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Role of adjuvant therapy in intermediate-risk cervical cancer patients – Subanalyses of the SCCAN study

  • David Cibula*
  • , Huseyin Akilli
  • , Jiri Jarkovsky
  • , Luc van Lonkhuijzen
  • , Giovanni Scambia
  • , Mehmet Mutlu Meydanli
  • , David Isla Ortiz
  • , Henrik Falconer
  • , Nadeem R. Abu-Rustum
  • , Diego Odetto
  • , Jaroslav Klát
  • , Ricardo dos Reis
  • , Ignacio Zapardiel
  • , Giampaolo di Martino
  • , Jiri Presl
  • , Rene Laky
  • , Aldo López
  • , Vit Weinberger
  • , Andreas Obermair
  • , Rene Pareja
  • Renata Poncová, Constantijne Mom, Nicolò Bizzarri, Martina Borčinová, Koray Aslan, Rosa Angélica Salcedo Hernandez, Guus Fons, Klára Benešová, Lukáš Dostálek, Ali Ayhan
*Corresponding author for this work
  • Charles University
  • Baskent University
  • Masaryk University
  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS
  • University of Health Sciences
  • Gynecology Oncology Center, National Institute of Cancerology Mexico, Mexico
  • Karolinska Institutet
  • Memorial Sloan-Kettering Cancer Center
  • Hospital Italiano de Buenos Aires
  • University of Ostrava
  • Hospital de Câncer de Barretos
  • Universidad Autónoma de Madrid
  • University of Milan - Bicocca
  • Medical University of Graz
  • Instituto Nacional de Enfermedades Neoplásicas
  • University of Queensland
  • Instituto Nacional De Cancerologia, Bogotá, Colombia
  • Amsterdam UMC - University of Amsterdam
  • Amsterdam University Medical Centers
  • National Institute of Cancerology Mexico
  • Karolinska University Hospital
  • Instituto Nacional de Cancerología

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Objective: The “intermediate-risk” (IR) group of early-stage cervical cancer patients is characterized by negative pelvic lymph nodes and a combination of tumor-related prognostic risk factors such as tumor size ≥2 cm, lymphovascular space invasion (LVSI), and deep stromal invasion. However, the role of adjuvant treatment in these patients remains controversial. We investigated whether adjuvant (chemo)radiation is associated with a survival benefit after radical surgery in patients with IR cervical cancer. Methods: We analyzed data from patients with IR cervical cancer (tumor size 2–4 cm plus LVSI OR tumor size >4 cm; N0; no parametrial invasion; clear surgical margins) who underwent primary curative-intent surgery between 2007 and 2016 and were retrospectively registered in the international multicenter Surveillance in Cervical CANcer (SCCAN) study. Results: Of 692 analyzed patients, 274 (39.6%) received no adjuvant treatment (AT−) and 418 (60.4%) received radiotherapy or chemoradiotherapy (AT+). The 5-year disease-free survival (83.2% and 80.3%; PDFS = 0.365) and overall survival (88.7% and 89.0%; POS = 0.281) were not significantly different between the AT− and AT+ groups, respectively. Adjuvant (chemo)radiotherapy was not associated with a survival benefit after adjusting for confounding factors by case-control propensity score matching or in subgroup analyses of patients with tumor size ≥4 cm and <4 cm. In univariable analysis, adjuvant (chemo)radiotherapy was not identified as a prognostic factor in any of the subgroups (full cohort: PDFS = 0.365; POS = 0.282). Conclusion: Among patients with IR early-stage cervical cancer, radical surgery alone achieved equal disease-free and overall survival rates to those achieved by combining radical surgery with adjuvant (chemo)radiotherapy.

Original languageEnglish
Pages (from-to)195-202
Number of pages8
JournalGynecologic oncology
Volume170
DOIs
Publication statusPublished - 1 Mar 2023

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adjuvant treatment
  • Cervical cancer
  • GOG criteria
  • Intermediate risk
  • Radial surgery
  • Radiotherapy

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