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Tocilizumab for Cytokine Release Syndrome Prophylaxis in Haploidentical Transplantation

Primary Purpose

Cytokine Release Syndrome, Stem Cell Transplant Complications

Status
Completed
Phase
Phase 1
Locations
Mexico
Study Type
Interventional
Intervention
Tocilizumab
Sponsored by
Hospital Universitario Dr. Jose E. Gonzalez
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cytokine Release Syndrome focused on measuring Tocilizumab, Haploidentical, Peripheral blood

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Haploidentical transplant recipients
  • Informed consent signature
  • Previous diagnosis of any neoplastic, metabolic or autoimmune disease

Exclusion Criteria:

  • History of immune deficiency virus infection
  • Hepatitis C or B virus infection
  • Documented bacterial of fungal infection prior to tocilizumab infusion
  • Previous use of tocilizumab

Sites / Locations

  • Hospital Universitario Dr. Jose E Gonzalez UANL

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Tocilizumab 4 mg/kg

Tocilizumab 8 mg/kg

Arm Description

Tocilizumab 4 mg/kg IV single dose day -1 prior to haploidentical transplantation

Tocilizumab 8 mg/kg IV single dose day -1 prior to haploidentical transplantation

Outcomes

Primary Outcome Measures

Cytokine release syndrome
Incidence of fever in the first seven days after haploidentical transplantation

Secondary Outcome Measures

Hospitalization rate
Incidence of hospitalization in the first seven days after haploidentical transplantation
Adverse effects
According to Common Terminology Criteria for Adverse Events v5.0
IL-6 concentration
Concentration of serum IL-6 prior and during the first week after transplantation|

Full Information

First Posted
May 10, 2018
Last Updated
March 5, 2021
Sponsor
Hospital Universitario Dr. Jose E. Gonzalez
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1. Study Identification

Unique Protocol Identification Number
NCT03533101
Brief Title
Tocilizumab for Cytokine Release Syndrome Prophylaxis in Haploidentical Transplantation
Official Title
Tocilizumab for Cytokine Release Syndrome Prophylaxis in Peripheral Blood Haploidentical Hematopoietic Stem Cell Transplantation With Post-transplant Cyclophosphamide
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
May 25, 2018 (Actual)
Primary Completion Date
May 15, 2019 (Actual)
Study Completion Date
June 15, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitario Dr. Jose E. Gonzalez

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Tocilizumab will be administered prior to transplantation in order to prevent the onset of cytokine release syndrome and its complications associated to peripheral blood haploidentical hematopoietic stem cell transplantation with post-transplant cyclophosphamide
Detailed Description
Cytokine release syndrome (CRS) is a common and potentially severe toxicity associated to haploidentical peripheral blood (PBSC) hematopoietic stem cell transplantation (Haplo-HSCT), which was described previously in the context of immunotherapies for acute lymphoblastic leukemia such as chimeric antigen receptor T-cells and blinatumomab. CRS is characterized by immune system activation with a high level of circulating inflammatory cytokines including IL-6. Haplo-HSCT recipients have a high incidence of post-transplant fever, with elevated IL-6 in absence of documented infection. CRS occurs more frequently when using PBSC, and severe cases have been associated to delayed engraftment, increased transplant-related mortality and lower survival. Tocilizumab an IL-6 receptor-targeted monoclonal antibody has been effectively used to treat CRS in several scenarios, including Haplo-HSCT. Therefore, there is considerable interest for the development of a successful strategy for CRS prevention with tocilizumab, potentially eliminating complications. However, it is currently unknown whether the use of this monoclonal antibody can adversely affect the outcome of Haplo-HSCT recipients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cytokine Release Syndrome, Stem Cell Transplant Complications
Keywords
Tocilizumab, Haploidentical, Peripheral blood

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Adaptive design using two different doses of tocilizumab prophylaxis
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tocilizumab 4 mg/kg
Arm Type
Experimental
Arm Description
Tocilizumab 4 mg/kg IV single dose day -1 prior to haploidentical transplantation
Arm Title
Tocilizumab 8 mg/kg
Arm Type
Active Comparator
Arm Description
Tocilizumab 8 mg/kg IV single dose day -1 prior to haploidentical transplantation
Intervention Type
Drug
Intervention Name(s)
Tocilizumab
Other Intervention Name(s)
Actemra, RoActemra
Intervention Description
IL-6 receptor antibody pre-transplant administration to avoid cytokine release syndrome
Primary Outcome Measure Information:
Title
Cytokine release syndrome
Description
Incidence of fever in the first seven days after haploidentical transplantation
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Hospitalization rate
Description
Incidence of hospitalization in the first seven days after haploidentical transplantation
Time Frame
1 week
Title
Adverse effects
Description
According to Common Terminology Criteria for Adverse Events v5.0
Time Frame
1 week
Title
IL-6 concentration
Description
Concentration of serum IL-6 prior and during the first week after transplantation|
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Haploidentical transplant recipients Informed consent signature Previous diagnosis of any neoplastic, metabolic or autoimmune disease Exclusion Criteria: History of immune deficiency virus infection Hepatitis C or B virus infection Documented bacterial of fungal infection prior to tocilizumab infusion Previous use of tocilizumab
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Gómez-Almaguer, MD
Organizational Affiliation
Hospital Universitario "Dr. José Eleuterio González"
Official's Role
Study Director
Facility Information:
Facility Name
Hospital Universitario Dr. Jose E Gonzalez UANL
City
Monterrey
State/Province
Nuevo Leon
ZIP/Postal Code
64460
Country
Mexico

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
27381687
Citation
Tanaka T, Narazaki M, Kishimoto T. Immunotherapeutic implications of IL-6 blockade for cytokine storm. Immunotherapy. 2016 Jul;8(8):959-70. doi: 10.2217/imt-2016-0020.
Results Reference
background
PubMed Identifier
27543158
Citation
Teachey DT, Grupp SA. Cytokine Release Syndrome after Haploidentical Stem Cell Transplantation. Biol Blood Marrow Transplant. 2016 Oct;22(10):1736-1737. doi: 10.1016/j.bbmt.2016.08.010. Epub 2016 Aug 16. No abstract available.
Results Reference
background
PubMed Identifier
29680516
Citation
Raj RV, Hamadani M, Szabo A, Pasquini MC, Shah NN, Drobyski WR, Shaw BE, Saber W, Rizzo JD, Jerkins J, Fenske TS, D'Souza A, Dhakal B, Zhang C, Konings S, Hari PN, Chhabra S. Peripheral Blood Grafts for T Cell-Replete Haploidentical Transplantation Increase the Incidence and Severity of Cytokine Release Syndrome. Biol Blood Marrow Transplant. 2018 Aug;24(8):1664-1670. doi: 10.1016/j.bbmt.2018.04.010. Epub 2018 Apr 19.
Results Reference
background
PubMed Identifier
27318038
Citation
Abboud R, Keller J, Slade M, DiPersio JF, Westervelt P, Rettig MP, Meier S, Fehniger TA, Abboud CN, Uy GL, Vij R, Trinkaus KM, Schroeder MA, Romee R. Severe Cytokine-Release Syndrome after T Cell-Replete Peripheral Blood Haploidentical Donor Transplantation Is Associated with Poor Survival and Anti-IL-6 Therapy Is Safe and Well Tolerated. Biol Blood Marrow Transplant. 2016 Oct;22(10):1851-1860. doi: 10.1016/j.bbmt.2016.06.010. Epub 2016 Jun 16.
Results Reference
result
PubMed Identifier
25456364
Citation
Kennedy GA, Varelias A, Vuckovic S, Le Texier L, Gartlan KH, Zhang P, Thomas G, Anderson L, Boyle G, Cloonan N, Leach J, Sturgeon E, Avery J, Olver SD, Lor M, Misra AK, Hutchins C, Morton AJ, Durrant ST, Subramoniapillai E, Butler JP, Curley CI, MacDonald KPA, Tey SK, Hill GR. Addition of interleukin-6 inhibition with tocilizumab to standard graft-versus-host disease prophylaxis after allogeneic stem-cell transplantation: a phase 1/2 trial. Lancet Oncol. 2014 Dec;15(13):1451-1459. doi: 10.1016/S1470-2045(14)71017-4. Epub 2014 Nov 14.
Results Reference
result
PubMed Identifier
29351985
Citation
Drobyski WR, Szabo A, Zhu F, Keever-Taylor C, Hebert KM, Dunn R, Yim S, Johnson B, D'Souza A, Eapen M, Fenske TS, Hari P, Hamadani M, Horowitz MM, Rizzo JD, Saber W, Shah N, Shaw B, Pasquini M. Tocilizumab, tacrolimus and methotrexate for the prevention of acute graft-versus-host disease: low incidence of lower gastrointestinal tract disease. Haematologica. 2018 Apr;103(4):717-727. doi: 10.3324/haematol.2017.183434. Epub 2018 Jan 19.
Results Reference
result

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Tocilizumab for Cytokine Release Syndrome Prophylaxis in Haploidentical Transplantation

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