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DOI 10.1158/1078-0432.ccr-07-1720

Медицинская библиотека · Clinical cancer research : an official journal of the American Association for Cancer Research · 2008

Predicting outcome in follicular lymphoma by using interactive gene pairs.

LeBrun David, Baetz Tara, Foster Cheryl, Farmer Patricia, Sidhu Roger, Guo Hong, Harrison Karen, Somogyi Roland, Greller Larry D, Feilotter Harriet

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

PURPOSE: Follicular lymphoma is a common lymphoma of adults. Although its course is often indolent, a substantial proportion of patients have a poor prognosis, often due to rapid progression or transformation to a more aggressive lymphoma. Currently available clinical prognostic scores, such as the follicular lymphoma international prognostic index, are not able to optimally predict transformation or poor outcome.

EXPERIMENTAL

DESIGN

Gene expression profiling was done on primary lymphoma biopsy samples.

RESULTS

Using a statistically conservative approach, predictive interaction analysis, we have identified pairs of interacting genes that predict poor outcome, measured as death within 5 years of diagnosis. The best gene pair performs >1,000-fold better than any single gene or the follicular lymphoma international prognostic index in our data set. Many gene pairs achieve outcome prediction accuracies exceeding 85% in extensive cross-validation and noise sensitivity computational analyses. Many genes repeatedly appear in top-ranking pairs, suggesting that they reproducibly provide predictive capability.

CONCLUSIONS

The evidence reported here may provide the basis for an expression-based, multi-gene test for predicting poor follicular lymphoma outcomes.

Для цитирования: LeBrun David, Baetz Tara, Foster Cheryl, Farmer Patricia, Sidhu Roger, Guo Hong, Harrison Karen, Somogyi Roland, Greller Larry D, Feilotter Harriet. Predicting outcome in follicular lymphoma by using interactive gene pairs.. Clinical cancer research : an official journal of the American Association for Cancer Research. 2008. DOI: 10.1158/1078-0432.ccr-07-1720.

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