+353-1-416-8900REST OF WORLD
+44-20-3973-8888REST OF WORLD
1-917-300-0470EAST COAST U.S
1-800-526-8630U.S. (TOLL FREE)
Sale

Progressive Multifocal Leukoencephalopathy - Epidemiology Forecast - 2032

  • PDF Icon

    Report

  • 58 Pages
  • July 2022
  • Region: Global
  • DelveInsight
  • ID: 5525601
UP TO OFF until Dec 31st 2024
This ‘Progressive Multifocal Leukoencephalopathy (PML) - Epidemiology Forecast - 2032' report delivers an in-depth understanding of the historical and forecasted epidemiology of progressive multifocal leukoencephalopathy (PML) in the United States, EU5 (Germany, Spain, Italy, France, and the United Kingdom), and Japan.

Progressive Multifocal Leukoencephalopathy (PML): Disease Understanding


Progressive Multifocal Leukoencephalopathy (PML) Overview


Progressive multifocal leukoencephalopathy (PML) is an opportunistic infection caused by the JC virus (JCV), involving infection of white matter (principally oligodendrocytes) and neurons in the brain and leading to irreversible demyelination and neuroaxonal damage.

The immunosuppressive conditions associated with PML are broad and heterogeneous, ranging from HIV-AIDS (relatively common before highly active antiretroviral therapy [HAART] was available) to disease-specific immunosuppressive therapies, including monoclonal antibodies. The causative agent is the polyomavirus JC which has a tropism for oligodendrocytes. The virus is widespread in up to 85% of the general adult population. Asymptomatic primary infection occurs in childhood, with the virus remaining latent in the kidneys and lymphoid tissue. With profound cellular immunosuppression, the virus reactivates and spreads to the CNS. Most common symptoms include limb weakness, cognitive deficits, speech and visual difficulties, ataxia, seizures, gait, sensory loss, and headache.

PML occurs at an estimated incidence of 0.2 per 100,000 patients with autoimmune diseases who did not have HIV or malignancy and at a very low incidence among patients with rheumatic diseases but can occur even in the absence of HIV or malignancy. The preferred diagnostic method is cerebral spinal fluid polymerase chain reaction (CSF PCR) to detect JC virus DNA. Stereotactic brain biopsy remains the reference standard for diagnosis. PML occurs almost exclusively in immunosuppressed patients, including those with AIDS (79%), hematologic malignancies (13%), organ transplants (5%), and autoimmune diseases on immunosuppressive therapy (3%). PML has rarely been reported in patients with occult immunosuppression such as hepatic cirrhosis and renal failure (Paul, 2019).

There is no specific treatment for JCV. Current treatment strategies are aimed at restoring immune function to improve survival successfully. In HIV-positive patients with PML, ART optimization is the best therapeutic option; in HIV-negative patients, removal or decrease of any potential source of immunosuppression is recommended. However, the prognosis for the majority of PML patients remains poor.

Despite the persistent risk of PML among patients with immunosuppressive conditions and a growing risk of PML among patients treated with immunomodulatory agents, no therapeutics are approved for the treatment of PML. However, the incidence and mortality of PML have decreased since the introduction of HAART, and the restoration of the host adaptive immune response has been shown to prolong survival.

Recently, genetic risk variants in patients with PML have been identified, which might help assess patients at risk, especially in those using immunosuppressant agents. However, outcomes in PML populations remain poor. Therefore, there is still a high unmet need for effective prophylaxis and treatment of PML.

Progressive Multifocal Leukoencephalopathy (PML): Epidemiology


The progressive multifocal leukoencephalopathy (PML) epidemiology division provides insights into the historical and current patient pool, along with the forecast trend for every seven major countries. It helps recognize the causes of current and forecasted trends by exploring numerous studies and views of key opinion leaders. This part of the report also provides the diagnosed patient pool and their trends, along with assumptions undertaken.

Key Findings


The disease epidemiology covered in the report provides historical and forecasted progressive multifocal leukoencephalopathy (PML) epidemiology segmented as the Diagnosed incident cases of progressive multifocal leukoencephalopathy, Age-specific cases of progressive multifocal leukoencephalopathy, and Incident cases of progressive multifocal leukoencephalopathy based on etiologies. The report includes the incident scenario of progressive multifocal leukoencephalopathy (PML) in the 7MM covering the United States, EU5 countries (Germany, France, Italy, Spain, and the United Kingdom), and Japan from 2019 to 2032.

Country-wise progressive multifocal leukoencephalopathy (PML) Epidemiology


The epidemiology segment also provides the progressive multifocal leukoencephalopathy (PML) epidemiology data and findings across the United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan.

The total diagnosed incident cases of progressive multifocal leukoencephalopathy (PML) in the 7MM countries was close to 3,900 cases in 2021.

As per the estimates, the United States had the highest diagnosed incident cases of progressive multifocal leukoencephalopathy (PML) in 2021. Among the EU5 countries, Germany had the highest diagnosed incident cases of progressive multifocal leukoencephalopathy (PML) with more than 400 cases, followed by France in 2021. On the other hand, Spain had the lowest diagnosed incident cases of progressive multifocal leukoencephalopathy (PML) close to 230 cases in 2021.

Scope of the Report

  • The progressive multifocal leukoencephalopathy report covers a detailed overview explaining its causes, symptoms and classification, pathophysiology, diagnosis, and treatment patterns.
  • The progressive multifocal leukoencephalopathy epidemiology report and model provide an overview of the risk factors and global trends of progressive multifocal leukoencephalopathy in the seven major markets (7MM: US, France, Germany, Italy, Spain, UK, and Japan).
  • The report provides insight into the historical and forecasted patient pool of progressive multifocal leukoencephalopathy in seven major markets covering the United States, EU5 (Germany, Spain, France, Italy, UK), and Japan.
  • The report helps recognize the growth opportunities in the 7MM concerning the patient population.
  • The report assesses the disease risk and burden and highlights the unmet needs of progressive multifocal leukoencephalopathy.
  • The report provides the segmentation of progressive multifocal leukoencephalopathy epidemiology by diagnosed incident cases of progressive multifocal leukoencephalopathy in the 7MM.
  • The report provides the segmentation of the progressive multifocal leukoencephalopathy epidemiology by age-specific cases of progressive multifocal leukoencephalopathy in the 7MM.
  • The report provides the segmentation of the progressive multifocal leukoencephalopathy epidemiology by incident cases of progressive multifocal leukoencephalopathy based on etiologies in the 7MM.

Report Highlights

  • 11-year Forecast of progressive multifocal leukoencephalopathy epidemiology
  • 7MM Coverage
  • Diagnosed incident cases of progressive multifocal leukoencephalopathy
  • Age-specific cases of progressive multifocal leukoencephalopathy
  • Incident cases of progressive multifocal leukoencephalopathy based on etiologies

KOL Views


The publisher interviews KOLs and obtain SME's opinions through primary research to fill the data gaps and validate our secondary research. The opinion helps understand the total patient population and current treatment pattern. This will support the clients in potential upcoming novel treatments by identifying the overall scenario of the indications.

Key Questions Answered

  • What are the major factors that will drive the change in the patient population in progressive multifocal leukoencephalopathy during the forecast period (2019-2032)?
  • What are the key findings pertaining to the progressive multifocal leukoencephalopathy epidemiology across 7MM, and which country will have the highest number of patients during the forecast period (2019-2032)?
  • What would be the total number of patients with progressive multifocal leukoencephalopathy across the 7MM during the forecast period (2019-2032)?
  • Among the EU5 countries, which country will have the highest number of patients during the forecast period (2019-2032)?
  • At what CAGR is the patient population expected to grow in the 7MM forecast period (2019-2032)?
  • What are the disease risk, burdens, and unmet needs of progressive multifocal leukoencephalopathy?
  • What are the currently available treatments for progressive multifocal leukoencephalopathy?

Reasons to Buy


Progressive Multifocal Leukoencephalopathy (PML) Epidemiology report will allow the user to:
  • Develop business strategies by understanding the trends shaping and driving the global progressive multifocal leukoencephalopathy (PML) market.
  • Quantify patient populations in the global progressive multifocal leukoencephalopathy market to improve product design, pricing, and launch plans.
  • Understand the magnitude of the progressive multifocal leukoencephalopathy population by its diagnosed incident cases.
  • Understand the magnitude of the progressive multifocal leukoencephalopathy population by its age-specific cases.
  • Understand the magnitude of the progressive multifocal leukoencephalopathy (PML) population by its incident cases of progressive multifocal leukoencephalopathy based on etiologies.
  • The progressive multifocal leukoencephalopathy (PML) epidemiology report and model were written and developed by Master's and Ph.D. level epidemiologists.
  • The progressive multifocal leukoencephalopathy (PML) Epidemiology Model developed by the publisher is easy to navigate, interactive with dashboards, and epidemiology based on transparent and consistent methodologies. Moreover, the model supports the data presented in the report and showcases disease trends over an 11-year forecast period using reputable sources.

Key Assessments

  • Patient Segmentation
  • Disease Risk and Burden
  • Risk of disease by the segmentation
  • Factors driving growth in a specific patient population

Geographies Covered

  • The United States
  • EU5 (Germany, France, Italy, Spain, and the United Kingdom)
  • Japan
Study Period: 2019-2032

Table of Contents

1. Key Insights2. Report Introduction
3. Progressive Multifocal Leukoencephalopathy (PML) Patient Share at a Glance
3.1. Patient Share (%) Distribution of PML in 2019
3.2. Patient Share (%) Distribution of PML in 2032
4. Executive Summary of Progressive Multifocal Leukoencephalopathy
5. Disease Background and Overview
5.1. Introduction
5.2. Causes and Risk factors
5.3. Signs and Symptoms
5.4. Pathophysiology
5.5. Diagnosis
5.6. Treatment
6. Epidemiology and Patient Population
6.1. Key Findings
6.2. Total Diagnosed Incidence of PML in 7MM
6.3. Assumptions and Rationale
6.4. The United States
6.4.1. Total Diagnosed Incident cases of PML in the United States
6.4.2. Age-specific cases of PML in the United States
6.4.3. Incidence of PML based on etiologies in the United States
6.5. EU5
6.5.1. Total Diagnosed Incidence of PML in EU5
6.5.2. Germany
6.5.2.1. Diagnosed incident cases of PML in Germany
6.5.2.2. Age-specific cases of PML in Germany
6.5.2.3. Incidence of PML based on etiologies in Germany
6.5.3. France
6.5.3.1. Diagnosed incident cases of PML in France
6.5.3.2. Age-specific cases of PML in France
6.5.3.3. Incidence of PML based on etiologies in France
6.5.4. Italy
6.5.4.1. Diagnosed incident cases of PML in Italy
6.5.4.2. Age-specific cases of PML in Italy
6.5.4.3. Incidence of PML based on etiologies in Italy
6.5.5. Spain
6.5.5.1. Diagnosed incident cases of PML in Spain
6.5.5.2. Age-specific cases of PML in Spain
6.5.5.3. Incidence of PML based on etiologies in Spain
6.5.6. The United Kingdom
6.5.6.1. Diagnosed incident cases of PML in the United Kingdom
6.5.6.2. Age-specific cases of PML in the United Kingdom
6.5.6.3. Incidence of PML based on etiologies in the United Kingdom
6.6. Japan
6.6.1. Diagnosed incident cases of PML in Japan
6.6.2. Age-specific cases of PML in Japan
6.6.3. Incidence of PML based on etiologies in Japan
7. Patient Journey8. KOL Views9. SWOT Analysis10. Unmet Needs
11. Appendix
11.1. Bibliography
11.2. Report Methodology
12. Publisher Capabilities13. Disclaimer14. About the Publisher
List of Tables
Table 1: Summary of Progressive Multifocal Leukoencephalopathy, Epidemiology, and Key Events (2019 to 2032)
Table 2: Therapeutic approaches to PML
Table 3: Diagnosed Incident cases of PML in the 7MM (2019 to 2032)
Table 4: Diagnosed incident cases of PML in the United States (2019 to 2032)
Table 5: Age-specific cases of PML in the United States (2019 to 2032)
Table 6: Incidence of PML based on etiologies in the United States (2019 to 2032)
Table 7: Diagnosed Incident cases of PML in EU5 (2019 to 2032)
Table 8: Diagnosed incident cases of PML in Germany (2019 to 2032)
Table 9: Age-specific cases of PML in Germany (2019 to 2032)
Table 10: Incidence of PML based on etiologies in Germany (2019 to 2032)
Table 11: Diagnosed incident cases of PML in France (2019 to 2032)
Table 12: Age-specific cases of PML in France (2019 to 2032)
Table 13: Incidence of PML based on etiologies in France (2019 to 2032)
Table 14: Diagnosed incident cases of PML in Italy (2019 to 2032)
Table 15: Age-specific cases of PML in Italy (2019 to 2032)
Table 16: Incidence of PML based on etiologies in Italy (2019 to 2032)
Table 17: Diagnosed incident cases of PML in Spain (2019 to 2032)
Table 18: Age-specific cases of PML in Spain (2019 to 2032)
Table 19: Incidence of PML based on etiologies in Spain (2019 to 2032)
Table 20: Diagnosed incident cases of PML in the United Kingdom (2019 to 2032)
Table 21: Age-specific cases of PML in the United Kingdom (2019 to 2032)
Table 22: Incidence of PML based on etiologies in the United Kingdom (2019 to 2032)
Table 23: Diagnosed incident cases of PML in Japan (2019 to 2032)
Table 24: Age-specific cases of PML in Japan (2019 to 2032)
Table 25: Incidence of PML based on etiologies in Japan (2019 to 2032)
List of Figures
Figure 1: White matter and Gray matter in the brain
Figure 2: Appearance of gradually demyelinating nerve cells (white matter) in the brain
Figure 3: Causes and risk factors of PML
Figure 4: Symptoms of PML
Figure 5: Pathophysiology of PML
Figure 6: Algorithm for diagnosing PML
Figure 7: Diagnosed Incident cases of PML in the 7MM (2019 to 2032)
Figure 8: Diagnosed Incident cases of PML in the United States (2019 to 2032)
Figure 9: Age-specific cases of PML in the United States (2019 to 2032)
Figure 10: Incidence of PML based on etiologies in the United States (2019 to 2032)
Figure 11: Diagnosed Incident cases of PML in EU5 (2019 to 2032)
Figure 12: Diagnosed Incident cases of PML in Germany (2019 to 2032)
Figure 13: Age-specific cases of PML in Germany (2019 to 2032)
Figure 14: Incidence of PML based on etiologies in Germany (2019 to 2032)
Figure 15: Diagnosed Incident cases of PML in France (2019 to 2032)
Figure 16: Age-specific cases of PML in France (2019 to 2032)
Figure 17: Incidence of PML based on etiologies in France (2019 to 2032)
Figure 18: Diagnosed Incident cases of PML in Italy (2019 to 2032)
Figure 19: Age-specific cases of PML in Italy (2019 to 2032)
Figure 20: Incidence of PML based on etiologies in Italy (2019 to 2032)
Figure 21: Diagnosed Incident cases of PML in Spain (2019 to 2032)
Figure 22: Age-specific cases of PML in Spain (2019 to 2032)
Figure 23: Incidence of PML based on etiologies in Spain (2019 to 2032)
Figure 24: Diagnosed Incident cases of PML in the United Kingdom (2019 to 2032)
Figure 25: Age-specific cases of PML in the United Kingdom (2019 to 2032)
Figure 26: Incidence of PML based on etiologies in the United Kingdom (2019 to 2032)
Figure 27: Diagnosed Incident cases of PML in Japan (2019 to 2032)
Figure 28: Age-specific cases of PML in Japan (2019 to 2032)
Figure 29: Incidence of PML based on etiologies in Japan (2019 to 2032)