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Stakeholder Insight: Multiple Sclerosis - Disease-modifying Efficacy and Side Effects Guide Treatment Choice


Description: The disease-modifying drugs are considered by physicians to represent a significant advance for the management of MS. However, none is fully effective and there are problems with regards to side effects, dosing regimens and cost. Tysabri, a novel once-monthly drug is expected to be an improvement in terms of efficacy; however, there remains a concern over side effects and long-term safety.

Scope of this title:
- Overview of epidemiology, presentation, referral and diagnostic assessment in MS
- Breakdown of first-line to fourth-line treatment regimens and treatment choice according to disease category
- Influences on treatment choice and perception of current drug therapies
- Evaluation of unmet needs and future outlook

Highlights of this title:
- Multiple sclerosis affects less than 1% of the population in the US and Europe. Despite the high level of general awareness of the disease, neurologists estimate less than half of individuals present at the time they suffer from first symptoms and it can take more than one year to receive an accurate diagnosis.
- Numerous strategies, including switching to an alternative interferon beta, are adopted as second-line therapy. Although not favored by opinion leaders or US neurologists, combining two disease-modifying drugs is popular in the 5EU markets. Given the willingness of neurologists to try this strategy, further trials are required.
- Tysabri is perceived by neurologists as offering a clear improvement in terms of disease-modifying efficacy. However, a lack of long-term safety data will ensure for the moment it remains positioned as a last-line therapy for relapse-remitting patients who have failed first- and second-line treatment with interferon beta or glatiramer acetate.

Reasons to order your copy:
- Target prescribers more effectively, through an understanding of prescribing behavior and its influences
- Validate new product forecasting based on diagnosis and treatment rates, and the likely rate of uptake for new products
- Benchmark brand awareness and perceptions surrounding product positioning in order to formulate competitive lifecycle management strategies


Contents:

Chapter 1.

Executive summary 3
Scope of the analysis 3
Our insight into the multiple sclerosis market 4



Chapter 2.

Introduction and scope 14
Coverage of the Stakeholder Insight Survey 14
Disease definition & epidemiology 14
Presentation and diagnosis 14
Treatment 14
Key prescribing influences 15
Unmet needs 15



Chapter 3.

Country treatment trees 16
US 17
France 18
Germany 19
Italy 20
Spain 21
UK 22



Chapter 4.

Epidemiology and patient segmentation 23
Disease definition 23
There is no universal course for multiple sclerosis 23
Researchers have attempted to classify multiple sclerosis according to the clinical course of the disease 23
Epidemiology of multiple sclerosis 25
Young female adults are most at risk of developing multiple sclerosis 25
Other genetic and environmental factors appear to play a role in onset of MS 27
Prevalence of multiple sclerosis 28
Over 800,000 individuals across the US and 5EU are estimated to suffer from MS 28
US 30
5EU 30
The majority of patients suffer from relapse remitting multiple sclerosis 34



Chapter 5.

Presentation and diagnosis 35
Presentation 35
Symptoms typically first emerge in relapsing-remitting course of multiple sclerosis 35
Fatigue and depression are most common symptoms 36
Less than half of new patients present to a physician at the time they suffer from first symptoms of MS 37
The majority of patients present to a primary care physician 41
Diagnosis 42
Diagnostic criteria 43
Only half of patients with multiple sclerosis symptoms receive an accurate diagnosis on initial presentation to a physician 45



Chapter 6.

Treatment options and guidelines 48
Treatment options 48
Symptomatic treatment 48
Disease-modifying drug treatments 49
Acute relapse treatment 52
Treatment guidelines 52
There are no official international guidelines for the chronic treatment of multiple sclerosis and use of disease-modifying therapies 52
Several treatment guidelines are in place for the management of acute relapses of multiple sclerosis 54



Chapter 7.

Prescribing trends in multiple sclerosis 56
Treatment of multiple sclerosis with disease-modifying drug treatments 56
Across all stages of MS, 53% of total diagnosed patients receive disease modifying therapies 56
First-line therapy 60
Approximately one third of patients prescribed first-line therapy move to second-line therapy 64
Second-line therapy 67
Approximately one quarter of patients prescribed second-line therapy move to third-line therapy 70
Third-line therapy 72
Only one fifth of patients prescribed third-line therapy move to fourth-line therapy 74
Fourth-line therapy 77
Summary of treatment lines according to country 79
Novantrone (mitoxantrone) 80
Novantrone is the only treatment US Food and Drug Association-approved treatment for worsening MS 80
Approximately half of respondents prescribe mitoxantrone to their patients 81
The majority of current mitoxantrone prescriptions are reserved for last line therapy 82
In the future, mitoxantrone is unlikely to change from being reserved as a last line therapy 85
Tysabri (natalizumab) 87
Tysabri is the first humanized monoclonal antibody approved for the treatment of multiple sclerosis 87
Cases of progressive multifocal leukoencephalopathy led to withdrawal after only three months on the market 87
Tysabri has been relaunched albeit under tight controls 88
The majority of interviewed neurologists would consider prescribing Tysabri 89
Tysabri administered as an infusion presents a small barrier to use 90
A potential risk of progressive multifocal leukoencephalopathy with Tysabri would create a barrier to its use 92
Respondents expect to prescribe Tysabri predominantly to their patients with RRMS 94
There is no clear point for when Tysabri will be prescribed in the treatment algorithm 95
Treatment for acute relapse of multiple sclerosis 98
Steroids have historically been the mainstay of treatment 98
Interviewed neurologists consider intravenous methylprednisolone the number one treatment for acute relapses 98
Interviewed neurologists use numerous other therapies 100
Oral steroids are used by almost a quarter of patients but may increase risk of side effects 101
Intravenous dexamethasone offers a cheaper alternative to intravenous methylprednisolone 101
Aspirin and nonsteroidal anti-inflammatory drugs may help reduce side effects 102
Plasmapheresis should be considered for patients who fail to respond to intravenous methylprednisolone 102
Use of intramuscular adrenocortropic hormone is no longer the preferred treatment for treating acute relapse 103
Intrathecal steroids are not recommended for treating acute relapse 103



Chapter 8.

Influencing factors on prescribing trends in multiple sclerosis 104
Current market overview 104
The disease-modifying drugs have continued to perform well in terms of revenues 104
Factors driving prescribing choice 106
Disease-modifying efficacy is the number one influential factor 106
Side effects are accepted as an inherent outcome of taking any disease-modifying drug but the nature and severity of the side effects are key influencers 107
Speed of onset of action is desirable 107
Ability to combine a drug with other therapies is heavily influenced by prescribing practices and trends 108
Drugs are used over a long period of time and must be considered safe for extended use 109
Dosing frequency and delivery methods may compromise patient compliance 111
In Europe cost typically has a greater influence on prescribing choice than formulary / reimbursement status 113
UK restricts use of disease-modifying drugs based on clinical versus cost-effectiveness 114
In the US formulary / reimbursement status is considered a greater influence on prescribing choice than cost 115



Chapter 9.

Improving treatment outcomes 117
Performance of prescribed drugs against attributes 117
Neurologists in the US and UK are most satisfied with current therapies 117
Avonex is perceived to perform slightly better across all attributes than the other disease-modifying therapies 118
Tysabri is perceived to perform best on disease modification efficacy 119
Higher dosed interferons are perceived to have a faster onset of action 121
None of the drugs are perceived to have a very good side-effect profile 123
Ability to combine with other therapies 126
A higher dosing frequency is perceived to more efficacious 127
Intravenous delivery methods are perceived less favorable 129
Interferons and Copaxone are considered safe for extended use 130
There is room to improve patient treatment compliance 131
Formulary / reimbursement status 132
Drugs with increased disease-modifying efficacy are considered to perform better on cost 133
Reasons for discontinuing therapy/switching to alternative drug therapy 135
Lack of efficacy and intolerable side effects are the key reasons for discontinuing or switching treatment 135
Occurrence of any side effect if poorly managed can lead to treatment discontinuation 137
Unmet needs 140

BIBLIOGRAPHY 143
References 143
Websites 149
APPENDIX A 152
Physician research methodology 152
Physician sample breakdown 152
US 152
France 153
Germany 153
Italy 154
Spain 154
UK 155
Contributing experts 155

APPENDIX B 156
The survey questionnaire 156
Physician details 156
Introduction 157
Section 1—Epidemiology and diagnosis of multiple sclerosis 157
Section 2—Treatment of multiple sclerosis 159
First-line therapy 160
Second-line therapy 162
Third-line therapy 164
Fourth-line therapy 166
Section 3—Key prescribing factors 170
Disclaimer 175






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