Sonographic, Demographic, and Clinical Characteristics of Pre- and Postmenopausal Women with Endometrial Cancer; Results from a Post Hoc Analysis of the IETA4 (International Endometrial Tumor Analysis) Multicenter Cohort
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
20150411
Avtal om Läkarutbildning och Forskning (ALF)
20190202
Avtal om Läkarutbildning och Forskning (ALF)
154112
Konung Gustaf V Jubileumsfond
181115
Konung Gustaf V Jubileumsfond
PubMed
38201310
PubMed Central
PMC10802150
DOI
10.3390/diagnostics14010001
PII: diagnostics14010001
Knihovny.cz E-zdroje
- Klíčová slova
- biometry, endometrial neoplasms, exploratory research, lifestyle, perimenopause, postmenopause, premenopause, risk factors, ultrasonography,
- Publikační typ
- časopisecké články MeSH
In this study, we conducted a comparative analysis of demographic, histopathological, and sonographic characteristics between pre- and postmenopausal women diagnosed with endometrial cancer, while also examining sonographic and anthropometric features in 'low' and 'intermediate/high-risk' cases, stratified by menopausal status. Our analysis, based on data from the International Endometrial Tumor Analysis (IETA) 4 cohort comprising 1538 women (161 premenopausal, 1377 postmenopausal) with biopsy-confirmed endometrial cancer, revealed that premenopausal women, compared to their postmenopausal counterparts, exhibited lower parity (median 1, IQR 0-2 vs. 1, IQR 1-2, p = 0.001), a higher family history of colon cancer (16% vs. 7%, p = 0.001), and smaller waist circumferences (median 92 cm, IQR 82-108 cm vs. 98 cm, IQR 87-112 cm, p = 0.002). Premenopausal women more often had a regular endometrial-myometrial border (39% vs. 23%, p < 0.001), a visible endometrial midline (23% vs. 11%, p < 0.001), and undefined tumor (73% vs. 84%, p = 0.001). Notably, despite experiencing a longer duration of abnormal uterine bleeding (median 5 months, IQR 3-12 vs. 3 months, 2-6, p < 0.001), premenopausal women more often had 'low' risk disease (78% vs. 46%, p < 0.001). Among sonographic and anthropometric features, only an irregular endometrial-myometrial border was associated with 'intermediate/high' risk in premenopausal women. Conversely, in postmenopausal women, multiple features correlated with 'intermediate/high' risk disease. Our findings emphasize the importance of considering menopausal status when evaluating sonographic features in women with endometrial cancer.
Department of Development and Regeneration KU Leuven 3000 Leuven Belgium
Department of Gynecological Oncology European Institute of Oncology IRCCS 20141 Milan Italy
Department of Obstetrics and Gynecology Catholic University of the Sacred Heart 00168 Rome Italy
Department of Obstetrics and Gynecology Södersjukhuset 118 83 Stockholm Sweden
Department of Obstetrics and Gynecology University Hospital Leuven 3000 Leuven Belgium
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Amant F., Mirza M.R., Koskas M., Creutzberg C.L. Cancer of the Corpus Uteri. Int. J. Gynecol. Obstet. 2015;131:S96–S104. doi: 10.1016/j.ijgo.2015.06.005. PubMed DOI
Ferlay J., Soerjomataram I., Dikshit R., Eser S., Mathers C., Rebelo M., Parkin D.M., Forman D., Bray F. Cancer Incidence and Mortality Worldwide: Sources, Methods and Major Patterns in GLOBOCAN 2012. Int. J. Cancer. 2015;136:E359–E386. doi: 10.1002/ijc.29210. PubMed DOI
National Cancer Institute (NIH) Cancer Stat Facts: Endometrial Cancer. [(accessed on 30 October 2019)]; Available online: https://seer.cancer.gov/statfacts/html/corp.html.
Cancer Research UK [(accessed on 30 October 2019)]. Available online: https://www.cancerresearchuk.org/health-professional/cancer-statistics/statistics-by-cancer-type/uterine-cancer/incidence#heading-One.
Socialstyrelsen, Statistikdatabas för Cancer. [(accessed on 30 October 2019)]. Available online: https://sdb.socialstyrelsen.se/if_can/val.aspx.
Pennant M.E., Mehta R., Moody P., Hackett G., Prentice A., Sharp S.J., Lakshman R. Premenopausal Abnormal Uterine Bleeding and Risk of Endometrial Cancer. BJOG. 2017;124:404–411. doi: 10.1111/1471-0528.14385. PubMed DOI PMC
Clarke M.A., Long B.J., Del Mar Morillo A., Arbyn M., Bakkum-Gamez J.N., Wentzensen N. Association of Endometrial Cancer Risk with Postmenopausal Bleeding in Women a Systematic Review and Meta-Analysis. JAMA Intern. Med. 2018;178:1201–1208. doi: 10.1001/jamainternmed.2018.2820. PubMed DOI PMC
Hernandez A.V., Pasupuleti V., Benites-Zapata V.A., Thota P., Deshpande A., Perez-Lopez F.R. Insulin Resistance and Endometrial Cancer Risk: A Systematic Review and Meta-Analysis. Eur. J. Cancer. 2015;51:2747–2758. doi: 10.1016/j.ejca.2015.08.031. PubMed DOI
McPherson C.P., Sellers T.A., Potter J.D., Bostick R.M., Folsom A.R. Reproductive Factors and Risk of Endometrial Cancer. The Iowa Women’s Health Study. Am. J. Epidemiol. 1996;143:1195–1202. doi: 10.1093/oxfordjournals.aje.a008707. PubMed DOI
Soliman P.T., Oh J.C., Schmeler K.M., Sun C.C., Slomovitz B.M., Gershenson D.M., Burke T.W., Lu K.H. Risk Factors for Young Premenopausal Women With Endometrial Cancer. Obstet. Gynecol. 2005;105:575–580. doi: 10.1097/01.AOG.0000154151.14516.f7. PubMed DOI
Wise M.R., Jordan V., Lagas A., Showell M., Wong N., Lensen S., Farquhar C.M. Obesity and Endometrial Hyperplasia and Cancer in Premenopausal Women: A Systematic Review. Am. J. Obstet. Gynecol. 2016;214:689.e1–689.e17. doi: 10.1016/j.ajog.2016.01.175. PubMed DOI
Schmeler K.M., Soliman P.T., Sun C.C., Slomovitz B.M., Gershenson D.M., Lu K.H. Endometrial Cancer in Young, Normal-Weight Women. Gynecol. Oncol. 2005;99:388–392. doi: 10.1016/j.ygyno.2005.06.029. PubMed DOI
Lee N.K., Cheung M.K., Shin J.Y., Husain A., Teng N.N., Berek J.S., Kapp D.S., Osann K., Chan J.K. Prognostic Factors for Uterine Cancer in Reproductive-Aged Women. Obstet. Gynecol. 2007;109:655–662. doi: 10.1097/01.AOG.0000255980.88205.15. PubMed DOI
Pellerin G.P., Finan M.A. Endometrial Cancer in Women 45 Years of Age or Younger: A Clinicopathological Analysis. Am. J. Obstet. Gynecol. 2005;193:1640–1644. doi: 10.1016/j.ajog.2005.05.003. PubMed DOI
Colombo N., Creutzberg C., Amant F., Bosse T., González-Martín A., Ledermann J., Marth C., Nout R., Querleu D., Mirza M.R., et al. ESMO-ESGO-ESTRO Consensus Conference on Endometrial Cancer: Diagnosis, Treatment and Follow-Up. Ann. Oncol. 2016;27:16–41. doi: 10.1093/annonc/mdv484. PubMed DOI PMC
Verbakel J.Y., Mascilini F., Wynants L., Fischerova D., Testa A.C., Franchi D., Frühauf F., Cibula D., Lindqvist P.G., Fruscio R., et al. Validation of Ultrasound Strategies to Assess Tumor Extension and to Predict High-Risk Endometrial Cancer in Women from the Prospective IETA (International Endometrial Tumor Analysis)-4 Cohort. Ultrasound Obstet. Gynecol. 2020;55:115–124. doi: 10.1002/uog.20374. PubMed DOI
Epstein E., Fischerova D., Valentin L., Testa A.C., Franchi D., Sladkevicius P., Frühauf F., Lindqvist P.G., Mascilini F., Fruscio R., et al. Ultrasound Characteristics of Endometrial Cancer as Defined by International Endometrial Tumor Analysis (IETA) Consensus Nomenclature: Prospective Multicenter Study. Ultrasound Obstet. Gynecol. 2018;51:818–828. doi: 10.1002/uog.18909. PubMed DOI
Eriksson L.S.E., Epstein E., Testa A.C., Fischerova D., Valentin L., Sladkevicius P., Franchi D., Frühauf F., Fruscio R., Haak L.A., et al. Ultrasound-Based Risk Model for Preoperative Prediction of Lymph-Node Metastases in Women with Endometrial Cancer: Model-Development Study. Ultrasound Obstet. Gynecol. 2020;56:443–452. doi: 10.1002/uog.21950. PubMed DOI
Green R.W., Valentin L., Alcazar J.L., Chiappa V., Erdodi B., Franchi D., Frühauf F., Fruscio R., Guerriero S., Graupera B., et al. Endometrial Cancer Off-Line Staging Using Two-Dimensional Transvaginal Ultrasound and Three-Dimensional Volume Contrast Imaging: Intermethod Agreement, Interrater Reliability and Diagnostic Accuracy. Gynecol. Oncol. 2018;150:438–445. doi: 10.1016/j.ygyno.2018.06.027. PubMed DOI
Leone F.P.G., Timmerman D., Bourne T., Valentin L., Epstein E., Goldstein S.R., Marret H., Parsons A.K., Gull B., Istre O., et al. Terms, Definitions and Measurements to Describe the Sonographic Features of the Endometrium and Intrauterine Lesions: A Consensus Opinion from the International Endometrial Tumor Analysis (IETA) Group. Ultrasound Obstet. Gynecol. 2010;35:103–112. doi: 10.1002/uog.7487. PubMed DOI
Installé A.J.F., Van Den Bosch T., De Moor B., Timmerman D. Clinical Data Miner: An Electronic Case Report Form System with Integrated Data Preprocessing and Machine-Learning Libraries Supporting Clinical Diagnostic Model Research. J. Med. Internet Res. 2014;16:e28. doi: 10.2196/medinform.3251. PubMed DOI PMC
Pecorelli S. Revised FIGO Staging for Carcinoma of the Vulva, Cervix, and Endometrium. Int. J. Gynecol. Obstet. 2009;105:103–104. doi: 10.1016/j.ijgo.2009.02.012. PubMed DOI
Kurman R.J., Carcangiu M.L., Herrington S.C., Young R.H. WHO Classification of Tumours of Female Reproductive Organs. 4th ed. International Agency for Research on Cancer; Lyon, France: 2014.
Alberti K.G.M.M., Eckel R.H., Grundy S.M., Zimmet P.Z., Cleeman J.I., Donato K.A., Fruchart J.C., James W.P.T., Loria C.M., Smith S.C. Harmonizing the Metabolic Syndrome: A Joint Interim Statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International. Circulation. 2009;120:1640–1645. doi: 10.1161/CIRCULATIONAHA.109.192644. PubMed DOI
Benjamini Y., Yekutieli D. The Control of the False Discovery Rate in Multiple Testing under Dependency. Ann. Stat. 2001;29:1165–1188. doi: 10.1214/aos/1013699998. DOI
Newson R. Multiple—Test Procedures and Smile Plots. Stata J. Promot. Commun. Stat. Stata. 2003;3:109–132. doi: 10.1177/1536867X0300300202. DOI
Gaus W. Interpretation of Statistical Significance-Exploratory Versus Confirmative Testing in Clinical Trials, Epidemiological Studies, Meta-Analyses and Toxicological Screening (Using Ginkgo Biloba as an Example) Clin. Exp. Pharmacol. 2015;5:1000182. doi: 10.4172/2161-1459.1000182. DOI
Breijer M.C., Peeters J.A.H., Opmeer B.C., Clark T.J., Verheijen R.H.M., Mol B.W.J., Timmermans A. Capacity of Endometrial Thickness Measurement to Diagnose Endometrial Carcinoma in Asymptomatic Postmenopausal Women: A Systematic Review and Meta-Analysis. Ultrasound Obstet. Gynecol. 2012;40:621–629. doi: 10.1002/uog.12306. PubMed DOI
Su D., Li L., Zhong M., Xia Y. Capacity of Endometrial Thickness Measurement to Diagnose Endometrial Carcinoma in Asymptomatic Postmenopausal Women: A Systematic Review and Meta-Analysis. Ann. Palliat. Med. 2021;10:10840–10848. doi: 10.21037/apm-21-2516. PubMed DOI
Tsuda H., Ito Y.M., Todo Y., Iba T., Tasaka K., Sutou Y., Hirai K., Dozono K., Dobashi Y., Manabe M., et al. Measurement of Endometrial Thickness in Premenopausal Women in Office Gynecology. Reprod. Med. Biol. 2018;17:29–35. doi: 10.1002/rmb2.12062. PubMed DOI PMC
Gao Y., Dai X., Lee A.C., Wise M.R., Shen F., Chen Q. Body Mass Index Is Negatively Associated with Endometrial Cancer Stage, Regardless of Subtype and Menopausal Status. J. Cancer. 2018;9:4756–4761. doi: 10.7150/jca.21137. PubMed DOI PMC
Arem H., Irwin M.L. Obesity and Endometrial Cancer Survival: A Systematic Review. Int. J. Obes. 2013;37:634–639. doi: 10.1038/ijo.2012.94. PubMed DOI PMC
Nevadunsky N.S., Van Arsdale A., Strickler H.D., Moadel A., Kaur G., Levitt J., Girda E., Goldfinger M., Goldberg G.L., Einstein M.H. Obesity and Age at Diagnosis of Endometrial Cancer. Obstet. Gynecol. 2014;124:300–306. doi: 10.1097/AOG.0000000000000381. PubMed DOI
Van Arsdale A., Miller D.T., Kuo D.Y., Isani S., Sanchez L., Nevadunsky N.S. Association of Obesity with Survival in Patients with Endometrial Cancer. Gynecol. Oncol. 2019;154:156–162. doi: 10.1016/j.ygyno.2019.03.258. PubMed DOI
Eurostat. [(accessed on 13 December 2019)]. Available online: https://ec.europa.eu/eurostat/data/database.
Santoro N., Lasley B., McConnell D., Allsworth J., Crawford S., Gold E.B., Finkelstein J.S., Greendale G.A., Kelsey J., Korenman S., et al. Body Size and Ethnicity Are Associated with Menstrual Cycle Alterations in Women in the Early Menopausal Transition: The Study of Women’s Health across the Nation (SWAN) Daily Hormone Study. J. Clin. Endocrinol. Metab. 2004;89:2622–2631. doi: 10.1210/jc.2003-031578. PubMed DOI
Benjamin D.J., Berger J.O., Johannesson M., Nosek B.A., Wagenmakers E.J., Berk R., Bollen K.A., Brembs B., Brown L., Camerer C., et al. Redefine Statistical Significance. Nat. Hum. Behav. 2018;2:6–10. doi: 10.1038/s41562-017-0189-z. PubMed DOI
Benjamini Y., Zeevi Y. It’s the Selection’s Fault—Not the p-Values’: A Comment on “The Role of p-Values in Judging the Strength of Evidence and Realistic Replication Expectations”. Stat. Biopharm. Res. 2020;13:22–25. doi: 10.1080/19466315.2020.1845790. DOI
Amrhein V., Greenland S., McShane B. Scientists Rise up against Statistical Significance. Nature. 2019;567:305–307. doi: 10.1038/d41586-019-00857-9. PubMed DOI
Dirnagl U. The p Value Wars (Again) Eur. J. Nucl. Med. Mol. Imaging. 2019;46:2421–2423. doi: 10.1007/s00259-019-04467-5. PubMed DOI
Ioannidis J.P.A. Retiring Statistical Significance Would Give Bias a Free Pass. Nature. 2019;567:461. doi: 10.1038/d41586-019-00969-2. PubMed DOI