Combination Chemotherapy in Treating Younger Patients With Hodgkin Lymphoma

Recruiting

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  • Source

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    Public Title Combination Chemotherapy in Treating Younger Patients With Hodgkin Lymphoma
    Acronym Sorry, not currently available
    Source of Record URL http://clinicaltrials.gov/show/NCT00666484
  • Trial

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    Health Condition(s) or Problem Lymphoma; Neurotoxicity
    Lay Summary RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. It is not yet known which regimen of combination chemotherapy is more effective for Hodgkin lymphoma. PURPOSE: This phase II trial is studying the side effects of three different regimens of combination chemotherapy and to see how well they work in treating younger patients with Hodgkin lymphoma. (from ClinicalTrials.gov)
    Who can enter the trial DISEASE CHARACTERISTICS: - Biopsy proven de-novo classical Hodgkin lymphoma - Any stage disease - No nodular lymphocyte-predominant Hodgkin lymphoma PATIENT CHARACTERISTICS: - No known or suspected HIV infection - No pre-existing neurological disorder - No serious comorbidity which may prevent administration of study treatment - No other previous malignancy - Not pregnant or nursing - Fertile patients must use effective contraception during and for up to 1 year after completion of study treatment - Creatinine = 1.5 times upper limit of normal (ULN) unless due to the lymphoma - ALT/AST = 1.5 times ULN unless due to the lymphoma - Bilirubin = 2 times ULN unless due to the lymphoma PRIOR CONCURRENT THERAPY: - No prior chemotherapy or radiotherapy - No prior organ transplant
    Who cannot enter the trial DISEASE CHARACTERISTICS: - Biopsy proven de-novo classical Hodgkin lymphoma - Any stage disease - No nodular lymphocyte-predominant Hodgkin lymphoma PATIENT CHARACTERISTICS: - No known or suspected HIV infection - No pre-existing neurological disorder - No serious comorbidity which may prevent administration of study treatment - No other previous malignancy - Not pregnant or nursing - Fertile patients must use effective contraception during and for up to 1 year after completion of study treatment - Creatinine = 1.5 times upper limit of normal (ULN) unless due to the lymphoma - ALT/AST = 1.5 times ULN unless due to the lymphoma - Bilirubin = 2 times ULN unless due to the lymphoma PRIOR CONCURRENT THERAPY: - No prior chemotherapy or radiotherapy - No prior organ transplant
    What will happen Drug; cyclophosphamide; Drug; doxorubicin hydrochloride; Drug; etoposide; Drug; prednisolone; Drug; procarbazine hydrochloride; Drug; vincristine sulfate; Radiation; radiation therapy
    Primary aim Neurotoxicity due to the intensive use of Vinca alkaloids
    Secondary Aim Response rate; No; Disease-free survival; No; Overall survival; No; Gonadal toxicity; Yes
    Participant Information Sheet Sorry, not currently available
    Website Sorry, not currently available
    Recruitment Status Recruiting
    Nation England
    Location Leeds, London, Newcastle upon Tyne, Northwood
  • Contact

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    Contact for Public Queries Kirit Ardeshna Principal Investigator University College London Hospitals
    Contact for Scientific Queries Sorry, not currently available
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