Journal of Clinical Oncology, Vol 16, 2070-2079, Copyright © 1998 by American Society of Clinical Oncology
Late effects in long-term survivors of high-grade non-Hodgkin's lymphomas
TB Haddy, MA Adde, J McCalla, MJ Domanski, M Datiles 3rd, SC Meehan, A Pikus, AT Shad, I Valdez, L Lopez Vivino and IT Magrath
Pediatric Oncology Branch, National Cancer Institute, Division of Epidemiology and Clinical Applications, National Institutes of Health, Bethesda, MD, USA.
PURPOSE: To evaluate long-term survivors of high-grade non-Hodgkin's
lymphomas (NHLs) for late effects and to attempt to assess the relative
contributions of the primary treatment modalities to these late effects.
PATIENTS AND METHODS: Of 103 young survivors followed up for 1 to 20 years,
74 patients were interviewed and underwent various investigations, and an
additional 12 patients were interviewed only. Of the 86 patients, 65 had
previously suffered from small non-cleaved-cell lymphoma, 16 from
lymphoblastic lymphoma, and five from large-cell lymphoma. RESULTS: Left
ventricular dysfunction was identified in eight of 57 (14.0%) patients who
had received doxorubicin (DOX) in doses greater than 200 mg/m2, of whom
four were symptomatic and four were asymptomatic. A ninth patient required
a pacemaker. Of the 86 patients, 23 (26.7%) reported pregnancies, 18 of
whom had 30 children. Two of the 86 (2.3%) patients developed second
cancers. Other major late effects included posttransfusion viral hepatitis,
eight patients; CNS toxicity, two patients; endocrine impairment, 14
patients; vitamin B12 deficiency, two patients; esophageal stricture, one
patient; urinary tract problems, two patients; and musculoskeletal defects,
three patients. Major late effects occurred in 11 of 21 (52.4%) patients
who had received radiation as well as chemotherapy, eight of 22 (36.4%)
patients who had surgical resections as well as chemotherapy, and 17 of 74
(23.0%) patients who had received chemotherapy alone. CONCLUSION: The
predominant major late effects observed were late cardiac toxicity related
to DOX therapy and hepatitis C virus infection that presumably resulted
from blood product transfusions administered before the introduction of
screening for the hepatitis C virus. Fertility was not greatly impaired,
and second malignancies were uncommon. No patient had clinically
significant impairment of growth. Radiation appeared to increase the
likelihood of late effects.

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