Blood cancer Awareness month
Each day throughout September, MPNRF will post a fact about MPNs on social media. The growing list will appear HERE.
The 30-day social media campaign will focus on:
- • The importance of clinical trials
- • What patients can learn about treatments currently in the clinical trial pipeline
- • How to know if you qualify
- • How to access potentially new treatments currently available only through a clinical trial
- • How researchers and practitioners can make an even greater impact on people living with an MPN by participating in or hosting a trial
Our commitment: funding the science that results in more options for people living with myeloproliferative neoplasms, the rare chronic blood cancers known as MPNs. Our investments in global, cutting edge, multi-center research have directly advanced knowledge about the causes of MPNs, while leading to the development of new treatments and improved quality of life for MPN patients.
MPN Awareness Day is September 8th
In honor of MPN Awareness Day 2022, the MPN Research Foundation proudly features a profile on Dr. Richard T. Silver, Director Emeritus, Silver MPN Center at Weill Cornell Medicine. Read HERE about his extraordinary research and clinical career, and what keeps him actively engaged in the MPN community into his 90s.
Donate to MPN research in honor of Blood Cancer Awareness Month
Table of Contents
WEEK 3 FACTS
MPNRF focuses on gaps in MPN research to better understand and treat ET, PV and MF, investing more than $16 million over the past two decades. You can be a part of the impact by making a gift toward MPN research here.
Hematology/Oncology doctors can play an important role in helping patients access new MPN treatments through clinical trials. More patients will consider enrolling in a trial if they are asked. So go ahead. Ask the question. And consider hosting a clinical trial. You don’t need to be at an academic institution. Contact MPNRF for more info: email@example.com
MPN patients can experience very different symptoms. If you or a loved one have an MPN and you are not satisfied with the information or course of treatment provided to you, consider finding a physician who sees many people with MPNs. Find a specialist here.
Ruxolitinib was approved in 2011 for myelofibrosis and has provided symptom relief for many patients. Because it isn’t enough for everyone, many current clinical trials are testing the effectiveness of drug combinations. One example is a phase 1/2 study of selinexor, a drug previously approved for multiple myeloma and lymphoma which, when combined with ruxolitinib, is showing significant reduction in spleen size and a rapid reduction in total symptom score (TSS). Read details here.
Clinical trials are not ONLY for patients seen at academic medical centers. Community-based practitioners can either refer patients to a site where a trial is offered, or they can consider hosting a trial at their institution. Clinical trials can offer better treatment options for ET, PV or MF. So communication is critically important between clinicians and their patients about potential eligibility and participation in a trial.
Research projects funded by MPNRF have led to important advances for people living with MPNs. These include discovery of the CALR mutation, understanding more about interferon and disease progression, and identifying possible new treatments. Read more about the 21-year MPN IMPACT here.
MPNRF looks at critical gaps in current MPN research that may move answers from the laboratory to the clinic, faster. The foundation plays a uniquely independent role in the MPN community, convening academia, industry, patients, advocates and regulatory agencies, ultimately to improve the lives of people living with MPNs. Hear what leading MPN specialists say about the IMPACT@21
MPN research investments in the lab lead to more MPN trials in the clinic, bringing more and better treatment options to people living with ET, PV and MF. Read how you can invest in future MPN research through planned giving. Details here.
Because symptoms can vary significantly among MPN patients, it is important to track changes in symptoms and their severity between doctor visits. Keep current on the latest MPN research updates and speak to your doctor about how changes in your symptoms may call for a change in treatment.
WEEK 2 FACTS
Current MPNs research studies and clinical trials focus on symptom relief and disease progression by understanding and targeting of biomarkers. The aim is to lead to more personalized treatments. Read here about Identifying and Validating Actionable Biomarkers in MPN
More medicines are now approved for MPNs: ruxolitinib, fedratinib and pacritinib for myelofibrosis, ruxolitinib and ropeginterferon alfa-2b for polycythemia vera. These approvals took years and the commitment of valued patients who participated in their clinical trials.
There are more clinical trials every year for people living with ET, PV or MF. Get a personalized list of trials that match your diagnosis and medical history, then share with the medical team that manages your MPN. Get started with the MPN Clinical Trial Finder
The safety and scientific validity of a clinical study are carefully considered by a study sponsor and investigators. A listed clinical study means it is being carefully evaluated by the health authorities. Along with the benefits of participating in a clinical trial, learn the potential risks. Speak to your MPN care team.
It’s a new day in MPNs – so many promising therapies, yet there is so much work to be done toward a cure. Biopharma is a partner in the fight. Thank you to our Blood Cancer Awareness Month sponsors.
An ongoing MPNRF-funded study is testing the feasibility of comparing stem cell transplantation with a non-transplant option in patients with high-risk myelofibrosis. What is unique is that participants choose the treatment they prefer, transplant or best available non-transplant treatment. Read about this work by Dr. Vikas Gupta and other recent MPN Challenge projects in the summer MPNRF Update.
Because MPNs are rare, the challenge of finding enough people with ET, PV and MF who are willing and able to participate in a clinical trial can slow new drug approvals. “My life-altering symptoms have nearly disappeared since starting a drug combination in a clinical trial. The drugs I’m on would not be available to me otherwise.” 64-yr. old MF patient. Ask your doctor what MPN trial might be a good match for you.
Your participation in a clinical trial helps advance new treatments for more patients like you. Learn more about what you need to consider and what current trials match your personal medical history and diagnosis with the MPN Clinical Trial Finder
WEEK 1 FACTS
Polycythemia vera #PV and essential thrombocythemia #ET are often found during routine bloodwork. It’s common for patients to have no symptoms or mild symptoms for years. Want to know more about these rare, chronic blood cancers? Visit MPN Research Impact And you can help increase awareness of MPN research and clinical trials by sharing our 30 FACTS About MPNs throughout September.
Bringing new treatments to MPN patients takes many years, from discovery in the lab, to pre-clinical research that tests for safety and effectiveness. Successful pre-clinical therapeutic candidates move to human clinical trials and ultimately require approval by a regulatory agency, such as the US Food and Drug Administration. Learn more here: Drug development & clinical trials . For a personalized list of MPN clinical trials that match your diagnosis click here: Trialjectory.
MPN clinical trials have gone beyond JAK inhibitors and are now looking at new targets and therapeutic pathways that will expand the universe of options for patients. This is especially promising for patients who could not tolerate JAK inhibitors or they stopped working. Read about MPNRF-funded research here: MPN Challenge.
Anemia is a major contributor to the hallmark fatigue associated with MPNs. Read about two recently reported clinical trials: how the need for phlebotomy was reduced or eliminated in polycythemia vera patients with rusfertide; and how momolottinib met the unique needs of myelofibrosis patients with enlarged spleen and anemia. 2022 ASCO Highlights
MPN research is rapidly accelerating our understanding of what causes these chronic diseases and how to treat them. While only a few MPN drug treatments are now approved, hundreds of clinical trials are underway across the globe, studying potential new and better treatment options. An MPN specialist can help you explore your eligibility to participate in one or more trials. Print and share a potential list of trials with your MPN care team here: Trialjectory.
Some 120 medicines are currently in clinical trial or awaiting approval by the US FDA for blood cancers, including for the rare MPNs essential thrombocythemia, polycythemia vera and myelofibrosis. Research and trials are gaining ground every year toward new, better treatments for MPN patients. Find out what clinical trials match your diagnosis and history here: MPN Clinical Trial Finder.
With research advancing so rapidly, many people living with an MPN find clinical trials offer a better treatment option for their disease symptoms, either after current therapies failed or were not fully effective. Talk to your doctor about MPN trials you might qualify for, then ask questions and consider your personal options.
Thank you to these generous Blood Cancer Awareness Month sponsors: