ASIA Down Syndrome Acute Lymphoblastic Leukemia 2016

Last updated: September 26, 2022
Sponsor: National Hospital Organization Nagoya Medical Center
Overall Status: Active - Recruiting

Phase

2

Condition

Cancer (Pediatric)

Retinoblastoma

Leukemia

Treatment

N/A

Clinical Study ID

NCT03286634
ASIA-DS-ALL-2016
  • Ages < 20
  • All Genders

Study Summary

To evaluate the outcome of a prednisolone and low dose methotrexate based protocol in Down syndrome children with ALL (DS-ALL) in an Asia-wide study. The treatment protocol was modified based upon backbone of Taiwan Pediatric Oncology Group (TPOG)-ALL protocol in which risk classification will be guided by level of flow minimal residual disease (MRD) instead.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Down syndrome diagnosed clinically or cytogenetically (including Mosaic Down)
  • Newly diagnosed ALL according to WHO 2016 classification.
  • Age < 21 years old at time of enrollment.
  • ECOG performance status (PS) score of 0-2.
  • Written informed consent obtained from legally acceptable representatives.

Exclusion

Exclusion Criteria:

  • Second malignancy.
  • Philadelphia positive ALL.
  • Mature B-ALL.
  • Mixed phenotype acute leukemia.
  • Any previous treatment with cytotoxic chemotherapy excluding treatment for TAM orradiation therapy. Patient pre-treated with short term steroid (< 7 days of durationwithin last 1 month prior to treatment start) can be enrolled into this study.
  • Renal dysfunction with creatinine >2x upper limit of normal (ULN). Patients whosecreatinine has improved to <2x ULN before treatment commencement can enrol subject todiscretion of site PI.
  • Liver dysfunction with direct bilirubin > 5x ULN.
  • Any serious uncontrolled medical condition or impending end organ dysfunction thatwould impair the ability of the subject to receive protocol therapy, including:
  1. History of coronary arterial disease, cardiomyopathy, heart failure, arrhythmia (other than sinus arrhythmia) or severe cardiac malformation which with residualabnormalities or requires further major corrective surgery within 2 years.
  2. Ongoing uncontrolled hypertension.
  3. Ongoing uncontrolled diabetes mellitus.
  4. Ongoing uncontrolled infection.
  5. History of congenital or acquired immunodeficiency including HIV infection.
  6. History of interstitial pneumonia, pulmonary fibrosis, bronchiectasis or severepulmonary emphysema.
  7. CNS hemorrhage.
  8. Psychiatric disorder.
  9. Other concurrent active neoplasms.
  • Pregnant or lactating women.
  • Doubtful compliance or ability to complete study therapy due to financial, social,familial or geographic reason, or in the judgement of site investigator.

Study Design

Total Participants: 60
Study Start date:
April 18, 2017
Estimated Completion Date:
March 31, 2033

Connect with a study center

  • Prince of Wales Hospital

    Shatin, New Territories
    Hong Kong

    Active - Recruiting

  • Prince of Wales Hospital

    Shatin, New Territories,
    Hong Kong

    Site Not Available

  • Kagoshima University Hospital

    Kagoshima, 890-8544
    Japan

    Active - Recruiting

  • University of Malaya Medical Centre

    Kuala Lumpur, 59100
    Malaysia

    Site Not Available

  • Subang Jaya Medical Centre

    Subang Jaya, 47500
    Malaysia

    Site Not Available

  • KK Women's and Children's Hospital

    Singapore, 229899
    Singapore

    Active - Recruiting

  • National University Hospital

    Singapore, 119074
    Singapore

    Active - Recruiting

  • Mackay Memorial Hospital

    Taipei, 10449
    Taiwan

    Active - Recruiting

  • National Taiwan University Children's Hospital

    Taipei, 100
    Taiwan

    Site Not Available

  • Chang Gung Memorial Hopsital, Linkou

    Taoyuan, 333
    Taiwan

    Site Not Available

  • Siriraj Hospital Mahidol University

    Bangkok, 10700
    Thailand

    Active - Recruiting

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