Risk Stratification of Stage I Grade 3 Endometrioid Endometrial Carcinoma in the Era of Molecular Classification

Author:

Zammarrelli William A.1ORCID,Kim Sarah H.1,Da Cruz Paula Arnaud1,Rios-Doria Eric V.1ORCID,Ehmann Sarah1,Yeoshoua Effi1,Hanlon Etta J.2,Zhou Qin3ORCID,Iasonos Alexia3ORCID,Alektiar Kaled M.4ORCID,Aghajanian Carol56,Makker Vicky56ORCID,Leitao Mario M.17ORCID,Abu-Rustum Nadeem R.17,Ellenson Lora H.2,Weigelt Britta2ORCID,Mueller Jennifer J.17ORCID

Affiliation:

1. Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY

2. Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY

3. Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY

4. Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY

5. Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY

6. Department of Medicine, Weill Cornell Medical College, New York, NY

7. Department of Obstetrics and Gynecology, Weill Cornell Medical College, New York, NY

Abstract

PURPOSE The role of adjuvant therapy in stage I grade 3 endometrioid endometrial carcinoma (EEC) is debatable. We sought to define the agreement between Post Operative Radiation Therapy in Endometrial Carcinoma 1 (PORTEC-1) high-intermediate risk (HIR) and Gynecologic Oncology Group (GOG)-99 HIR criteria, assess their concordance with The Cancer Genome Atlas molecular subtypes, and evaluate oncologic outcomes in this population. METHODS We identified patients with stage I grade 3 EECs who underwent surgical staging at our institution from January 2014 to January 2020. Patients were stratified into PORTEC-1 HIR, GOG-99 HIR, and The Cancer Genome Atlas molecular subtypes. Adjuvant treatment, and progression-free survival (PFS), and overall survival (OS) were analyzed. RESULTS Seventy-five patients were included. The agreement between PORTEC-1 and GOG-99 HIR classification was 68% (95% CI, 56.2 to 78.3), with a kappa of 0.36 ( P = .001). There was no agreement between PORTEC-1 or GOG-99 HIR classification and a dichotomized molecular classification (copy number-high [CN-H] v other subtypes), with a kappa of 0.03 ( P = .39) and −0.03 ( P = .601), respectively. There was no difference in PFS between PORTEC-1 HIR and non-HIR (HR, 10.9; 95% CI, 0.28 to 4.21) or between GOG-99 HIR and non-HIR (HR, 1.22; 95% CI, 0.32 to 4.6) stage I grade 3 EECs. Patients with CN-H compared with non-CN-H EEC had worse PFS (HR, 5.67; 95% CI, 1.73 to 18.63) and OS (HR, 5.05; 95% CI, 1.13 to 22.5). CONCLUSION In surgically staged patients with stage I grade 3 EEC, PORTEC-1 and GOG-99 HIR criteria were not prognostic and did not identify CN-H patients. Patients with CN-H EEC had worse PFS and OS compared with those with other molecular subtypes. The integration of the molecular classification with recognized clinicopathologic factors may identify patients with higher-risk stage I grade 3 EEC who benefit from additional therapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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