Journal of Clinical Oncology, Vol 15, 3060-3066, Copyright © 1997 by American Society of Clinical Oncology
Clinical presentation and outcome in lymphocyte-predominant Hodgkin's disease
S Bodis, MD Kraus, G Pinkus, B Silver, ME Kadin, GP Canellos, LN Shulman, NJ Tarbell and PM Mauch
Department of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
PURPOSE: The patterns of presentation, histologic pattern (nodular or
diffuse), treatment, and long-term outcome were studied in patients with
lymphocyte-predominant (LP) Hodgkin's disease (HD) to determine whether
these patients should be treated differently than patients with other
subtypes of HD. PATIENTS AND METHODS: Pathology was reviewed for 97
patients with an initial diagnosis of LPHD made between 1970 and 1993.
Seventy-five patients had LPHD on review: 55 had nodular LPHD, 14 had
diffuse LPHD, and six had LP histology without subclassification. There
were 60 males (80%) and 15 females (20%). Sixty-six patients (88%),
presented with clinical stage (CS) I or II disease. Seventy-one patients
were treated at the Joint Center for Radiation Therapy (JCRT) and were
considered for analysis of treatment outcome. Sixty-one of these 71 were
treated with radiation (RT) alone; 17 received mantle RT alone, 27 mantle
and paraaortic RT, and seven total-nodal irradiation (TNI). Ten patients
with subdiaphragmatic HD received pelvic and paraaortic RT. Of the 10
remaining patients, four were treated with RT and chemotherapy (CT) and six
were treated with CT alone. The median follow-up time was 10.8 years.
RESULTS: The 10-year actuarial freedom- from-first-relapse (FFR) and
10-year overall survival rates for the 71 patients with LPHD treated at the
JCRT were 80% and 93%, respectively. The 10-year actuarial FFR by nodular
(n = 51), diffuse (n = 14), and unspecified (n = 6) histologic pattern was
74%, 100%, and 60%, respectively. Overall, 14 of 71 patients have relapsed:
nine of 61 with stage IA, IB, or IIA disease and five of 10 with stage IIB
to IVB disease have relapsed. The median time to relapse was 53 months.
Nine of 71 patients have died. Only one death has been from HD: five
patients died of second cancers, two of cardiac disease, and one of
alcoholic liver cirrhosis. Of seven patients with second malignancies, five
died. None of the second malignancies were non-Hodgkin's lymphoma (NHL).
CONCLUSION: Patients with LPHD have different patterns of presentation, sex
and age distribution, and likelihood of occult abdominal disease than
patients with nodular-sclerosing (NS) or mixed- cellularity (MC) disease.
The median time to relapse for LP patients was later than reported for
other histologic subtypes; however, there was no pattern of continuous late
relapse. With pathologic staging and standard treatment, mortality from
LPHD is low; nearly all deaths have been cardiac- or second tumor-related.
This suggests that less aggressive treatment for LPHD might continue to
yield excellent results, while perhaps lowering the long-term risk of
complications.
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