Journal of Clinical Oncology, Vol 14, 925-934, Copyright © 1996 by American Society of Clinical Oncology
Adults and children with small non-cleaved-cell lymphoma have a similar excellent outcome when treated with the same chemotherapy regimen
I Magrath, M Adde, A Shad, D Venzon, N Seibel, J Gootenberg, J Neely, C Arndt, M Nieder, E Jaffe, RA Wittes and ID Horak
Pediatric Branch, National Cancer Institute, Bethesda, MD, USA.
PURPOSE: We have used identical treatment protocols for adults and children
with small non-cleaved-cell lymphoma (SNCL) for many years and report here
the results of two successive treatment regimens in these age groups.
PATIENTS AND METHODS: Seventy-two patients (39 adults and 33 children) were
treated with protocol 77-04 between 1977 and 1985. All patients, except
those with resected abdominal disease, received 15 cycles of a combination
of cyclophosphamide (CTX), doxorubicin (ADR), prednisone (PRED),
vincristine (VCR), high-dose methotrexate (MTX), and intrathecal (IT)
therapy. Forty-one patients (20 adults and 21 children) were treated with
protocol 89-C-41, which has been used since 1989. High-risk patients
received four alternating cycles (with a total duration of 12 to 15 weeks)
of an intensified version of protocol 77-04 without PRED (CODOX-M), and a
new drug combination consisting of ifosfamide, etoposide, high-dose
cytarabine (ara-C), and IT MTX (IVAC). Low-risk patients received three
cycles of the CODOX-M regimen. High- risk patients were randomized to
either receive or not receive granulocyte-macrophage colony-stimulating
factor (GM-CSF). RESULTS: Event-free survival (EFS) in protocol 77-04 was
56% at 2 years and beyond. EFS in protocol 89-C-41 was 92% at 2 years and
beyond. GM-CSF was associated with increased thrombocytopenia. CONCLUSION:
Adults and children with SNCL have a similar prognosis when treated with
the same chemotherapy. EFS in high-risk patients has been markedly improved
by including IVAC in protocol 89-C-41, and excellent results can be
achieved with only four cycles of therapy. In protocol 89-C-41, GM-CSF was
not beneficial.

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