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

Biswanath Majumder(Mitra Biotech (India)), Ulaganathan Baraneedharan(Mitra Biotech (India)), Saravanan Thiyagarajan(Mitra Biotech (India)), Padhma Radhakrishnan(Mitra Biotech (India)), Harikrishna Narasimhan(Indian Institute of Science Bangalore), Muthu Dhandapani(Mitra Biotech (India)), Nilesh Brijwani(Mitra Biotech (India)), Dency D. Pinto(Mitra Biotech (India)), Arun Prasath(Mitra Biotech (India)), Basavaraja Shanthappa(Mitra Biotech (India)), Allen Thayakumar(Mitra Biotech (India)), Rajagopalan Surendran(Stanley Medical College), Govind K Babu(Kidwai Memorial Institute of Oncology), Ashok M. Shenoy(Kidwai Memorial Institute of Oncology), Moni Abraham Kuriakose(Mazumdar Shaw Medical Foundation), Guillaume Bergthold(Broad Institute), Peleg Horowitz(Broad Institute), Massimo Loda(Broad Institute), Rameen Beroukhim(Brigham and Women's Hospital), Shivani Agarwal(Indian Institute of Science Bangalore), Shiladitya Sengupta(Brigham and Women's Hospital), Mallikarjun Sundaram(Mitra Biotech (India)), Pradip K. Majumder(Mitra Biotech (India))
Nature Communications
February 27, 2015
Cited by 307Open Access
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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.


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