Y. Yan et al., CLINICAL AND PROGNOSTIC-SIGNIFICANCE OF BONE-MARROW INVOLVEMENT IN PATIENTS WITH DIFFUSE AGGRESSIVE B-CELL LYMPHOMA, Journal of clinical oncology, 13(6), 1995, pp. 1336-1342
Purpose: We studied the effect of morphology and extent of bone marrow
(BM) infiltrate on the survival of patients with diffuse aggressive B
-cell non-Hodgkin's lymphoma (NHL), along with clinical features. Pati
ents and Methods: Sixty adult patients with diffuse aggressive B-cell
NHL and BM involvement at the time of presentation were studied. All p
atients were uniformly staged and treated with a curative high-dose ch
emotherapy regimen. BM involvement was assessed according to the cytol
ogy, pattern of infiltration, and extent of involvement, and was corre
lated with overall survival (OS) and failure-free survival (FFS). Resu
lts: Patients with BM involvement that consisted of greater than or eq
ual to 50% large cells or BM involvement of greater than or equal to 7
0% had a poorer OS (P=.065 and P=.055, respectively). Those who presen
ted with an infiltrate of less than 50% large cells and an internation
al prognostic index (IPI) of less than or equal to 3 had a significant
ly longer postrelapse survival time (P=.003). A diffuse or interstitia
l pattern of BM involvement was predictive of both poor OS and FFS (P=
.008 and .009, respectively). Multivariate analysis indicated that onl
y IPI (P=.0005) and pattern of BM infiltration (P=.009) were independe
nt predictors of OS, and only the former was predictive of FFS (P=.03)
. Conclusion: The IPI is predictive of OS and FFS, while BM involvemen
t with a diffuse or interstitial pattern is associated with significan
tly poorer OS. Patients with BM infiltration that involved greater tha
n or equal to 70% of the marrow or contained greater than or equal to
50% large cells had poor OS, but more patients need to be studied to d
etermine the significance. Two parameters, IPI less than or equal to 3
and BM large cells less than 50%, identify a group of patients with l
ong-term survival after relapse. (C) 1995 by American Society of Clini
cal Oncology.