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Radiomics analysis for predicting pembrolizumab response in patients with advanced rare cancers.
Colen, Rivka R; Rolfo, Christian; Ak, Murat; Ayoub, Mira; Ahmed, Sara; Elshafeey, Nabil; Mamindla, Priyadarshini; Zinn, Pascal O; Ng, Chaan; Vikram, Raghu; Bakas, Spyridon; Peterson, Christine B; Rodon Ahnert, Jordi; Subbiah, Vivek; Karp, Daniel D; Stephen, Bettzy; Hajjar, Joud; Naing, Aung.
Afiliação
  • Colen RR; Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA anaing@mdanderson.org colenrr@upmc.edu.
  • Rolfo C; Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
  • Ak M; Department of Thoracic Medical Oncology, University of Maryland, Baltimore, Maryland, USA.
  • Ayoub M; Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Ahmed S; Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
  • Elshafeey N; Department of Radiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Mamindla P; Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
  • Zinn PO; Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Ng C; Department of Breast Imaging, Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Vikram R; Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
  • Bakas S; Department of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
  • Peterson CB; Abdominal Imaging Department, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Rodon Ahnert J; Abdominal Imaging Department, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Subbiah V; Radiology, Pathology, and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Karp DD; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Stephen B; Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Hajjar J; Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Naing A; Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
J Immunother Cancer ; 9(4)2021 04.
Article em En | MEDLINE | ID: mdl-33849924
ABSTRACT

BACKGROUND:

We present a radiomics-based model for predicting response to pembrolizumab in patients with advanced rare cancers.

METHODS:

The study included 57 patients with advanced rare cancers who were enrolled in our phase II clinical trial of pembrolizumab. Tumor response was evaluated using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 and immune-related RECIST (irRECIST). Patients were categorized as 20 "controlled disease" (stable disease, partial response, or complete response) or 37 progressive disease). We used 3D-slicer to segment target lesions on standard-of-care, pretreatment contrast enhanced CT scans. We extracted 610 features (10 histogram-based features and 600 second-order texture features) from each volume of interest. Least absolute shrinkage and selection operator logistic regression was used to detect the most discriminatory features. Selected features were used to create a classification model, using XGBoost, for the prediction of tumor response to pembrolizumab. Leave-one-out cross-validation was performed to assess model performance.

FINDINGS:

The 10 most relevant radiomics features were selected; XGBoost-based classification successfully differentiated between controlled disease (complete response, partial response, stable disease) and progressive disease with high accuracy, sensitivity, and specificity in patients assessed by RECIST (94.7%, 97.3%, and 90%, respectively; p<0.001) and in patients assessed by irRECIST (94.7%, 93.9%, and 95.8%, respectively; p<0.001). Additionally, the common features of the RECIST and irRECIST groups also highly predicted pembrolizumab response with accuracy, sensitivity, specificity, and p value of 94.7%, 97%, 90%, p<0.001% and 96%, 96%, 95%, p<0.001, respectively.

CONCLUSION:

Our radiomics-based signature identified imaging differences that predicted pembrolizumab response in patients with advanced rare cancer.

INTERPRETATION:

Our radiomics-based signature identified imaging differences that predicted pembrolizumab response in patients with advanced rare cancer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Interpretação de Imagem Radiográfica Assistida por Computador / Tomografia Computadorizada por Raios X / Doenças Raras / Anticorpos Monoclonais Humanizados / Antineoplásicos Imunológicos / Inibidores de Checkpoint Imunológico / Neoplasias Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Interpretação de Imagem Radiográfica Assistida por Computador / Tomografia Computadorizada por Raios X / Doenças Raras / Anticorpos Monoclonais Humanizados / Antineoplásicos Imunológicos / Inibidores de Checkpoint Imunológico / Neoplasias Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article