Myeloproliferative neoplasm medical therapy: Difference between revisions
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Imatinib | Imatinib<ref name="pmid28254862">{{cite journal| author=Valent P, Akin C, Hartmann K, Nilsson G, Reiter A, Hermine O et al.| title=Advances in the Classification and Treatment of Mastocytosis: Current Status and Outlook toward the Future. | journal=Cancer Res | year= 2017 | volume= 77 | issue= 6 | pages= 1261-1270 | pmid=28254862 | doi=10.1158/0008-5472.CAN-16-2234 | pmc=5354959 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28254862 }} </ref> | ||
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Tyrosine kinase inhibitor that inhibits wild-type ''c-kit''; not effective for ''c-kit'' ''D816V'' mutation | Tyrosine kinase inhibitor that inhibits wild-type ''c-kit''; not effective for ''c-kit'' ''D816V'' mutation | ||
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Midostaurin | Midostaurin<ref name="pmid28254862">{{cite journal| author=Valent P, Akin C, Hartmann K, Nilsson G, Reiter A, Hermine O et al.| title=Advances in the Classification and Treatment of Mastocytosis: Current Status and Outlook toward the Future. | journal=Cancer Res | year= 2017 | volume= 77 | issue= 6 | pages= 1261-1270 | pmid=28254862 | doi=10.1158/0008-5472.CAN-16-2234 | pmc=5354959 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28254862 }} </ref> | ||
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Tyrosine kinase inhibitor that inhibits wild-type ''c-kit'' and mutant ''c-kit'' ''D816V'' | Tyrosine kinase inhibitor that inhibits wild-type ''c-kit'' and mutant ''c-kit'' ''D816V'' |
Revision as of 23:14, 23 June 2018
Myeloproliferative Neoplasm Microchapters |
Differentiating myeloproliferative neoplasm from other Diseases |
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Diagnosis |
Treatment |
Case Studies |
Myeloproliferative neoplasm medical therapy On the Web |
American Roentgen Ray Society Images of Myeloproliferative neoplasm medical therapy |
Directions to Hospitals Treating Myeloproliferative neoplasm |
Risk calculators and risk factors for Myeloproliferative neoplasm medical therapy |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Mohamad Alkateb, MBBCh [2] Shyam Patel [3]
Overview
The mainstay of therapy for myeloproliferative neoplasm is chemotherapy, aspirin, and palliative care. Treatment is directed at reducing the excessive numbers of blood cells.[1]
Medical Therapy
Medical therapy for myeloproliferative neoplasm is based on the specific subtype of myeloproliferative neoplasm.
Polycythemia vera
Therapy | Mechanism of Action | Dosing | Adverse Effects |
---|---|---|---|
Aspirin |
Irreversibly inhibits cyclooxygenase-1 and -2 (COX-1 and COX-2) |
81mg PO daily |
Mucosal bleeding Gastrointestinal bleeding |
Hydroxyurea |
Inhibits ribonucleotide reductase |
20mg/kg PO daily |
Anemia, thrombocytopenia, ulcerations, secondary cancers |
Ruxolitinib |
Inhibits JAK2 (tyrosine kinase inhibitor) |
10mg PO twice daily |
Weight gain, zoster, non-melanoma skin cancers, cytopenias |
Phlebotomy |
Mechanically removes red blood cells from circulation |
|
Iron deficiency anemia, fatigue, vasovagal episodes, pain at phlebotomy site |
Essential thrombocythemia
Treatment of essential thrombocythemia is based on risk assessment and prognostication:
Prognostic Group | Defining Features | Therapy |
---|---|---|
Very low risk[2] |
|
or
|
Low risk[2] |
|
or
|
Intermediate risk[2] |
|
|
High risk[2] |
|
or
|
Therapy | Mechanism of Action | Dosing | Adverse Effects |
---|---|---|---|
Anagrelide |
|
0.5mg PO every 6 hours or 1mg every 12 hours |
Headache, palpitations, diarrhea, edema, nausea |
Hydroxyurea |
Inhibits ribonucleotide reductase |
20mg/kg PO daily |
Anemia, thrombocytopenia, ulcerations, secondary cancers |
Aspirin |
Irreversibly inhibits cyclooxygenase-1 and -2 (COX-1 and COX-2) |
81mg PO twice daily |
Mucosal bleeding Gastrointestinal bleeding |
Ruxolitinib |
Inhibits JAK2 (tyrosine kinase inhibitor) |
10mg PO twice daily |
Weight gain, zoster, non-melanoma skin cancers, cytopenias |
Plateletpheresis |
Mechanically removes platelets from circulation |
Daily until platelet count returns to normal range |
Hypotension, thrombocytopenia |
Pegylated interferon alpha 2a |
Immunomodulatory agent; anti-angiogenic agent |
45mcg/week |
Hypotension, infusion reaction |
Primary myelofibrosis
Therapy | Mechanism of Action | Dosing | Adverse Effects |
---|---|---|---|
Hydroxyurea |
Inhibits ribonucleotide reductase |
20mg/kg PO daily |
Anemia, thrombocytopenia, ulcerations, secondary cancers |
Ruxolitinib |
Inhibits JAK2 (tyrosine kinase inhibitor) |
10mg PO twice daily |
Weight gain, zoster, non-melanoma skin cancers, cytopenias |
Radiation therapy |
Unknown mechanism |
0.5 Gy to spleen 5 days weekly |
Fatigue, secondary cancers, nausea, cytopenias |
Chronic myeloid leukemia
Therapy | Mechanism of Action | Dosing | Adverse Effects |
---|---|---|---|
Imatinib |
Inhibits BCR-ABL tyrosine kinase |
400mg PO daily |
Edema, periorbital swelling, nausea, anasarca |
Dasatinib |
Inhibits BCR-ABL tyrosine kinase |
100mg PO daily |
Pleural effusions, edema, periorbital swelling, facial edema |
Nilotinib |
Inhibits BCR-ABL tyrosine kinase |
400mg PO twice daily |
Occlusive arterial disease, peripheral vascular disease, cytopenias, nausea |
Bosutinib |
Inhibits BCR-ABL tyrosine kinase |
400mg PO daily |
Edema, chest pain, fatigue, diarrhea |
Ponatinib |
Inhibits BCR-ABL tyrosine kinase |
45mg PO daily |
Hypertension, arterial ischemia, fatigue, constipation |
Omacetaxine |
Inhibits protein synthesis |
|
Peripheral edema, fatigue, nausea, thrombocytopenia |
Chronic neutrophilic leukemia
Therapy | Mechanism of Action | Dosing | Adverse Effects |
---|---|---|---|
Hydroxyurea |
Inhibits ribonucleotide reductase |
20mg/kg PO daily |
Anemia, thrombocytopenia, ulcerations, secondary cancers |
Pegylated interferon alpha 2a |
Immunomodulatory agent; anti-angiogenic agent |
45mcg/week |
Hypotension, infusion reaction |
Systemic mastocytosis
Therapy | Mechanism of Action | Dosing | Adverse Effects |
---|---|---|---|
Imatinib[3] |
Tyrosine kinase inhibitor that inhibits wild-type c-kit; not effective for c-kit D816V mutation |
400mg PO daily |
Edema, periorbital swelling, nausea, anasarca |
Midostaurin[3] |
Tyrosine kinase inhibitor that inhibits wild-type c-kit and mutant c-kit D816V |
10mg PO twice daily |
Nausea, hypocalcemia, mucositis, headache, epistaxis, hypernatremia |
References
- ↑ National Cancer Institute. Physician Data Query Database 2015.http://www.cancer.gov/types/leukemia/hp/cml-treatment-pdq#section/_19
- ↑ 2.0 2.1 2.2 2.3 Tefferi A, Vannucchi AM, Barbui T (2018). "Essential thrombocythemia treatment algorithm 2018". Blood Cancer J. 8 (1): 2. doi:10.1038/s41408-017-0041-8. PMC 5802626. PMID 29321520.
- ↑ 3.0 3.1 Valent P, Akin C, Hartmann K, Nilsson G, Reiter A, Hermine O; et al. (2017). "Advances in the Classification and Treatment of Mastocytosis: Current Status and Outlook toward the Future". Cancer Res. 77 (6): 1261–1270. doi:10.1158/0008-5472.CAN-16-2234. PMC 5354959. PMID 28254862.