Article Data

  • Views 771
  • Dowloads 144

Original Research

Open Access

Uterine Cancer Normogram to Predict Lymph Node Metastasis: Comparison to the Mayo Algorithm and an External Vali ation of a Model in a North American Population

  • Michelle F. Benoit1,*,
  • Kristy K. Ward1

1Gynecologic Oncology, Kaiser Permanente Washington, United States

DOI: 10.31083/j.ejgo.2020.05.5401 Vol.41,Issue 5,October 2020 pp.681-684

Submitted: 24 October 2018 Accepted: 17 April 2019

Published: 15 October 2020

*Corresponding Author(s): Michelle F. Benoit E-mail: benoitmf1@yahoo.com

Abstract

Objective: We sought to compare two intraoperative uterine cancer normograms for prediction of lymph node (LN) metastasis. We used the widely known Mayo criteria, comparing it to an algorithm provided by Koskas et al. to predict likelihood of LN metastasis. Design: 490 uterine cancer patients from a single practice provider were included in the review. Data was abstracted to include age, race, stage, tumor size, grade, histologic subtype, depth of invasion, cervical involvement, lymphovascular space involvement (LVSI), and microsatellite instability (MSI). Patient comorbidities were analyzed to include body mass index (BMI), diabetes, and hypertension. Laboratories for these comorbidities were included. Those patients staged 1, 2, and 3 were included in final analysis. Results: The receiver operator curve (ROC) for the Koskas normogram was 0.78 when 4% was used as the cutoff for LN metastasis, with a sensitivity of 78% and specificity of 60%. When a 5% cutoff was used, the ROC was 0.71. For every percentage point that the French score rose, the chance of being LN positive increased by 0.8% (p < 0.001). The three point Mayo criteria odds ratio (OR) was 7.4 and the ROC was 0.57. Lymph node metastasis also correlated with MSI as seen on immunohistochemistry (IHC) testing. Conclusions: The Koskas normogram provided a better predictive algorithm for risk assessment of LN metastasis. Our results are comparable with those previously published by Koskas et al. providing an external validation of this normogram previously used in an European population. These intraoperative variables can be incorporated into real time risk assessment for LN metastasis and operative decision making. Mayo criteria, not using tumor size, could spare an additional 40% of patients an unnecessary LND compared to standard 3 point Mayo criteria–with better predictive value.


Keywords

Uterine cancer; Endometrial cancer; Lymph node metastasis; Mayo; Algorithm; Prediction.


Cite and Share

Michelle F. Benoit,Kristy K. Ward. Uterine Cancer Normogram to Predict Lymph Node Metastasis: Comparison to the Mayo Algorithm and an External Vali ation of a Model in a North American Population. European Journal of Gynaecological Oncology. 2020. 41(5);681-684.

References

[1] Siegel R.L., Miller K.D., Jemal A.: “Cancer statistics, 2020”. Ca. Cancer J. Clin., 2020, 70, 7-30.

[2] NCCN Uterine Cancer Guidelines: https://www.nccn.org/professionals/physician_gls/pdf/uterine.pdf Accessed March 10, 2020.

[3] Mariani A., Dowdy S.C., Cliby W.A., Gostout B.S., Jones M.B., Wilson T.O., et al.: “Prospective assessment of lymphatic dissemi-nation in endometrial cancer: A paradigm shift in surgical staging”. Gynecol. Oncol., 2008, 109, 11-18.

[4] Bendifallah S, Genin A.S., Koskas M., Naoura I., Buffet N.C., Chapelon F.C., et al.: “A normogram for predicting lymph node metastasis of presumed stage I and II endometrial cancer”. Am J Obstet Gynecol, 2012, 207, 197.

[5] Walker J.L., Piedmonte M.R., Spirtos N.M., Eisenkop S.M., Schlaerth J.B., Mannel R.S., et al.: “Recurrence and Survival AfterRandom Assignment to Laparoscopy Versus Laparotomy for Comprehensive Surgical Staging of Uterine Cancer: Gynecologic Oncology Group LAP2 Study”. J. Clin. Oncol., 2012, 30, 695-700.

[6] THOMAS M., MARIANI A., CLIBY W., KEENEY G., PODRATZ K., DOWDY S.: “Role of cytoreduction in stage III and IV uterine papillary serous carcinoma”. Gynecol. Oncol., 2007, 107, 190-193.

[7] Bokhman J.V.: “Two pathogenetic types of endometrial carcinoma”. Gynecol. Oncol., 1983, 15, 10-17.

[8] Kwon J.S., Scott J.L., Gilks C.B., Daniels M.S., Sun C.C., Lu K.H.: “Testing Women With Endometrial Cancer to Detect Lynch Syndrome”. J. Clin. Oncol., 2011, 29, 2247-2252.

[9] Koskas M., Fourneir M., Vanderstraeten A., Walker F., Timmerman D., Vergote L., et al.: “Evaluation of models to predict lymph node metastasis in endometrial cancer: A multicenter study”. Eur J Cancer, 2016, 61, 52-60.

[10] Yost K.J., Cheville A.L., Al-Hilli M.M., Mariani A., Barrette B.A., McGree M.E., et al.: “Lymphedema after surgery for endometrial cancer: prevalence, risk factors, and quality of life”. Obstet. Gynecol., 2014, 124, 307-315.

[11] Stewart K.I., Eska J.S., Harrison R.F., Suidan R., Abraham A., Chisholm G.B., et al.: “Implementation of a sentinel lymph node mapping algorithm for endometrial cancer: surgical outcomes and hospital charges”. International Journal of Gynecologic Cancer, 2020, 30, 352-357.

[12] Suidan R.S., Sun C.C., Cantor S.B., Mariani A., Soliman P.T., Westin S.N., et al.: “Three Lymphadenectomy Strategies in Low-Risk Endometrial Carcinoma”. Obstetrics & Gynecology, 2018, 132, 52-58.

[13] Chapel D.B., Yamada S.D., Cowan M., Lastra R.R.: “Immunohis-tochemistry for mismatch repair protein deficiency in endometrioid endometrial carcinoma yields equivalent results when performed on endometrial biopsy/curettage or hysterectomy specimens”. Gynecol. Oncol., 2018, 149, 570-574.

[14] Timmerman S., Van Rompuy A.S., Van Gorp T., Vanden Bempt I., Brems H., Van Nieuwenhuysen E., et al.: “Analysis of 108 patients with endometrial carcinoma using the PROMISE classification and additional genetic analyses for MMR-D”. Gynecol. Oncol., 2020, 157, 245-251.

[15] Zhang M., Isaksson R., Rivard C.: “Evaluating the Use of a Mod-ified Mayo Criteria for Early Stage Endometrial Cancer”. Gynecol Oncol, 2017, 147, 230.


Abstracted / indexed in

Science Citation Index Expanded (SciSearch) Created as SCI in 1964, Science Citation Index Expanded now indexes over 9,500 of the world’s most impactful journals across 178 scientific disciplines. More than 53 million records and 1.18 billion cited references date back from 1900 to present.

Biological Abstracts Easily discover critical journal coverage of the life sciences with Biological Abstracts, produced by the Web of Science Group, with topics ranging from botany to microbiology to pharmacology. Including BIOSIS indexing and MeSH terms, specialized indexing in Biological Abstracts helps you to discover more accurate, context-sensitive results.

Google Scholar Google Scholar is a freely accessible web search engine that indexes the full text or metadata of scholarly literature across an array of publishing formats and disciplines.

JournalSeek Genamics JournalSeek is the largest completely categorized database of freely available journal information available on the internet. The database presently contains 39226 titles. Journal information includes the description (aims and scope), journal abbreviation, journal homepage link, subject category and ISSN.

Current Contents - Clinical Medicine Current Contents - Clinical Medicine provides easy access to complete tables of contents, abstracts, bibliographic information and all other significant items in recently published issues from over 1,000 leading journals in clinical medicine.

BIOSIS Previews BIOSIS Previews is an English-language, bibliographic database service, with abstracts and citation indexing. It is part of Clarivate Analytics Web of Science suite. BIOSIS Previews indexes data from 1926 to the present.

Journal Citation Reports/Science Edition Journal Citation Reports/Science Edition aims to evaluate a journal’s value from multiple perspectives including the journal impact factor, descriptive data about a journal’s open access content as well as contributing authors, and provide readers a transparent and publisher-neutral data & statistics information about the journal.

Submission Turnaround Time

Conferences

Top