Efficiency Study of Low Dose of IL-2 to Prevent Relapse in Standard Risk Leukemia After Transplantation

NCT ID: NCT01517347

Last Updated: 2016-10-24

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 90 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-01-31
• Study Completion Date: 2015-08-31

Brief Summary

Hematopoietic stem cell transplantation (HSCT) is one of the best, and sometimes the only, option for the treatment of leukemia. However, relapse rate was still the key question to influence the overall survival after transplantation, even in standard risk leukemia.There were good evidences that natural killer cells and T regulatory cells, which were expanded and stimulated by the application of IL-2, could mediate protection against GvHD while maintaining graft anti-tumor activity as a positive side effect. Meanwhile, it was found in our previous pilot study that low-dose IL-2 subcutaneous administration from 100 days for a prolonged period could be a safe and effective strategy to prevent relapse in acute lymphoblastic malignancy patients with high risk of recurrence after unmanipulated allo-HSCT.

The study hypothesis:

Prevention of relapse using low dose IL-2 following hematopoietic stem cell transplantation in patients with standard risk acute leukemia can

• reduce relapse rate
• improve survival

Detailed Description

Standard risk patients over 15 years old(except Ph+ ALL, AML t(8;21) and T-ALL) undergone unmanipulated blood and marrow transplantation following day 60 post-transplantation were randomized into treated group (with low dose IL-2 treatment) or controlled group (without any intervention post-transplantation). The end points were safety and clinical and immunologic response.Following time is 24 months.

Primary Outcome Measures:

*To determine the feasibility and efficacy of administering an 6 course of subcutaneous IL-2 in this patient population. [ Time Frame: 2 years ]

Secondary Outcome Measures:

*To assess the immunologic impact of ultra-low dose subcutaneous IL-2 in patients after transplantation [ Time Frame: 2 years ] Estimated Enrollment:360 Study Start Date:Jan 2012 Estimated Study Completion Date:Jan 2016

Intervention Details Description:

*Drug: Interleukin-2 Dose will vary depending upon when participant enters the trial: Given as a daily injection under the skin for 8 weeks.

Detailed Description:

• Patients receive low dose interleukin-2(Daily 1×106 IU per square meter of body-surface area) on days 60 after unmanipulated blood and marrow transplantation. Interleukin-2 treatment repeats every 14 days for 6 courses in the absence of disease progression or unacceptable toxicity.
• Participants will be seen periodically while they are receiving IL-2. Physical exams and blood tests will be performed weekly for the first two weeks and then every other week until the completion of 6 course therapy.

Eligibility Ages Eligible for Study:15 Years and older Genders Eligible for Study:Both Accepts Healthy Volunteers:No Criteria

Inclusion Criteria:

• Standard risk of Recipients of allogeneic stem cell transplantation with myeloablative conditioning regimens
• Standard risk of Recipients: CR1 or CR 2 of AML/ALL before transplantation
• Ph+ ALL，AML with t(8;21) and T-ALL were excepted
• Patients were at least 60 days post-transplantation
• Bone marrow monitoring was still Complete Remission (CR) and minor residual disease (MRD) was negative
• 15 years of age or older
• No serious infection

Exclusion Criteria:

• Exposure to any other clinical trials prior to enrollment
• Active malignant disease relapse
• Active, uncontrolled infection
• Inability to comply with IL-2 treatment regimen

Conditions

Leukemia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Interleukin-2

Interleukin-2 post-transplantation to prevent relapse of standard risk leukemia

Group Type: EXPERIMENTAL

Interleukin-2

Intervention Type: DRUG

Patients receive low dose interleukin-2(Daily 1×106 IU per square meter of body-surface area) on days 60 after unmanipulated blood and marrow transplantation. Interleukin-2 treatment repeats every 14 days for 6 courses in the absence of disease progression or unacceptable toxicity.

controlled group

controlled standard risk leukemia received regular transplantation without IL-2 intervention

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Interleukin-2

Patients receive low dose interleukin-2(Daily 1×106 IU per square meter of body-surface area) on days 60 after unmanipulated blood and marrow transplantation. Interleukin-2 treatment repeats every 14 days for 6 courses in the absence of disease progression or unacceptable toxicity.

Intervention Type: DRUG

Other Intervention Names

IL-2

Eligibility Criteria

Inclusion Criteria

• Standard risk of Recipients (CR1 or CR 2 of AML/ALL before transplantation except Ph+ ALL and T-ALL) of allogeneic stem cell transplantation with myeloablative conditioning regimens
• Standard risk of Recipients: CR1 or CR 2 of AML/ALL before transplantation
• Ph+ ALL, AML with t(8;21) and T-ALL were excepted
• Patients were at least 60 days post-transplantation
• Bone marrow monitoring was still Complete Remission (CR) and minor residual disease (MRD) was negative
• 15 years of age or older
• No serious infection

Exclusion Criteria

• Exposure to any other clinical trials prior to enrollment
• Active malignant disease relapse
• Active, uncontrolled infection
• Inability to comply with IL-2 treatment regimen

• Minimum Eligible Age: 15 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Peking University People's Hospital

OTHER

Sponsor Role: lead

Responsible Party

Xiaojun Huang

Chief of Peking University Institute of Hematology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Xiaojun Huang, MD

Role: PRINCIPAL_INVESTIGATOR

Peking University Institute of Hematology

Locations

Xiaosu Zhao

Beijing, Beijing Municipality, China

Countries

China

Other Identifiers

PUPH IRB [2012] (09）

Identifier Type: -

Identifier Source: org_study_id