Treatment outcome of mucosa-associated lymphoid tissue/marginal zone non-Hodgkin’s lymphoma

Purpose: To evaluate the treatment outcome in patients with mucosa-associated lymphoid tissue (MALT)/marginal zone (MZ) non-Hodgkin’s lymphoma (NHL). Methods and Materials: Between 1986 and 2000, 66 patients with clinical stage (CS) I–IV MALT/MZ NHL were treated; these comprise the study population....

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2002-03, Vol.52 (4), p.1058-1066
Hauptverfasser: Hitchcock, Stacie, Ng, Andrea K, Fisher, David C, Silver, Barbara, Bernardo, M.Patricia, Dorfman, David M, Mauch, Peter M
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Sprache:eng
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Zusammenfassung:Purpose: To evaluate the treatment outcome in patients with mucosa-associated lymphoid tissue (MALT)/marginal zone (MZ) non-Hodgkin’s lymphoma (NHL). Methods and Materials: Between 1986 and 2000, 66 patients with clinical stage (CS) I–IV MALT/MZ NHL were treated; these comprise the study population. The progression-free survival (PFS) and overall survival (OS) were calculated using the Kaplan-Meier technique. Forty-five patients (68%) had CS I–II and 21 (32%) had CS III–IV disease. Twenty-nine of the 45 CS I–II patients received radiation therapy (RT) alone, and 6 patients had surgery and RT. The median RT dose was 3350 cGy. Among the 21 CS III–IV patients, treatment included chemotherapy alone (15), chemotherapy + RT (3), surgery (1), surgery + chemotherapy (1), and RT alone (1). Median follow-up was 48 months. Results: All 35 early-stage and all 4 advanced-stage patients who received RT as part of initial treatment achieved local control. Among the 63 evaluable patients, the 5-year OS and PFS were 90 and 57%, respectively. The 5-year OS was 93% and PFS was 75% among CS I–II patients; the corresponding estimates in CS III–IV patients were 83% and 14%, respectively. Conclusions: Modest doses of RT provide excellent local control in patients with MALT/MZ NHL. The poor PFS in advanced-stage patients suggests the need to develop alternative systemic treatment strategies for this disease.
ISSN:0360-3016
1879-355X
DOI:10.1016/S0360-3016(01)02714-6