- Blood. 2001 Aug
15;98(4):945-51.
Comment in:
- Blood. 2002 Apr 1;99(7):2624-5.
Expression of a single gene, BCL-6,
strongly predicts survival in patients with diffuse large
B-cell lymphoma.
Lossos IS, Jones CD, Warnke R, Natkunam Y, Kaizer H, Zehnder
JL, Tibshirani R, Levy R.
Department of Medicine, Division of Oncology, Stanford
University Medical Center, CA 94305-5151, USA.
Diffuse large B-cell lymphoma (DLBCL) is characterized by a
marked degree of morphologic and clinical heterogeneity.
Establishment of parameters that can predict outcome could
help to identify patients who may benefit from risk-adjusted
therapies. BCL-6 is a proto-oncogene commonly implicated in
DLBCL pathogenesis. A real-time reverse
transcription-polymerase chain reaction assay was
established for accurate and reproducible determination of
BCL-6 mRNA expression. The method was applied to evaluate
the prognostic significance of BCL-6 expression in DLBCL.
BCL-6 mRNA expression was assessed in tumor specimens
obtained at the time of diagnosis from 22 patients with
primary DLBCL. All patients were subsequently treated with
anthracycline-based chemotherapy regimens. These patients
could be divided into 2 DLBCL subgroups, one with high BCL-6
gene expression whose median overall survival (OS) time was
171 months and the other with low BCL-6 gene expression
whose median OS was 24 months (P =.007). BCL-6 gene
expression also predicted OS in an independent validation
set of 39 patients with primary DLBCL (P =.01). BCL-6
protein expression, assessed by immunohistochemistry, also
predicted longer OS in patients with DLBCL. BCL-6 gene
expression was an independent survival predicting factor in
multivariate analysis together with the elements of the
International Prognostic Index (IPI) (P =.038). By contrast,
the aggregate IPI score did not add further prognostic
information to the patients' stratification by BCL-6 gene
expression. High BCL-6 mRNA expression should be considered
a new favorable prognostic factor in DLBCL and should be
used in the stratification and the design of risk-adjusted
therapies for patients with DLBCL. (Blood. 2001;98:945-951)
PMID: 11493437 [PubMed - indexed for MEDLINE]
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