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NCT Number: NCT06390306

The Efficacy and Safety of Third-generation TKIs Combined With Azacitidine and Bcl-2 Inhibitor in Patients With CML-MBP

This is a prospective multi-center study to investigate efficacy and safety of the third generation tyrosine kinase inhibitors (TKIs) combined with azacitidine and B-cell lymphoma-2 (Bcl-2) inhibitor in patients with myeloid blast phase chronic myeloid leukemia (CML-MBP).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Peking university people's hospital, Beijing, Beijing Municipality, China

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About this study

CML-MBP has dismal outcome. Currently, there is no standardized induction treatment approach in CML-MBP. The European LeukemiaNet (ELN) recommendations and NCCN guideline recommended the combination of TKI and chemotherapy in CML-MBP. The previous study revealed that TKI combined with hypomethylating agents had promising efficacy. However, imatinib and second generation TKI are the most widely applied in combination treatment, there is limited data in third generation TKI.

Currently, venetoclax in combination with hypomethylating agents such as azacitidine is standard treatment for patients with AML unsuitable for intensive induction chemotherapy. Maiti et al. reported that TKI combined with venetoclax and detectable had promising efficacy in CML-MBP. Therefore, the investigator conducted a study to explore the efficacy and safety of a third generation TKI in combination with azacitidine and Bcl-2 inhibitor in CML-MBP and multi-omics exploratory analysis was performed to identify potential biomarkers correlated with the outcome.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age ≥ 18 years old;
  • philadelphia chromosome (Ph)-positive or BCR::ABL-positive;
  • serum creatinine ≤ 1.5 × upper limit of normal (ULN) or 24h creatinine clearance ≥ 50 mL/min when serum creatinine was > 1.5 × ULN;
  • serum total bilirubin ≤ 1.5 × ULN;
  • aspartate aminotransferase and alanine aminotransferase ≤ 2.5 × ULN;
  • amylase ≤ 1.5 × ULN; (7) lipase ≤ 1.5 × ULN;
  • ejection fraction > 50%; corrected QT interval on electrocardiographic evaluation was ≤ 450 ms in men or ≤ 470 ms in women.

Exclusion criteria

  • concurrent diseases requiring treatment(s) with potential to interact with 3G-TKI;
  • diagnosis of other primary malignancies;
  • history of allogeneic HSCT;
  • extramedullary disease only.

Treatment and study plan

Ponatinib

Drug

Ponatinib is recommended orally (PO) daily continuously on days 1-28 in 28-day cycle. Treatment repeats every 28 days in the absence of disease progression, unacceptable toxicity or HSCT.

Azacitidine

Drug

Azacitidine is recommended 75mg/m2 subcutaneously on days 1-7 in 28-day cycle. Treatment repeats every 28 days in the absence of disease progression, unacceptable toxicity or HSCT.

Venetoclax

Drug

Venetoclax is recommended orally (PO) daily on days 1-14 in 28-day cycle. Treatment repeats every 28 days in the absence of disease progression, unacceptable toxicity or HSCT.

Olverembatinib

Drug

Olverembatinib is recommended orally (PO) every other day on days 1-28 in 28-day cycle. Treatment repeats every 28 days in the absence of disease progression, unacceptable toxicity or HSCT.

Primary outcomes

  1. Major hematologic response (MaHR)

    Time frame: At the end of Cycle 2 (each cycle is 28 days)

    either a complete hematologic response (CHR) or no evidence of leukemia (NEL).

Secondary outcomes

  1. Return to chronic phase

    Time frame: At the end of Cycle 2 (each cycle is 28 days)

    < 10% blasts in blood and bone marrow with no extra-medullary leukemia and last for ≥ 4 weeks

  2. Major cytogenetic response (MCyR)

    Time frame: Up to 3 years

    Ph-positive cells ≤ 35%

  3. Complete cytogenetic response (CCyR)

    Time frame: Up to 3 years

    no Ph-positive cell

  4. Major molecular response (MMR)

    Time frame: Up to 3 years

    BCR::ABL1IS ≤ 0.1%

  5. Event-free survival (EFS)

    Time frame: Up to 3 years

    interval from therapy start to lacking RCP after 1 cycle, MaHR after 2 cycles, loss of hematologic response, progression to blast phase again, or death from any causes

  6. CML-related survival

    Time frame: Up to 3 years

    interval from therapy start to death from blast phase, or censored at the last follow-up

  7. Survival

    Time frame: Up to 3 years

    interval from therapy start to death from any cause or censored at the last follow-up

  8. Incidence of adverse events

    Time frame: Up to 3 years

    Adverse effects (AEs) were graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0. and assessed continuously.

Study contacts

Contact information is provided by the study sponsor or research team.

Qian Jiang, MD

CONTACT

[email protected]

+861088326006

Sponsors and collaborators

Lead sponsor

Peking University People's Hospital

Other

Collaborators

  • Beijing Chuiyangliu Hospital
  • Henan Cancer Hospital
  • Nanfang Hospital, Southern Medical University
  • Peking Union Medical College
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
  • Zhejiang University

Registry information

Official study title

The Efficacy and Safety of Third Generation Tyrosine Kinase Inhibitors Combined With Azacitidine and B-cell Lymphoma-2 Inhibitor in Patients With Myeloid Blast Phase Chronic Myeloid Leukemia

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Apr 30, 2024
Registry last updated
Jun 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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