activity of epcoritamab + R-CHOP. III. To evaluate duration of response (DOR), progression-free survival (PFS), and overall survival (OS).
EXPLORATORY OBJECTIVES:
I. To evaluate changes in serum cytokine levels with epcoritamab treatment and explore their association with the incidence and severity of CRS.
II. To characterize peripheral T-cell subsets and activation states and explore phenotypic profiles associated with CRS.
OUTLINE:
Participants will receive epcoritamab combined with R-CHOP chemotherapy and dexamethasone. The treatment will be delivered in up to 8 cycles in an outpatient setting. participants are followed at Week 8 and every 3 months for up to one year, or until improvement or stabilization, or until new therapy begins, whichever occurs first.
연구 유형
등록 (추정된)
단계
- 2 단계
연락처 및 위치
연구 연락처
- 이름: UCSF Hematopoietic Malignancies Clinical Trial Recruitment
- 전화번호: 877-827-3222
- 이메일: HDFCCC.Heme@ucsf.edu
연구 연락처 백업
- 이름: Clinical Trial Recruitment
- 이메일: cancertrials@ucsf.edu
연구 장소
-
-
California
-
San Francisco, California, 미국, 94143
- University of California, San Francisco
-
연락하다:
-
연락하다:
- UCSF Hematopoietic Malignancies Clinical Trial Recruitment
- 전화번호: 877-827-3222
- 이메일: HDFCCC.Heme@ucsf.edu
-
수석 연구원:
- Mwanasha Merrill, MD
-
San Francisco, California, 미국, 94110
- Zuckerberg San Francisco General
-
연락하다:
- UCSF Hematopoietic Malignancies Clinical Trial Recruitment
- 전화번호: 877-827-3222
- 이메일: HDFCCC.Heme@ucsf.edu
-
연락하다:
- Clinical Trial Recruitment
- 전화번호: cancertrials@ucsf.edu
-
수석 연구원:
- Mwanasha Merrill, MD
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Participants must have confirmed CD20-positive aggressive B-cell lymphoma, including de novo or transformed diffuse large B-cell lymphoma (DLBCL), not otherwise specified (NOS); high-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangement; primary mediastinal large B-cell lymphoma (PMBCL); T-cell/histiocyte-rich large B-cell lymphoma (THRLBCL); Epstein-Barr virus-positive DLBCL, NOS; or follicular lymphoma grade 3b.
- Measurable disease per Lugano 2014 criteria.
- No prior therapy for DLBCL or FL G3B other than corticosteroids or palliative radiotherapy. Of note, a cycle of anthracycline-containing regimen (given as standard of care prior to study enrollment) is allowed, provided that patients will receive a total of six cycles of chemotherapy as part of their treatment plan. Patients who received one cycle of an anthracycline-containing regimen prior to enrollment will proceed directly to Cycle 2 on study.
- Age ≥18 years
- Participants must have an International Prognostic Index (IPI) score of 2-5.
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 (Karnofsky ≥ 60%)
Demonstrates adequate organ function as defined below:
Adequate bone marrow function:
absolute neutrophil count platelets
- 1.0 × 10⁹/Litre (L) (with growth factor use allowed)
- 75 × 10⁹/L
Exceptions:
Patients may be enrolled despite not meeting the thresholds above if either of the following applies, provided the Absolute Neutrophil Count (ANC) is ≥0.75 × 10⁹/L:
- The patient has received one prior cycle of chemotherapy off study, and cytopenias at Cycle 2, Day 1 of protocol therapy are believed to be due to recent chemotherapy, provided there is evidence of marrow recovery and no other contraindications.
- The patient has documented bone marrow involvement by lymphoma, and cytopenias are believed to be disease-related rather than indicative of poor marrow reserve or unrelated pathology. In such cases, enrollment is permitted at the discretion of the investigator if the patient is otherwise eligible and deemed safe to proceed.
Adequate hepatic function:
Total bilirubin
≤2 × upper limit of normal (ULN) (unless due to Gilbert's)
Aspartate aminotransferase (AST) Serum glutamic-oxaloacetic transaminase (SGOT)
≤3 × institutional upper limit of normal
Alanine aminotransferase (ALT) Serum glutamic-pyruvic transaminase (SGPT)
≤3 × institutional upper limit of normal
Adequate renal function:
As assessed by estimated glomerular filtration rate (eGFR)
Coagulation:
Prothrombin time (PT) International Normalized Ratio (INR) and Activated partial thromboplastin time aPTT
≤1.5 × ULN, unless receiving anticoagulation therapy
- Left ventricular ejection fraction (LVEF) ≥50% by multigated acquisition (MUGA) or echocardiography at screening.
- Ability to understand and the willingness to sign a written informed consent document.
.Human immunodeficiency virus (HIV)-infected individuals are eligible if the following criteria are met:
- Serum HIV viral load is < lower limit of detection (LLD) and controlled with antiretroviral therapy for at least 1 year prior to enrollment, with confirmatory testing at screening;
- CD4 count ≥ 200 cells/microliter (μL) at screening;
- Subject is receiving antiretroviral regimens in accordance with current International Acquired Immunodeficiency Syndrome (AIDS) Society guidelines;
- No evidence of AIDS-defining illnesses (other than lymphoma diagnosis) or active opportunistic infections;
- Antiretroviral therapy does not interfere with study medications.
- For participants with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated.
- Individuals with a history of hepatitis C virus (HCV) infection must have been treated and cured. For individuals with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load.
- Individuals with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.
- The effects of epcoritamab on the developing human fetus are unknown. For this reason, and because bispecific antibodies may be teratogenic, women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control, or abstinence). Woman with reproductive potential must agree to use adequate contraception during the trial, and for 12 months after the last administration of epcoritamab or according to the local prescribing information of the standard of care (SOC) regimens, whichever is the longest. Adequate contraception is defined as highly effective methods of contraception. Also refer to the local prescribing information for information regarding contraceptive requirements for the SOC regimens.
- A woman of childbearing potential must have a negative serum (beta-hCG) pregnancy test at screening and a negative urine pregnancy test before treatment administration on Day 1 of every cycle.
- A woman must agree not to donate eggs (ova, oocytes) for the purposes of assisted reproduction during the trial and for 12 months after receiving the last dose of epcoritamab or according to the local prescribing information of the SOC regimens, whichever is the longest.
- A man who is sexually active with a woman of childbearing potential and has not had a vasectomy must agree to use a barrier method of birth control, eg, either condom with spermicidal foam/gel/film/cream/suppository or partner with occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository, and all men must also not donate sperm during the trial and for 12 months after receiving the last dose of epcoritamab or according to the local prescribing information of the SoC regimens, whichever is the longest.
- Participants must agree not to donate blood for 60 days after receiving the last dose of trial treatment.
- Participants must have a treating physician at University of California, San Francisco (UCSF) or Zuckerberg San Francisco General Hospital (ZSFGH), receive study treatment under the supervision of the study Principal Investigator or qualified study sub-investigators at the enrolling site, and be willing to comply with study procedures.
Exclusion Criteria:
- History of severe allergic or anaphylactic reactions to anti-CD20 mAb therapy or known allergy or intolerance to any component or excipient of epcoritamab.
- Any prior treatment with a bispecific antibody targeting CD3 and CD20.
- Treatment with an investigational drug within 4 weeks or 5 half-lives, whichever is longer, prior to the first dose of epcoritamab.
- Requiring immunosuppressive therapy for an ongoing baseline medical condition. For corticosteroids, prednisolone >10 mg daily (or equivalent) qualifies as immunosuppressive and thus be excluded for this use. Note: corticosteroids at any dose are permitted for control of lymphoma related symptoms, including during screening, and for any adverse events (AE) management during study.
- Vaccination with live vaccines within 28 days prior to the first dose of epcoritamab.
Clinically significant cardiovascular disease, including:
- Myocardial infarction within 6 months prior to the first dose of epcoritamab, or unstable or uncontrolled disease/condition related to or affecting cardiac function (eg, unstable angina, congestive heart failure New York Heart Association Class III-IV), cardiac arrhythmia (NCI Common Terminology Criteria for Adverse Events (CTCAE) Version 5 Grade 3 or higher), or clinically significant electrocardiogram (ECG) abnormalities
- Screening 12-lead ECG showing a baseline QT Corrected for Heart Rate using Fridericia's Formula (QTcF) >470 msec
- Stroke within 6 months prior to first epcoritamab dose
- Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds) at trial enrolment or significant infections within 2 weeks prior to the first dose of epcoritamab.
- Active hepatitis B Virus (HBV) (Deoxyribonucleic Acid Polymerase Chain Reaction (DNA PCR) -positive) or hepatitis C (Ribonucleic Acid Polymerase Chain Reaction (RNA PCR) -positive infection). Subjects with evidence of prior HBV but who are PCR-negative are permitted in the trial but should receive prophylactic antiviral therapy. Subjects who received treatment for Hepatitis C Virus (HCV) that was intended to eradicate the virus may participate if hepatitis C Ribonucleic acid (RNA) levels are undetectable.
Known past or current malignancy other than inclusion diagnosis, except for:
- Cervical carcinoma of Stage 1B or less
- Non-invasive basal cell or squamous cell skin carcinoma
- Non-invasive, superficial bladder cancer
- Prostate cancer with a current Prostate-Specific Antigen (PSA) level < 0.1 ng/milliliter (mL)
- Any curable cancer with a complete response (CR) of > 2 years duration.
- Neuropathy > grade 1 with the exception of neuropathy directly related to lymphoma (e.g., direct nerve compression from tumor).
- . Female who is pregnant, breast-feeding, or planning to become pregnant while enrolled in this trial or within 12 months after the last dose of epcoritamab; female subjects must also agree not to breastfeed during the entire trial and until 12 months after the last administration of study drug.
- Male who plans to father a child while enrolled in this trial or within 12 months after the last dose of epcoritamab.
- Contraindication to any of the individual drugs of the R-CHOP regimen.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위화되지 않음
- 중재 모델: 순차적 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Arm A: Treatment with Standard Dexamethasone (First 6 participants)
Participants will receive 8 cycles of rituximab, cyclophosphamide, hydroxydaunorubicin, oncovin, prednisolone (R-CHOP) chemotherapy combined with epcoritamab.
A standard dose of dexamethasone is given in Cycle 2. Treatment includes six 21-day cycles: Cycle 1 consists of R-CHOP alone; Cycles 2-5 include R-CHOP on Day 1 with epcoritamab on Days 1, 8, and 15.
In Cycle 2, dexamethasone is given on epcoritamab treatment days and for 3 subsequent days.
In Cycle 6, both R-CHOP and epcoritamab are given on Day 1 only.
This is followed by two 28-day consolidation cycles (Cycles 7-8) with epcoritamab on Day 1. Safety follow-up occurs at Week 8 and every 3 months for up to one year.
Participants who discontinue due to adverse events will be followed until improvement or stabilization, or until new therapy begins, whichever occurs first.
|
구두로 주어진
Given orally and intravenously (IV)
다른 이름들:
Given subcutaneously (SC)
다른 이름들:
Undergo imaging
Perform Blood work
Participants complete European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30)
Undergo Imaging
|
|
실험적: Arm B: Treatment with Modified Dexamethasone
Participants will receive 8 cycles of rituximab, cyclophosphamide, hydroxydaunorubicin, oncovin, prednisolone (R-CHOP) chemotherapy combined with epcoritamab.
A modified dose of dexamethasone will be given in Cycle 2. Treatment includes six 21-day cycles: Cycle 1 consists of R-CHOP alone; Cycles 2-5 include R-CHOP on Day 1 with epcoritamab on Days 1, 8, and 15.
In Cycle 2, dexamethasone is administered on epcoritamab treatment days and the following day.
In Cycle 6, both R-CHOP and epcoritamab are given on Day 1 only.
This is followed by two 28-day consolidation cycles (Cycles 7-8) with epcoritamab on Day 1. Safety follow-up occurs at Week 8 and every 3 months for up to one year.
Participants who discontinue due to adverse events will be followed until improvement or stabilization, or until new therapy begins, whichever occurs first.
|
구두로 주어진
Given orally and intravenously (IV)
다른 이름들:
Given subcutaneously (SC)
다른 이름들:
Undergo imaging
Perform Blood work
Participants complete European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30)
Undergo Imaging
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Cytokine Release Syndrome (CRS) Rate
기간: Up to day 42
|
The cytokine release syndrome (CRS) rate is defined as the incidence of CRS of any grade during Cycle 2, graded according to the American Society for Transplantation and Cellular Therapy (ASTCT) consensus criteria.
The proportion and corresponding 95% confidence interval will be reported.
|
Up to day 42
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Proportion of Participants with Treatment-emergent Adverse Events
기간: Up to 60 days after treatment
|
Proportion of participants with treatment-emergent adverse events, classified according to the NCI Common Terminology Criteria for Adverse Events (CTCAE) v5.0.
The proportion and 95% confidence interval will be reported.
|
Up to 60 days after treatment
|
|
Overall Response (OR)
기간: Up to 2 years
|
Overall response (OR) is defined as the proportion of treated participants who obtained an radiographic objective response confirmed complete response (CR) or confirmed partial response (PR) per Lugano Classification.
The proportion and 95% confidence interval will be reported.
|
Up to 2 years
|
|
Duration of Overall Response
기간: Up to 2 years
|
Duration of overall response is defined as the time from first documentation of complete response (CR) or partial response (PR) to the first occurrence of disease progression, recurrence, or death, whichever occurs first.
Patients without progression who are alive at the clinical cutoff will be censored at the date of their last disease assessment.
Median, estimates and 95% confidence interval will be reported using the Kaplan-Meier method and Brookmeyer and Crowley method.
|
Up to 2 years
|
|
Median Progression-Free Survival (PFS)
기간: Up to 2 years
|
Progression-free survival (PFS) is the time from the first dose of treatment until disease progression or death, whichever occurs first.
If neither event occurs, PFS is measured up to the last adequate disease assessment.
If a patient is alive but has no tumor assessments after starting treatment, PFS is measured up to the first dose date.
Median, estimates and 95% confidence interval will be reported using the Kaplan-Meier method and Brookmeyer and Crowley method.
|
Up to 2 years
|
|
Median Overall Survival (OS)
기간: Up to 2 years.
|
Overall survival (OS) is the time from the first dose of treatment until death from any cause.
Patients who are still alive will be followed up to their last known contact date.
Median, estimates and 95% confidence interval will be reported using the Kaplan-Meier method and Brookmeyer and Crowley method.
|
Up to 2 years.
|
공동 작업자 및 조사자
수사관
- 수석 연구원: Mwanasha Merrill, MD, University of California, San Francisco
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
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
- 신생물
- 면역계 질환
- 조직학적 유형에 따른 신생물
- 림프계 질환
- 림프 증식 장애
- 면역증식성 장애
- 림프종
- 헴 및 림프병
- 림프종, B세포
- 림프종, 대형 B세포, 미만성
- 림프종, 비호지킨
- 건강 관리 품질, 접근 및 평가
- 아미노산, 펩티드 및 단백질
- 단백질
- 유기 화학 물질
- 이종 사이 클릭 화합물
- 이종 사이 클릭 화합물, 2- 링
- 이종 사이 클릭 화합물, 융합 링
- 조사 기술
- 역학적 방법
- 시편 처리
- 임상 실험실 기술
- 진단 기술 및 절차
- 진단
- 구멍
- 수술 절차, 수술
- 탄화수소
- 탄화수소, 순환
- 데이터 수집
- 건강 관리 평가 메커니즘
- 건강 관리의 질
- 공중 위생
- 환경 및 공중 보건
- 탄수화물
- 알칼로이드
- 다 환식 방향족 탄화수소
- 탄화수소, 방향족
- 다 환식 화합물
- 글리코 사이드
- 인돌
- 항체, 모노클로 날
- 항체
- 면역 글로불린
- 면역 단백질
- 혈액 단백질
- 혈청 글로불린
- 글로불린
- Pretadienes
- 임신
- 스테로이드
- 융합 링 화합물
- 스테로이드, 불소
- 화학 기술, 분석
- 스펙트럼 분석
- 포스 포 아미드 머스타드
- 질소 머스타드 화합물
- 겨자 화합물
- 탄화수소, 할로겐화
- 포스 포 아미드
- 유기 인 화합물
- Pregnadienetriols
- Vinca 알칼로이드
- Secologanin Tryptamine 알칼로이드
- 인돌 알칼로이드
- 인돌리 지딘
- 인도인
- 안트라 사이클린
- 나프 타센
- 아미노 글리코 시드
- 항체, 모노클로 날, 뮤린 유래
- Daunorubicin
- 리툭시맙
- 덱사메타손
- 프레드니솔론
- 시클로포스파미드
- 독소루비신
- 빈크리스틴
- 설문 조사 및 설문지
- 자기 공명 분광법
- 혈액 표본 수집
기타 연구 ID 번호
- 252526
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
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. .
미만성 거대 B세포 림프종(DLBCL)에 대한 임상 시험
-
Millennium Pharmaceuticals, Inc.완전한GCB(Non-Germinal B-cell-like) 미만성 거대 B-세포 림프종(DLBCL)미국
-
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
덱사메타손에 대한 임상 시험
-
Ain Shams University완전한건설자 Spinae 평면 블록 | 수술 후 통증 | 고관절 전치환술(THA)이집트
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Johns Hopkins All Children's Hospital아직 모집하지 않음
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The Hospital for Sick ChildrenCanadian Institutes of Health Research (CIHR)아직 모집하지 않음
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Al Salam University모집하지 않고 적극적으로수술 후 통증 | 트리스무스 | 얼굴 붓기 | 하악 세 번째 어금니에 영향을 미쳤다이집트
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Vanderbilt University Medical Center종료됨
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Poznan University of Medical Sciences모병
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Eye & ENT Hospital of Fudan UniversityShanghai Zhongshan Hospital; Shanghai Jiao Tong University Affiliated Sixth People's Hospital아직 모집하지 않음