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==Acute promyelocytic leukemia risk factors==
==Acute promyelocytic leukemia risk factors==
*'''Advanced age''': This is the most common [[risk factor]] for acute leukemia. [[Old age|Elderly]] [[Patient|patients]] are more likely to develop [[myeloid leukemia]], due to a longer duration and opportunity for [[Mutation|mutations]] to accumulate in [[Cell (biology)|cells]]. These [[Mutation|mutations]] are more likely to accumulate in [[hematopoietic]] [[Stem cell|stem cells]] through a process called clonal evolution.<ref name="pmid25056697">{{cite journal| author=Grove CS, Vassiliou GS| title=Acute myeloid leukaemia: a paradigm for the clonal evolution of cancer? | journal=Dis Model Mech | year= 2014 | volume= 7 | issue= 8 | pages= 941-51 | pmid=25056697 | doi=10.1242/dmm.015974 | pmc=4107323 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25056697  }} </ref>
*'''Advanced age'''
*'''Benzene''': [[Benzene]] is a [[chemical]] [[solvent]] and [[aromatic]] [[hydrocarbon]], for which exposure is a significant [[risk factor]] for [[acute leukemia]].<ref name="pmid22166497">{{cite journal| author=McHale CM, Zhang L, Smith MT| title=Current understanding of the mechanism of benzene-induced leukemia in humans: implications for risk assessment. | journal=Carcinogenesis | year= 2012 | volume= 33 | issue= 2 | pages= 240-52 | pmid=22166497 | doi=10.1093/carcin/bgr297 | pmc=3271273 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22166497  }} </ref>
**This is the most common [[risk factor]] for acute leukemia.
*'''Prior myelodysplastic syndrome''': [[Myelodysplastic syndrome]] is a [[Disorder (medicine)|disorder]] characterized by ineffective [[hematopoiesis]], defective [[maturation]] of [[Blood cell|blood cells]], and peripheral [[Cytopenia|cytopenias]]. Antecedant [[myelodysplastic syndrome]] is implicated in some forms of [[acute leukemia]], such as [[acute myeloid leukemia]]. [[Myelodysplastic syndrome]] is a [[precursor]] for [[leukemia]], as this [[disease]] is characterized by the presence of [[Dysplasia|dysplastic]] or [[cancerous]] [[cells]] that do not meet the requirements for a formal [[diagnosis]] of [[leukemia]].<ref name="pmid23980065">{{cite journal| author=Malcovati L, Hellström-Lindberg E, Bowen D, Adès L, Cermak J, Del Cañizo C et al.| title=Diagnosis and treatment of primary myelodysplastic syndromes in adults: recommendations from the European LeukemiaNet. | journal=Blood | year= 2013 | volume= 122 | issue= 17 | pages= 2943-64 | pmid=23980065 | doi=10.1182/blood-2013-03-492884 | pmc=3811170 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23980065  }} </ref>
**[[Old age|Elderly]] [[Patient|patients]] are more likely to develop [[myeloid leukemia]], due to a longer duration and opportunity for [[Mutation|mutations]] to accumulate in [[Cell (biology)|cells]].  
*'''Germline mutations''': In general, [[germline]] [[predisposition]] to [[acute promyelocytic leukemia]] is rare. In [[patient]]<nowiki/>s with [[acute myeloid leukemia]], [[germline]] [[Mutation|mutations]] in the ''[[RUNX1]]'' gene can predispose to the development of the [[cancer]].<ref name="pmid28179279">{{cite journal| author=Sood R, Kamikubo Y, Liu P| title=Role of RUNX1 in hematological malignancies. | journal=Blood | year= 2017 | volume= 129 | issue= 15 | pages= 2070-2082 | pmid=28179279 | doi=10.1182/blood-2016-10-687830 | pmc=5391618 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28179279  }} </ref>
**These [[Mutation|mutations]] are more likely to accumulate in [[hematopoietic]] [[Stem cell|stem cells]] through a process called clonal evolution.<ref name="pmid25056697">{{cite journal| author=Grove CS, Vassiliou GS| title=Acute myeloid leukaemia: a paradigm for the clonal evolution of cancer? | journal=Dis Model Mech | year= 2014 | volume= 7 | issue= 8 | pages= 941-51 | pmid=25056697 | doi=10.1242/dmm.015974 | pmc=4107323 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25056697  }} </ref>
*'''Benzene'''
**[[Benzene]] is a [[chemical]] [[solvent]] and [[aromatic]] [[hydrocarbon]], for which exposure is a significant [[risk factor]] for [[acute leukemia]].<ref name="pmid22166497">{{cite journal| author=McHale CM, Zhang L, Smith MT| title=Current understanding of the mechanism of benzene-induced leukemia in humans: implications for risk assessment. | journal=Carcinogenesis | year= 2012 | volume= 33 | issue= 2 | pages= 240-52 | pmid=22166497 | doi=10.1093/carcin/bgr297 | pmc=3271273 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22166497  }} </ref>
*'''Prior myelodysplastic syndrome''':  
**[[Myelodysplastic syndrome]] is a [[Disorder (medicine)|disorder]] characterized by ineffective [[hematopoiesis]], defective [[maturation]] of [[Blood cell|blood cells]], and peripheral [[Cytopenia|cytopenias]].
**Antecedant [[myelodysplastic syndrome]] is implicated in some forms of [[acute leukemia]], such as [[acute myeloid leukemia]].  
**[[Myelodysplastic syndrome]] is a [[precursor]] for [[leukemia]], as this [[disease]] is characterized by the presence of [[Dysplasia|dysplastic]] or [[cancerous]] [[cells]] that do not meet the requirements for a formal [[diagnosis]] of [[leukemia]].<ref name="pmid23980065">{{cite journal| author=Malcovati L, Hellström-Lindberg E, Bowen D, Adès L, Cermak J, Del Cañizo C et al.| title=Diagnosis and treatment of primary myelodysplastic syndromes in adults: recommendations from the European LeukemiaNet. | journal=Blood | year= 2013 | volume= 122 | issue= 17 | pages= 2943-64 | pmid=23980065 | doi=10.1182/blood-2013-03-492884 | pmc=3811170 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23980065  }} </ref>
*'''Germline mutations'''
**In general, [[germline]] [[predisposition]] to [[acute promyelocytic leukemia]] is rare. In [[patient|patie]]<nowiki/>[[patient|nt]]<nowiki/>s with [[acute myeloid leukemia|acute myeloid]]<nowiki/> [[acute myeloid leukemia|leukemia]], [[germline]] [[Mutation|mutations]] in the ''[[RUNX1]]'' gene can predispose to the development of the [[cancer]].<ref name="pmid28179279">{{cite journal| author=Sood R, Kamikubo Y, Liu P| title=Role of RUNX1 in hematological malignancies. | journal=Blood | year= 2017 | volume= 129 | issue= 15 | pages= 2070-2082 | pmid=28179279 | doi=10.1182/blood-2016-10-687830 | pmc=5391618 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28179279  }} </ref>


==References==
==References==

Revision as of 19:23, 13 March 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2] Associate Editor(s)-in-Chief: Sogand Goudarzi, MD [3]

Overview

Risk factors for acute promyelocytic leukemia are similar to risk factors for acute myeloid leukemia. These include advanced age, benzene exposure, prior myelodysplastic syndrome, and germline mutations.

Acute promyelocytic leukemia risk factors

References

  1. Grove CS, Vassiliou GS (2014). "Acute myeloid leukaemia: a paradigm for the clonal evolution of cancer?". Dis Model Mech. 7 (8): 941–51. doi:10.1242/dmm.015974. PMC 4107323. PMID 25056697.
  2. McHale CM, Zhang L, Smith MT (2012). "Current understanding of the mechanism of benzene-induced leukemia in humans: implications for risk assessment". Carcinogenesis. 33 (2): 240–52. doi:10.1093/carcin/bgr297. PMC 3271273. PMID 22166497.
  3. Malcovati L, Hellström-Lindberg E, Bowen D, Adès L, Cermak J, Del Cañizo C; et al. (2013). "Diagnosis and treatment of primary myelodysplastic syndromes in adults: recommendations from the European LeukemiaNet". Blood. 122 (17): 2943–64. doi:10.1182/blood-2013-03-492884. PMC 3811170. PMID 23980065.
  4. Sood R, Kamikubo Y, Liu P (2017). "Role of RUNX1 in hematological malignancies". Blood. 129 (15): 2070–2082. doi:10.1182/blood-2016-10-687830. PMC 5391618. PMID 28179279.

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