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Receiving a diagnosis of multiple sclerosis (MS) can be a life-altering event, bringing with it many questions about the future. MS is a condition of the central nervous system that disrupts communication between the brain and the body. Its effects vary widely from person to person, but recent progress in medical science offers more hope and better outcomes than ever before. The focus of care has expanded from simply managing symptoms to actively slowing the condition's progression and improving overall quality of life.
Modern approaches to managing MS have transformed what it means to live with the condition. With a growing range of therapies, people with MS now have more opportunities to maintain their independence and continue participating in the activities they enjoy. These developments reflect a deeper recognition of how the disease works, leading to more targeted and convenient treatment plans.
Freepix image[/caption]
Receiving a diagnosis of multiple sclerosis (MS) can be a life-altering event, bringing with it many questions about the future. MS is a condition of the central nervous system that disrupts communication between the brain and the body. Its effects vary widely from person to person, but recent progress in medical science offers more hope and better outcomes than ever before. The focus of care has expanded from simply managing symptoms to actively slowing the condition's progression and improving overall quality of life.
Modern approaches to managing MS have transformed what it means to live with the condition. With a growing range of therapies, people with MS now have more opportunities to maintain their independence and continue participating in the activities they enjoy. These developments reflect a deeper recognition of how the disease works, leading to more targeted and convenient treatment plans.
Dr. Cortese[/caption]
Marianna Cortese, MD, PhD
Senior Research Scientist











Dr. Mathias Buttmann[/caption]
PD Dr. Mathias Buttmann
Senior Consultant Neurologist and Head of the Multiple Sclerosis Outpatient Clinic
University of Wuerzburg
Wuerzburg, Germany
MedicalResearch.com: What is the background for this study? What are the main findings?
Dr. Buttmann: The synthetic anthracenedione mitoxantrone is approved for disease-modifying treatment of patients with aggressive forms of relapsing or secondary progressive multiple sclerosis (MS). It has been known for years that this DNA-intercalating agent increases the risk of acute myeloid leukemia. We performed a retrospective cohort study to investigate whether mitoxantrone also increases the risk for other types of malignancies. We included all 677 mitoxantrone-treated multiple sclerosis patients who were seen at our large German academic MS centre between 1994 and 2007 and collected follow-up information on the occurrence of malignancies, death and causes of death as of 2011. Follow-up was complete in 676 patients. The median age at mitoxantrone initiation was 41 years and the median follow-up duration was 8.7 years. We identified 37 patients with a malignancy after mitoxantrone initiation, among them 4 cases of acute myeloic leukemia and 7 cases of colorectal cancer.
Compared to the general population matched for sex, age and year of occurrence, we calculated an 1.5-fold increased incidence of any type of malignancy, a tenfold increased incidence of acute myeloic leukemia and a threefold increased incidence of colorectal cancer, while the incidence of other types of malignancies was not increased. Higher age at mitoxantrone initiation but neither higher cumulative mitoxantrone dose nor treatment with other immuosuppressive agents was identified as a malignancy risk factor. Fifty-five patients had died, among them 12 from a malignancy. Our study confirmed previous reports on an increased incidence of acute myeloic leukemia after mitoxantrone treatment and newly described an association between mitoxantrone therapy and an increased incidence of colorectal cancer.
Dr. Jennifer Graves[/caption]
Jennifer Graves, MD, PhD, MAS
Adult and Pediatric Multiple Sclerosis Centers
UCSF
MedicalResearch.com: What is the background for this study? What are the main findings?
Dr. Graves: Cessation of medications with effects on immune trafficking may be more likely to cause rebound inflammatory activity in autoimmune diseases such as multiple sclerosis. We observed 5 strikingly severe relapses consistent with rebound events following cessation of fingolimod treatment and identified several similar cases in the literature. At our center the rebound events occurred with an approximate 10% frequency.
MedicalResearch.com: What should clinicians and patients take away from your report?
Dr. Graves: Fingolimod cessation may be complicated by rebound phenomena in some patients, similar to what has been observed with natalizumab. Both of these medications have effects on immune cell trafficking, likely explaining the association with rebound events. Careful consideration must be taken in stopping these medications.
