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Completed

NCT Number: NCT00193973

Idarubicin Based Combined Modality Therapy in Primary CNS Lymphoma

Idarubicin combined with high dose methotrexate and moderate dose radiotherapy will achieve similar survival outcomes but with reduced neurotoxicity compared to regimens using methotrexate with high dose radiotherapy.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

The Canberra Hospital, Garran, Australian Capital Territory, Australia

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About this study

Combined modality therapy in PCNSL has improved survival outcomes but at the cost of unacceptable rates of neurotoxicity when high dose radiotherapy is used. Idarubicin has activity in systemic lymphomas and crosses the blood brain barrier and may add to the efficacy of methotrexate. By combining these 2 drugs with moderate dose radiotherapy survival outcomes should be optimal but with lower rates of neurotoxicity.

Comparison: TROG has previously performed a phase 2 study using methotrexate with high dose radiotherapy and this will allow comparison of survival and neurotoxicity rates.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically proven primary CNS lymphoma.
  • Absence of disease outside the CNS.
  • ECOG performance status 0-3
  • Negative HIV status.
  • Peripheral blood counts with granulocytes >1.5 x 109L and platelets > 100 x 109L. Serum creatinine <150mmol/L. Serum bilirubin <1.5 times and AST <2 times upper limit of normal.
  • Age >18 and <=70 years.
  • Patients must give written informed consent.
  • Corticosteroids prior to histological diagnosis are allowed.

Exclusion criteria

  • Previous history of malignancy (other than non-melanomatous skin carcinoma, or carcinoma in situ of cervix completely excised).
  • Patients who are pregnant or lactating.
  • NYHA (New York State Heart Association classification) cardiac failure grade 3
  • Macroscopic spinal thecal or spinal cord disease.

Treatment and study plan

Idarubicin, Methotrexate, Filgrastim, intrathecal Ara-C

Drug

Idarubicin 15mg/m2 days 1, 22. Filgrastim 5mcg/kg until neutrophil recovery days 2, 23. Methotrexate 1g/m2 days 15, 36 and 50.

radiation therapy

Radiation

Whole brain Irradiation, 30Gy in 20 fractions over 4 weeks

Other names: Radiation, Radiotherapy

Primary outcomes

  1. To estimate the median and 2 year overall survival.

    Time frame: Estimate of survival at 2 years and at 5 years.

Secondary outcomes

  1. Assess acute toxicity.

    Time frame: Interim actute toxicity analyses will be performed at accrual points: 5, 10, 15, 20 and 25 patients.

  2. Assess functional indices of living in patients with PCNSL.

    Time frame: Analysis will be at 5 years.

  3. To estimate the risk of late neurotoxicity relative to results achieved in TROG 92.01.

    Time frame: Analysis at 3 years.

Sponsors and collaborators

Lead sponsor

Trans Tasman Radiation Oncology Group

Other

Collaborators

  • Australasian Leukaemia and Lymphoma Group

Registry information

Official study title

A Phase 2 Study of Idarubicin Based Combined Modality Therapy in Primary Central Nervous System Lymphoma

Important dates

Study start
2001
Primary completion
2008
Study completion
2013
First posted
Sep 19, 2005
Registry last updated
Feb 17, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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