PURPOSE: Gleason score strongly predicts prostate cancer mortality; however, scoring varies among pathologists, and many men are diagnosed with intermediate-risk Gleason score 7. We previously developed a 157-gene signature for Gleason score using a limited gene panel. Using a new whole-transcriptome expression dataset, we verified the previous signature's performance and developed a new Gleason signature to improve lethal outcome prediction among men with Gleason score 7. EXPERIMENTAL DESIGN: We generated mRNA expression data from prostate tumor tissue from men in the Physicians' Health Study and Health Professionals Follow-Up Study (N = 404) using the Affymetrix Human Gene 1.0 ST microarray. The Prediction Analysis for Microarrays method was used to develop a signature to distinguish high (≥8) versus low (≤6) Gleason score. We evaluated the signature's ability to improve prediction of lethality among men with Gleason score 7, adjusting for 3 + 4/4 + 3 status, by quantifying the area under the receiver operating characteristic (ROC) curve (AUC). RESULTS: We identified a 30-gene signature that best distinguished Gleason score ≤6 from ≥8. The AUC to predict lethal disease among Gleason score 7 men was 0.76 [95% confidence interval (CI), 0.67-0.84] compared with 0.68 (95% CI, 0.59-0.76) using 3 + 4/4 + 3 status alone (P = 0.0001). This signature was a nonsignificant (P = 0.09) improvement over our previous signature (AUC = 0.72). CONCLUSIONS: Our new 30-gene signature improved prediction of lethality among men with Gleason score 7. This signature can potentially become a useful prognostic tool for physicians to improve treatment decision making.

Prognostic Utility of a New mRNA expression Signature of Gleason Score / Sinnott JA; Peisch S; Tyekucheva S; Gerke TA; Lis RT; Rider JR; Fiorentino M; Stampfer MJ; Mucci LA; Loda M; Penney KL.. - In: CLINICAL CANCER RESEARCH. - ISSN 1078-0432. - STAMPA. - 23:1(2017), pp. clincanres.1245.2016.81-clincanres.1245.2016.87. [10.1158/1078-0432.CCR-16-1245]

Prognostic Utility of a New mRNA expression Signature of Gleason Score.

FIORENTINO, MICHELANGELO;
2017

Abstract

PURPOSE: Gleason score strongly predicts prostate cancer mortality; however, scoring varies among pathologists, and many men are diagnosed with intermediate-risk Gleason score 7. We previously developed a 157-gene signature for Gleason score using a limited gene panel. Using a new whole-transcriptome expression dataset, we verified the previous signature's performance and developed a new Gleason signature to improve lethal outcome prediction among men with Gleason score 7. EXPERIMENTAL DESIGN: We generated mRNA expression data from prostate tumor tissue from men in the Physicians' Health Study and Health Professionals Follow-Up Study (N = 404) using the Affymetrix Human Gene 1.0 ST microarray. The Prediction Analysis for Microarrays method was used to develop a signature to distinguish high (≥8) versus low (≤6) Gleason score. We evaluated the signature's ability to improve prediction of lethality among men with Gleason score 7, adjusting for 3 + 4/4 + 3 status, by quantifying the area under the receiver operating characteristic (ROC) curve (AUC). RESULTS: We identified a 30-gene signature that best distinguished Gleason score ≤6 from ≥8. The AUC to predict lethal disease among Gleason score 7 men was 0.76 [95% confidence interval (CI), 0.67-0.84] compared with 0.68 (95% CI, 0.59-0.76) using 3 + 4/4 + 3 status alone (P = 0.0001). This signature was a nonsignificant (P = 0.09) improvement over our previous signature (AUC = 0.72). CONCLUSIONS: Our new 30-gene signature improved prediction of lethality among men with Gleason score 7. This signature can potentially become a useful prognostic tool for physicians to improve treatment decision making.
2017
Prognostic Utility of a New mRNA expression Signature of Gleason Score / Sinnott JA; Peisch S; Tyekucheva S; Gerke TA; Lis RT; Rider JR; Fiorentino M; Stampfer MJ; Mucci LA; Loda M; Penney KL.. - In: CLINICAL CANCER RESEARCH. - ISSN 1078-0432. - STAMPA. - 23:1(2017), pp. clincanres.1245.2016.81-clincanres.1245.2016.87. [10.1158/1078-0432.CCR-16-1245]
Sinnott JA; Peisch S; Tyekucheva S; Gerke TA; Lis RT; Rider JR; Fiorentino M; Stampfer MJ; Mucci LA; Loda M; Penney KL.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/577805
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