Ritchie reflects on research underway in Myeloproliferative Neoplasms
Investigators are in the midst of exploring novel therapeutic regimens for patients with myeloproliferative neoplasms (MPNs), as well as working to obtain a deeper understanding of the biology of these rare conditions.
With the FDA-approved agents available for these rare malignancies, such as interferon and ruxolitinib (Jakafi), researchers are now looking to combine these therapies with other biologic agents to improve response rates and quality of life (QOL).
Moreover, innovative single agents are being explored, including SL-401—a targeted therapy directed to the interleukin-3 receptor CD-123—which is being tested in a phase I/II trial for patients with advanced, high-risk MPNs, including systemic mastocytosis, advanced symptomatic hypereosinoophic disorder, myelofibrosis, and chronic myelomonocytic leukemia (NCT02268253).
“MPNs are rare diseases and we have a lot to learn about these diseases and, as a community oncologist, you might not see many of these diseases in a lifetime,” said Ellen K. Ritchie, M.D.
Ritchie gave a lecture on the landscape of MPNs at the 2017 OncLive® State of the Science Summit on Hematologic Malignancies. In an interview during the meeting, she highlighted the collaborations at Weill Cornell Medicine/NewYork-Presbyterian Hospital with MPN research, current and emerging novel treatments, and the possibility of using immunotherapy to treat these patients. An excerpt of her interview with OncLive is below; read the full story here.
OncLive®: Can you provide an overview of your presentation on MPNs?
Ritchie: This talk was to introduce this audience to our program at Weill Cornell Medicine. Dr Richard T. Silver—who has been at Weill Cornell Medicine forever—really piloted the use of interferon in patients with myeloproliferative diseases and we are trying to expand. We are an institution that has the longest experience in treating patients who have MPNs with interferon.
We were really excited to move into some of the newer longer-acting interferons, and combining interferon with other agents to treat [patients with] myeloproliferative diseases. We are also looking at new ways to support patients with myeloproliferative disease, including programs looking at the association of pulmonary hypertension in patients who have MPNs, as well as collaborating with our other departments at Weill Cornell Medicine—such as cardiology—to come up with better ways to recognize this problem and treat this problem in patients.
Young patients actually get these diseases [too] and we have patients on medications that affect their fertility, so I am working with our Department of Urology looking at male infertility in particular and how we can allow young patients with these diseases to have families, go forward, and not interrupt their treatment too much. That is another exciting area that we are delving into.
With our gastrointestinal (GI) group, we are looking at a connection between patients with inflammatory bowel diseases and myeloproliferative disorders, and we are excited doing exploratory work in this particular area. We are interested in looking at new drugs to treat these diseases; our leukemia group is really exploring the use of immunotherapy in treatment of patients with acute myeloid leukemia. We are hoping to piggyback on that and look at some of these immunotherapies in myeloproliferative diseases, as well.
We are very lucky that we are in a major medical center in Manhattan, so for a disease that affects many different organs and organ systems, we have excellent teams of cardiology, urology, GI, and leukemia experts to collaborate with to help these patients through all phases of disease and support them.
Are there any known risk factors for MPNs?
No, it is really hard to say. There probably are genetic risk factors. That is something that, as we learn more about the different genes—which are involved in myeloid diseases and we start to look at families—we are going to see more of these genetic risk factors for these diseases. Certainly, modern life exposes us to a lot of things, and what the relationship of these exposures are to the development of cancer [is something that] we still are sorting out.