Myeloproliferative neoplasm overview: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Myeloproliferative disease}} | {{Myeloproliferative disease}} | ||
{{CMG}}{{AE}}{{MJK}} {{shyam}} | {{CMG}}{{AE}}{{MJK}} {{shyam}} | ||
==Overview== | ==Overview== | ||
Myeloproliferative neoplasm are a group of eight disease subtypes of the [[bone marrow]] in which excess cells are produced. Myeloproliferative neoplasm may be classified according to the World Health Organization into eight subtypes, including [[polycythemia vera]], [[essential thrombocythemia]], [[primary myelofibrosis]], [[chronic myelogenous leukemia]], [[chronic neutrophilic leukemia]], [[chronic eosinophilic leukemia]], myeloproliferative neoplasm not otherwise specified, and [[mastocytosis]].They are related to, or may evolve into, [[myelodysplastic syndrome]] and [[acute myeloid leukemia]], although the myeloproliferative diseases on the whole have a much better prognosis than these conditions. Clinical and pathologic features in the myeloproliferative neoplasms are due to dysregulated proliferation and expansion of [[myeloid]] [[progenitors]] in the [[bone marrow]], resulting in altered populations of [[granulocytes]], [[erythrocytes]], or [[platelets]] in the peripheral blood. Myeloproliferative neoplasm is caused by a mutational events in the ''[[BCR]]-[[ABL]]'', [[''Janus kinase 2'']] (''JAK2''), [[''calreticulin'']] (''CALR''), or ''myeloproliferative leukemia'' (''MPL'') genes. Patients may be [[asymptomatic]] at diagnosis. However, if symptoms present, symptoms of myeloproliferative neoplasm include [[fever]], [[fatigue]], and [[bleeding]]. The mainstay of therapy for myeloproliferative neoplasm is [[chemotherapy]], [[cytoreduction]], [[aspirin]], and palliative care. | |||
[[chronic eosinophilic leukemia]], not otherwise specified, | |||
[[mastocytosis]] | |||
==Historical Perspective== | ==Historical Perspective== | ||
The first description of myeloproliferative neoplasm dates back to the late 19th century, when Sir Louis Vasquez studied a patient with excess red blood cells. Myeloproliferative neoplasm was first brought to attention as an important clinical entity by Dr. William Dameshek, an American hematologist, in 1951. In 2005, the link between the JAK2 mutation and polycythemia vera was discovered. The World Health Organization created diagnostic criteria for myeloproliferative neoplasms in 2008, and this was revised in 2016. | The first description of myeloproliferative neoplasm dates back to the late 19th century, when Sir Louis Vasquez studied a patient with excess [[red blood cells]]. Myeloproliferative neoplasm was first brought to attention as an important clinical entity by Dr. William Dameshek, an American hematologist, in 1951. In 2005, the link between the ''[[Janus kinase|JAK2]]'' mutation and [[polycythemia vera]] was discovered. The World Health Organization created diagnostic criteria for myeloproliferative neoplasms in 2008, and this was revised in 2016. | ||
==Classification== | ==Classification== | ||
Myeloproliferative neoplasm may be classified according to the World Health Organization into eight subtypes: [[polycythemia vera]], [[essential thrombocythemia]], [[primary myelofibrosis]], [[chronic myelogenous leukemia]], [[chronic neutrophilic leukemia]], [[chronic eosinophilic leukemia]], myeloproliferative neoplasms unclassifiable, and [[mastocytosis]]. Each subtypes is based on a distinct malignant cell, and each subtype has different criteria for diagnosis. | Myeloproliferative neoplasm may be classified according to the World Health Organization into eight subtypes: [[polycythemia vera]], [[essential thrombocythemia]], [[primary myelofibrosis]], [[chronic myelogenous leukemia]], [[chronic neutrophilic leukemia]], [[chronic eosinophilic leukemia]], myeloproliferative neoplasms unclassifiable, and [[mastocytosis]]. Each subtypes is based on a distinct [[Malignant|malignant cell]], and each subtype has different criteria for diagnosis. | ||
==Pathophysiology== | ==Pathophysiology== | ||
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Myeloproliferative neoplasm is caused by mutations in various genes. Different gene mutations are responsible for each of the 8 subtypes of myeloproliferative neoplasms. Importantly, multiple different gene mutations can cause a single disease. | Myeloproliferative neoplasm is caused by mutations in various genes. Different gene mutations are responsible for each of the 8 subtypes of myeloproliferative neoplasms. Importantly, multiple different gene mutations can cause a single disease. | ||
==Differentiating Myeloproliferative Neoplasm from | ==Differentiating Myeloproliferative Neoplasm from Other Diseases== | ||
Myeloproliferative neoplasm must be differentiated from [[myelodysplastic syndrome]], [[acute myelogenous leukemia]], [[acute lymphoblastic leukemia, [[Waldenstrom's macroglobulinemia]], and [[lymphoproliferative disorder]]. Each of these conditions has unique set of causes, laboratory abnormalities, physical exam findings, and therapies. | Myeloproliferative neoplasm must be differentiated from [[myelodysplastic syndrome]], [[acute myelogenous leukemia]], [[acute lymphoblastic leukemia, [[Waldenstrom's macroglobulinemia]], and [[lymphoproliferative disorder]]. Each of these conditions has a unique set of causes, laboratory abnormalities, physical exam findings, and therapies. | ||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
The incidence of myeloproliferative neoplasm is approximately 7.8 per 100,000 individuals worldwide. | The incidence of myeloproliferative neoplasm is approximately 7.8 per 100,000 individuals worldwide. The different subtypes of myeloproliferative neoplasm have different incidence and prevalence statistics. Males are more commonly affected than females, and older persons are more commonly affected than younger persons. | ||
==Risk | |||
There are | ==Risk Factors== | ||
There are four major categories of risk factors for myeloproliferative neoplasm. Genetic mutational events comprise the most common risk factor. Other risk factors include advanced age, prior cytotoxic chemotherapy, and autoimmune disease. | |||
==Screening== | ==Screening== | ||
There are currently no guidelines for screening for myeloproliferative neoplasm. Monitoring of the complete blood count is done routinely. | |||
==Natural History, Complications and Prognosis== | ==Natural History, Complications and Prognosis== | ||
The natural history of myeloproliferative neoplasm begins with weight loss, fever, and night sweats. The natural history depends on the subtype of myeloproliferative neoplasm. Common complications of myeloproliferative neoplasm include [[splenomegaly]], bleeding, [[thrombosis]], bone marrow fibrosis, and acute leukemia. Prognosis depends on the subtype of myeloproliferative neoplasm. Each subtype has its own prognostic scoring system. In general, patients with [[polycythemia vera]], [[essential thrombocythemia]], and [[chronic myeloid leukemia]] have better prognosis than patients with [[primary myelofibrosis]]. The prognosis is generally good with treatment. | |||
==Diagnosis== | ==Diagnosis== | ||
===History and Symptoms=== | ===History and Symptoms=== | ||
Patients may be [[asymptomatic]] at diagnosis. However, if symptoms present, symptoms of myeloproliferative neoplasm include [[fever]], [[fatigue]], and [[bleeding]]. | Patients may be [[asymptomatic]] at diagnosis. However, if symptoms present, symptoms of myeloproliferative neoplasm include [[fever]], [[fatigue]], and [[bleeding]]. | ||
===Physical Examination=== | ===Physical Examination=== | ||
Patients with myeloproliferative neoplasm are usually well-appearing. Physical examination of patients with chronic myelogenous leukemia is usually remarkable for skin [[bruising]] , [[fever]], [[splenomegaly]], and [[lymphadenopathy]]. | Patients with myeloproliferative neoplasm are usually well-appearing. Physical examination of patients with chronic myelogenous leukemia is usually remarkable for skin [[bruising]], [[fever]], [[splenomegaly]], and [[lymphadenopathy]]. | ||
===Laboratory Findings=== | ===Laboratory Findings=== | ||
Patients with myeloproliferative neoplasm are usually well-appearing. Physical examination of patients with chronic myelogenous leukemia is usually remarkable for skin [[bruising]], [[fever]], [[splenomegaly]], and [[lymphadenopathy]]. | |||
===Chest X-Ray=== | ===Chest X-Ray=== | ||
The chest x-ray may be helpful in the diagnosis of myeloproliferative neoplasm and can reveal pleural effusions, pneumonia, and pulmonary edema. | |||
=== | |||
Abdominal and chest CT scan may be helpful in the diagnosis of myeloproliferative neoplasm. Findings on CT scan suggestive of myeloproliferative neoplasm include enlarged lymph nodes, [[ | ===CT=== | ||
=== | Abdominal and chest CT scan may be helpful in the diagnosis of myeloproliferative neoplasm. Findings on CT scan suggestive of myeloproliferative neoplasm include enlarged lymph nodes, [[hepatosplenomegaly]], splanchnic venous thrombosis, and [[pulmonary embolism]]. | ||
Brain MRI | |||
=== | ===MRI=== | ||
Brain MRI is helpful in the detection of thrombotic events, such as ischemic stroke, in patients with myeloproliferative neoplasm. Abdominal MRI is helpful in the detection of mesenteric thrombosis in patients with myeloproliferative neoplasm. | |||
===Ultrasound=== | |||
Ultrasound may be helpful in the diagnosis of myeloproliferative neoplasm. Findings on abdominal ultrasound suggestive of myeloproliferative neoplasm include enlarged [[lymph nodes]], [[hepatosplenomegaly]], and ascites. Findings on extremity ultrasound include thrombosis. | |||
===Other Imaging Findings=== | |||
Other imaging studies for myeloproliferative neoplasm include [[positron emission tomography]] ([[PET]]) scan, which helps to detect metastasis in bone marrow and to follow up medical treatment. | |||
===Other Diagnostic Studies=== | ===Other Diagnostic Studies=== | ||
Other diagnostic studies for myeloproliferative neoplasm include [[bone marrow aspiration]] and [[biopsy|trephine biopsy]], [[lumbar puncture]], and [[lymph node biopsy]]. | Other diagnostic studies for myeloproliferative neoplasm include [[bone marrow aspiration]] and [[biopsy|trephine biopsy]], [[erythropoietin]] level, [[lumbar puncture]], and [[lymph node biopsy]]. | ||
==Treatment== | ==Treatment== | ||
===Medical Therapy=== | ===Medical Therapy=== | ||
The mainstay of therapy for myeloproliferative neoplasm is [[chemotherapy]], [[aspirin]], and palliative care. | Medical therapy for myeloproliferative neoplasm is based on the specific subtype of myeloproliferative neoplasm. The mainstay of therapy for myeloproliferative neoplasm is [[chemotherapy]], [[cytoreduction]], [[aspirin]], and palliative care. Treatment is directed at reducing the excessive numbers of blood cells. | ||
===Surgery=== | ===Surgery=== | ||
Surgical intervention is recommended for the management of chronic myelogenous leukemia | |||
Surgical intervention is usually not recommended for the management of chronic myelogenous leukemia unless there is [[splenomegaly]]. | |||
===Primary Prevention=== | ===Primary Prevention=== | ||
There is no established method for prevention of myeloproliferative neoplasm. | |||
There is no established method for primary prevention of myeloproliferative neoplasm. | |||
===Secondary Prevention=== | ===Secondary Prevention=== | ||
Secondary prevention measures include routine monitoring of laboratory values, including [[complete blood count]] (CBC) and metabolic panel. | |||
===Future of Investigational Therapies=== | |||
Future or investigational therapies in myeloproliferative neoplasms include BLU-285, JQ1, and suberoylanilide hydroxamic acid. Each of these investigational agents carries a unique mechanism of action on myeloid cells. The agents are currently in clinical trials. | |||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category: | [[Category:Medicine]] | ||
[[Category:Hematology]] | |||
[[Category:Oncology]] | [[Category:Oncology]] | ||
[[Category: | [[Category:Up-To-Date]] | ||
Latest revision as of 22:51, 29 July 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Mohamad Alkateb, MBBCh [2] Shyam Patel [3]
Overview
Myeloproliferative neoplasm are a group of eight disease subtypes of the bone marrow in which excess cells are produced. Myeloproliferative neoplasm may be classified according to the World Health Organization into eight subtypes, including polycythemia vera, essential thrombocythemia, primary myelofibrosis, chronic myelogenous leukemia, chronic neutrophilic leukemia, chronic eosinophilic leukemia, myeloproliferative neoplasm not otherwise specified, and mastocytosis.They are related to, or may evolve into, myelodysplastic syndrome and acute myeloid leukemia, although the myeloproliferative diseases on the whole have a much better prognosis than these conditions. Clinical and pathologic features in the myeloproliferative neoplasms are due to dysregulated proliferation and expansion of myeloid progenitors in the bone marrow, resulting in altered populations of granulocytes, erythrocytes, or platelets in the peripheral blood. Myeloproliferative neoplasm is caused by a mutational events in the BCR-ABL, ''Janus kinase 2'' (JAK2), ''calreticulin'' (CALR), or myeloproliferative leukemia (MPL) genes. Patients may be asymptomatic at diagnosis. However, if symptoms present, symptoms of myeloproliferative neoplasm include fever, fatigue, and bleeding. The mainstay of therapy for myeloproliferative neoplasm is chemotherapy, cytoreduction, aspirin, and palliative care.
Historical Perspective
The first description of myeloproliferative neoplasm dates back to the late 19th century, when Sir Louis Vasquez studied a patient with excess red blood cells. Myeloproliferative neoplasm was first brought to attention as an important clinical entity by Dr. William Dameshek, an American hematologist, in 1951. In 2005, the link between the JAK2 mutation and polycythemia vera was discovered. The World Health Organization created diagnostic criteria for myeloproliferative neoplasms in 2008, and this was revised in 2016.
Classification
Myeloproliferative neoplasm may be classified according to the World Health Organization into eight subtypes: polycythemia vera, essential thrombocythemia, primary myelofibrosis, chronic myelogenous leukemia, chronic neutrophilic leukemia, chronic eosinophilic leukemia, myeloproliferative neoplasms unclassifiable, and mastocytosis. Each subtypes is based on a distinct malignant cell, and each subtype has different criteria for diagnosis.
Pathophysiology
The pathophysiology of myeloproliferative neoplasms is based on the specific subtype of myeloproliferative neoplasm. Each of the 8 different myeloproliferative neoplasms have a slightly different pathophysiologic basis. Primary cytogenetic abnormalities have not been identified in the majority of myeloproliferative neoplasms. Aberrant activation of tyrosine kinases and associated signaling pathways is frequently implicated as the disease-initiating event for many of the myeloproliferative neoplasms. Clinical and pathologic features in the myeloproliferative neoplasms are due to dysregulated proliferation and expansion of myeloid progenitors in the bone marrow, resulting in altered populations of granulocytes, erythrocytes, or platelets in the peripheral blood.
Causes
Myeloproliferative neoplasm is caused by mutations in various genes. Different gene mutations are responsible for each of the 8 subtypes of myeloproliferative neoplasms. Importantly, multiple different gene mutations can cause a single disease.
Differentiating Myeloproliferative Neoplasm from Other Diseases
Myeloproliferative neoplasm must be differentiated from myelodysplastic syndrome, acute myelogenous leukemia, [[acute lymphoblastic leukemia, Waldenstrom's macroglobulinemia, and lymphoproliferative disorder. Each of these conditions has a unique set of causes, laboratory abnormalities, physical exam findings, and therapies.
Epidemiology and Demographics
The incidence of myeloproliferative neoplasm is approximately 7.8 per 100,000 individuals worldwide. The different subtypes of myeloproliferative neoplasm have different incidence and prevalence statistics. Males are more commonly affected than females, and older persons are more commonly affected than younger persons.
Risk Factors
There are four major categories of risk factors for myeloproliferative neoplasm. Genetic mutational events comprise the most common risk factor. Other risk factors include advanced age, prior cytotoxic chemotherapy, and autoimmune disease.
Screening
There are currently no guidelines for screening for myeloproliferative neoplasm. Monitoring of the complete blood count is done routinely.
Natural History, Complications and Prognosis
The natural history of myeloproliferative neoplasm begins with weight loss, fever, and night sweats. The natural history depends on the subtype of myeloproliferative neoplasm. Common complications of myeloproliferative neoplasm include splenomegaly, bleeding, thrombosis, bone marrow fibrosis, and acute leukemia. Prognosis depends on the subtype of myeloproliferative neoplasm. Each subtype has its own prognostic scoring system. In general, patients with polycythemia vera, essential thrombocythemia, and chronic myeloid leukemia have better prognosis than patients with primary myelofibrosis. The prognosis is generally good with treatment.
Diagnosis
History and Symptoms
Patients may be asymptomatic at diagnosis. However, if symptoms present, symptoms of myeloproliferative neoplasm include fever, fatigue, and bleeding.
Physical Examination
Patients with myeloproliferative neoplasm are usually well-appearing. Physical examination of patients with chronic myelogenous leukemia is usually remarkable for skin bruising, fever, splenomegaly, and lymphadenopathy.
Laboratory Findings
Patients with myeloproliferative neoplasm are usually well-appearing. Physical examination of patients with chronic myelogenous leukemia is usually remarkable for skin bruising, fever, splenomegaly, and lymphadenopathy.
Chest X-Ray
The chest x-ray may be helpful in the diagnosis of myeloproliferative neoplasm and can reveal pleural effusions, pneumonia, and pulmonary edema.
CT
Abdominal and chest CT scan may be helpful in the diagnosis of myeloproliferative neoplasm. Findings on CT scan suggestive of myeloproliferative neoplasm include enlarged lymph nodes, hepatosplenomegaly, splanchnic venous thrombosis, and pulmonary embolism.
MRI
Brain MRI is helpful in the detection of thrombotic events, such as ischemic stroke, in patients with myeloproliferative neoplasm. Abdominal MRI is helpful in the detection of mesenteric thrombosis in patients with myeloproliferative neoplasm.
Ultrasound
Ultrasound may be helpful in the diagnosis of myeloproliferative neoplasm. Findings on abdominal ultrasound suggestive of myeloproliferative neoplasm include enlarged lymph nodes, hepatosplenomegaly, and ascites. Findings on extremity ultrasound include thrombosis.
Other Imaging Findings
Other imaging studies for myeloproliferative neoplasm include positron emission tomography (PET) scan, which helps to detect metastasis in bone marrow and to follow up medical treatment.
Other Diagnostic Studies
Other diagnostic studies for myeloproliferative neoplasm include bone marrow aspiration and trephine biopsy, erythropoietin level, lumbar puncture, and lymph node biopsy.
Treatment
Medical Therapy
Medical therapy for myeloproliferative neoplasm is based on the specific subtype of myeloproliferative neoplasm. The mainstay of therapy for myeloproliferative neoplasm is chemotherapy, cytoreduction, aspirin, and palliative care. Treatment is directed at reducing the excessive numbers of blood cells.
Surgery
Surgical intervention is usually not recommended for the management of chronic myelogenous leukemia unless there is splenomegaly.
Primary Prevention
There is no established method for primary prevention of myeloproliferative neoplasm.
Secondary Prevention
Secondary prevention measures include routine monitoring of laboratory values, including complete blood count (CBC) and metabolic panel.
Future of Investigational Therapies
Future or investigational therapies in myeloproliferative neoplasms include BLU-285, JQ1, and suberoylanilide hydroxamic acid. Each of these investigational agents carries a unique mechanism of action on myeloid cells. The agents are currently in clinical trials.