Journal of Clinical Oncology, Vol 1, 11-16, Copyright © 1983 by American Society of Clinical Oncology
Histologic conversion in the non-Hodgkin's lymphomas
B Acker, RT Hoppe, TV Colby, RS Cox, HS Kaplan and SA Rosenberg
Between July 1, 1971 and December 31, 1978, 150 patients with favorable
subtypes of non-Hodgkin's lymphoma [nodular poorly differentiated
lymphocytic (NLPD), nodular mixed, or diffuse well differentiated
lymphocytic] were entered into prospective randomized clinical trials at
Stanford University. Treatments included involved field, total lymphoid, or
whole body irradiation, single alkylating agent chemotherapy, combination
chemotherapy with cyclophosphamide, vincristine and prednisone (CVP) or
with cyclophosphamide, vincristine, procarbazine, and prednisone (C-MOPP),
or various combinations of chemotherapy and irradiation. The initial
complete response rate (CR) was 79%. Among patients who achieved a CR, 31%
later relapsed. There were 78 patients who either failed to achieve a CR or
achieved a CR and later relapsed. Histologic conversion (change from
initially favorable to an unfavorable subtype of non-Hodgkin's lymphoma)
was documented in 22/78 patients (28%). However, the actuarial risk for
conversion was actually much greater (60% at 8 yr). The median time to
documentation of conversion was 51 mo. The most common type of histologic
conversion was from NLPD to diffuse histiocytic lymphoma. Documented
histologic conversion was often associated with a more aggressive clinical
behavior of the lymphoma, and the median survival after conversion was less
than 1 yr. However, those patients who achieved a CR after conversion had a
more favorable outcome (actuarial survival 75% at 5 yr). No specific risk
factors predictive of histologic conversion could be identified.
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