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Predicting clinical response to anticancer drugs using an ex vivo platform that captures tumour heterogeneity

Authors :
Harvard University--MIT Division of Health Sciences and Technology
Sengupta, Shiladitya
Majumder, Biswanath
Baraneedharan, Ulaganathan
Thiyagarajan, Saravanan
Radhakrishnan, Padhma
Narasimhan, Harikrishna
Dhandapani, Muthu
Brijwani, Nilesh
Pinto, Dency D.
Prasath, Arun
Shanthappa, Basavaraja U.
Thayakumar, Allen
Surendran, Rajagopalan
Babu, Govind K.
Shenoy, Ashok M.
Kuriakose, Moni A.
Bergthold, Guillaume
Horowitz, Peleg
Loda, Massimo
Beroukhim, Rameen
Agarwal, Shivani
Sundaram, Mallikarjun
Majumder, Pradip K.
Harvard University--MIT Division of Health Sciences and Technology
Sengupta, Shiladitya
Majumder, Biswanath
Baraneedharan, Ulaganathan
Thiyagarajan, Saravanan
Radhakrishnan, Padhma
Narasimhan, Harikrishna
Dhandapani, Muthu
Brijwani, Nilesh
Pinto, Dency D.
Prasath, Arun
Shanthappa, Basavaraja U.
Thayakumar, Allen
Surendran, Rajagopalan
Babu, Govind K.
Shenoy, Ashok M.
Kuriakose, Moni A.
Bergthold, Guillaume
Horowitz, Peleg
Loda, Massimo
Beroukhim, Rameen
Agarwal, Shivani
Sundaram, Mallikarjun
Majumder, Pradip K.
Source :
Nature Publishing Group
Publication Year :
2015

Abstract

Predicting clinical response to anticancer drugs remains a major challenge in cancer treatment. Emerging reports indicate that the tumour microenvironment and heterogeneity can limit the predictive power of current biomarker-guided strategies for chemotherapy. Here we report the engineering of personalized tumour ecosystems that contextually conserve the tumour heterogeneity, and phenocopy the tumour microenvironment using tumour explants maintained in defined tumour grade-matched matrix support and autologous patient serum. The functional response of tumour ecosystems, engineered from 109 patients, to anticancer drugs, together with the corresponding clinical outcomes, is used to train a machine learning algorithm; the learned model is then applied to predict the clinical response in an independent validation group of 55 patients, where we achieve 100% sensitivity in predictions while keeping specificity in a desired high range. The tumour ecosystem and algorithm, together termed the CANScript technology, can emerge as a powerful platform for enabling personalized medicine.

Details

Database :
OAIster
Journal :
Nature Publishing Group
Notes :
application/pdf, en_US
Publication Type :
Electronic Resource
Accession number :
edsoai.on1141892397
Document Type :
Electronic Resource