Tailoring postoperative management through sentinel lymph node biopsy in low- and intermediate-risk endometrial cancer - the SENTRY clinical trial

Klin Onkol. 2024;38(2):126-133. doi: 10.48095/ccko2024126.

Abstract

Background: While total hysterectomy and bilateral salpingo-oophorectomy without lymph node staging are standard for low- and intermediate-risk endometrial cancer, certain histopathologic factors revealed after surgery can necessitate additional interventions. Our study assessed the influence of sentinel lymph node biopsy on postoperative decision-making.

Materials and methods: In the SENTRY trial (July 2021 - February 2023), we enrolled patients with International Federation of Gynaecology and Obstetrics (FIGO) stage IA-IB low-grade endometrioid endometrial cancer. Laparoscopic sentinel lymph node mapping using indocyanine green was performed alongside total hysterectomy with bilateral salpingo-oophorectomy. Subsequent management changes based on sentinel lymph node biopsy results were evaluated. The trial was registered at ClinicalTrials.gov (NCT04972682).

Results: Of the 100 enrolled participants, a bilateral detection rate of 91% was observed with a median detection time of 10 min (interquartile range 8-13 min). Sentinel lymph node metastases were found in 8% (N = 8) of participants. Postoperative FIGO staging increased in 15% (N = 15) and decreased in 5% (N = 5) of patients. Sentinel lymph node biopsy results altered the adjuvant treatment plan for 20% (N = 20): external beam radiotherapy was omitted in 12% (N = 12) while 6% (N = 6) had external beam radiotherapy +/- systemic chemotherapy added due to sentinel lymph node metastases. In 2% (N = 2), the external beam radiotherapy field was expanded with the paraaortic region. No intraoperative complications were reported and no 30-day major morbidity and mortality occurred. Throughout a median follow-up of 14 (95% CI 12-15 months, neither patient-reported lymphedema nor pelvic recurrence surfaced in the cohort.

Conclusions: Sentinel lymph node biopsy using indocyanine green is a safe procedure and allows tailoring adjuvant therapy in presumed low- and intermediate-risk endometrial cancer. It assists in avoiding external beam radiotherapy overtreatment and introducing additional modalities when necessary.

Keywords: Drug therapy; Hysterectomy; Uterine cancer; adjuvant treatment; gynecological cancer; indocyanine green; radiotherapy; sentinel lymph node.

Publication types

  • Clinical Trial

MeSH terms

  • Aged
  • Carcinoma, Endometrioid / pathology
  • Carcinoma, Endometrioid / surgery
  • Carcinoma, Endometrioid / therapy
  • Endometrial Neoplasms* / pathology
  • Endometrial Neoplasms* / surgery
  • Endometrial Neoplasms* / therapy
  • Female
  • Humans
  • Hysterectomy
  • Indocyanine Green
  • Laparoscopy
  • Lymphatic Metastasis
  • Middle Aged
  • Neoplasm Staging
  • Postoperative Care
  • Salpingo-oophorectomy
  • Sentinel Lymph Node Biopsy*

Substances

  • Indocyanine Green

Associated data

  • ClinicalTrials.gov/NCT04972682