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NCT Number: NCT05272293

Immunotherapy With ex Vivo Expanded Haploidentical Natural Killer Cells for Children/Young Adults With AML

The purpose of this study is to estimate the efficacy of immunotherapy with ex vivo expanded haploidentical NK cells for children/young adults with primary high risk or refractory AML and relapsed AML.

Recruiting

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Key information

Age range

6 month–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Belarussian Research Center for Pediatric Oncology, Hematology and Immunology

Minsk, Minsk Oblast, 223053, Belarus

Location status: Recruiting

Location contact

Mariya Naumovich

CONTACT

[email protected]

+375293563846

Olga Aleinikova, MD, Prof

PRINCIPAL_INVESTIGATOR

Tatsiana Shman

CONTACT

[email protected]

+37529 6341853

About this study

Immunotherapy with NK cells may improve the treatment results in AML. For better efficiency high cell doses or several infusions of NK cells are required. For this purpose, donor NK cells are expanded in the presence of feeder K562-mbIL21-41BBL cell line.

For patients with high-risk primary AML a cycle of immunotherapy includes chemotherapy (HD-ARA-C+IDA) followed by three doses of NK cells infusion.

For patients with refractory/relapsed AML a cycle of immunotherapy includes chemotherapy (FLAG - fludarabine, cytarabine, G-CSF) followed by three doses of NK cells infusion.

A 2nd cycle of therapy may be administered if a recipient continues to meet the eligibility criteria.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Patients:

  • primary high risk AML
  • primary refractory AML
  • relapsed AML
  • Karnofsky or Lansky performance scale greater or equal to 70
  • written informed consent

Donors:

  • haploidentical family donor
  • donor suitable for cell donation and apheresis according to standard criteria
  • written informed consent

Exclusion criteria

Patients:

  • uncontrolled infection
  • severe hepatic dysfunction: SGOT or SCPT >=5x upper limit of normal for age
  • positive serology for human immunodeficiency virus (HIV)

Donors:

  • pregnancy
  • positive serology for HIV, hepatitis B or C

Treatment and study plan

NK cell infusions

Biological

Three doses of expanded haploidentical NK cells (30-100 x 10^6 cells /kg).

Primary outcomes

  1. Objective Response Rate (ORR) (PR+ MLFS+CRi +CR)

    Time frame: 30 days after every a course of NK immunotherapy

    The proportion of patients with complete remission (CR), CR with incomplete hematologic recovery (CRi), morphologic leukemia-free state (MLFS), and partial remission (PR) as measured by response criteria definitions for acute myeloid leukemia.

  2. Leukemia-free survival (LFS)

    Time frame: 1 year

    Time from achievement of CR/CRi/MLFS to the time of relapse, death in remission, or last follow-up.

  3. Overall survival (OS)

    Time frame: 1 year

    The proportion of patients with overall survival

Secondary outcomes

  1. Duration of persistence of infused NK cells

    Time frame: 21 days after the first infusion

    Days of persistence of donor NK cells

  2. Number of T, B, NK, activated T and NK cells after immunotherapy

    Time frame: 30 days after the first infusion

    Analysis of T, B, NK, activated T and NK cells numbers (cells/microL) after NK infusions.

Study contacts

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

Mariya Naumovich, MD

CONTACT

[email protected]

+375293563846

Tatsiana Shman, PhD

CONTACT

[email protected]

+375296341853

Sponsors and collaborators

Lead sponsor

Belarusian Research Center for Pediatric Oncology, Hematology and Immunology

Other

Registry information

Official study title

Immunotherapy With ex Vivo Expanded Haploidentical Natural Killer Cells for Children/Young Adults With High-risk, Refractory or Relapsed AML

Important dates

Study start
2021
Primary completion
2025
Study completion
2026
First posted
Mar 9, 2022
Registry last updated
Aug 28, 2024

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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