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A Nomogram to Predict Distant Metastases After Multimodality Therapy for Patients With Localized Esophageal Cancer.
Sudo, Kazuki; Wang, Xuemei; Xiao, Lianchun; Wadhwa, Roopma; Shiozaki, Hironori; Elimova, Elena; Rice, David C; Lee, Jeffrey H; Weston, Brian; Bhutani, Manoop S; Hiremath, Adarsh; Charalampakis, Nikolaos; Komaki, Ritsuko; Blum, Mariela A; Swisher, Stephen G; Maru, Dipen M; Skinner, Heath D; Garris, Jeana L; Rogers, Jane E; Hofstetter, Wayne L; Ajani, Jaffer A.
Afiliação
  • Sudo K; Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Wang X; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Xiao L; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Wadhwa R; Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Shiozaki H; Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Elimova E; Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Rice DC; Department of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Lee JH; Department of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Weston B; Department of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Bhutani MS; Department of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Hiremath A; Department of Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Charalampakis N; Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Komaki R; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Blum MA; Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Swisher SG; Department of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Maru DM; Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Skinner HD; Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Garris JL; Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Rogers JE; Department of The University of Pharmacy Clinical Programs, Texas MD Anderson Cancer Center, Houston, Texas
  • Hofstetter WL; Department of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Ajani JA; Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
J Natl Compr Canc Netw ; 14(2): 173-9, 2016 02.
Article em En | MEDLINE | ID: mdl-26850487
ABSTRACT

BACKGROUND:

Among patients with localized esophageal cancer (LEC), 35% or more develop distant metastases (DM) as first relapse, most in the first 24 months after local therapy. Implementation of novel strategies may be possible if DM can be predicted reliably. We hypothesized that clinical variables could help generate a DM nomogram. PATIENTS AND

METHODS:

Patients with LEC who completed multimodality therapy were analyzed. Various statistical methods were used, including multivariate analysis to generate a nomogram. A concordance index (c-index) was established and validated using the bootstrap method.

RESULTS:

Among 629 patients analyzed (356 trimodality/273 bimodality), 36% patients developed DM as first relapse. The median overall survival from DM was only 8.6 months (95% CI, 7.0-10.2). In a multivariate analysis, the variables associated with a higher risk for developing DM were poorly differentiated histology (hazard ratio [HR], 1.76; P<.0001), baseline T3/T4 primary (HR, 3.07; P=.0006), and baseline N+ LEC (HR, 2.01; P<.0001). Although variables associated with a lower risk for DM were age of 60 years or older (HR, 0.75; P=.04), squamous cell carcinoma (HR, 0.54; P=.013), and trimodality therapy (HR, 0.58; P=.0001), the bias-corrected c-index was 0.67 after 250 bootstrap resamples.

CONCLUSIONS:

Our nomogram identified patients with LEC who developed DM with a high probability. The model needs to be refined (tumor and blood biomarkers) and validated. This type of model will allow implementation of novel strategies in patients with LEC.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Esofágicas / Metástase Neoplásica Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Natl Compr Canc Netw Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Esofágicas / Metástase Neoplásica Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Natl Compr Canc Netw Assunto da revista: NEOPLASIAS Ano de publicação: 2016 Tipo de documento: Article