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Complete pathologic response in esophageal adenocarcinoma: does it make a difference?
Donato, Britton B; Campany, Megan E; Brady, Justin T; Jenkins, J Asher; Armstrong, Valerie; Butterfield, Richard; Reck Dos Santos, Pedro; D'Cunha, Jonathan.
Afiliación
  • Donato BB; Department of Surgery, Mayo Clinic, Phoenix, AZ, USA.
  • Campany ME; Division of Cardiothoracic Surgery, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Brady JT; Mayo Clinic Alix School of Medicine, Mayo Clinic, Scottsdale AZ, USA.
  • Jenkins JA; Department of Colorectal Surgery, Mayo Clinic, Phoenix, AZ, USA.
  • Armstrong V; Department of Surgery, Mayo Clinic, Phoenix, AZ, USA.
  • Butterfield R; Department of Surgery, Mayo Clinic, Phoenix, AZ, USA.
  • Reck Dos Santos P; Department of Quantitative Health Sciences, Mayo Clinic, Phoenix, AZ, USA.
  • D'Cunha J; Department of Cardiothoracic Surgery, Mayo Clinic, Phoenix, AZ, USA.
Dis Esophagus ; 2024 Aug 22.
Article en En | MEDLINE | ID: mdl-39169845
ABSTRACT
Advancements in neoadjuvant regimens for esophageal adenocarcinoma have enabled some patients to achieve complete pathologic response at time of esophagectomy. There are currently limited data detailing this trend or the implications of complete pathologic response on survival. The National Cancer Database was used to identify 16,169 patients with esophageal adenocarcinoma that received trimodal therapy including esophagectomy between 2006 and 2020. Of these, 11.4% had complete pathologic response at esophagectomy. Patient factors, staging characteristics, and survival trends were evaluated. In patients diagnosed between 2016 and 2020, the rate of complete pathologic response was 17.5%. Female sex (OR 1.295, 95% CI 1.134-1.481, p = 0.0001), Black race (OR 1.729, 95% CI 1.362-2.196, p = 0.0002), Hispanic ethnicity (OR 1.418, 95% CI 1.073-1.875, p = 0.0141), and later era of diagnosis (2016-2020 OR 2.898, 95% CI 2.508-3.349, p < 0.0001) were independent predictors of complete pathologic response. Clinical stage II disease was associated with an increased probability of complete pathologic response (OR 1.492, 95% CI 1.19-1.871) while clinical stage III disease had a decreased probability of complete pathologic response (OR 0.762, 95% CI 0.621-0.936, p < 0.0001). Complete pathologic response conveyed a strong survival benefit, with a median survival of 86.4 months (95% CI 73.9-102.1) versus 30.7 months (95% CI 29.8-31.7, p < 0.0001) in those without complete pathologic response. Four-year median survival was also higher in those with complete pathologic response (63.3%, 95% CI 60.8-66.0% vs. 39.2%, 95% CI 38.4-40.1%, p < 0.0001). In summary, complete pathologic response is associated with a profound survival advantage in patients with esophageal adenocarcinoma. Such knowledge carries implications for patient counseling, prognostication, and surveillance and demonstrates a need for improved identification of complete clinical response prior to esophagectomy.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Dis Esophagus Asunto de la revista: GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Dis Esophagus Asunto de la revista: GASTROENTEROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos