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Erschienen in: Journal of Cancer Research and Clinical Oncology 12/2015

01.12.2015 | Original Article – Cancer Research

Changing incidence of myeloproliferative neoplasms: trends and subgroup risk profiles in the USA, 1973–2011

verfasst von: Melissa A. Deadmond, Julie A. Smith-Gagen

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 12/2015

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Abstract

Purpose

Recent diagnostic and cancer reporting changes influencing myeloproliferative neoplasms (MPNs) encourage the assessment of trends and examination of the recently identified MPN subtypes: polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF), across the age continuum by race and ethnicity.

Methods

Surveillance, Epidemiology, and End Results data provided MPN incidence data since 1973 and MPN subtype data since 2001. Joinpoint regression estimated annual percent changes. Poisson regression estimated risk ratios.

Results

The 2005 JAK2 V617F discovery and the 2008 WHO diagnostic guideline for the JAK2 V617F mutation coincide with a 31 % increase in ET and a 21 % decrease in PV incidence rates. We found that younger women had a 13–33 % higher ET risk and that women under the age of 34 had a 58 % higher PMF risk, relative to men. Blacks, aged 35–49 with a higher ET risk, also had a 69 % higher PMF risk relative to whites.

Conclusion

Demographic characteristic of ET and PMF patients may be useful for improving risk prediction and informing clinical screening and treatment strategies. Changing guidelines, new discoveries, and in-depth analysis of a large population-based study have implications for accurately identifying incident cases of MPNs, MPN subgroups, and health resource planning.
Literatur
Zurück zum Zitat Alvarez-Larrán BB, Pereira A, Kerguelen A, Hernández-Boluda JC, Martínez-Avilés L et al (2014) JAK2V617F monitoring in polycythemia vera and essential thrombocythemia: clinical usefulness for predicting myelofibrotic transformation and thrombotic events. Am J Hematol 89:517–523CrossRefPubMed Alvarez-Larrán BB, Pereira A, Kerguelen A, Hernández-Boluda JC, Martínez-Avilés L et al (2014) JAK2V617F monitoring in polycythemia vera and essential thrombocythemia: clinical usefulness for predicting myelofibrotic transformation and thrombotic events. Am J Hematol 89:517–523CrossRefPubMed
Zurück zum Zitat Anderson LA, McMullin MF (2014) Epidemiology of MPN: what do we know. Curr Hematol Malig Rep 9:340–349CrossRefPubMed Anderson LA, McMullin MF (2014) Epidemiology of MPN: what do we know. Curr Hematol Malig Rep 9:340–349CrossRefPubMed
Zurück zum Zitat Bain BJ (2004) The World Health Organization classification of myeloproliferative and myelodysplastic syndromes. Curr Diagn Pathol 10:394–403CrossRef Bain BJ (2004) The World Health Organization classification of myeloproliferative and myelodysplastic syndromes. Curr Diagn Pathol 10:394–403CrossRef
Zurück zum Zitat Bhayat F, Das-Gupta E, Smith C, McKeever T, Hubbard R (2009) The incidence of and mortality from leukaemias in the UK: a general population-based study. BMC Cancer 9:252PubMedCentralCrossRefPubMed Bhayat F, Das-Gupta E, Smith C, McKeever T, Hubbard R (2009) The incidence of and mortality from leukaemias in the UK: a general population-based study. BMC Cancer 9:252PubMedCentralCrossRefPubMed
Zurück zum Zitat Chasseriau J, Rivet J, Bilan F, Chomel J-C, Guilhot F, Bourmeyster N, Kitzis A (2004) Characterization of the different BCR–ABL transcripts with a single multiplex RT-PCR. J Mol Diagn 6:343–347PubMedCentralCrossRefPubMed Chasseriau J, Rivet J, Bilan F, Chomel J-C, Guilhot F, Bourmeyster N, Kitzis A (2004) Characterization of the different BCR–ABL transcripts with a single multiplex RT-PCR. J Mol Diagn 6:343–347PubMedCentralCrossRefPubMed
Zurück zum Zitat Craig BM, Rollison DE, List AF, Cogle CR (2011) Diagnostic testing, treatment, cost of care, and survival among registered and non-registered patients with myelodysplastic syndromes. Leuk Res 35:1453–1456PubMedCentralCrossRefPubMed Craig BM, Rollison DE, List AF, Cogle CR (2011) Diagnostic testing, treatment, cost of care, and survival among registered and non-registered patients with myelodysplastic syndromes. Leuk Res 35:1453–1456PubMedCentralCrossRefPubMed
Zurück zum Zitat Craig BM, Rollison DE, List AF, Cogle CR (2012) Underreporting of myeloid malignancies by united states cancer registries. Cancer epidemiology, biomarkers & prevention: a publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology 21:474–481 Craig BM, Rollison DE, List AF, Cogle CR (2012) Underreporting of myeloid malignancies by united states cancer registries. Cancer epidemiology, biomarkers & prevention: a publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology 21:474–481
Zurück zum Zitat Heisterkamp N, Stephenson JR, Groffen J, Hansen PF, de Klein A, Bartram CR, Grosveld G (1983) Localization of the c-ABL oncogene adjacent to a translocation breakpoint in chronic myelocytic leukaemia. Nature 306:239–242CrossRefPubMed Heisterkamp N, Stephenson JR, Groffen J, Hansen PF, de Klein A, Bartram CR, Grosveld G (1983) Localization of the c-ABL oncogene adjacent to a translocation breakpoint in chronic myelocytic leukaemia. Nature 306:239–242CrossRefPubMed
Zurück zum Zitat Heisterkamp N, Stam K, Groffen J, de Klein A, Grosveld G (1985) Structural organization of the BCR gene and its role in the Ph’ translocation. Nature 315:758–761CrossRefPubMed Heisterkamp N, Stam K, Groffen J, de Klein A, Grosveld G (1985) Structural organization of the BCR gene and its role in the Ph’ translocation. Nature 315:758–761CrossRefPubMed
Zurück zum Zitat James C, Ugo V, Le Couedic J, Staerk J, Delhommeau F, Lacout C et al (2005) A unique clonal JAK2 mutation leading to constitutive signaling causes polycythaemia vera. Nature 434:1144–1148CrossRefPubMed James C, Ugo V, Le Couedic J, Staerk J, Delhommeau F, Lacout C et al (2005) A unique clonal JAK2 mutation leading to constitutive signaling causes polycythaemia vera. Nature 434:1144–1148CrossRefPubMed
Zurück zum Zitat Joinpoint Regression Program, Version 4.1.1.4—February (2015) Statistical Methodology and Applications Branch, Surveillance Research Program, National Cancer Institute Joinpoint Regression Program, Version 4.1.1.4—February (2015) Statistical Methodology and Applications Branch, Surveillance Research Program, National Cancer Institute
Zurück zum Zitat Jones AV, Kreil S, Zoi K, Waghorn K, Curtis C, Zhang L et al (2005) Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. Blood 106:2162–2168CrossRefPubMed Jones AV, Kreil S, Zoi K, Waghorn K, Curtis C, Zhang L et al (2005) Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. Blood 106:2162–2168CrossRefPubMed
Zurück zum Zitat Kim H, Fay MP, Yu B, Barrett MJ, Feuer EJ (2004) Comparability of segmented line regression models. Biometrics 60:1005–1014CrossRefPubMed Kim H, Fay MP, Yu B, Barrett MJ, Feuer EJ (2004) Comparability of segmented line regression models. Biometrics 60:1005–1014CrossRefPubMed
Zurück zum Zitat Kramárová E, Stiller CA (1996) The international classification of childhood cancer. Int J Cancer 68:759–765CrossRefPubMed Kramárová E, Stiller CA (1996) The international classification of childhood cancer. Int J Cancer 68:759–765CrossRefPubMed
Zurück zum Zitat Kvasnicka HM (2013) WHO classification of myeloproliferative neoplasms (MPN): a critical update. Curr Hematol Malig Rep 8:333–341CrossRefPubMed Kvasnicka HM (2013) WHO classification of myeloproliferative neoplasms (MPN): a critical update. Curr Hematol Malig Rep 8:333–341CrossRefPubMed
Zurück zum Zitat Ma X, Does M, Raza A, Mayne ST (2007) Myelodysplastic syndromes: incidence and survival in the United States. Cancer 109:1536–1542CrossRefPubMed Ma X, Does M, Raza A, Mayne ST (2007) Myelodysplastic syndromes: incidence and survival in the United States. Cancer 109:1536–1542CrossRefPubMed
Zurück zum Zitat NAACCR Race and Ethnicity Work Group (2014) NAACCR Guideline for enhancing hispanic/latino identification: revised NAACCR hispanic/latino identification algorithm[NHIA v2.2.1].Springfield (IL): North American Association of Central Cancer Registries NAACCR Race and Ethnicity Work Group (2014) NAACCR Guideline for enhancing hispanic/latino identification: revised NAACCR hispanic/latino identification algorithm[NHIA v2.2.1].Springfield (IL): North American Association of Central Cancer Registries
Zurück zum Zitat Price GL, Davis KL, Karve S, Pohl G, Walgren RA (2014) Survival patterns in United States (US) medicare enrollees with non-CML myeloproliferative neoplasms (MPN). PLoS One. 9(3):e90299PubMedCentralCrossRefPubMed Price GL, Davis KL, Karve S, Pohl G, Walgren RA (2014) Survival patterns in United States (US) medicare enrollees with non-CML myeloproliferative neoplasms (MPN). PLoS One. 9(3):e90299PubMedCentralCrossRefPubMed
Zurück zum Zitat Rollison DE, Howlader N, Smith MT, Strom SS, Merritt WD et al (2008) Epidemiology of myelodysplastic syndromes and chronic myeloproliferative disorder in the United States, 2001-2004, using data from the NAACCR and SEER programs. Blood 112:45–52CrossRefPubMed Rollison DE, Howlader N, Smith MT, Strom SS, Merritt WD et al (2008) Epidemiology of myelodysplastic syndromes and chronic myeloproliferative disorder in the United States, 2001-2004, using data from the NAACCR and SEER programs. Blood 112:45–52CrossRefPubMed
Zurück zum Zitat SAS/STAT software, Version 9.3 of the SAS System for PC. (2014) SAS Institute Inc., Cary, NC, USA SAS/STAT software, Version 9.3 of the SAS System for PC. (2014) SAS Institute Inc., Cary, NC, USA
Zurück zum Zitat Selinger HA, Ma X (2009) Jakking up tumor registry reporting of the myeloproliferative neoplasms. Am J Hematol 84:124–126CrossRefPubMed Selinger HA, Ma X (2009) Jakking up tumor registry reporting of the myeloproliferative neoplasms. Am J Hematol 84:124–126CrossRefPubMed
Zurück zum Zitat Spivak JL, Silver RT (2008) The revised WHO Organization diagnostic criteria for polycythemia vera, essential thrombocytosis, and primary myelofibrosis: an alternative proposal. Blood 112:231–239CrossRefPubMed Spivak JL, Silver RT (2008) The revised WHO Organization diagnostic criteria for polycythemia vera, essential thrombocytosis, and primary myelofibrosis: an alternative proposal. Blood 112:231–239CrossRefPubMed
Zurück zum Zitat Steliarova-Foucher E, Stiller C, Lacour B, Kaatsch P (2005) International classification of childhood cancer, third edition. Cancer 103:1457–1467CrossRefPubMed Steliarova-Foucher E, Stiller C, Lacour B, Kaatsch P (2005) International classification of childhood cancer, third edition. Cancer 103:1457–1467CrossRefPubMed
Zurück zum Zitat Surveillance, Epidemiology, and End Results (SEER) Program (www.seer.cancer.gov) SEER*Stat Database: incidence—SEER 9 Regs Research Data, Nov 2013 Sub (1973–2011) <Katrina/Rita Population Adjustment>- Linked To County Attributes—Total US, 1969-2012 Counties, National Cancer Institute, DCCPS, Surveillance Research Program, Surveillance Systems Branch, released April 2014, based on the November 2013 submission. www.seer.cancer.gov. Accessed 16 Sept 2014 Surveillance, Epidemiology, and End Results (SEER) Program (www.​seer.​cancer.​gov) SEER*Stat Database: incidence—SEER 9 Regs Research Data, Nov 2013 Sub (1973–2011) <Katrina/Rita Population Adjustment>- Linked To County Attributes—Total US, 1969-2012 Counties, National Cancer Institute, DCCPS, Surveillance Research Program, Surveillance Systems Branch, released April 2014, based on the November 2013 submission. www.​seer.​cancer.​gov. Accessed 16 Sept 2014
Zurück zum Zitat Swerdlow AJ, Schoemaker MJ, Higgins CD, Wright AF, Jacobs PA (2008) Cancer risk in patients with constitutional chromosome deletions: a nationwide British cohort study. Br J Cancer 98:1929–1933PubMedCentralCrossRefPubMed Swerdlow AJ, Schoemaker MJ, Higgins CD, Wright AF, Jacobs PA (2008) Cancer risk in patients with constitutional chromosome deletions: a nationwide British cohort study. Br J Cancer 98:1929–1933PubMedCentralCrossRefPubMed
Zurück zum Zitat Tefferi A, Lasho TL, Finke CM, Knudson RA, Ketterling R, Hanson Ch et al (2014) CALR vs JAK2 vs MPL-mutated or triple-negative myelofibrosis: clinical, cytogenetic and molecular comparisons. Leukemia 28:1472–1477CrossRefPubMed Tefferi A, Lasho TL, Finke CM, Knudson RA, Ketterling R, Hanson Ch et al (2014) CALR vs JAK2 vs MPL-mutated or triple-negative myelofibrosis: clinical, cytogenetic and molecular comparisons. Leukemia 28:1472–1477CrossRefPubMed
Zurück zum Zitat Titmarsh GL, Duncombe AS, McMullin MF, O’Rorke M, Mesa R, De Vocht F et al (2014) How common are myeloproliferative neoplasms? A systematic review and meta-analysis. Am J Hematol 112:581–587CrossRef Titmarsh GL, Duncombe AS, McMullin MF, O’Rorke M, Mesa R, De Vocht F et al (2014) How common are myeloproliferative neoplasms? A systematic review and meta-analysis. Am J Hematol 112:581–587CrossRef
Zurück zum Zitat Vardiman JW, Thiele J, Arber DA, Brunning RD, Borowitz MJ, Porwit A et al (2009) The 2008 revision of the world health organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood 114:937–951CrossRefPubMed Vardiman JW, Thiele J, Arber DA, Brunning RD, Borowitz MJ, Porwit A et al (2009) The 2008 revision of the world health organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes. Blood 114:937–951CrossRefPubMed
Zurück zum Zitat Yacoub A, Odenike O, Verstovsek S (2014) Ruxolitinib: long-term management of patients with myelofibrosis and future directions in the treatment of myeloproliferative neoplasms. Curr Hematol Malig Rep 9:350–359PubMedCentralCrossRefPubMed Yacoub A, Odenike O, Verstovsek S (2014) Ruxolitinib: long-term management of patients with myelofibrosis and future directions in the treatment of myeloproliferative neoplasms. Curr Hematol Malig Rep 9:350–359PubMedCentralCrossRefPubMed
Zurück zum Zitat Zhang SP, Li H, Lai RS (2015) Detection of JAK2 V617F mutation increases the diagnosis of myeloproliferative neoplasms. Oncol Lett 9:735–738PubMedCentralPubMed Zhang SP, Li H, Lai RS (2015) Detection of JAK2 V617F mutation increases the diagnosis of myeloproliferative neoplasms. Oncol Lett 9:735–738PubMedCentralPubMed
Metadaten
Titel
Changing incidence of myeloproliferative neoplasms: trends and subgroup risk profiles in the USA, 1973–2011
verfasst von
Melissa A. Deadmond
Julie A. Smith-Gagen
Publikationsdatum
01.12.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 12/2015
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-015-1983-5

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