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관해 중인 AML 환자의 유지 요법으로서 AZA + 베네토클락스

2026년 10월 13일 업데이트: M.D. Anderson Cancer Center

관해 중인 AML 환자의 유지 요법으로서 5-아자시티딘(AZA) + 베네토클락스의 제2상 연구

This phase II trial studies how well azacitidine and venetoclax work in treating patients with acute myeloid leukemia that is in remission. Drugs used in chemotherapy, such as azacitidine and venetoclax, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading.

연구 개요

상세 설명

PRIMARY OBJECTIVES:

I. To assess relapse-free survival (RFS) of patients (pts) with acute myeloid leukemia (AML) treated with 5-azacytidine (azacitidine; AZA) combined with venetoclax (VEN) as maintenance therapy after achieving remission.

SECONDARY OBJECTIVES:

I. To assess modified RFS of pts with AML treated with 5-azacytidine combined with venetoclax as maintenance therapy.

II. To assess overall survival (OS) of pts with AML treated with 5-azacytidine combined with venetoclax as maintenance therapy.

III. To assess event-free survival (EFS) of pts with AML treated with 5-azacytidine combined with venetoclax as maintenance therapy.

IV. To assess the duration of remission (CRd) of pts with AML treated 5-azacytidine combined with venetoclax as maintenance therapy.

V. To assess toxicity and safety of 5-azacytidine combined with venetoclax as maintenance therapy in pts with AML.

VI. To assess the effects of 5-azacytidine combined with venetoclax on dynamics of minimal residual disease (MRD) and their relationship to outcomes.

OUTLINE:

Patients receive azacitidine subcutaneously (SC) or intravenously (IV) over 1 hour daily on days 1-5, and venetoclax orally (PO) daily on days 1-14. Treatment repeats every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up at 30 days and then every 6-12 months thereafter.

연구 유형

중재적

등록 (실제)

36

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Texas
      • Houston, Texas, 미국, 77030
        • M D Anderson Cancer Center

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  1. Patients aged >/= 18 years AML who have achieved their FIRST CR or CRi and are not immediately candidates for allogeneic stem cell transplant.

  2. Patients who have received intensive therapy (defined as receiving standard or higher dose cytarabine-based therapy) to achieve remission (CR/CRi) should have received remission induction therapy and at least 1 consolidation cycle. These patients are eligible as long as they are not greater than 2 months from their last consolidation therapy and will be enrolled in COHORT 1.

  3. Patients who have received lower intensity therapy (defined as receiving low-dose cytarabine (LDAC) or hypomethylating agent (HMA)-based therapy) to achieve remission should have received at least 2 cycles of lower intensity therapy between the time they have achieved CR/CRi and enrollment on this protocol. They will be treated on COHORT 2.

  4. For either subgroup (lower or higher intensity), patients who have measurable residual disease may be enrolled on their respective cohort at any time without maximum 'time from consolidation' requirement.

  5. ECOG performance status of < or = 3

  6. Adequate organ function as follows:

    1. Serum total bilirubin < or = to 1.5 X the Upper Limit of Normal (ULN)
    2. Serum creatinine < or = to 2.5 x ULN
  7. Adequate BM reserve:

    1. Absolute neutrophil count (ANC) > 0.5 x k/uL
    2. Platelet count > or = 30 x k/uL
  8. For females of childbearing age, they may participate if they:

    1. Have a negative serum or urine pregnancy test within 10 to 14 days of enrolling
    2. Agree to either abstinence or 2 effective contraceptive methods (such as barrier methods or hormonal contraception) throughout the treatment period and up to 30 days after discontinuing treatment.
  9. For male patients with a female partner of childbearing age, they may participate if they agree to either abstinence or 2 effective contraceptive methods throughout the treatment period and up to 30 days after discontinuing treatment.

  10. Ability to understand and sign informed consent.

Exclusion Criteria:

  1. Diagnosis of acute promyelocytic leukemia (APL), AML - M3 by FAB classification based on morphology, immunophenotype, molecular, or cytogenetic s studies.
  2. Diagnosis of AML associated t(15;17) or APL variant. Patients with t(9;22) are also ineligible unless they are unable or unwilling to receive therapy with a tyrosine kinase inhibitor.
  3. Uncontrolled intercurrent illness including, but not limited to active uncontrolled infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
  4. Patients with active CNS (central nervous system) disease.
  5. Patients with documented hypersensitivity to any components of the study program.
  6. Females who are pregnant or lactating or intending to become pregnant during the study.
  7. Patients with history of extramedullary AML, except for CNS involvement that is currently controlled, will not be eligible for enrollment.
  8. Patient should be removed from current trial if they wish to participate and get treatment on another trial.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

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
실험적: Treatment (azacytidine, venetoclax)

Patients receive azacitidine SC or IV over 1 hour daily on days 1-5, and venetoclax PO daily on days 1-14. Treatment repeats every 28 days for up to 24 cycles in the absence of disease progression or unacceptable toxicity.

Given PO

다른 이름들:
  • 벤클렉스타
  • ABT-0199
  • ABT-199
  • ABT199
  • GDC-0199
  • RG7601
  • 벤클릭스토

Given SC or IV

다른 이름들:
  • 5 AZC
  • 5-AC
  • 5-아자시티딘
  • 5-AZC
  • 아자시티딘
  • 아자시티딘, 5-
  • 라다카마이신
  • 마일로사르
  • U-18496
  • 비다자

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Relapse-free survival (RFS)
기간: From date of complete remission (CR) or complete remission with incomplete count recovery (CRi), assessed for up to 10 years

The study will be continuously monitored for the primary endpoint, RFS, using the method of Thall, Wooten, and Tannir (2005). Will also summarize the posterior distribution of lambda-E (i.e., median RFS) assuming posterior mean and 95% credible interval.

From date of complete remission (CR) or complete remission with incomplete count recovery (CRi), assessed for up to 10 years

2차 결과 측정

결과 측정
측정값 설명
기간
Incidence of toxicity
기간: Up to 10 years

Toxicities are defined as any treatment -related clinically significant grade 3 or 4 non-hematologic adverse events occurred during cycles 1-2 of the trial. Will continuously monitor treatment-related toxicities using the Bayesian approach of Thall, Simon, Estey (1995).

Up to 10 years
Modified RFS
기간: Time from enrollment on study until date of first objective documentation of relapse or death, assessed for up to 10 years

Distribution assessed using Kaplan-Meier method.

Time from enrollment on study until date of first objective documentation of relapse or death, assessed for up to 10 years
Overall survival (OS)
기간: From the start of study treatment until date of death due to any cause, assessed for up to 10 years

Distribution assessed using Kaplan-Meier method.

From the start of study treatment until date of death due to any cause, assessed for up to 10 years
Event free survival (EFS)
기간: From the start of study treatment until date of first confirmed relapse, withdrawal from study due to adverse event, or death due to any cause, assessed for up to 10 years

Distribution assessed using Kaplan-Meier method.

From the start of study treatment until date of first confirmed relapse, withdrawal from study due to adverse event, or death due to any cause, assessed for up to 10 years
Complete remission duration (CRd)
기간: Time from CR or CRi until date of first objective documentation of confirmed relapse, assessed for up to 10 years

Distribution assessed using Kaplan-Meier method.

Time from CR or CRi until date of first objective documentation of confirmed relapse, assessed for up to 10 years

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Tapan M Kadia, M.D. Anderson Cancer Center

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2019년 9월 13일

기본 완료 (실제)

2026년 10월 12일

연구 완료 (실제)

2026년 10월 12일

연구 등록 날짜

최초 제출

2019년 8월 16일

QC 기준을 충족하는 최초 제출

2019년 8월 16일

처음 게시됨 (실제)

2019년 8월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 10월 16일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 10월 13일

마지막으로 확인됨

2026년 10월 1일

추가 정보

이 연구와 관련된 용어

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

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. .

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