Addition of Etanercept and Extracorporeal Photopheresis (ECP) to Standard Graft-Versus-Host Disease (GVHD) Prophylaxis in Stem Cell Transplant

NCT ID: NCT00639717

Last Updated: 2017-08-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-03-31
• Study Completion Date: 2016-04-30

Brief Summary

This research study investigates the benefits and possible risks of adding both etanercept (Enbrel) and ECP (extracorporeal photopheresis) to the conventional preventative (or prophylactic) treatments for graft-versus-host disease (GVHD). GVHD is a common, serious, and too often fatal, complication after matched unrelated donor stem cell transplantation, regardless of the pre-transplant conditioning regimen used (full or reduced intensity).

Reduced intensity transplants which employ lower doses of chemotherapy during the conditioning phase of the transplant, are less toxic than full intensity transplants. Reduced intensity transplants may extend the unrelated donor transplant option to older patients or to patients with existing medical conditions or illness, where a full intensity transplant is not possible. To be successful, reduced intensity transplants need to offset any lower effectiveness in killing cancer cells during the conditioning phase, with the establishment of a donor cell, graft-versus-leukemia effect (GVL). The GVL effect and GVHD are associated with each other and therefore, the goal of GVHD prophylaxis for this study is not so much to prevent all GVHD, but rather to prevent serious and fatal acute GVHD.

Most GVHD-related deaths are either the direct consequence of severe GVHD or from infections associated with intense immunosuppression, a consequence of the standard treatments for acute GVHD, which almost always include high-dose steroids. A more effective prophylaxis therapy that allows for the GVL effect to develop, while limiting the exposure to high-dose steroids may reduce transplant mortality and morbidity. We also will study how key chemical and cellular factors relate to clinical outcome.

Conditions

Graft Versus Host Disease

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Etanercept and ECP

Etanercept and ECP (Extracorporeal Photopheresis) in addition to standard GVHD prevention:

Etanercept will be given twice weekly by subcutaneous injection starting on the day of HSCT (Hematopoietic stem cell transplantation) conditioning until 8 weeks post transplant. ECP treatments will begin at once weekly starting at 4 weeks post transplant and continue at less frequent intervals until 6 months post transplant.

GVHD prophylaxis will consist of a standard two drug regimen: mycophenolate for 4 weeks and tacrolimus (titrated to a therapeutic level) for 8 weeks, then weaned over 4 months with discontinuation by 6 months post-transplant.

Group Type: EXPERIMENTAL

stem cell transplant

Intervention Type: PROCEDURE

reduced intensity, matched unrelated donor stem cell transplant

tacrolimus (standard GVHD prophylaxis)

Intervention Type: DRUG

Tacrolimus(or cyclosporine when necessary)

Tacrolimus will begin on day -3, IV or oral.

Target trough level for tacrolimus is 8-12 ng/ml.

In the absence of GVHD, tacrolimus tapering will begin on day +56 post transplant

mycophenolate (standard GVHD prophylaxis)

Intervention Type: DRUG

Mycophenolate will begin on day 0 at 10 mg/kg/dose (up to 1 gram per dose) every 8 hours orally or intravenously and will continue until day 28.

etanercept

Intervention Type: DRUG

Etanercept will be given at a dose 0.4 mg/kg (actual weight) up to a maximum dose of 25 mg, subcutaneously, twice weekly from day 0 to day 56 (16 doses)

methoxsalen

Intervention Type: DRUG

Methoxsalen (UVADEX) treatments by Extracorporeal photopheresis (ECP) will be started day +28 post transplant and given weekly.

On day +70 post transplant ECP frequency will be given every other week.

On day +100 post transplant ECP will be given monthly until day +180 and stopped.

Interventions

stem cell transplant

reduced intensity, matched unrelated donor stem cell transplant

Intervention Type: PROCEDURE

tacrolimus (standard GVHD prophylaxis)

Tacrolimus(or cyclosporine when necessary)

Tacrolimus will begin on day -3, IV or oral.

Target trough level for tacrolimus is 8-12 ng/ml.

In the absence of GVHD, tacrolimus tapering will begin on day +56 post transplant

Intervention Type: DRUG

mycophenolate (standard GVHD prophylaxis)

Mycophenolate will begin on day 0 at 10 mg/kg/dose (up to 1 gram per dose) every 8 hours orally or intravenously and will continue until day 28.

Intervention Type: DRUG

etanercept

Etanercept will be given at a dose 0.4 mg/kg (actual weight) up to a maximum dose of 25 mg, subcutaneously, twice weekly from day 0 to day 56 (16 doses)

Intervention Type: DRUG

methoxsalen

Methoxsalen (UVADEX) treatments by Extracorporeal photopheresis (ECP) will be started day +28 post transplant and given weekly.

On day +70 post transplant ECP frequency will be given every other week.

On day +100 post transplant ECP will be given monthly until day +180 and stopped.

Intervention Type: DRUG

Other Intervention Names

Enbrel; UVADEX

Eligibility Criteria

Inclusion Criteria

• Candidate for unrelated donor (allogeneic) HSCT for hematologic conditions, either malignant or non-malignant.
• Donor can be unrelated marrow, blood or cord blood.
• Any disease for which unrelated donor transplant is appropriate is eligible except:

• Progressive or poorly controlled malignancies for which the likelihood of durable disease control [i.e., patients expected to have at least 6 months PFS from date of transplant] is <25%.
• This determination of likelihood of durable disease control must take into account the patient's disease status and consideration of the agents and doses used in the reduced intensity conditioning regimen.
• The determination of adequate disease control will be certified by the PI or designee on the eligibility checklist.
• Patients may be consented to this trial based on disease control at the time of consent, but later removed from the trial prior to initiation of transplant conditioning regimen if disease status confirmation between consenting and transplant changes. In the event this occurs these patients will be replaced.
• Must be receiving a recognized reduced intensity transplant as determined by the University of Michigan Blood and Marrow Transplantation Program.
• Patients age 50 or older are eligible based on age.
• Patients may be <50 years old if they are eligible for a reduced intensity conditioning regimen based on disease type (eg, indolent lymphoma) or if comorbidities preclude a full-intensity transplant.
• Patients must have adequate venous access by either peripheral vein or central line so that ECP can be performed.
• Patients must be expected to tolerate the fluid shifts associated with ECP. The primary reason for expected intolerance of ECP is small size (ie, <30kg weight), but other factors may also be considered in this determination.

Exclusion Criteria

• Not a candidate for a reduced intensity transplant conditioning regimen (based on the current U-M BMT program clinical guidelines).
• Patient has a suitable related donor available for transplant.
• Karnofsky or Lansky performance status of < 50% at the time of admission for HSCT
• Patients with evidence of HIV infection or other opportunistic infection including but not limited to Tuberculosis and Histoplasmosis.
• Patients with active bacterial, fungal or viral infection not responding to treatment.
• Any medical or psychological conditions that would keep the patient from complying with the protocol and/or would markedly increase the morbidity and mortality from the procedure.
• Pregnancy.
• T-cell depleted allograft

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Mallinckrodt

INDUSTRY

Sponsor Role: collaborator

Amgen

INDUSTRY

Sponsor Role: collaborator

University of Michigan Rogel Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Gregory Yanik, MD

Role: PRINCIPAL_INVESTIGATOR

University of Michigan Rogel Cancer Center

Locations

University of Michigan Cancer Center

Ann Arbor, Michigan, United States

Countries

United States

Other Identifiers

umcc 2008.003

Identifier Type: -

Identifier Source: org_study_id