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Use of Machine-Learning Algorithms in Intensified Preoperative Therapy of Pancreatic Cancer to Predict Individual Risk of Relapse.
Sala Elarre, Pablo; Oyaga-Iriarte, Esther; Yu, Kenneth H; Baudin, Vicky; Arbea Moreno, Leire; Carranza, Omar; Chopitea Ortega, Ana; Ponz-Sarvise, Mariano; Mejías Sosa, Luis D; Rotellar Sastre, Fernando; Larrea Leoz, Blanca; Iragorri Barberena, Yohana; Subtil Iñigo, Jose C; Benito Boíllos, Alberto; Pardo, Fernando; Rodríguez Rodríguez, Javier.
Affiliation
  • Sala Elarre P; Department of Medical Oncology, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. psala@unav.es.
  • Oyaga-Iriarte E; Department of Mathematics and Statistics, Pharmamodelling, Noain, 31110 Navarra, Spain. eoyaga@pharmamodelling.es.
  • Yu KH; Gastrointestinal Oncology Service, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. YuK1@mskcc.org.
  • Baudin V; Weill Cornell Medical College, New York, NY 10065, USA. YuK1@mskcc.org.
  • Arbea Moreno L; Human Oncology and Pathogenesis Program, Collaborative Research Centers, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. baudinv@mskcc.org.
  • Carranza O; Department of Radiation Oncology, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. larbea@unav.es.
  • Chopitea Ortega A; Department of Medical Oncology, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. ocarranza@hotmail.com.
  • Ponz-Sarvise M; Department of Medical Oncology, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. chopitea@unav.es.
  • Mejías Sosa LD; Department of Medical Oncology, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. mponz@unav.es.
  • Rotellar Sastre F; Department of Pathology, Hospital Universitario Rey Juan Carlos, Móstoles, 28933 Madrid, Spain. luis.mejiass@hospitalreyjuancarlos.es.
  • Larrea Leoz B; Department of HPB Surgery, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. frotellar@unav.es.
  • Iragorri Barberena Y; Department of HPB Surgery, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. blarreal@unav.es.
  • Subtil Iñigo JC; Department of Medical Oncology, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. yiragorri@unav.es.
  • Benito Boíllos A; Department of Gastroenterology, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. jcsubtil@unav.es.
  • Pardo F; Department of Radiology, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. albenitob@unav.es.
  • Rodríguez Rodríguez J; Department of HPB Surgery, Clínica Universidad de Navarra, Pamplona, 31008 Navarra, Spain. fpardo@unav.es.
Cancers (Basel) ; 11(5)2019 Apr 30.
Article in En | MEDLINE | ID: mdl-31052270
ABSTRACT

BACKGROUND:

Although surgical resection is the only potentially curative treatment for pancreatic cancer (PC), long-term outcomes of this treatment remain poor. The aim of this study is to describe the feasibility of a neoadjuvant treatment with induction polychemotherapy (IPCT) followed by chemoradiation (CRT) in resectable PC, and to develop a machine-learning algorithm to predict risk of relapse.

METHODS:

Forty patients with resectable PC treated in our institution with IPCT (based on mFOLFOXIRI, GEMOX or GEMOXEL) followed by CRT (50 Gy and concurrent Capecitabine) were retrospectively analyzed. Additionally, clinical, pathological and analytical data were collected in order to perform a 2-year relapse-risk predictive population model using machine-learning techniques.

RESULTS:

A R0 resection was achieved in 90% of the patients. After a median follow-up of 33.5 months, median progression-free survival (PFS) was 18 months and median overall survival (OS) was 39 months. The 3 and 5-year actuarial PFS were 43.8% and 32.3%, respectively. The 3 and 5-year actuarial OS were 51.5% and 34.8%, respectively. Forty-percent of grade 3-4 IPCT toxicity, and 29.7% of grade 3 CRT toxicity were reported. Considering the use of granulocyte colony-stimulating factors, the number of resected lymph nodes, the presence of perineural invasion and the surgical margin status, a logistic regression algorithm predicted the individual 2-year relapse-risk with an accuracy of 0.71 (95% confidence interval [CI] 0.56-0.84, p = 0.005). The model-predicted outcome matched 64% of the observed outcomes in an external dataset.

CONCLUSION:

An intensified multimodal neoadjuvant approach (IPCT + CRT) in resectable PC is feasible, with an encouraging long-term outcome. Machine-learning algorithms might be a useful tool to predict individual risk of relapse. A small sample size and therapy heterogeneity remain as potential limitations.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Cancers (Basel) Year: 2019 Document type: Article Affiliation country: Spain

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Cancers (Basel) Year: 2019 Document type: Article Affiliation country: Spain