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Completed

NCT Number: NCT02452099

Impact of DMSO Concentrations on Hematopoietic Recovery After Autologous HSC Transplantation.

The main aim of the study was to evaluate the clinical impact of different DMSO concentrations in cryopreservation mixture (5%, 7.5%, 10%) on reconstitution of hematopoiesis after autologous hematopoietic stem cell transplantation.

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Key information

About this study

The procedure of autologous hematopoietic stem cell (HSC) transplantation requires cryopreservation of HSCs. Addition of DMSO (dimethyl sulfoxide) is necessary to secure the viability of such cells, but this cryoprotectant is potentially toxic to stem cell recipient. The concentrations of DMSO in cryopreservation mixture vary strongly between protocols in different transplant centers. Usually, the HSCs are stored in mixtures containing 10% DMSO, but there is no sufficient evidence that this concentration of DMSO is indeed optimal.

The main aim of the study is to evaluate the clinical impact of reduction of DMSO concentration in cryopreservation mixture on engraftment after autologous hematopoietic stem cell transplantation. 150 consecutive patients will be randomly assigned to one of three study arms (50 patients each). HSCs obtained by leukapheresis will be cryopreserved in three concentrations of DMSO: 5%, 7.5%, 10%, respectively. Evaluation of the mixtures will be carried out by monitoring reconstitution of hematopoiesis and the frequency the side effects in patients. The most important aspect of our evaluation will be the speed of neutrophil recovery after transplantation (defined by the first day, when absolute neutrophil count in peripheral blood will be higher than 0.5 G/L). The investigators will also evaluate the toxicity of cell suspension by monitoring the frequency of infusion-related adverse events (like nausea or vomiting) during infusion and 24 hours after transplantation.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with hematological malignancies or solid tumors, refered for autologous HSC transplantation
  • Written informed consent

Treatment and study plan

Cryopreservation of HSCs using 5% DMSO concentration

Procedure

Cryopreservation of HSCs obtained by leukapheresis will be performed using 5% DMSO concentration.

Cryopreservation of HSCs using 7,5% DMSO concentration

Procedure

Cryopreservation of HSCs obtained by leukapheresis will be performed using 7,5% DMSO concentration.

Cryopreservation of HSCs using 10% DMSO concentration

Procedure

Cryopreservation of HSCs obtained by leukapheresis will be performed using 10% DMSO concentration.

Primary outcomes

  1. The median time to neutrophils recovery after autoHSC transplantation.

    Time frame: The first from 3 consecutive days, on which absolute neutrophil count in peripheral blood will be higher than 0.5 G/L

Secondary outcomes

  1. The median time to platelets recovery after autoHSC transplantation.

    Time frame: The first from 3 consecutive days, on which platelet count in peripheral blood will be higher than 20 G/L, without platelet transfusion 7 days prior.

  2. Adverse reactions related with transplantation procedure

    Time frame: 24 hours after transplantation

Sponsors and collaborators

Lead sponsor

Maria Sklodowska-Curie National Research Institute of Oncology

Other

Registry information

Official study title

Impact of Different DMSO Concentrations in Cryopreservation Mixture on Hematopoietic Recovery After Autologous Transplantation of Hematopoietic Stem Cells.

Acronym: DMSOconc3

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
May 22, 2015
Registry last updated
Jan 18, 2017

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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