PRIMARY MEDIASTINAL LARGE-CELL LYMPHOMA IS CHARACTERIZED BY AN INVERTED PATTERN OF LARGE TUMORAL MASS AND LOW BETA(2) MICROGLOBULIN LEVELS IN SERUM AND FREQUENTLY ELEVATED LEVELS OF SERUM LACTATE-DEHYDROGENASE
J. Rodriguez et al., PRIMARY MEDIASTINAL LARGE-CELL LYMPHOMA IS CHARACTERIZED BY AN INVERTED PATTERN OF LARGE TUMORAL MASS AND LOW BETA(2) MICROGLOBULIN LEVELS IN SERUM AND FREQUENTLY ELEVATED LEVELS OF SERUM LACTATE-DEHYDROGENASE, Annals of oncology, 5(9), 1994, pp. 847-849
Background: Primary mediastinal large cell lymphoma (PMLCL) is an emer
ging entity. New parameters can help define it. Materials and methods:
Retrospective analysis of medical records from 35 patients treated at
The University of Texas M.D. Anderson Cancer Center from 1985 to 1990
. Immunohistochemical evaluation of tissue specimens. Determination of
survival (S) and time to treatment failure (TTF). Results: The median
age was 34 years and 69% were females. Eighty-three percent presented
with symptoms of mediastinal involvement. While 100% of the patients
presented with bulky mediastinal disease and 72% had elevated pretreat
ment serum lactate dehydrogenase, only 6% presented with an elevated p
retreatment serum beta(2) microglobulin. The lymphoma cells lacked CD2
1 staining. For the 18 patients treated initially at M.D. Anderson Can
cer Center, S and TTF curves rates after doxorubicin-based regimens (p
lus radiotherapy in 14 cases) were 72% and 61%, respectively, at 5 yea
rs follow-up (median, 42 months). Four out of six patients who receive
d autologous bone marrow transplant as salvage therapy are currently a
live without disease at followup times of 21, 25, 32, and 54 months. C
onclusion: Primary mediastinal large cell lymphoma has characteristic
clinicopathological features to which another can be added, that of an
inverted pattern of bulky disease, high LDH and low beta(2)M in serum
. The response to therapy is comparable to that of intermediate-grade
lymphomas, although the numbers in the study are small. Our preliminar
y data suggest a possible role for autologous bone marrow transplantat
ion (ABMT) as salvage therapy.