Pan-cancer Transcriptomic Predictors of Perineural Invasion Improve Occult Histopathologic Detection

被引:20
作者
Guo, Jimmy A. [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Hoffman, Hannah, I [1 ,2 ,3 ,4 ]
Shroff, Stuti G. [8 ]
Chen, Peter [9 ]
Hwang, Peter G. [10 ]
Kim, Daniel Y. [11 ]
Kim, Daniel W. [4 ]
Cheng, Stephanie W. [12 ]
Zhao, Daniel [13 ]
Mahal, Brandon A. [14 ]
Alshalalfa, Mohammed [15 ]
Niemierko, Andrzej [4 ]
Wo, Jennifer Y. [4 ]
Loeffler, Jay S. [4 ]
Fernandez-del Castillo, Carlos [16 ]
Jacks, Tyler [2 ,3 ]
Aguirre, Andrew J. [1 ,7 ]
Hong, Theodore S. [4 ]
Mino-Kenudson, Mari [8 ]
Hwang, William L. [1 ,2 ,3 ,4 ]
机构
[1] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[2] MIT, Koch Inst Integrat Canc Res, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] MIT, Howard Hughes Med Inst, Dept Biol, Cambridge, MA USA
[4] Massachusetts Gen Hosp, Dept Radiat Oncol, Boston, MA 02114 USA
[5] Harvard Med Sch, Program Biol & Biomed Sci, Boston, MA 02115 USA
[6] Univ Calif San Francisco, Sch Med, San Francisco, CA USA
[7] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[8] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[9] Raytheon Technol, Brooklyn, NY USA
[10] MIT, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[11] Massachusetts Gen Hosp, Mol Pathol Unit, Charlestown, MA 02114 USA
[12] Harvard Univ, Cambridge, MA 02138 USA
[13] New York Med Coll, Valhalla, NY 10595 USA
[14] Miller Sch Med, Dept Radiat Oncol, Miami, FL USA
[15] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[16] Massachusetts Gen Hosp, Dept Surg, Boston, MA 02114 USA
关键词
CELL; MECHANISMS; EXPRESSION; SURVIVAL; IMPACT;
D O I
10.1158/1078-0432.CCR-20-4382
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Perineural invasion (PNI) is associated with aggressive tumor behavior, recurrence, and metastasis, and can influence the administration of adjuvant treatment. However, standard histopathologic examination has limited sensitivity in detecting PNI and does not provide insights into its mechanistic underpinnings. Experimental Design: A multivariate Cox regression was performed to validate associations between PNI and survival in 2,029 patients across 12 cancer types. Differential expression and gene set enrichment analysis were used to learn PNI-associated programs. Machine learning models were applied to build a PNI gene expression classifier. A blinded re-review of hematoxylin and eosin (H&E) slides by a board-certified pathologist helped determine whether the classifier could improve occult histopathologic detection of PNI. Results: PNI associated with both poor overall survival [HR, 1.73; 95% confidence interval (CI), 1.27-2.36; P < 0.001] and disease-free survival (HR, 1.79; 95% CI, 1.38-2.32; P < 0.001). Neural-like, prosurvival, and invasive programs were enriched in PNI-positive tumors (P-adj < 0.001). Although PNI-associated features likely reflect in part the increased presence of nerves, many differentially expressed genes mapped specifically to malignant cells from single-cell atlases. A PNI gene expression classifier was derived using random forest and evaluated as a tool for occult histopathologic detection. On a blinded H&E re-review of sections initially described as PNI negative, more specimens were reannotated as PNI positive in the high classifier score cohort compared with the low-scoring cohort (P = 0.03, Fisher exact test). Conclusions: This study provides salient biological insights regarding PNI and demonstrates a role for gene expression classifiers to augment detection of histopathologic features.
引用
收藏
页码:2807 / 2815
页数:9
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