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Overall survival after definitive chemoradiotherapy for patients with esophageal cancer: a retrospective cohort study.
van der Zijden, Charlène J; Bouwman, Anna; Mostert, Bianca; Nuyttens, Joost J M E; van der Sluis, Pieter C; Spaander, Manon C W; Mens, Jan Willem M; Homs, Marjolein Y V; van Doorn, Leni; Wijnhoven, Bas P L; Lagarde, Sjoerd M.
  • van der Zijden CJ; Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Bouwman A; Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Mostert B; Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Nuyttens JJME; Department of Radiation Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • van der Sluis PC; Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Spaander MCW; Department of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Mens JWM; Department of Radiation Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Homs MYV; Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • van Doorn L; Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Wijnhoven BPL; Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Lagarde SM; Department of Surgery, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Dis Esophagus ; 2024 Jun 05.
Article en En | MEDLINE | ID: mdl-38836354
ABSTRACT
Definitive chemoradiotherapy (dCRT) is a potentially curative therapy for esophageal cancer. As indications for dCRT differ widely, it is challenging to draw conclusions on outcomes and survival. The aim of this study was to evaluate overall survival (OS) and recurrence patterns according to indications for treatment. Patients who underwent dCRT (50.4 Gy concomitant with carboplatin/paclitaxel) for esophageal cancer between 2012 and 2022 were identified. Indications for dCRT were cervical tumor, irresectable disease, unfit for surgery, and patient and/or physician preference. The primary endpoint was OS calculated with the Kaplan-Meier method. Secondary endpoints included the proportion of patients that completed the dCRT regimen, 30- and 90-day mortality, and disease recurrence. One hundred and fifty-seven patients were included (72.6% esophageal squamous cell carcinoma) with a median follow-up of 20 months (IQR 10.0-43.9). The full dCRT regimen was completed by 116 patients (73.9%). Thirty- and 90-day mortality were 2.5% and 8.3%, respectively. Median and 5-year OS for all patients were 22.9 months (95% CI 18.0-27.9) and 31.4%, respectively. The median OS per indication was 23.7 months (95% CI 6.5-40.8) for patients with cervical tumors, 10.9 months (95% 0.0-23.2) for irresectable disease, 28.2 months (95% CI 12.3-44.0) for unfit patients, and 22.9 months (95% CI 15.4-30.5) for patients' preference for dCRT (P = 0.11). Disease recurrence was observed in 74 patients (46%), located locoregionally (46%), distant (19%), or combined (35%). Patients who underwent dCRT had a 5-year OS of 31.4%, but OS differed according to indications for treatment with patients who had irresectable disease having the worst prognosis.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article