EMA Restricts Tofacitinib Dosing Save
The Pharmacovigilance Risk Assessment Committee (PRAC) of the European Medicines Agency (EMA) issued recommendations limiting the use of Xeljanz (tofacitinib) 10 mg twice daily in patients with ulcerative colitis (UC) in the EU, primarily because of a risk of pulmonary embolism.
The new recommendations are temporary while PRAC undertakes a review of all available evidence on the safety and efficacy of tofacitinib. The review follows warnings of an increased risk of pulmonary embolism (PE) and death from the U.S. Food and Drug Administration based on Pfizer's large post-marketing safety study (in high risk rheumatoid arthritis (RA) patients with one or more underlying cardiovascular risk factors) wherein those receiving in tofacitinib 10 mg twice daily in study A3921133 had more PE and mortalities than comparator groups (tofacitinib 5 mg bid or adalimumab).
In Europe, (tofacitinib) 10 mg twice daily is not an approved dose for RA patients, but has been approved for those with severe ulcerative colitis (just as in the USA).
The EMA’s safety committee is recommending that doctors must not prescribe the 10 mg twice daily dose of tofacitinib in patients who are at high risk of blood clots in the lungs. This includes patients who have heart failure, cancer, inherited blood clotting disorders or a history of blood clots, as well as patients who take combined hormonal contraceptives, are receiving hormone replacement therapy or are undergoing major surgery.
In addition, doctors should consider other factors that may increase the risk of blood clots in the lungs including age, obesity, smoking or immobilisation.
The details of the Pfizer ongoing study, A3921133, wherein RA patients had these events are not currently available but are going to be further analyzed by the FDA and the EMA.
The PRAC directive for the EU audience is that patients at high risk for venous thromboembolic events (VTE) taking this dose of tofacitinib must either be switched to alternative treatments.
These new recommendations are temporary and follow previous PRAC advice not to exceed the recommended 5 mg twice daily dose when treating rheumatoid arthritis. The PRAC will now carry out a review of all available evidence, and updated guidance will be provided to patients and healthcare professionals once the review is concluded.
Information for patients
An ongoing study in patients with rheumatoid arthritis showed that when Xeljanz was given at a dose of 10 mg twice daily there was an increased risk of dangerous blood clots in the lungs and death.
This dose is higher than the approved dose of 5 mg twice daily for rheumatoid arthritis. However, this dose is used for the initial treatment of patients with ulcerative colitis (for up to 16 weeks) and may also be used in some patients when continuing treatment.
While an in-depth review of Xeljanz is ongoing, if you are being treated with Xeljanz 10 mg twice daily and you are at high risk of blood clots in the lungs, your doctor may switch you to an alternative treatment.
You may be at high risk of blood clots in the lungs if you:
- have heart failure (when the heart does not work as well as it should)
- have inherited blood clotting disorders
- have had blood clots in the veins
- are taking combined hormonal contraceptives or hormone replacement therapy
- have cancer
- will have or have recently had major surgery.
Your doctor will also take into account your age, whether you are obese (your body mass index is above 30), smoke or are immobilised when evaluating your risk of blood clots.
If you are being treated with Xeljanz, you should not change the dose or stop taking the medicine without discussing it with your doctor.
You should seek medical attention immediately if you experience the following symptoms which may be signs of a blood clot in your lungs: difficulty breathing, chest pain or pain in your upper back, coughing up blood, excessive sweating and bluish skin.
If you have any concerns about your medicine, you should discuss them with a healthcare professional.
Information for healthcare professionals
An increased risk of pulmonary embolism and overall mortality has been observed in a study with tofacitinib 10 mg twice daily in rheumatoid arthritis.
These results come from study A3921133, an ongoing open-label clinical trial evaluating the safety of tofacitinib 5 mg twice daily and tofacitinib 10 mg twice daily compared with a tumour necrosis factor (TNF) inhibitor in patients with rheumatoid arthritis. Patients in the study are 50 years of age or older with at least one additional cardiovascular risk factor.
The preliminary results of the study showed that there were 19 cases of pulmonary embolism out of 3,884 patient-years in the tofacitinib 10 mg twice daily arm of the study compared with 3 cases out of 3,982 in the TNF inhibitor arm. Additionally, there were 45 deaths from all causes out of 3,884 patient-years in the 10 mg twice daily arm compared with 25 cases out of 3,982 patient-years in the TNF inhibitor group.
While an in-depth review of these risks is ongoing, doctors must not prescribe the 10 mg twice daily dose in patients:
- with heart failure
- with inherited coagulation disorders
- who have had venous thromboembolism, either deep venous thrombosis or pulmonary embolism
- who use combined hormonal contraceptives or hormone replacement therapy
- with malignancy
- who are undergoing major surgery.
Additionally, other risk factors to be considered when prescribing tofacitinib 10 mg twice daily include age, obesity (BMI>30), smoking and immobilisation.
Patients who are already treated with the 10 mg twice daily dose and are at high risk of pulmonary embolism should be switched to alternative treatments.
While further assessment of the study results continues, prescribers should continue to adhere to the authorised dose of 5 mg twice daily for the treatment of rheumatoid arthritis and psoriatic arthritis.
Patients receiving tofacitinib, irrespective of indication, should be monitored for the signs and symptoms of pulmonary embolism, and be advised to seek medical attention immediately if they experience them.
A letter is being sent to all healthcare professionals expected to prescribe the medicine to inform them of the temporary treatment recommendations.