Adjuvant therapy for grade 3, deeply invasive endometrioid adenocarcinoma of the uterus Journal Article


Authors: Onstad, M.; Ducie, J.; Fellman, B. M.; Abu-Rustum, N. R.; Leitao, M.; Mariani, A.; Multinu, F.; Lu, K. H.; Soliman, P.
Article Title: Adjuvant therapy for grade 3, deeply invasive endometrioid adenocarcinoma of the uterus
Abstract: Background Patients with grade 3, deeply invasive endometrioid adenocarcinoma are typically managed with primary surgery. The role and type of adjuvant therapy used is controversial. We sought to evaluate the role of adjuvant radiation and/or chemotherapy in women with deeply invasive grade 3 endometrioid tumors. Methods A multi-center retrospective chart review was performed at three large medical institutions in the United States. Patients with grade 3 endometrioid adenocarcinoma invading >50% of the myometrium were included. Medical records were queried to evaluate whether lymph node assessment was performed, the status of the lymph nodes, adjuvant treatment strategy used, and dates of death or recurrence. Results Between 1984 and 2013, 257 patients were identified with a median follow-up of 3.08 years. Most patients (84.7%) had evaluation of pelvic and/or para-aortic lymph nodes and 43% had positive lymph nodes. For node negative patients, there was no difference in overall survival (OS) between those who received adjuvant pelvic radiation +/-vaginal brachytherapy (n=52) vs brachytherapy alone (n=46) (5-year probabilities were 0.73 vs 0.70, P=0.729). Among patients with positive lymph nodes (n=92), the adjuvant treatment strategy utilized impacted OS, with women undergoing a combination of chemotherapy and external beam radiation having the best outcomes (P=0.003). Conclusions Among women with grade 3, deeply invasive endometrioid adenocarcinoma, vaginal cuff brachytherapy alone resulted in similar survival when compared with pelvic radiation in node negative patients. The combination of chemotherapy with external beam radiation was associated with improved OS for women with positive nodes. © 2020 IGCS and ESGO. No commercial re-use. See rights and permissions. Published by BMJ.
Keywords: immunohistochemistry; human tissue; protein expression; aged; unclassified drug; gene mutation; major clinical study; exon; cancer patient; endometrial neoplasms; lymph nodes; radiotherapy; epidermal growth factor receptor 2; protein; cohort analysis; genetic variation; pathology; brca2 protein; retrospective study; in situ hybridization; mismatch repair; microsatellite instability; phosphatidylinositol 3,4,5 trisphosphate 3 phosphatase; atm protein; dna sequence; estrogen receptor; progesterone receptor; k ras protein; fibroblast growth factor receptor 2; uterus carcinoma; carcinosarcoma; protein kinase b beta; uterine carcinosarcoma; high throughput sequencing; human; female; priority journal; article; rna sequencing; nf1 protein; rb1 protein; mutational load; pik3ca protein; kmt2d protein; f box/wd repeat containing protein 7; molecular fingerprinting; kmt2c protein; ccne1 protein; dicer1 protein; ppp2r1a protein; top2a protein; ts protein; tubb3 protein
Journal Title: International Journal of Gynecological Cancer
Volume: 30
Issue: 4
ISSN: 1048-891X
Publisher: Lippincott Williams & Wilkins  
Date Published: 2020-04-01
Start Page: 485
End Page: 490
Language: English
DOI: 10.1136/ijgc-2019-000807
PUBMED: 31980487
PROVIDER: scopus
PMCID: PMC8270113
DOI/URL:
Notes: Article -- Export Date: 1 June 2020 -- Source: Scopus
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  1. Mario Leitao
    575 Leitao
  2. Jennifer A Ducie
    18 Ducie