Precision Medicine for Relapsed Multiple Myeloma on the Basis of an Integrative Multiomics Approach

被引:21
|
作者
Lagana, Alessandro [1 ]
Beno, Itai [1 ]
Melnekoff, David [1 ]
Leshchenko, Violetta [1 ]
Madduri, Deepu [1 ]
Ramdas, Dennis [1 ]
Sanchez, Larysa [1 ]
Niglio, Scot [1 ]
Perumal, Deepak [1 ]
Kidd, Brian A. [1 ]
Miotto, Riccardo [1 ]
Shaknovich, Rita [2 ]
Chari, Ajai [1 ]
Cho, Hearn Jay [1 ]
Barlogie, Bart [1 ]
Jagannath, Sundar [1 ]
Dudley, Joel T. [1 ]
Parekh, Samir [1 ]
机构
[1] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[2] Canc Genet, Rutherford, NJ USA
基金
美国国家卫生研究院;
关键词
CLONAL HETEROGENEITY; TARGETED THERAPY; VENETOCLAX; EFFICACY;
D O I
10.1200/PO.18.00019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Multiple myeloma (MM) is a malignancy of plasma cells, with a median survival of 6 years. Despite recent therapeutic advancements, relapse remains mostly inevitable, and the disease is fatal in the majority of patients. A major challenge in the treatment of patients with relapsed MM is the timely identification of treatment options in a personalized manner. Current approaches in precision oncology aim at matching specific DNA mutations to drugs, but incorporation of genome-wide RNA profiles has not yet been clinically assessed. Methods We have developed a novel computational platform for precision medicine of relapsed and/or refractory MM on the basis of DNA and RNA sequencing. Our approach expands on the traditional DNA-based approaches by integrating somatic mutations and copy number alterations with RNA-based drug repurposing and pathway analysis. We tested our approach in a pilot precision medicine clinical trial with 64 patients with relapsed and/or refractory MM. Results We generated treatment recommendations in 63 of 64 patients. Twenty-six patients had treatment implemented, and 21 were assessable. Of these, 11 received a drug that was based on RNA findings, eight received a drug that was based on DNA, and two received a drug that was based on both RNA and DNA. Sixteen of the 21 evaluable patients had a clinical response (ie, reduction of disease marker 25%), giving a clinical benefit rate of 76% and an overall response rate of 66%, with five patients having ongoing responses at the end of the trial. The median duration of response was 131 days. Conclusion Our results show that a comprehensive sequencing approach can identify viable options in patients with relapsed and/or refractory myeloma, and they represent proof of principle of how RNA sequencing can contribute beyond DNA mutation analysis to the development of a reliable drug recommendation tool. (C) 2018 by American Society of Clinical Oncology
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页码:1 / 17
页数:16
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