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Radiomics analysis for predicting pembrolizumab response in patients with advanced rare cancers

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 Res...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051405/
https://www.ncbi.nlm.nih.gov/pubmed/33849924
http://dx.doi.org/10.1136/jitc-2020-001752
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author 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
author_facet 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
author_sort Colen, Rivka R
collection PubMed
description 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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spelling pubmed-80514052021-04-26 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 J Immunother Cancer Clinical/Translational Cancer Immunotherapy 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. BMJ Publishing Group 2021-04-13 /pmc/articles/PMC8051405/ /pubmed/33849924 http://dx.doi.org/10.1136/jitc-2020-001752 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Clinical/Translational Cancer Immunotherapy
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
Radiomics analysis for predicting pembrolizumab response in patients with advanced rare cancers
title Radiomics analysis for predicting pembrolizumab response in patients with advanced rare cancers
title_full Radiomics analysis for predicting pembrolizumab response in patients with advanced rare cancers
title_fullStr Radiomics analysis for predicting pembrolizumab response in patients with advanced rare cancers
title_full_unstemmed Radiomics analysis for predicting pembrolizumab response in patients with advanced rare cancers
title_short Radiomics analysis for predicting pembrolizumab response in patients with advanced rare cancers
title_sort radiomics analysis for predicting pembrolizumab response in patients with advanced rare cancers
topic Clinical/Translational Cancer Immunotherapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051405/
https://www.ncbi.nlm.nih.gov/pubmed/33849924
http://dx.doi.org/10.1136/jitc-2020-001752
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