Determining therapeutic susceptibility in multiple myeloma by single-cell mass accumulation

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作者
Arif E. Cetin
Mark M. Stevens
Nicholas L. Calistri
Mariateresa Fulciniti
Selim Olcum
Robert J. Kimmerling
Nikhil C. Munshi
Scott R. Manalis
机构
[1] Massachusetts Institute of Technology,Koch Institute for Integrative Cancer Research
[2] Harvard Medical School,Department of Medical Oncology, Dana
[3] Dana-Farber Cancer Institute,Farber Cancer Institute
[4] Harvard Medical School,Jerome Lipper Multiple Myeloma Center, Department of Medical Oncology
[5] Massachusetts Institute of Technology,Veterans Affairs Boston Healthcare System
[6] Massachusetts Institute of Technology,Department of Biological Engineering
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Nature Communications | / 8卷
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摘要
Multiple myeloma (MM) has benefited from significant advancements in treatment that have improved outcomes and reduced morbidity. However, the disease remains incurable and is characterized by high rates of drug resistance and relapse. Consequently, methods to select the most efficacious therapy are of great interest. Here we utilize a functional assay to assess the ex vivo drug sensitivity of single multiple myeloma cells based on measuring their mass accumulation rate (MAR). We show that MAR accurately and rapidly defines therapeutic susceptibility across human multiple myeloma cell lines to a gamut of standard-of-care therapies. Finally, we demonstrate that our MAR assay, without the need for extended culture ex vivo, correctly defines the response of nine patients to standard-of-care drugs according to their clinical diagnoses. This data highlights the MAR assay in both research and clinical applications as a promising tool for predicting therapeutic response using clinical samples.
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