search
Back to results

Applying Pediatric Regimens to Younger Adult Patients With Acute Lymphoblastic Leukemia (ALL)

Primary Purpose

Lymphoblastic Leukemia, Acute

Status
Unknown status
Phase
Phase 2
Locations
Japan
Study Type
Interventional
Intervention
Methotrexate
Prednisolone
Dexamethasone
Vincristine
Pirarubicin
Cyclophosphamide
L-asparaginase
Cytarabine
Hydrocortisone
Mercaptopurine
Sponsored by
Japan Adult Leukemia Study Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lymphoblastic Leukemia, Acute focused on measuring acute lymphoblastic leukemia, newly diagnosed, BCR-ABL-negative

Eligibility Criteria

15 Years - 24 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Previously untreated BCR-ABL-negative ALL Age between 15 and 24 years Performance status between 0 and 3 (ECOG criteria) Adequate functioning of the liver (serum bilirubin level < 2.0 mg/dL); kidneys (serum creatinine level < 2.0 mg/dL); and heart (left ventricular ejection fraction greater than 50% and no severe abnormalities detected on electrocardiograms and echocardiographs). Written informed consent to participate in the trial Exclusion Criteria: Uncontrolled active infection Another severe and/or life-threatening disease Positive for HIV antibody and/or hepatitis B surface (HBs) antigen tests Another primary malignancy which is clinically active and/or requires medical interventions Pregnant and/or lactating women Past history of renal failure

Sites / Locations

  • Department of Hematology, Nagoya University Graduate School of MedicineRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

A

Arm Description

Outcomes

Primary Outcome Measures

Disease-free survival

Secondary Outcome Measures

The rate of complete remission

Full Information

First Posted
August 15, 2005
Last Updated
November 13, 2008
Sponsor
Japan Adult Leukemia Study Group
search

1. Study Identification

Unique Protocol Identification Number
NCT00131053
Brief Title
Applying Pediatric Regimens to Younger Adult Patients With Acute Lymphoblastic Leukemia (ALL)
Official Title
Phase 2 Study of Applying Pediatric Regimens to Younger Adult Patients With BCR-ABL-Negative Acute Lymphoblastic Leukemia
Study Type
Interventional

2. Study Status

Record Verification Date
November 2008
Overall Recruitment Status
Unknown status
Study Start Date
September 2002 (undefined)
Primary Completion Date
May 2011 (Anticipated)
Study Completion Date
September 2011 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Japan Adult Leukemia Study Group

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to investigate the efficacy and safety for treating adult ALL patients with the pediatric protocol.
Detailed Description
The prognosis for adult acute lymphoblastic leukemia (ALL) remains poor, which contrasts with that for pediatric ALL. It is regarded that the prognostic diversity is attributable to several differences between adults and children with respect to biological characteristics of leukemic cells, tolerance to anticancer drugs, treatment itself, and so on. It has been reported that adolescent ALL patients who were treated according to the pediatric protocol had a significantly better survival than those who were treated according to the adult protocol, indicating that the difference of treatment may be of considerable importance. To test the hypothesis, the Japan Adult Leukemia Study Group (JALSG) has planned a phase 2 study to treat younger ALL patients who are negative for BCR-ABL with the pediatric regimen which was used by the Japan Association of Childhood Leukemia Study. Those who are positive for BCR-ABL can participate in a separate protocol. The regimen is especially characterized by dose-intensified L-asparaginase, high-dose methotrexate, and intensified maintenance therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphoblastic Leukemia, Acute
Keywords
acute lymphoblastic leukemia, newly diagnosed, BCR-ABL-negative

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Methotrexate
Intervention Type
Drug
Intervention Name(s)
Prednisolone
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Intervention Type
Drug
Intervention Name(s)
Vincristine
Intervention Type
Drug
Intervention Name(s)
Pirarubicin
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Intervention Type
Drug
Intervention Name(s)
L-asparaginase
Intervention Type
Drug
Intervention Name(s)
Cytarabine
Intervention Type
Drug
Intervention Name(s)
Hydrocortisone
Intervention Type
Drug
Intervention Name(s)
Mercaptopurine
Primary Outcome Measure Information:
Title
Disease-free survival
Time Frame
3 years
Secondary Outcome Measure Information:
Title
The rate of complete remission
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Previously untreated BCR-ABL-negative ALL Age between 15 and 24 years Performance status between 0 and 3 (ECOG criteria) Adequate functioning of the liver (serum bilirubin level < 2.0 mg/dL); kidneys (serum creatinine level < 2.0 mg/dL); and heart (left ventricular ejection fraction greater than 50% and no severe abnormalities detected on electrocardiograms and echocardiographs). Written informed consent to participate in the trial Exclusion Criteria: Uncontrolled active infection Another severe and/or life-threatening disease Positive for HIV antibody and/or hepatitis B surface (HBs) antigen tests Another primary malignancy which is clinically active and/or requires medical interventions Pregnant and/or lactating women Past history of renal failure
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fumihiko Hayakawa, MD
Email
bun-hy@med.nagoya-u.ac.jp
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fumihiko Hayakawa, MD
Organizational Affiliation
Nagoya University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Tomoki Naoe, MD
Organizational Affiliation
Nagoya University
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Hematology, Nagoya University Graduate School of Medicine
City
Nagoya
ZIP/Postal Code
466-8550
Country
Japan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fumihiko Hayakawa, MD
Email
bun-hy@med.nagoya-u.ac.jp
First Name & Middle Initial & Last Name & Degree
Fumihiko Hayakawa, MD

12. IPD Sharing Statement

Links:
URL
http://www.jalsg.jp/
Description
The JALSG homepage

Learn more about this trial

Applying Pediatric Regimens to Younger Adult Patients With Acute Lymphoblastic Leukemia (ALL)

We'll reach out to this number within 24 hrs