Colombian consensus for the molecular diagnosis of endometrial cancer

Authors

  • Marc Edy Pierre Centro de tratamiento e investigación sobre el Cáncer Luis Carlos Sarmiento (CTIC), Bogotá, Colombia. https://orcid.org/0000-0003-2119-9840
  • Angélica Viviana Fletcher Prieto Centro de Investigaciones Clínica San Diego-CIOSAD, Bogotá, Colombia. Centro Internacional de Alta Tecnología (CLINALTEC), Ibagué, Colombia. https://orcid.org/0000-0001-8634-6261
  • Juliana Rodríguez Fundación Santa Fe de Bogotá, Bogotá, Colombia. Grupo de Investigación Clínica y Epidemiológica del Cáncer (GICEC), Instituto Nacional de Cancerología, Bogotá, Colombia. Departamento de Obstetricia y Ginecología, Universidad Nacional de Colombia, Bogotá, Colombia. https://orcid.org/0000-0002-5472-4093
  • Abraham Hernández Blanquisett Hospital Serena del Mar, Cartagena, Colombia. https://orcid.org/0000-0002-0258-5888
  • Ana Milena Gómez Camacho Hospital Universitario San Ignacio, Bogotá, Colombia. Fundación Santa Fe de Bogotá, Bogotá, Colombia.
  • Rafael Parra Medina Instituto Nacional de Cancerología, Bogotá, Colombia. Fundación Universitaria de Ciencias de la Salud, Bogotá, Colombia.
  • Lucrecia Mojica Silva Liga contra el Cáncer. Villavicencio, Colombia.
  • Robinson Fernández Clínica La Asunción. Barranquilla, Colombia.
  • Pedro Hernando Calderón Quiroz Instituto Nacional de Cancerología, Bogotá, Colombia. Hospital Universitario Clínica San Rafael, Bogotá, Colombia. https://orcid.org/0000-0003-3672-4820

DOI:

https://doi.org/10.18597/rcog.4060

Abstract

Objective: The Cancer Genome Atlas research program (TCGA) developed the molecular classification for endometrial cancer with prognostic and therapeutic utility, which was replaced by the ProMisE (Proactive Molecular Risk Classifier for Endometrial Cancer) classification by consensus and international guidelines due to its high cost. This article aims to present national recommendations from an expert consensus that allows unification and implementation of the molecular classification for women with endometrial cancer nationwide, with a rational use of resources and technology.

Methods: Consensus of 36 experts in clinical oncology, oncological gynecology, pathology, and genetics, with clinical practice in the national territory. The leader group performed a literature review and structuring of questions rated 1 to 9 points. A modified nominal group technique was used. There was a face-to-face meeting with master presentations, deliberative dialogue, and Google Forms (Google LLC, Mountain View, CA, USA) questionnaire voting with analysis and discussion of responses. The non-consensual responses led to a second round of voting. The final manuscript was finally prepared and revised.

Results: Seven recommendations were formulated integrating the panelist responses based on evidence, but adjusted to the Colombian context and reality.

Recommendation 1. The molecular classification is recommended in all the endometrial cancers using the immunohistochemistry markers as subrogated results from the molecular profile initially proposed in the TCGA classification.

Recommendation 2. The sequential test strategy is recommended, starting with the immunohistochemistry markers (p53, MLH1, MSH 2, MSH6, PMS2) simultaneously in all the patients, defining to request POLE (DNA polymerase epsilon) (if available) according to the risk classification based on the surgical piece.

Recommendation 3. It is recommended, that the gynecologist oncologist should be the one to request the POLE (if available) according to the final pathology report. This test must be requested for all endometrial cancers stage I-II, except in low risk (stage IA low grade endometrioid histology without linfovascular invasion normal p53) and, stages III-IV without residual disease, without affecting the request of subrogated immunohistochemistry molecular markers upon histology.

The consensus proposes that the POLE is requested after the immunohistochemistry and according to the categories in the risk classification established by the 2020 ESGO/ESTRO/ESP guidelines.

Recommendation 4. It is recommended to perform immunohistochemistry for hormonal receptors for all women with endometrial cancer and the HER2 in patients with p53abn, simultaneously with the others immunohistochemistry markers.

Recommendation 5. It is recommended to perform the immunohistochemistry markers (p53, MLH1, MSH2, MSH6 y PMS2) in an initial endometrial biopsy or curettage when the specimen is adequate and available. In case the initial immunohistochemistry is inconclusive, or there are histological discrepancies between the initial and definitive pathology, it is recommended to repeat the molecular profile in the surgical pathology. The immunohistochemistry markers must be reported in the pathology report according to the CAP (College of American Pathologists) recommendations, independently of the type of sample.

Recommendation 6. It is recommended to perform MLH1 promoter methylation testing in patients who exhibit loss of expression of MLH1 in immunohistochemistry whether it is accompanied or not with loss of expression of PMS2. All the patients with deficient MMR (mismatch repair), should be sent for genetic counseling to rule out Lynch syndrome.

Recommendation 7. It is recommended to consider the molecular classification in addition to the classical histopathological criteria when making adjuvant judgments, as incorporated by the classification of prognostic groups of the 2020 ESGO/ESTRO/ESP guidelines.

Conclusions: It is necessary to implement the molecular classification of endometrial cancer in clinical practice in accordance to the Colombian context, due to its prognostic and probably predictive value. This will enable the characterization of the Colombian population in order to offer individualized guided treatments. This is an academic and nonregulatory document.

References

Lu KH, Broaddus RR. Endometrial Cancer. Longo DL, editor. New England Journal of Medicine. 2020;383(21):2053–64. https://doi.org/10.1056/NEJMra1514010

Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021;71(3):209–49. ttps://doi.org/10.3322/caac.21660

International Agency for Research on Cancer. Cancer Today- Globocan [Internet]. 2022 Disponible en: https://gco.iarc.who.int/today/en/dataviz/tables?mode=population&sexes=2&cancers=24&types=0&group_populations=0&multiple_populations=1&populations=124_152_191_196_203_208_233_246_250_258_276_300_316_348_352_36_372_376_380_392_40_410_414_428_44_440_442_470_48_512_52_528_540_554_56_578_616_620_630_634_682_702_703_705_724_752_756_780_784_826_840_858_96&multiple_cancers=1

Gu B, Shang X, Yan M, Li X, Wang W, Wang Q, et al. Variations in incidence and mortality rates of endometrial cancer at the global, regional, and national levels, 1990-2019. Gynecol Oncol. 2021;161(2):573–80. https://doi.org/10.1016/j.ygyno.2021.01.036

Bokhman J V. Two pathogenetic types of endometrial carcinoma. Gynecol Oncol. 1983;15(1):10–7. https://doi.org/10.1016/0090-8258(83)90111-7

Colombo N, Creutzberg C, Amant F, Bosse T, González-Martón A, Ledermann J, et al. ESMO-ESGO-ESTRO Consensus Conference on Endometrial Cancer: diagnosis, treatment and follow-up†. Annals of Oncology. 2016;27(1):16–41. https://doi.org/10.1093/annonc/mdv484

Gilks CB, Oliva E, Soslow RA. Poor interobserver reproducibility in the diagnosis of high-grade endometrial carcinoma. American Journal of Surgical Pathology. 2013;37(6):874–81. https://doi.org/10.1097/PAS.0b013e31827f576a

Jamieson A, Barroilhet LM, McAlpine JN. Molecular classification in endometrial cancer: Opportunities for precision oncology in a changing landscape. Cancer. 2022;128(15):2853–7. https://doi.org/10.1002/cncr.34328

Getz G, Gabriel SB, Cibulskis K, Lander E, Sivachenko A, Sougnez C, et al. Integrated genomic characterization of endometrial carcinoma. Nature. 2013;497(7447):67–73. https://doi.org/10.1038/nature12113

Alexa M, Hasenburg A, Battista MJ. The TCGA Molecular Classification of Endometrial Cancer and Its Possible Impact on Adjuvant Treatment Decisions. Cancers (Basel). 2021;13(6): 1478. https://doi.org/10.3390/cancers13061478

Talhouk A, McConechy MK, Leung S, Li-Chang HH, Kwon JS, Melnyk N, et al. A clinically applicable molecular-based classification for endometrial cancers. Br J Cancer. 2015;113(2):299–310. https://doi.org/10.1038/bjc.2015.190

Talhouk A, McConechy MK, Leung S, Yang W, Lum A, Senz J, et al. Confirmation of ProMisE: A simple, genomics-based clinical classifier for endometrial cancer. Cancer. 2017;123(5):802–13. https://doi.org/10.1002/cncr.30496

Kommoss S, McConechy MK, Kommoss F, Leung S, Bunz A, Magrill J, et al. Final validation of the ProMisE molecular classifier for endometrial carcinoma in a large population-based case series. Ann Oncol. 2018;29(5):1180–8. https://doi.org/10.1093/annonc/mdy058

Leon-Castillo A, De Boer SM, Powell ME, Mileshkin LR, Mackay HJ, Leary A, et al. Molecular Classification of the PORTEC-3 Trial for High-Risk Endometrial Cancer: Impact on Prognosis and Benefit From Adjuvant Therapy. J Clin Oncol. 2020;38(29):3388–97. https://doi.org/10.1200/JCO.20.00549

Léon-Castillo A. Update in the molecular classification of endometrial carcinoma. International Journal of Gynecologic Cancer. 2023;33(3):333–42. https://doi.org/10.1136/ijgc-2022-003772

León-Castillo A, Britton H, McConechy MK, McAlpine JN, Nout R, Kommoss S, et al. Interpretation of somatic POLE mutations in endometrial carcinoma. J Pathol. 2020;250(3):323–35. https://doi.org/10.1002/path.5372

McAlpine JN, Chiu DS, Nout RA, Church DN, Schmidt P, Lam S, et al. Evaluation of treatment effects in patients with endometrial cancer and POLE mutations: An individual patient data meta-analysis. Cancer. 2021;127(14):2409–22. https://doi.org/10.1002/cncr.33516

Stelloo E, Nout RA, Osse EM, Jürgenliemk-Schulz IJ, Jobsen JJ, Lutgens LC, et al. Improved Risk Assessment by Integrating Molecular and Clinicopathological Factors in Early-stage Endometrial Cancer-Combined Analysis of the PORTEC Cohorts. Clin Cancer Res. 2016;22(16):4215–24. https://doi.org/10.1158/1078-0432.CCR-15-2878

Stelloo E, Bosse T, Nout RA, Mackay HJ, Church DN, Nijman HW, et al. Refining prognosis and identifying targetable pathways for high-risk endometrial cancer; a TransPORTEC initiative. Mod Pathol. 2015;28(6):836–44. https://doi.org/10.1038/modpathol.2015.43

Singh N, Piskorz AM, Bosse T, Jimenez-Linan M, Rous B, Brenton JD, et al. p53 immunohistochemistry is an accurate surrogate for TP53 mutational analysis in endometrial carcinoma biopsies. J Pathol. 2020; 250(3):336–45. https://doi.org/10.1002/path.5375

Jamieson A, Thompson EF, Huvila J, Gilks CB, McAlpine JN. p53abn Endometrial Cancer: understanding the most aggressive endometrial cancers in the era of molecular classification. International Journal of Gynecologic Cancer. 2021;31(6):907–13. https://doi.org/10.1136/ijgc-2020-002256

Soussi T, Leroy B, Taschner PEM. Recommendations for Analyzing and Reporting TP53 Gene Variants in the High-Throughput Sequencing Era. Hum Mutat. 2014; 35(6):766–78. https://doi.org/10.1002/humu.22561

Proctor L, Pradhan M, Leung S, Cheng A, Lee CH, Soslow RA, et al. Assessment of DNA Ploidy in the ProMisE molecular subgroups of endometrial cancer. Gynecol Oncol. 2017;146(3):596–602. https://doi.org/10.1016/j.ygyno.2017.06.020

León-Castillo A, Gilvazquez E, Nout R, Smit VT, Mcalpine JN, Mcconechy M, et al. Clinicopathological and molecular characterisation of “multiple-classifier” endometrial carcinomas Multiple-classifier endometrial carcinoma. J Pathol. 2020; 250(3):312-322. https://doi.org/10.1002/path.5373

Herrington CS, (ed.), Editorial Board WHOCOT. WHO Classification of Tumours Female Genital Tumours. 5th ed. International Agency for Research on Cancer, 2020.

NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Uterine Neoplasms Version 2 [Internet]. 2024. Disponible en: https://www.nccn.org/professionals/physician_gls/pdf/uterine.pdf

Concin N, Matias-Guiu X, Vergote I, Cibula D, Mirza MR, Marnitz S, et al. ESGO/ESTRO/ESP guidelines for the management of patients with endometrial carcinoma. Int J Gynecol Cancer. 2021; 31(1):12–39. https://doi.org/10.1136/ijgc-2020-002230

Oaknin A, Bosse TJ, Creutzberg CL, Giornelli G, Harter P, Joly F, Lorusso D, Marth C, Makker V, Mirza MR, Ledermann JA, Colombo N; ESMO Guidelines Committee. Electronic address: clinicalguidelines@esmo.org. Endometrial cancer: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up. Ann Oncol. 2022 Sep;33(9):860-877. https://doi.org/10.1016/j.annonc.2022.05.009

Murali R, Delair DF, Bean SM, Abu-Rustum NR, Soslow RA. Evolving Roles of Histologic Evaluation and Molecular/Genomic Profiling in the Management of Endometrial Cancer. J Natl Compr Canc Netw. 2018; 16(2):201–9. https://doi.org/10.6004/jnccn.2017.7066

Berek JS, Matias-Guiu X, Creutzberg C, Fotopoulou C, Gaffney D, Kehoe S, et al. FIGO staging of endometrial cancer: 2023. International Journal of Gynecology and Obstetrics. 2023;162(2):383–94. https://doi.org/10.1002/ijgo.14923

Orellana TJ, Kim H, Beriwal S, Bhargava R, Berger J, Buckanovich RJ, et al. Cost-effectiveness analysis of tumor molecular classification in high-risk early-stage endometrial cancer. Gynecol Oncol. 2022;164(1):129–35. https://doi.org/10.1016/j.ygyno.2021.10.071

Orellana T, Kim H, Beriwal S, Taylor S, Smith K, Lesnock J. Cost-effectiveness analysis of tumor molecular testing in stage III endometrial cancer. Gynecol Oncol. 2023; (173):81–7. https://doi.org/10.1016/j.ygyno.2023.04.010

Motter A, Frederick P, Gaffney DK, Giuntoli RI, Han E, Huh WK, et al. NCCN Guidelines Version 1.2021 Cervical Cancer Continue NCCN Guidelines. 2021.

Eskander RN, Sill MW, Beffa L, Moore RG, Hope JM, Musa FB, et al. Pembrolizumab plus Chemotherapy in Advanced Endometrial Cancer. New England Journal of Medicine. 2023;388(23):2159–70. https://doi.org/10.1056/NEJMoa2302312

Mirza MR, Chase DM, Slomovitz BM, dePont Christensen R, Novák Z, Black D, et al. Dostarlimab for Primary Advanced or Recurrent Endometrial Cancer. New England Journal of Medicine. 2023;388(23):2145–58. https://doi.org/10.1056/NEJMoa2216334

Oaknin A, Dusa L, Sullivan R, Pothuri B, Ellard S, Leath C. Preliminary safety, efficacy, and pharmacokinetic/pharmacodynamic characterization from GARNET, a phase I/II clinical trial of the anti–PD-1 monoclonal antibody, TSR-042, in patients with recurrent or advanced MSI-h and MSS endometrial cancer. Gynecol Oncol. 2019;154. https://doi.org/10.1016/j.ygyno.2019.04.04437. Bethesda (MD): National Library of Medicine (US), editor. Lenvatinib in combination with pembrolizumab versus treatment of physician’s choice in participants with advanced endometrial cancer (MK-3475-775/E7080-G000-309 Per Merck Standard Convention [KEYNOTE-775]) . In 2018.

Marabelle A, Le DT, Ascierto PA, Di Giacomo AM, de Jesus-Acosta A, Delord JP, et al. Efficacy of pembrolizumab in patients with noncolorectal high microsatellite instability/ mismatch repair–deficient cancer: Results from the phase II KEYNOTE-158 study. Journal of Clinical Oncology. 2020;38(1):1–10. https://doi.org/10.1200/JCO.19.02105

Favier A, Varinot J, Uzan C, Duval A, Brocheriou I, Canlorbe G. The Role of Immunohistochemistry Markers in Endometrial Cancer with Mismatch Repair Deficiency: A Systematic Review. Cancers (Basel). 2022;14(15):3783. https://doi.org/10.3390/cancers14153783

Xiao JP, Wang JS, Zhao YY, Du J, Wang YZ. Microsatellite instability as a marker of prognosis: a systematic review and meta-analysis of endometrioid endometrial cancer survival data. Arch Gynecol Obstet. 2023;307(2):573-582. https://doi.org/10.1007/s00404-022-06636-8

Cho KR, Cooper K, Croce S, Djordevic B, Herrington S, Howitt B, Hui P, Ip P, Koebel M, Lax S, Quade BJ, Shaw P, Vidal A, Yemelyanova A, Clarke B, Hedrick Ellenson L, Longacre TA, Shih IM, McCluggage WG, Malpica A, Oliva E, Parkash V, Matias-Guiu X. International Society of Gynecological Pathologists (ISGyP) Endometrial Cancer Project: Guidelines From the Special Techniques and Ancillary Studies Group. Int J Gynecol Pathol. 2019 Jan;38 Suppl 1(Iss 1 Suppl 1):S114-S122. https://doi.org/10.1097/PGP.0000000000000496

Modica I, Soslow RA, Black D, Tornos C, Kauff N, Shia J. Utility of immunohistochemistry in predicting microsatellite instability in endometrial carcinoma. Am J Surg Pathol. 2007;31(5):744–51. https://doi.org/10.1097/01.pas.0000213428.61374.06

Uribe AG, Julio N, Muñoz M, Ruiz Gómez F, Ospina Martínez ML, Gómez Lopez MG. Informe Tecnico. Sexta Edicion. Desigualdades Sociales en Salud en Colombia. 2015.

Ricaurte Guerrero O, Sarmiento Lacera L. Manejo Inicial de Muestras Para Estudios de Anatomía Patológica. Manual de Procedimientos. Instituto Nacional de Salud. Santa Fe de Bogotá; 1993.

Gómez López A, Eliana I, Arellano S, Aponte CP. Orientaciones técnicas para la implementación de la RIAS para la población con riesgo o presencia de cáncer con enfoques diferenciales en el marco de los elementos estratégicos de APS. Bogotá D.C.; 2022.

Imboden S, Nastic D, Ghaderi M, Rydberg F, Siegenthaler F, Mueller MD, et al. Implementation of the 2021 molecular ESGO/ESTRO/ESP risk groups in endometrial cancer. Gynecol Oncol 2021;162(2):394–400. https://doi.org/10.1016/j.ygyno.2021.05.026

Betella I, Fumagalli C, Rafaniello Raviele P, Schivardi G, De Vitis LA, Achilarre MT, et al. A novel algorithm to implement the molecular classification according to the new ESGO/ESTRO/ESP 2020 guidelines for endometrial cancer. Int J Gynecol Cancer. 2022;32(8):993–1000. https://doi.org/10.1136/ijgc-2022-003480

Talhouk A, Jamieson A, Crosbie E, Taylor A, Chiu D, Leung S, et al. Targeted Molecular Testing in Endometrial Carcinoma: Validation of a Clinically Driven Selective ProMisE Testing Protocol: International Journal of Gynecological Pathology. International Journal of Gynecological Pathology. Int J Gynecol Pathol. 2023;42(4):353-363. https://doi.org/10.1097/PGP.0000000000000898

Consortium RR. Refining adjuvant treatment in endometrial cancer based on molecular features: the RAINBO clinical trial program. International Journal of Gynecologic Cancer. 2023 Jan 1;33(1):109–17. https://doi.org/10.1136/ijgc-2022-004039

Van Den Heerik ASVM, Horeweg N, Nout RA, Lutgens LCHW, Van Der Steen-Banasik EM, Westerveld GH, et al. PORTEC-4a: International randomized trial of molecular profile-based adjuvant treatment for women with high-intermediate risk endometrial cancer. International Journal of Gynecological Cancer. 2020;30(12):2002–7. https://doi.org/10.1136/ijgc-2020-001929

Tailored Adjuvant Therapy in POLE-mutated and p53-wildtype Early Stage Endometrial Cancer - Full Text View - ClinicalTrials.gov [Internet]. Disponible en: https://clinicaltrials.gov/ct2/show/NCT04705649

Makker V, Rasco D, Vogelzang NJ, Brose MS, Cohn AL, Mier J, et al. Lenvatinib plus pembrolizumab in patients with advanced endometrial cancer: an interim analysis of a multicentre, open-label, single-arm, phase 2 trial. Lancet Oncol. 2019;20(5):711–8. https://doi.org/10.1016/S1470-2045(19)30020-8

Uterine Cancer — Cancer Stat Facts [Internet]. Disponible en: https://seer.cancer.gov/statfacts/html/corp.html

Devereaux KA, Steiner DF, Ho C, Gomez AJ, Gilks B, Longacre TA, et al. A Multiplex SNaPshot Assay is a Rapid and Cost-Effective Method for Detecting POLE Exonuclease Domain Mutations in Endometrial Carcinoma. Int J Gynecol Pathol. 2022;41(6):541–51. https://doi.org/10.1097/PGP.0000000000000841

Kanopiene D, Smailyte G, Vidugiriene J, Bacher J. Impact of microsatellite instability on survival of endometrial cancer patients. Medicina (Kaunas). 2014 ;50(4):216–21. https://doi.org/10.1016/j.medici.2014.09.002

Ruz-Caracuel I, Ramón-Patino JL, López-Janeiro Á, Yébenes L, Berjón A, Hernández A, et al. Myoinvasive Pattern as a Prognostic Marker in Low-Grade, Early-Stage Endometrioid Endometrial Carcinoma. Cancers (Basel). 2019;11(12). https://doi.org/10.3390/cancers11121845

Haruma T, Nagasaka T, Nakamura K, Haraga J, Nyuya A, Nishida T, et al. Clinical impact of endometrial cancer stratified by genetic mutational profiles, POLE mutation, and microsatellite instability. PLoS One. 2018;13(4). https://doi.org/10.1371/journal.pone.0195655

Fitzgibbons PL, Bartley AN, Longacre TA, Broaddus R, Chuang LT, Cohen MB, et al. Template for Reporting Results of Biomarker Testing of Specimens From Patients With Carcinoma of the Endometrium Version: Endometrium Biomarkers 1.2.0.1 Template With guidance from the CAP Cancer and CAP Pathology Electronic Reporting Committees. Summary of Changes v1.2.0.1 Updated the Background Documentation (Notes) v1.2.0.0 Added HER2 Reporting Changed IHC Interpretation to include “for Mismatch Repair.” [Internet]. 2019. Disponible en: https://documents.cap.org/protocols/cp-femalereproductive-endometrium-biomarker-19-1200.pdf

Zhang Y, Zhao D, Gong C, Zhang F, He J, Zhang W, et al. Prognostic role of hormone receptors in endometrial cancer: A systematic review and meta-analysis. World J Surg Oncol [Internet]. 2015 Jun 25;13(1):1–12. doi: https://doi.org/10.1186/s12957-015-0619-1

Vermij L, Powell M, Leon-Castillo A, et al 397 Molecular profiling of NSMP high-risk endometrial cancers of the PORTEC-3 trial – prognostic refinement and druggable targets International Journal of Gynecologic Cancer 2021;31:A89-A90. https://doi.org/10.1136/ijgc-2021-ESGO.137

van Weelden WJ, Massuger LFAG; ENITEC; Pijnenborg JMA, Romano A. Anti-estrogen Treatment in Endometrial Cancer: A Systematic Review. Front Oncol. 2019 May 7;9:359. https://doi.org/10.3389/fonc.2019.00359

Togami S, Sasajima Y, Oi T, Ishikawa M, Onda T, Ikeda SI, et al. Clinicopathological and prognostic impact of human epidermal growth factor receptor type 2 (HER2) and hormone receptor expression in uterine papillary serous carcinoma. Cancer Sci. 2012;103(5):926–32. https://doi.org/10.1111/j.1349-7006.2012.02240.x

Zhao S, Choi M, Overton JD, Bellone S, Roque DM, Cocco E, et al. Landscape of somatic single-nucleotide and copy-number mutations in uterine serous carcinoma. Proc Natl Acad Sci U S A. 2013; 110(8):2916–21. https://doi.org/10.1073/pnas.1222577110

Vermij L, Horeweg N, Leon-Castillo A, Rutten TA, Mileshkin LR, Mackay HJ, et al. HER2 Status in High-Risk Endometrial Cancers (PORTEC-3): Relationship with Histotype, Molecular Classification, and Clinical Outcomes. Cancers (Basel). 2020;13(1):1–14. https://doi.org/10.3390/cancers13010044

Buza N. HER2 Testing in Endometrial Serous Carcinoma: Time for Standardized Pathology Practice to Meet the Clinical Demand. Arch Pathol Lab Med. 2021;145(6):687–91. https://doi.org/10.5858/arpa.2020-0207-RA

Erickson BK, Najjar O, Damast S, Blakaj A, Tymon-Rosario J, Shahi M, et al. Human epidermal growth factor 2 (HER2) in early stage uterine serous carcinoma: A multi-institutional cohort study. Gynecol Oncol. 2020; 159(1):17–22. https://doi.org/10.1016/j.ygyno.2020.07.016

Fader AN, Roque DM, Siegel E, Buza N, Hui P, Abdelghany O, et al. Randomized Phase II Trial of Carboplatin-Paclitaxel Compared with Carboplatin-Paclitaxel-Trastuzumab in Advanced (Stage III-IV) or Recurrent Uterine Serous Carcinomas that Overexpress Her2/Neu (NCT01367002): Updated Overall Survival Analysis. Clin Cancer Res. 2020;26(15):3928–35. https://doi.org/10.1158/1078-0432.CCR-20-0953

Meric-Bernstam F, Makker V, Oaknin A, Oh DY, Banerjee S, González-Martín A, et al. Efficacy and Safety of Trastuzumab Deruxtecan in Patients With HER2-Expressing Solid Tumors: Primary Results From the DESTINY-PanTumor02 Phase II Trial. Journal of Clinical Oncology. 2024;42(1):47–58. https://doi.org/10.1200/JCO.23.02005

Talhouk A, Hoang LN, McConechy MK, Nakonechny Q, Leo J, Cheng A, et al. Molecular classification of endometrial carcinoma on diagnostic specimens is highly concordant with final hysterectomy: Earlier prognostic information to guide treatment. Gynecol Oncol. 2016;143(1):46–53. https://doi.org/10.1016/j.ygyno.2016.07.090

Chapel DB, Yamada SD, Cowan M, Lastra RR. Immunohistochemistry 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(3):570–4. https://doi.org/10.1016/j.ygyno.2018.04.005

Weiss JM, Gupta S, Burke CA, Axell L, Chen LM, Chung DC, et al. NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 1.2021: Featured Updates to the NCCN Guidelines. Journal of the National Comprehensive Cancer Network. 2021;19(10):1122–32. https://doi: 10.1164/jnccn.2021.0048

Holter S, Hall MJ, Hampel H, Jasperson K, Kupfer SS, Larsen Haidle J, et al. Risk assessment and genetic counseling for Lynch syndrome – Practice resource of the National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer. J Genet Couns. 2022;31(3):568–83. https://doi.org/10.1002/jgc4.1546

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Pierre ME, Fletcher Prieto AV, Rodríguez J, Hernández Blanquisett A, Gómez Camacho AM, Parra Medina R, et al. Colombian consensus for the molecular diagnosis of endometrial cancer. Rev. colomb. obstet. ginecol. [Internet]. 2024 Jun. 17 [cited 2024 Jun. 19];75(1). Available from: https://revista.fecolsog.org/index.php/rcog/article/view/4060

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