Low cost arthritis drug can effectively treat blood cancer sufferers

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A simple arthritis drug could be an effective, low cost solution to treat patients with blood cancers such as polycythemia vera and essential thrombocythemia), a breakthrough study from the universities of Sheffield , Oxford and Cambridge has shown.

Led by Dr Martin Zeidler, from the University of Sheffield's department of biomedical science and Dr Sebastian Francis from the department of haematology at the Royal Hallamshire Hospital, as well as the Universities of Oxford and Cambridge, the study results show that methotrexate (MTX) – a drug on the World Health Organisation list of essential medicines that is commonly used to treat rheumatoid arthritis – significantly reduces the symptoms associated with the disease.

Every year around 6,000 people in the UK are diagnosed with either PV or ET, related blood cancers that cause an overproduction of red blood cells (PV) or blood-clotting platelets (ET). Patients often suffer with itching, headaches, weight loss, fatigue and night sweats. Although current treatments are usually able to control the increased blood counts, they provide little relief from sometimes debilitating symptoms that can often have a significant impact on quality of life.

Building on previous Medical Research Council-funded work in the Zeidler lab that identified methotrexate as an inhibitor of the JAK/STAT signalling pathway, this study examined hospital records to identify existing ET and PV patients already taking methotrexate for other diseases.

Despite the small numbers involved and the presence of background rheumatoid arthritis, these patients reported significantly lower symptom scores than patients not taking methotrexate.

The mis-regulation of the JAK/STAT signalling pathway in humans is central to the development of Myeloproliferative neoplasms (MPNs), the collective term for progressive blood cancers like ET and PV and is also central to many inflammatory processes such as those associated with rheumatoid arthritis.

Lab-based results showed that low doses of methotrexate acted as a powerful suppressor of JAK/STAT pathway activation – even in cells carrying the mutated gene responsible for MPNs in patients. Zeidler said: "While we still need to undertake a clinical trial to validate these findings, our results are very encouraging and suggest that a simple drug that has been used for nearly 40 years to treat arthritis can provide significant relief to blood cancer sufferers.

"Patients we tested showed a pronounced improvement in symptoms, something conventional treatments have been unable to provide.

"Given the very low cost of MTX, this research could offer an effective therapy on a budget accessible to healthcare systems throughout the world – marking a potentially substantial clinical and health economic benefit."

An 81-year-old PV patient based in California commented: "Methotrexate seemed to do a very nice job of controlling itching and night sweats. My subjective experience of MTX was of a PV holiday."

MTX has been used for 40 years to treat inflammatory diseases including rheumatoid arthritis, Crohn's disease and psoriasis. Even though the mechanisms by which MTX acts in these diseases had not previously been understood, the safety and effectiveness of MTX is well documented and many millions of patients regularly take the drug. Diseases such as rheumatoid arthritis all feature inflammatory processes driven by JAK/STAT activity and the effectiveness of MTX in these inflammatory diseases may well be a consequence of its ability to dampen the JAK/STAT pathway.

We recently identified low‐dose methotrexate (MTX) as a JAK/STAT pathway inhibitor and have demonstrated its activity in humanised animal models of myeloproliferative neoplasms (MPNs) (Thomas et al, 2015; Chinnaiya et al, 2017). Here, we describe a retrospective service evaluation of 11 MPN patients treated with low‐dose MTX for unrelated co‐morbidities. Three showed haematological changes following initiation/interruption of MTX while standardised symptom assessments suggested that MTX‐treated MPN patients suffer significantly decreased constitutional symptoms. Given the inflammatory nature of MPN symptoms we suggest that low‐dose MTX may represent a low cost, safe and effective treatment for the wider MPN population and propose further studies to test this hypothesis.

Sebastian Francis, Sally Thomas, Robert Luben, Nikolaos Sousos, Adam Mead, John A Snowden, Martin P Zeidler

University of Sheffield material British Journal of Haematology abstract

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