Association of p16 expression with prognosis varies across ovarian carcinoma histotypes: an Ovarian Tumor Tissue Analysis consortium study

Peter Rambau(University of Calgary), Robert A. Vierkant(Mayo Clinic), Maria P. Intermaggio(UNSW Sydney), Linda E. Kelemen(Medical University of South Carolina), Marc T. Goodman(Cedars-Sinai Medical Center), Esther Herpel(Heidelberg University), Paul D.P. Pharoah(University of Cambridge), Stefan Kommoss(University Children's Hospital Tübingen), Mercedes Jimenez‐Liñan(Addenbrooke's Hospital), Beth Y. Karlan(Cedars-Sinai Medical Center), Aleksandra Gentry‐Maharaj(Breast Cancer Now), Usha Menon(Breast Cancer Now), Susanna Hernando Polo(Hospital Universitario Fundación Alcorcón), Francisco José Cândido dos Reis(Universidade de São Paulo), Jennifer A. Doherty(University of Utah), Simon A. Gayther(University of Southern California), Raghwa Sharma(The University of Sydney), Melissa C. Larson(Mayo Clinic), Paul R. Harnett(The University of Sydney), Emma Hatfield(University of Calgary), Jurandyr Moreira de Andrade(Universidade de São Paulo), Gregg Nelson(University of Calgary), Helen Steed(Royal Alexandra Hospital), Joellen M. Schildkraut(University of Virginia), Micheal E Carney(University of Hawaiʻi at Mānoa), Estrid Høgdall(University of Copenhagen), Alice S. Whittemore(Stanford Health Care), Martin Widschwendter(Breast Cancer Now), Catherine J. Kennedy(The University of Sydney), Frances Wang(Duke Medical Center), Qin Wang(University of Cambridge), Chen Wang(Mayo Clinic in Florida), Sebastian M. Armasu(Mayo Clinic), Frances Daley(Institute of Cancer Research), Penny Coulson(Institute of Cancer Research), Michael E. Jones(Institute of Cancer Research), Michael S. Anglesio(University of British Columbia), Christine Chow(University of British Columbia), Anna de Fazio(The University of Sydney), Montserrat García‐Closas(Institute of Cancer Research), Sara Y. Brucker(University of Tübingen), Cezary Cybulski(Pomeranian Medical University), Holly R. Harris(Karolinska Institutet), Andreas D. Hartkopf(University Children's Hospital Tübingen), Tomasz Huzarski(Pomeranian Medical University), Allan Jensen(Danish Cancer Society), Jan Lubiński(Pomeranian Medical University), Oleg Oszurek(International Hereditary Cancer Center), Javier Benı́tez(Spanish National Cancer Research Centre), Fady Mina(University of Calgary), Annette Staebler(University Children's Hospital Tübingen), Florin‐Andrei Taran(University Children's Hospital Tübingen), J Pasternak(University Children's Hospital Tübingen), Aline Talhouk(BC Cancer Agency), Mary Anne Rossing(University of Washington), Joy Hendley(Peter MacCallum Cancer Centre), AOCS Group(University of Pittsburgh), Robert P. Edwards(University of Pittsburgh), Sián Fereday(University of Pittsburgh), Francesmary Modugno(The University of Texas MD Anderson Cancer Center), Roberta B. Ness(The University of Texas MD Anderson Cancer Center), Weiva Sieh(Hammersmith Hospital), Mona El‐Bahrawy(Hammersmith Hospital), Stacey J. Winham(Cedars-Sinai Medical Center), Jenny Lester(University of Copenhagen), Susanne K. Kjær(Copenhagen University Hospital), Jacek Gronwald(Heidelberg University), Hans‐Peter Sinn(University of California, Los Angeles), Peter A. Fasching(Universität Hamburg), Jenny Chang‐Claude(Roswell Park Comprehensive Cancer Center), Kirsten B. Moysich(Roswell Park Comprehensive Cancer Center), David D.L. Bowtell(University of Hawaiʻi at Mānoa), Brenda Y. Hernandez(University of Hawaiʻi at Mānoa), Hugh Luk(University of Hawaiʻi at Mānoa), Sabine Behrens(German Cancer Research Center), Mitul Shah(German Cancer Research Center), Audrey Jung(University of Calgary), Prafull Ghatage(University of Calgary), Jennifer Alsop(University of Cambridge), Kathryn Alsop(Peter MacCallum Cancer Centre), Jesús García-Donás(Cedars-Sinai Medical Center), Pamela J. Thompson(Cedars-Sinai Medical Center), Anthony J. Swerdlow(Institute of Cancer Research), Chloe Karpinskyj(Cancer Research UK), Alicia Cazorla(Spanish National Cancer Research Centre), María J. García(Nottingham University Hospitals NHS Trust), Susha Deen(University of Hawaiʻi at Mānoa), Lynne R. Wilkens(University of Hawaiʻi at Mānoa), José Palacios(Universidad de Alcalá), Andrew Berchuck(Alberta Health Services), Jennifer M. Koziak(Alberta Health Services), James D. Brenton(Alberta Health Services), Linda S. Cook(Alberta Health Services), Ellen L. Goode(BC Cancer Agency), David G. Huntsman(BC Cancer Agency), Susan J. Ramus(Garvan Institute of Medical Research), Martin Köbel(University of Calgary)
The Journal of Pathology Clinical Research
July 30, 2018
Cited by 99Open Access
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Abstract

We aimed to validate the prognostic association of p16 expression in ovarian high-grade serous carcinomas (HGSC) and to explore it in other ovarian carcinoma histotypes. p16 protein expression was assessed by clinical-grade immunohistochemistry in 6525 ovarian carcinomas including 4334 HGSC using tissue microarrays from 24 studies participating in the Ovarian Tumor Tissue Analysis consortium. p16 expression patterns were interpreted as abnormal (either overexpression referred to as block expression or absence) or normal (heterogeneous). CDKN2A (which encodes p16) mRNA expression was also analyzed in a subset (n = 2280) mostly representing HGSC (n = 2010). Association of p16 expression with overall survival (OS) was determined within histotypes as was CDKN2A expression for HGSC only. p16 block expression was most frequent in HGSC (56%) but neither protein nor mRNA expression was associated with OS. However, relative to heterogeneous expression, block expression was associated with shorter OS in endometriosis-associated carcinomas, clear cell [hazard ratio (HR): 2.02, 95% confidence (CI) 1.47-2.77, p < 0.001] and endometrioid (HR: 1.88, 95% CI 1.30-2.75, p = 0.004), while absence was associated with shorter OS in low-grade serous carcinomas (HR: 2.95, 95% CI 1.61-5.38, p = 0.001). Absence was most frequent in mucinous carcinoma (50%), and was not associated with OS in this histotype. The prognostic value of p16 expression is histotype-specific and pattern dependent. We provide definitive evidence against an association of p16 expression with survival in ovarian HGSC as previously suggested. Block expression of p16 in clear cell and endometrioid carcinoma should be further validated as a prognostic marker, and absence in low-grade serous carcinoma justifies CDK4 inhibition.


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