Abstract

BackgroundThe aim of the present study was to investigate the long-term survival outcomes and toxicities associated with our experienced early administration of adjuvant concurrent chemoradiotherapy (CCRT).MethodsNinety-eight patients with pelvic lymph node metastasis, positive resection margin, and/or parametrial invasion who received adjuvant CCRT between 1995 and 2011 were analyzed retrospectively. The first cycle of platinum-based adjuvant chemotherapy was initiated within 2–3 weeks after surgery (median, 12 days) and continued every 4 weeks for a total of 4 cycles. Adjuvant radiotherapy was performed during the second and third cycles of chemotherapy.ResultsAfter a median follow-up period of 119 months for survivors, 13 patients (13.3%) experienced recurrence and 11 patients died of cancer during the follow-up period. The 5-year recurrence-free survival and cancer specific survival rates were 87.6% and 90.6%, respectively. Ninety-four patients (95.9%) received ≥3 cycles of chemotherapy. Total radiation dose of ≥45 Gy was delivered in 91 patients (92.9%). Grade 3–4 hematologic and gastrointestinal toxicities developed in 37 (37.8%) and 14 (14.3%) patients during CCRT, respectively.ConclusionThe present study confirmed the long-term safety and encouraging survival outcomes of early administration of adjuvant CCRT, suggesting the benefits of early time to initiation of adjuvant treatments.

Highlights

  • The aim of the present study was to investigate the long-term survival outcomes and toxicities associated with our experienced early administration of adjuvant concurrent chemoradiotherapy (CCRT)

  • We previously reported the feasibility and promising results of the early administration of adjuvant CCRT, with a 5-year progression-free survival rate of 88.7% and a 5-yearoverall survival rate of 96.7% [24]

  • We reported the long-term outcomes and toxicities associated with the early administration of adjuvant CCRT for high-risk, early stage uterine cervical cancer

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Summary

Introduction

The aim of the present study was to investigate the long-term survival outcomes and toxicities associated with our experienced early administration of adjuvant concurrent chemoradiotherapy (CCRT). The primary treatment for International Federation of Gynecology and Obstetrics (FIGO) stage IA2–IIA uterine cervical cancer is either radical hysterectomy or external beam radiotherapy with or without concurrent platinum-based chemotherapy [1] Both treatment modalities have similar survival rates, radical hysterectomy is preferred in some young patients because of thorough evaluation of pelvic lymph nodes, prevention of premature and avoidance of radiation-induced late toxicities. Kim et al BMC Cancer (2017) 17:297 between adjuvant radiotherapy alone and adjuvant concurrent chemoradiotherapy (CCRT) in high-risk, early stage uterine cervical cancer patients [13] This trial (GOG 109/SWOG 8797/RTOG 91–12) demonstrated the beneficial effects of the concomitant administration of platinum-based chemotherapy on the survival rates, as well as the disadvantage of increased treatmentrelated toxicities

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