Journal of Clinical Oncology, Vol 10, 390-397, Copyright © 1992 by American Society of Clinical Oncology
Effect of recombinant human granulocyte-macrophage colony-stimulating factor in patients with Hodgkin's disease: a phase I/II study
DJ Hovgaard and NI Nissen
Department of Hematology, University Hospital, Rigshospital, Copenhagen, Denmark.
PURPOSE: As bone marrow toxicity is the major limitation of the optimal
administration of chemotherapy, we investigated whether recombinant human
granulocyte-macrophage colony-stimulating factor (rhGM-CSF) could prevent
myelotoxicity or accelerate hematopoietic recovery after mechlorethamine,
vincristine, procarbazine, and prednisone (MOPP) chemotherapy. PATIENTS AND
METHODS: Twenty-four previously untreated patients with Hodgkin's disease
were included in a phase I/II study in which standard MOPP chemotherapy was
followed by 5 days of GM-CSF at every other cycle. Patients were entered
sequentially to receive one of four dosc levels (2, 4, 8, and 16
micrograms/kg of glycoprotein; 1.4, 2.8, 5.5, and 11.0 micrograms/kg of
protein) and were randomly allocated to either 24-hour continuous
intravenous (IV) infusion or twice daily subcutaneous (SC) injection of
rhGM-CSF. RESULTS: WBC counts (mainly neutrophils, eosinophils, and
monocytes) were significantly higher in cycles with rhGM-CSF than in cycles
with MOPP alone. The total number of days of leukopenia (WBC count less
than or equal to 2.0 x 10(9)/L) and neutropenia (absolute neutrophil count
[ANC] less than or equal to 1.0 x 10(9)/L) was reduced in cycles with
rhGM-CSF from 6.3 to 0.8 days and from 5.4 to 1.0 days, respectively. All
dose levels of rhGM-CSF were effective in increasing the ANC, but only at
the dose levels of 8 and 16 micrograms/kg did this significantly affect the
scheduling of chemotherapy. Mild and reversible adverse reactions included
low-grade fever, chest/bone pain, myalgias, erythemia, headache, fatigue,
and periorbital edema. CONCLUSIONS: rhGM-CSF can be administered safely to
patients with Hodgkin's disease and results in improved hematologic
recovery after MOPP. Full-dose chemotherapy can be administered on time,
resulting in an increase in the overall tolerated dose of myelosuppressive
drugs when compared with historical controls. SC administration proved to
be at least as effective as continuous IV infusion and should be preferred.