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ASH 2018: Determining Multiple Myeloma Risk and Survival Rates
ASH 2018: Determining Multiple Myeloma Risk and Survival Rates image
ASH 2018: Determining Multiple Myeloma Risk and Survival Rates
Posted Dec 05, 2018

A need exists to further stratify myeloma patients according to genetic and blood signatures in order to better predict patient survival rates, according to Dr. Dirk Hose (Hoe-zeh), from the University of Heidelberg, Germany, at the annual ASH meeting in San Diego on Sunday, December 2.

Hose led off six lectures on possible biological measurements to use genetic information to better classify treatment response and survival among patients who share the same molecular characteristics.

The Heidelberg study compared patients who had various kinds of induction therapy, but all shared an exposure to bortezomib (Velcade) at some point in their therapy.  Future studies may stratify patients more specifically.

Hose noted the various national, study group, or institutional standards used to determine high and standard-risk patient classifications do not agree on a set of standards, making it more difficult to create a reliable and treatment-determining prognosis that doctors and patients can use.

Because myeloma is highly heterogenous—i.e., with very different features from person to person—it makes the homogeneous categories of standard- and high-risk confusing to patients and physicians alike.

In her talk on drug resistance in myeloma, Dr. Larissa Haertle, from the University of Würzburg, Germany, noted that more studies were looking at the role that specific genes contribute to drug resistance against protease inhibiters and iMiDs.  Her remarks echoed those of Dr. Ceri Bygrave, from the University Hospital of Wales in Cardiff, on Saturday, December 1, who noted that early relapse can become an agreed-upon marker of high-risk disease.

Dr. Bygrave noted that the plasma cell “creates a lot of diseases” and noted that the ability to differentiate among genetic characteristics of patients is fertile ground for future research to inform practicing clinicians.

Dr. Benjamin Barwick of the Winship Cancer Institute at Emory University reported on a study that found a correlation between Igl translocations and resistance to iMiDs that led to poorer outcomes.

All agreed it was important to reassess individual genetic information after a treatment cycle since the overwhelming findings of research have confirmed that myeloma’s genetic features change with each treatment cycle.

Dr. Hose’s study found that a standard approach to risk assessment, even if it pointed to high-risk disease, would aid physicians to get the most effective treatments to patients more efficiently.  This might also lessen potential drug resistance.

The author Greg Brozeit

about the author
Greg Brozeit

Greg Brozeit has been engaged in myeloma patient advocacy since 1998. He began working with the Myeloma Crowd in 2015. Prior to that, he consulted with Dr. Bart Barlogie at the University of Arkansas after working with the International Myeloma Foundation for 15 years, where he inaugurated the public policy advocacy program, patient support group outreach and IMF Europe, organizing more than 100 physician and patient education programs. He earned his BA in political science from Loyola University in New Orleans and lives in northeast Ohio.

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