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Completed

NCT Number: NCT04327037

Safety of Expanded Haploidentical Natural Killer Cells for Leukemia

The purpose of this study is to estimate the safety of ex vivo expanded haploidentical natural killer (NK) cells for patients with leukemia.

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Key information

Age range

1 year–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Belarussian Research Center for Pediatric Oncology, Hematology and Immunology

Minsk, Minsk Oblast, 223053, Belarus

About this study

Immunotherapy with natural killer (NK) cells may improve the results of treatment for patients with cancer. However, for better efficiency high doses of NK cells are required. For this purpose, NK cells were expanded in the presence of feeder K562 cells gene-modified for expression 4-1BBL and membrane bound IL-21. In the result of expansion, large number of activated NK cells are obtained.

Protocol of immunotherapy includes conditioning (fludarabine + cyclophosphamide or any other protocol of chemotherapy) followed by expanded NK cells intravenous infusion. To sustain proliferation of donor NK cells in vivo patients receive 6 doses of Il-2 every second day. 10 patients will be enrolled in phase I to test different doses of NK cells: 20, 50, 70, 100 and >100 x 10^6/kg.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Patients:

  • Relapsed acute myeloid or lymphoblastic leukemia
  • Primary refractory myeloid or lymphoblastic leukemia
  • Karnofsky or Lansky performance scale greater or equal to 70
  • Written informed consent

Donor:

  • Haploidentical family donor
  • > 18 years old
  • 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 or breast feeding
  • Positive serology for HIV, hepatitis B or C.

Treatment and study plan

Expanded Haploidentical Natural Killer cells

Biological

One dose (from 20x to >100x 10^6 /kg) of expanded haploidentical NK cells

IL-2

Drug

6 doses of IL-2 (1 × 10^6 units/m2) from -1 day every other day.

Other names: Ronkoleukinum

Primary outcomes

  1. Incidence of Treatment-Emergent Adverse Events

    Time frame: 1 months

    Adverse events will be graded according to the CTCAE v4.0

Secondary outcomes

  1. Days of persistence of adoptively-transferred haploidentical NK cells

    Time frame: 1 months

    Analysis of donor chimerism at +2, 6, 10, 14, 21, 28 days after NK infusion.

  2. Occurrence of disease response

    Time frame: 1 months post infusion

    Analysis of blast cells content in bone marrow by cytomorphology or detection of MRD level by flow/PCR before and after immunotherapy.

  3. Median time to leukocytes and platelets recovery

    Time frame: 2 months post infusion

    Days of platelets (>50x10^9/L) and leukocytes (>1x10^9/L) recovery.

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

    Time frame: 1 months post infusion

    Analysis of T, B, NK, activated T and NK cells numbers (cells/microL) at +2, 6, 10, 14, 21, 28 days after NK infusion.

Sponsors and collaborators

Lead sponsor

Belarusian Research Center for Pediatric Oncology, Hematology and Immunology

Other

Registry information

Official study title

Pilot Study of Immunotherapy With ex Vivo Expanded Haploidentical Natural Killer Cells for Leukemia

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Mar 30, 2020
Registry last updated
Mar 2, 2022

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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