Granulocyte-Macrophage Colony-Stimulating Factor (GM-CSF) as Adjunct Therapy in Relapsed Hodgkin Disease

  1. Subhash C. Gulati, MD, PhD; and
  2. Charles L. Bennett, MD, PhD

    Excerpt

    Objective: To determine the clinical and economic effects of granulocyte macrophage colony-stimulating factor (GM-CSF) as adjunct therapy in relapsed or refractory Hodgkin disease.

    Design: A randomized, double-blind, phase III clinical trial.

    Setting: A tertiary referral center.

    Patients: Twenty-four patients (twelve of whom were controls) treated with high-dose chemotherapy and autologous bone marrow transplantation.

    Main Results:The 12 patients treated with GM-CSF, when compared with placebo recipients, had shorter periods of neutropenia (median duration of an absolute neutrophil count of less than 1000 cells/mm3, 16 days compared with 27 days; P = 0.02), shorter periods of platelet-transfusion dependency (median duration, 13.5 days compared with 21 days; P = 0.03), and shorter hospitalizations (median hospital stay, 32 days compared with 40.5 days; P = 0.004). Other clinical outcomes, such as frequency and severity of toxicities, development of pneumonia or infection, in-hospital death, and response rate were similar in the two groups. Actuarial long-term disease-free survival was 64% for patients treated with GM-CSF and 58% for patients who received placebo after 32 months of follow-up (P = 0.15). The group treated with GM-CSF had lower total charges after infusion of autologous marrow than the placebo group (median in-hospital charges, $39 800 compared with $62 500; P = 0.005) because of lower post-infusion charges for room and board, antibiotic therapy, transfusions, laboratory tests, and physical therapy visits.

    Conclusions: Administration of GM-CSF was associated with acceleration of myeloid and platelet recovery and was cost effective in the treatment of patients with relapsed Hodgkin disease who received intensive chemotherapy.

    This 100-word excerpt has been provided in the absence of an abstract.

    Acknowledgments

    Acknowledgments: The authors thank He-Jing Wang and Robert Elash-off for statistical support, Nancy Elwood and Barbara Yarber for secretarial assistance, and Eric Bonnern for help with all phases of the study.

    Article and Author Information

    • From Memorial Sloan-Kettering Cancer Center, New York, New York; Duke University School of Medicine and Durham Veterans Affairs Hospital, Durham, North Carolina; and the RAND Corporation, Santa Monica, California. For current author addresses, see end of text.

    • Grant Support: In part by a grant from Schering-Plough and Sandoz Corporation. Dr. Bennett is supported by a Career Investigator Award from the Veterans Administration Health Services Research and Development.

    • Requests for Reprints: Charles L. Bennett, MD, PhD, Veterans Affairs Medical Center, Health Services Research and Development (152), 508 Fulton Street, Durham, NC 27705.

    • Current Author Addresses: Dr. Gulati: Division of Hematology-Oncology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021.

      Dr. Bennett: Veterans Affairs Medical Center, Health Services Research and Development (152), 508 Fulton Street, Durham, NC 27705.

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