Autologous Unselected Hematopoietic Stem Cell Transplantation for Refractory Crohn's Disease (AutoChron)

This study evaluates the safety and clinical benefits of a therapeutic approach using the cyclophosphamide (Cy) + thymoglobulin® (ATG) + granulocyte colony-stimulating factor (G-CSF) conditioning regimen followed by autologous hematopoietic stem cell transplantation (HSCT) rescue in the treatment of refractory Crohn's disease. Adverse events, and clinical and endoscopic conditions will be assessed at different short and long-term time points.

Study Overview

• Status: Active, not recruiting
• Conditions: Gastroenteritis; Inflammatory Bowel Diseases; Crohn's Disease
• Intervention / Treatment: Procedure: Autologous Hematopoietic Stem Cell Transplantation

Detailed Description

Crohn's disease (CD) is a chronic, refractory inflammatory bowel disease that affects the entire digestive tract associated with intestinal and extra intestinal manifestations or other autoimmune diseases. Conventional therapy for Crohn's disease includes anti-inflammatory, immunosuppressant and/or biologic drugs/corticosteroids. This treatment benefits the majority of patients. However, a proportion of patients fail to achieve complete and long-term disease control and often require multiple intestinal surgeries with a risk of developing short bowel syndrome.

Hematopoietic stem cell transplantation (HSCT) has been proposed to cause lymphoablation and reset of the immune system as an alternative strategy to induce long-term disease control in this high-risk population.

This study enrolled Crohn's disease patients not responsive to conventional therapy.

Initially safety and the clinical outcome will be evaluated. The selected patients will be admitted to the bone marrow transplant (BMT) unit for the mobilization regimen using cyclophosphamide (Cy - 60 mg/kg) and G-CSF (10 mcg/kg/day) from the 5th day after Cy administration until harvesting progenitor cells from peripheral blood by leukapheresis.

After seven days of rest, the conditioning regimen consists of Cy (200 mg/kg total dose for four days), rabbit antithymocyte globulin (6.5 mg/kg total dose for four days) and methylprednisolone (500 mg/day).

The clinical course of patients with refractory Crohn´s disease will be evaluated to determine the efficacy of HSCT as a therapeutic tool including the adverse aspects of the procedure, clinical outcome and quality of life.

• Study Type: Interventional
• Enrollment (Anticipated): 50
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Brazil
  • SP
    • Sao Jose do Rio Preto, SP, Brazil, 15015-750
      • Beneficência Portuguesa

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 14 years to 70 years (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Age between 14 and 50 years (patients aged 50 - 70 can participate at the principal investigators discretion).

2. Confirmed diagnosis of active Crohn's disease:

   • Diagnosis of Crohn's disease based on typical radiological findingsand or typical histology at least 6 months prior to screening.

   • Active disease at the time of registration to the trial, defined as

     *Crohn's Disease Activity Index (CDAI) > 150, and ii) Two of the following:

   • Harvey Bradshaw Index > 4
   • Endoscopic evidence of active disease confirmed by histology
   • Clear evidence of active small bowel Crohn's disease on computed tomography (CT) or magnetic resonance (MR) enterography.
3. Unsatisfactory course despite immunosuppressive agents (usually azathioprine, methotrexate and two biologic agents (normally infliximab, adalimumab and/or certolizumab) in addition to corticosteroids. Patients should have relapsing and refractory disease despite thiopurines, methotrexate and/or infliximab/adalimumab/certolizumab maintenance therapy or clear demonstration of intolerance / toxicity to these drugs.
4. Current problems unsuitable for surgery or patient at risk for developing short bowel syndrome.

5. Informed consent:

   • Prepared to undergo additional study procedures as per trial schedule
   • Patient has undergone intensive counseling about risks

Exclusion Criteria:

1. Pregnancy or unwillingness to use adequate contraception during the study, in women of childbearing age. Unwillingness of using appropriate contraceptive measures in males.

2. Concomitant severe disease

   • renal: creatinine clearance < 30 mL/min (measured or estimated)
   • cardiac: clinical evidence of refractory congestive heart failure; left ventricular ejection fraction < 40% by multigated radionuclide angiography (MUGA) or cardiac echo; chronic atrial fibrillation necessitating oral anticoagulation; uncontrolled ventricular arrhythmia; pericardial effusion with hemodynamic consequences as evaluated by an experienced echo cardiographer.
   • pulmonary: diffusion capacity <40%
   • psychiatric disorders including active drug or alcohol abuse
   • concurrent or recent history of malignant disease (excluding non-melanoma skin cancer)
   • uncontrolled hypertension, defined as resting systolic blood pressure ≥ 140 and/or resting diastolic pressure ≥ 90 despite at least 2 anti-hypertensive agents.
   • uncontrolled acute or chronic infection with HIV, Human T-lymphotropic virus (HTLV-1 or 2), hepatitis viruses or any other infection the investigators consider a contraindication to participation.
   • other chronic disease causing significant organ failure.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Hematopoietic Stem Cell Transplantation; High doses immunosuppression Cyclophosphamide (200 mg/kg total dose for four days) and rabbit antithymocyte globulin (6.5 mg/kg total dose for four days) followed by unselected autologous hematopoietic stem cell transplantation rescue.	Procedure: Autologous Hematopoietic Stem Cell Transplantation; Hematopoietic stem cell transplantation Lymphoablation followed by hematopoietic stem cell transplantation to rescue the immune system.; Other Names: Bone Marrow Transplantation; Hematopoietic Stem Cell Transplatation

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Safety of unselected autologous HSCT in refractory Crohn´s disease patients	HHSCT safety will be analyzed by laboratory tests and treatment-related adverse events. Safety will be evaluated by treatment-related adverse events. All adverse events will be recorded in a standardized way and their relationship to the study protocol will be assessed at different short- and long-term time points.	12 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Crohn´s Disease Activity Index (CDAI)	Duration of disease remission, defined as a CDAI ≤ 150, will be assessed at 1, 3, 6, 12 and 24 months after transplant.	12 months
CRAIG Crohn´s Severity Score (CSS)	The CRAIG CSS will be assessed at 1, 3, 6, 12 and 24 months after transplant.	12 months
Inflammatory Bowel Disease Questionnaire (IBDQ)	The IBDQ will be administered at 1, 3, 6, 12 and 24 months after transplant.	24 months
Short Form-36 Health Survey (SF-36)	The SF-36 will be administered at 1, 3, 6, 12 and 24 months after transplant.	24 months
Simple Endoscopic Activity Score (SES)	The SES will be assessed at 6, 12 and 24 months after HSCT.	24 months
Crohn's Disease Endoscopic Index of Severity (CDEIS)	The CDEIS will be assessed at 6, 12 and 24 months after HSCT.	24 months
Rutgeerts endoscopic score	Rutgeerts endoscopic score will be assessed at 6, 12 and 24 months after HSCT.	24 months
Harvey & Bradshaw Index (HBI)	The HBI will be assessed at 1, 3, 6, 12 and 24 months after HSCT.	24 months

Collaborators and Investigators

• Sponsor: Beneficência Portuguesa de São Paulo
• Investigators: Principal Investigator: Milton A Ruiz, MD, PhD, Beneficência Portuguesa

Study record dates

Study Major Dates

• Study Start: October 1, 2013
• Primary Completion (Actual): December 1, 2017
• Study Completion (Anticipated): December 1, 2024

Study Registration Dates

• First Submitted: December 9, 2016
• First Submitted That Met QC Criteria: December 21, 2016
• First Posted (Estimate): December 22, 2016

Study Record Updates

• Last Update Posted (Actual): January 15, 2021
• Last Update Submitted That Met QC Criteria: January 13, 2021
• Last Verified: January 1, 2021

More Information

Terms related to this study

• Keywords: immune system; autologous; Bone marrow transplant; lymphoablation; hematopoetic stem cell transplant
• Additional Relevant MeSH Terms: Digestive System Diseases; Gastrointestinal Diseases; Intestinal Diseases; Inflammatory Bowel Diseases; Crohn Disease; Gastroenteritis
• Other Study ID Numbers: autocrohnproject1

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Yes
• IPD Plan Description: The main objective is to observe the safety and clinical benefit of autologous HSCT therapy in refractory patients with Crohn's disease. Evaluation during transplant period and 1, 3, 6, 12 and 24 months post-transplant. Safety be evaluated by the amount of treatment-related adverse events. Record adverse events in a standardized way. Secondary outcome measures will be disease remission: 1, 3, 6, 12 and 24 months post-transplant both clinical and endoscopic remission. The percentage of patients in sustained disease remission at 1, 3, 6, 12 and 24 months post HSCT will be determined. Sustained disease remission is defined as a CDAI < 150; HBI <4, CCSI< 16, without the use of corticosteroids, immunosuppressant or biologic agents. Mucosal healing will be assessed during ileocolonoscopy at 6, 12, and 24 months following HSCT using SES, CDEIS and Rutgeerts endoscopy index. Heath Quality life, Short Form 36 and IBDQ at 1 3 6 12 and 24 months post-Transplant.