Assessing Epidemiological Differences in Myelofibrosis: A Comparative Study of a Single-Center Cohort and the SEER National Database

Background Myelofibrosis (MF) is a rare class of BCR-ABL negative myeloproliferative neoplasms characterized by clonal proliferation of hematopoietic stem cells and progressive fibrosis of the bone marrow. This study attempts to elucidate epidemiological discrepancies in survival outcomes between MF...

Full description

Saved in:
Bibliographic Details
Published inBlood Vol. 142; no. Supplement 1; p. 7426
Main Authors Yan, John, Wei, John X, Verma, Amit, Shah, Nishi, Goel, Swati
Format Journal Article
LanguageEnglish
Published Elsevier Inc 02.11.2023
Online AccessGet full text
ISSN0006-4971
1528-0020
DOI10.1182/blood-2023-184932

Cover

Abstract Background Myelofibrosis (MF) is a rare class of BCR-ABL negative myeloproliferative neoplasms characterized by clonal proliferation of hematopoietic stem cells and progressive fibrosis of the bone marrow. This study attempts to elucidate epidemiological discrepancies in survival outcomes between MF patients at a single tertiary care center from an underserved population in the Bronx (which ranks last in health outcomes amongst 62 New York state counties) versus the Survival, Epidemiology, and End Results (SEER) national cancer registry by analyzing different population parameters. Methods Our retrospectively constructed single center database included 96 patients with biopsy confirmed primary or secondary MF who were age ≥20 diagnosed after 2000. 75 remained for analysis after excluding subjects without known race or date of diagnosis. The SEER [SEER research plus data, 17 registries, Nov 2022 Sub (2000-2020)] dataset comprised of 5254 patients with microscopically confirmed primary MF (ICD code: 9661.3) diagnosed between 2000 and 2015, had age of diagnosis ≥20, and whose deaths were attributable to MF diagnosis. Both cohorts were independently analyzed via log-rank testing and/or cox proportional hazards (cox-PH) regression with death as event outcome. Results Mean age of our single-center cohort was 65.87 years. Males [37 (49.3%)] and females [38 (50.7%)] were approximately evenly distributed. Races included non-hispanic white (NHW) [26 (34.7%)], NH black (NHB) [20 (26.7%)], NH asian and pacific islanders (NH-API) [6 (8.0%)], and hispanics of all races [23 (30.7%)]. Primary [40 (53.3%)] and secondary [35 (46.7%)] MF were approximately even. Log rank testing detected significance in race (p=.05) but not sex (p=.2) or type (p=.7). Significant univariate cox-PH findings include increased mortality within the NHB group [hazard ratio (HR) 2.69, p=.04] and increased mortality with age (HR 1.07, p=.005) (Table 1). Low event size precluded multivariate analysis. In the SEER cohort, age was grouped into 4 categories: ≤44 years old [214 (4.1%)], 45-64 [1,590 (30.3%)], 65-84 [3,051 (58.1%)], and ≥85 [399 (7.6%)]. There were more females [3,159 (60.1%)] than males [2,095 (39.9%)]. NHW [3,995 (76.0%)] comprised the overwhelming majority of races reported, followed by NHB [441 (8.4%)], hispanic [420 (8.0%)], and NH-API [398 (7.6%)]. Median household income (MHI) data (inflation adjusted to 2021) was divided into <$70,000 and ≥$70,000 (table 2). Univariate cox-PH noted improved survival in NH-APIs (HR .75, p<.001) and MHI ≥$70K (HR .92, p=.05). However this significance disappeared upon adjustment for age and race. In multivariate cox-PH, age demonstrated significance for each category (45-64 HR 2.20; 65-84 HR 4.45; ≥85 HR 6.59, p < .001). Female patients had better survival compared to males (HR .73, p<.001) (Table 2). Conclusion In this comparison study of MF cohorts from an underserved tertiary center and SEER, we found differences in demographic features and their impact on disease mortality. NHW patients constitute the overwhelming majority of subjects in the SEER dataset while the tertiary cohort has nearly equal distribution of NHW, NHB, and hispanic patients. NHB patients from the single-center cohort tended to do worse while SEER showed no differential survival based on race. Possible explanations for this include differences in racial distribution, healthcare accessibility, and other socioeconomic factors. Median income in the Bronx is 36% lower than the national average and the poverty rate is 2.3x higher. Unexpectedly, no significant association was found between MHI and survival in SEER when adjusted for age and race. Also notable is that improved survival in NH-APIs per SEER data disappeared upon adjustment for age, which may suggest that the NH-API group tends to be younger at diagnosis given that age serves as a negative prognostic marker. Further research is warranted. Regarding sex, SEER data suggests that female patients have a decreased mortality risk compared to males which is consistent with literature. Caution in interpretation is necessary given the low tertiary center sample size and the inherent limitations of the SEER dataset. Verma:Novartis: Other: Scientific Advisor; Bakx: Current equity holder in private company, Other: Scientific Advisor; Stelexis: Current equity holder in private company, Honoraria, Other: Scientific Advisor; Eli Lilly: Research Funding; Curis: Research Funding; Medpacto: Research Funding; Incyte: Research Funding; GSK: Research Funding; BMS: Research Funding; Prelude: Research Funding; Acceleron: Other: Scientific Advisor; Celgene: Other: Scientific Advisor; Janssen: Honoraria; Throws Exception: Current equity holder in private company. [Display omitted]
AbstractList Background Myelofibrosis (MF) is a rare class of BCR-ABL negative myeloproliferative neoplasms characterized by clonal proliferation of hematopoietic stem cells and progressive fibrosis of the bone marrow. This study attempts to elucidate epidemiological discrepancies in survival outcomes between MF patients at a single tertiary care center from an underserved population in the Bronx (which ranks last in health outcomes amongst 62 New York state counties) versus the Survival, Epidemiology, and End Results (SEER) national cancer registry by analyzing different population parameters. Methods Our retrospectively constructed single center database included 96 patients with biopsy confirmed primary or secondary MF who were age ≥20 diagnosed after 2000. 75 remained for analysis after excluding subjects without known race or date of diagnosis. The SEER [SEER research plus data, 17 registries, Nov 2022 Sub (2000-2020)] dataset comprised of 5254 patients with microscopically confirmed primary MF (ICD code: 9661.3) diagnosed between 2000 and 2015, had age of diagnosis ≥20, and whose deaths were attributable to MF diagnosis. Both cohorts were independently analyzed via log-rank testing and/or cox proportional hazards (cox-PH) regression with death as event outcome. Results Mean age of our single-center cohort was 65.87 years. Males [37 (49.3%)] and females [38 (50.7%)] were approximately evenly distributed. Races included non-hispanic white (NHW) [26 (34.7%)], NH black (NHB) [20 (26.7%)], NH asian and pacific islanders (NH-API) [6 (8.0%)], and hispanics of all races [23 (30.7%)]. Primary [40 (53.3%)] and secondary [35 (46.7%)] MF were approximately even. Log rank testing detected significance in race (p=.05) but not sex (p=.2) or type (p=.7). Significant univariate cox-PH findings include increased mortality within the NHB group [hazard ratio (HR) 2.69, p=.04] and increased mortality with age (HR 1.07, p=.005) (Table 1). Low event size precluded multivariate analysis. In the SEER cohort, age was grouped into 4 categories: ≤44 years old [214 (4.1%)], 45-64 [1,590 (30.3%)], 65-84 [3,051 (58.1%)], and ≥85 [399 (7.6%)]. There were more females [3,159 (60.1%)] than males [2,095 (39.9%)]. NHW [3,995 (76.0%)] comprised the overwhelming majority of races reported, followed by NHB [441 (8.4%)], hispanic [420 (8.0%)], and NH-API [398 (7.6%)]. Median household income (MHI) data (inflation adjusted to 2021) was divided into <$70,000 and ≥$70,000 (table 2). Univariate cox-PH noted improved survival in NH-APIs (HR .75, p<.001) and MHI ≥$70K (HR .92, p=.05). However this significance disappeared upon adjustment for age and race. In multivariate cox-PH, age demonstrated significance for each category (45-64 HR 2.20; 65-84 HR 4.45; ≥85 HR 6.59, p < .001). Female patients had better survival compared to males (HR .73, p<.001) (Table 2). Conclusion In this comparison study of MF cohorts from an underserved tertiary center and SEER, we found differences in demographic features and their impact on disease mortality. NHW patients constitute the overwhelming majority of subjects in the SEER dataset while the tertiary cohort has nearly equal distribution of NHW, NHB, and hispanic patients. NHB patients from the single-center cohort tended to do worse while SEER showed no differential survival based on race. Possible explanations for this include differences in racial distribution, healthcare accessibility, and other socioeconomic factors. Median income in the Bronx is 36% lower than the national average and the poverty rate is 2.3x higher. Unexpectedly, no significant association was found between MHI and survival in SEER when adjusted for age and race. Also notable is that improved survival in NH-APIs per SEER data disappeared upon adjustment for age, which may suggest that the NH-API group tends to be younger at diagnosis given that age serves as a negative prognostic marker. Further research is warranted. Regarding sex, SEER data suggests that female patients have a decreased mortality risk compared to males which is consistent with literature. Caution in interpretation is necessary given the low tertiary center sample size and the inherent limitations of the SEER dataset.
Background Myelofibrosis (MF) is a rare class of BCR-ABL negative myeloproliferative neoplasms characterized by clonal proliferation of hematopoietic stem cells and progressive fibrosis of the bone marrow. This study attempts to elucidate epidemiological discrepancies in survival outcomes between MF patients at a single tertiary care center from an underserved population in the Bronx (which ranks last in health outcomes amongst 62 New York state counties) versus the Survival, Epidemiology, and End Results (SEER) national cancer registry by analyzing different population parameters. Methods Our retrospectively constructed single center database included 96 patients with biopsy confirmed primary or secondary MF who were age ≥20 diagnosed after 2000. 75 remained for analysis after excluding subjects without known race or date of diagnosis. The SEER [SEER research plus data, 17 registries, Nov 2022 Sub (2000-2020)] dataset comprised of 5254 patients with microscopically confirmed primary MF (ICD code: 9661.3) diagnosed between 2000 and 2015, had age of diagnosis ≥20, and whose deaths were attributable to MF diagnosis. Both cohorts were independently analyzed via log-rank testing and/or cox proportional hazards (cox-PH) regression with death as event outcome. Results Mean age of our single-center cohort was 65.87 years. Males [37 (49.3%)] and females [38 (50.7%)] were approximately evenly distributed. Races included non-hispanic white (NHW) [26 (34.7%)], NH black (NHB) [20 (26.7%)], NH asian and pacific islanders (NH-API) [6 (8.0%)], and hispanics of all races [23 (30.7%)]. Primary [40 (53.3%)] and secondary [35 (46.7%)] MF were approximately even. Log rank testing detected significance in race (p=.05) but not sex (p=.2) or type (p=.7). Significant univariate cox-PH findings include increased mortality within the NHB group [hazard ratio (HR) 2.69, p=.04] and increased mortality with age (HR 1.07, p=.005) (Table 1). Low event size precluded multivariate analysis. In the SEER cohort, age was grouped into 4 categories: ≤44 years old [214 (4.1%)], 45-64 [1,590 (30.3%)], 65-84 [3,051 (58.1%)], and ≥85 [399 (7.6%)]. There were more females [3,159 (60.1%)] than males [2,095 (39.9%)]. NHW [3,995 (76.0%)] comprised the overwhelming majority of races reported, followed by NHB [441 (8.4%)], hispanic [420 (8.0%)], and NH-API [398 (7.6%)]. Median household income (MHI) data (inflation adjusted to 2021) was divided into <$70,000 and ≥$70,000 (table 2). Univariate cox-PH noted improved survival in NH-APIs (HR .75, p<.001) and MHI ≥$70K (HR .92, p=.05). However this significance disappeared upon adjustment for age and race. In multivariate cox-PH, age demonstrated significance for each category (45-64 HR 2.20; 65-84 HR 4.45; ≥85 HR 6.59, p < .001). Female patients had better survival compared to males (HR .73, p<.001) (Table 2). Conclusion In this comparison study of MF cohorts from an underserved tertiary center and SEER, we found differences in demographic features and their impact on disease mortality. NHW patients constitute the overwhelming majority of subjects in the SEER dataset while the tertiary cohort has nearly equal distribution of NHW, NHB, and hispanic patients. NHB patients from the single-center cohort tended to do worse while SEER showed no differential survival based on race. Possible explanations for this include differences in racial distribution, healthcare accessibility, and other socioeconomic factors. Median income in the Bronx is 36% lower than the national average and the poverty rate is 2.3x higher. Unexpectedly, no significant association was found between MHI and survival in SEER when adjusted for age and race. Also notable is that improved survival in NH-APIs per SEER data disappeared upon adjustment for age, which may suggest that the NH-API group tends to be younger at diagnosis given that age serves as a negative prognostic marker. Further research is warranted. Regarding sex, SEER data suggests that female patients have a decreased mortality risk compared to males which is consistent with literature. Caution in interpretation is necessary given the low tertiary center sample size and the inherent limitations of the SEER dataset. Verma:Novartis: Other: Scientific Advisor; Bakx: Current equity holder in private company, Other: Scientific Advisor; Stelexis: Current equity holder in private company, Honoraria, Other: Scientific Advisor; Eli Lilly: Research Funding; Curis: Research Funding; Medpacto: Research Funding; Incyte: Research Funding; GSK: Research Funding; BMS: Research Funding; Prelude: Research Funding; Acceleron: Other: Scientific Advisor; Celgene: Other: Scientific Advisor; Janssen: Honoraria; Throws Exception: Current equity holder in private company. [Display omitted]
Author Yan, John
Wei, John X
Verma, Amit
Goel, Swati
Shah, Nishi
Author_xml – sequence: 1
  givenname: John
  surname: Yan
  fullname: Yan, John
  organization: Montefiore Medical Center, East Brunswick, NJ
– sequence: 2
  givenname: John X
  surname: Wei
  fullname: Wei, John X
  organization: Montefiore Medical Center, New York, NY
– sequence: 3
  givenname: Amit
  surname: Verma
  fullname: Verma, Amit
  organization: Department of Medical Oncology, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY
– sequence: 4
  givenname: Nishi
  surname: Shah
  fullname: Shah, Nishi
  organization: Department of Oncology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY
– sequence: 5
  givenname: Swati
  surname: Goel
  fullname: Goel, Swati
  organization: Department of Oncology, Montefiore Medical Center and Albert Einstein College of Medicine, Bronx, NY
BookMark eNp9kMtOwzAQRS1UJNrCB7DzDwT8yMOBVRXCQyog0e4jx560Rqld2aFS93w4DmXNajb33Jk5MzSxzgJC15TcUCrYbds7pxNGGE-oSEvOztCUZkwkhDAyQVNCSJ6kZUEv0CyET0Joylk2Rd-LECAEYze43hsNO-N6tzFK9vjBdB14sAoCNha_HqF3nWm9Cybc4QWu3G4vvRzMAfBq-NJH7Dos8Sp29ZBUYAfwMbR1fsDSajxsY66uP_BbZJwdN8hBtjLAJTrvZB_g6m_O0fqxXlfPyfL96aVaLBNVpizJu1ynItMZI6rlguRZLkBxLlSp2rYoeMol01mZQ5FJlslctmkOrCQtcBEhPkf0VKviD8FD1-y92Ul_bChpRovNr8VmtNicLEbm_sRAvOtgwDdBmdGJNh7U0Ghn_qF_APYGfRg
ContentType Journal Article
Copyright 2023 The American Society of Hematology
Copyright_xml – notice: 2023 The American Society of Hematology
DBID AAYXX
CITATION
DOI 10.1182/blood-2023-184932
DatabaseName CrossRef
DatabaseTitle CrossRef
DatabaseTitleList CrossRef

DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Chemistry
Biology
Anatomy & Physiology
EISSN 1528-0020
EndPage 7426
ExternalDocumentID 10_1182_blood_2023_184932
S0006497123140225
GroupedDBID ---
-~X
.55
0R~
1CY
23N
2WC
34G
39C
4.4
53G
5GY
5RE
6J9
AAEDW
AALRI
AAXUO
ABOCM
ACGFO
ADBBV
AENEX
AFETI
AFOSN
AITUG
AKRWK
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
BAWUL
BTFSW
CS3
DIK
DU5
E3Z
EBS
EJD
EX3
F5P
FDB
FRP
GS5
GX1
IH2
K-O
KQ8
L7B
LSO
MJL
N9A
OK1
P2P
R.V
RHF
RHI
ROL
SJN
THE
TR2
TWZ
W2D
WH7
WOQ
WOW
X7M
YHG
YKV
5VS
AAYWO
AAYXX
ACVFH
ADCNI
AEUPX
AFPUW
AGCQF
AIGII
AKBMS
AKYEP
CITATION
H13
W8F
ID FETCH-LOGICAL-c942-6f6d485d520cb3806568ec338c9cbb77343a2d596e75a25a6ab46e290be385203
ISSN 0006-4971
IngestDate Tue Jul 01 02:45:52 EDT 2025
Sat Oct 26 15:43:10 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue Supplement 1
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c942-6f6d485d520cb3806568ec338c9cbb77343a2d596e75a25a6ab46e290be385203
PageCount 1
ParticipantIDs crossref_primary_10_1182_blood_2023_184932
elsevier_sciencedirect_doi_10_1182_blood_2023_184932
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2023-11-02
PublicationDateYYYYMMDD 2023-11-02
PublicationDate_xml – month: 11
  year: 2023
  text: 2023-11-02
  day: 02
PublicationDecade 2020
PublicationTitle Blood
PublicationYear 2023
Publisher Elsevier Inc
Publisher_xml – name: Elsevier Inc
SSID ssj0014325
Score 2.435301
Snippet Background Myelofibrosis (MF) is a rare class of BCR-ABL negative myeloproliferative neoplasms characterized by clonal proliferation of hematopoietic stem...
SourceID crossref
elsevier
SourceType Index Database
Publisher
StartPage 7426
Title Assessing Epidemiological Differences in Myelofibrosis: A Comparative Study of a Single-Center Cohort and the SEER National Database
URI https://dx.doi.org/10.1182/blood-2023-184932
Volume 142
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9NAEF6FIqAXBCmIlof2gDgQGZzd9drmFkpQBWolSIDcrN31WrGUJqhND-XMb-F3Mvty7D4kysVyVvHYznyZ984g9LJKYyXKXEUqUzwCDTGMpE7iqKJUykqDWJa22uKIH3xjn2bJrNf706paOlvLN-rXlftK_oersAZ8Nbtkb8DZhigswDnwF47AYTj-E49dxtY4--PNoFcvySq_kc_Wux6e6wXcSYJKrE_DZvRN2-9J6CwtBhOgttCRCfrqE_jSHMzzpspyMh5_HRyF8OEHsRYyJHdCXnjhh89bSeKCq-1q3x-6DkuDWVj8brSDFVLHdVOFM5mLuYPq6bxuxyYItZv0SEfecjPDzqFHexFremLHJO7IYEZaYLMDTW10dDBsCVfw4nlLUYePl5VAZprKusJ_91QZy30UtdNw-4IibMoTrWOUkcKSKAyJwpG4hW6TNLXlAJ-_bLJVjBI3KcO_rc-eA4m3l57iavunZdNMH6D73hnBI4esh6inl320M1qK9er4HL_CtjzY5l366M77cHZvPwwJ7KO7h742Ywf9btCIL6ARt9CI6yXuoPEdHuEWFrHFIl5VWOAOFrHDIgYsYsAiNljEAYs4YPERmn4cT_cPIj_jI1I5IxGveMmypExIrCQ1SX6eaUVppnIlZZpSRgUpk5zrNBEkEVxIxjXJY6lpBhfRx2hruVrqJwjHUknwVypWlty0jMrSckiBW4wyTaUSu-h1-OGLn66TS3Eto3cRC6wpvCnqTMwCQHb9ZXs3ucdTtL35zzxDW-uTM_0cLNy1fGHh9RdxJaVY
linkProvider Colorado Alliance of Research Libraries
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Assessing+Epidemiological+Differences+in+Myelofibrosis%3A+A+Comparative+Study+of+a+Single-Center+Cohort+and+the+SEER+National+Database&rft.jtitle=Blood&rft.au=Yan%2C+John&rft.au=Wei%2C+John+X&rft.au=Verma%2C+Amit&rft.au=Shah%2C+Nishi&rft.date=2023-11-02&rft.issn=0006-4971&rft.eissn=1528-0020&rft.volume=142&rft.issue=Supplement+1&rft.spage=7426&rft.epage=7426&rft_id=info:doi/10.1182%2Fblood-2023-184932&rft.externalDBID=n%2Fa&rft.externalDocID=10_1182_blood_2023_184932
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0006-4971&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0006-4971&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0006-4971&client=summon