Prognostic discrimination in "good-risk" chronic granulocytic leukemia
The prognostic significance of disease features recorded at the time of diagnosis was examined among 813 patients with Philadelphia chromosome- positive, nonblastic chronic granulocytic leukemia (CGL) collected from six European and American series. The survival pattern for this population was typic...
Saved in:
Published in: | Blood Vol. 63; no. 4; pp. 789 - 799 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
01-04-1984
|
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Abstract | The prognostic significance of disease features recorded at the time of diagnosis was examined among 813 patients with Philadelphia chromosome- positive, nonblastic chronic granulocytic leukemia (CGL) collected from six European and American series. The survival pattern for this population was typical of “good-risk” patients, and median survival was 47 mo. There were multiple interrelationships among different disease features, which led to highly significant correlations with survival for some that had no primary prognostic significance, such as hematocrit. Multivariable regression analysis indicated that spleen size and the percentage of circulating blasts were the most important prognostic indicators. These features, and age, behaved as continuous variables with progressively unfavorable import at higher values. The platelet count did not influence survival significantly at values below 700 X 10(9)/liter but was increasingly unfavorable above this level. Basophils plus eosinophils over 15%, more than 5% marrow blasts, and karyotypic abnormalities in addition to the Ph1 were also significant unfavorable signs. The Cox model, generated with four variables representing percent blasts, spleen size, platelet count, and age, provided a useful representation of risk status in this population, with good fit between predicted and observed survival over more than a twofold survival range. A hazard function derived from half of the patient population successfully segregated the remainder into three groups with significantly different survival patterns. We conclude that it should be possible to identify a lower risk group of patients with a 2-yr survival of 90%, subsequent risk averaging somewhat less than 20%/yr and median survival of 5 yr, an intermediate group, and a high- risk group with a 2-yr survival of 65%, followed by a death rate of about 35%/yr and median survival of 2.5 yr. |
---|---|
AbstractList | The prognostic significance of disease features recorded at the time of diagnosis was examined among 813 patients with Philadelphia chromosome- positive, nonblastic chronic granulocytic leukemia (CGL) collected from six European and American series. The survival pattern for this population was typical of “good-risk” patients, and median survival was 47 mo. There were multiple interrelationships among different disease features, which led to highly significant correlations with survival for some that had no primary prognostic significance, such as hematocrit. Multivariable regression analysis indicated that spleen size and the percentage of circulating blasts were the most important prognostic indicators. These features, and age, behaved as continuous variables with progressively unfavorable import at higher values. The platelet count did not influence survival significantly at values below 700 X 10(9)/liter but was increasingly unfavorable above this level. Basophils plus eosinophils over 15%, more than 5% marrow blasts, and karyotypic abnormalities in addition to the Ph1 were also significant unfavorable signs. The Cox model, generated with four variables representing percent blasts, spleen size, platelet count, and age, provided a useful representation of risk status in this population, with good fit between predicted and observed survival over more than a twofold survival range. A hazard function derived from half of the patient population successfully segregated the remainder into three groups with significantly different survival patterns. We conclude that it should be possible to identify a lower risk group of patients with a 2-yr survival of 90%, subsequent risk averaging somewhat less than 20%/yr and median survival of 5 yr, an intermediate group, and a high- risk group with a 2-yr survival of 65%, followed by a death rate of about 35%/yr and median survival of 2.5 yr. |
Author | Sokal, JE Robertson, JE Gomez, GA Baccarani, M Tso, CY Braun, TJ Cox, EB Tura, S Clarkson, BD Cervantes, F |
Author_xml | – sequence: 1 givenname: JE surname: Sokal fullname: Sokal, JE – sequence: 2 givenname: EB surname: Cox fullname: Cox, EB – sequence: 3 givenname: M surname: Baccarani fullname: Baccarani, M – sequence: 4 givenname: S surname: Tura fullname: Tura, S – sequence: 5 givenname: GA surname: Gomez fullname: Gomez, GA – sequence: 6 givenname: JE surname: Robertson fullname: Robertson, JE – sequence: 7 givenname: CY surname: Tso fullname: Tso, CY – sequence: 8 givenname: TJ surname: Braun fullname: Braun, TJ – sequence: 9 givenname: BD surname: Clarkson fullname: Clarkson, BD – sequence: 10 givenname: F surname: Cervantes fullname: Cervantes, F |
BookMark | eNpl0E1PwzAMBuAIDYlu8B-qHZFanK82OcLEAGkSHIBrlKZpydYlKFkP-_d0gxsny5b9ynrmaOaDtwjdYigxFuSuGUJoy8-KlqyshSzP_TaM0euhomwaXaAMcyIKAAIzlAFAVTBZ4ys0T2kLgBklPEPrtxh6H9LBmbx1yUS3d14fXPC58_myn2KL6NJumZuvGPy01UftxyGY4-lksOPO7p2-RpedHpK9-asL9LF-fF89F5vXp5fV_aYwFAtZNB3IjvJWN6attewAg2AGBNENMJBGQAeV5KbRhFe8rWvWWEsNkS3HGrSlC_Twm2tiSCnaTn1PH-t4VBjUSUadJdQko5iaGNR_GfoDxPNiHA |
CitedBy_id | crossref_primary_10_1182_blood_2015_06_648667 crossref_primary_10_1182_bloodadvances_2018017772 crossref_primary_10_1182_blood_2013_05_501569 crossref_primary_10_1007_s00508_020_01690_1 crossref_primary_10_1182_blood_2014_06_581173 crossref_primary_10_1182_bloodadvances_2017006825 crossref_primary_10_1182_blood_2008_07_170449 crossref_primary_10_1182_bloodadvances_2017011858 crossref_primary_10_1182_blood_2012_03_380147 crossref_primary_10_1182_blood_2013_04_495598 crossref_primary_10_1093_jjco_hyv064 crossref_primary_10_1182_blood_2009_11_254680 crossref_primary_10_1182_blood_2005_12_028456 crossref_primary_10_1182_blood_2010_01_267013 crossref_primary_10_1182_blood_2011_01_330332 crossref_primary_10_1182_asheducation_2009_1_453 crossref_primary_10_1182_blood_2009_07_232595 crossref_primary_10_3324_haematol_2021_280175 crossref_primary_10_1182_blood_2007_04_038943 crossref_primary_10_1182_blood_2010_02_267906 crossref_primary_10_1182_blood_2008_12_191254 crossref_primary_10_1182_blood_2010_12_319038 crossref_primary_10_1182_blood_2011_02_336685 crossref_primary_10_1038_sj_onc_1208866 crossref_primary_10_20515_otd_978914 crossref_primary_10_1182_blood_2007_06_093617 crossref_primary_10_1182_blood_2011_10_388967 crossref_primary_10_1182_blood_2011_08_358135 crossref_primary_10_1182_blood_2010_12_324228 crossref_primary_10_1016_j_ajoc_2019_02_003 crossref_primary_10_1182_blood_2005_05_2155 crossref_primary_10_1200_JCO_2010_32_7114 crossref_primary_10_18632_aging_100420 crossref_primary_10_1182_blood_2014_07_590315 crossref_primary_10_2169_naika_108_547 crossref_primary_10_1182_blood_V92_11_4059_423k34_4059_4065 crossref_primary_10_1182_asheducation_V2000_1_90_20000090 crossref_primary_10_1182_blood_2006_02_004325 crossref_primary_10_1182_blood_2007_08_103499 crossref_primary_10_1182_blood_2011_10_383711 crossref_primary_10_1182_blood_2009_03_210732 crossref_primary_10_1182_blood_2006_02_001495 crossref_primary_10_1182_blood_2014_09_601674 crossref_primary_10_3960_jslrt_56_34 crossref_primary_10_1182_blood_2012_03_378919 crossref_primary_10_1182_blood_2009_08_237115 |
ContentType | Journal Article |
DBID | AAYXX CITATION |
DOI | 10.1182/blood.V63.4.789.bloodjournal634789 |
DatabaseName | CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | CrossRef |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Chemistry Biology Anatomy & Physiology |
EISSN | 1528-0020 |
EndPage | 799 |
ExternalDocumentID | 10_1182_blood_V63_4_789_bloodjournal634789 |
GroupedDBID | --- -~X .55 .GJ 0R~ 1CY 23N 2WC 4.4 53G 5GY 5RE 5VS 6J9 AAEDW AALRI AAXUO AAYXX ABOCM ABVKL ACGFO ADBBV ADVLN AENEX AFFNX AFOSN AI. AITUG AKRWK ALMA_UNASSIGNED_HOLDINGS AMRAJ BAWUL BTFSW C1A CITATION CS3 DIK DU5 E3Z EBS EJD EX3 F5P FDB FRP GS5 GX1 H13 IH2 J5H K-O KQ8 L7B LSO MJL MVM N9A OHT OK1 P2P R.V RHF RHI ROL SJN THE TR2 TWZ UCJ VH1 W2D W8F WH7 WOQ WOW X7M ZGI ZXP |
ID | FETCH-LOGICAL-c3189-bf09f35dabcd7a9f01084c082ab0409c80f0695cba2565d774bee3c29d51a0ae3 |
ISSN | 0006-4971 |
IngestDate | Thu Nov 21 22:16:05 EST 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 4 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c3189-bf09f35dabcd7a9f01084c082ab0409c80f0695cba2565d774bee3c29d51a0ae3 |
OpenAccessLink | https://ashpublications.org/blood/article-pdf/63/4/789/213004/789.pdf |
PageCount | 11 |
ParticipantIDs | crossref_primary_10_1182_blood_V63_4_789_bloodjournal634789 |
PublicationCentury | 1900 |
PublicationDate | 1984-04-01 |
PublicationDateYYYYMMDD | 1984-04-01 |
PublicationDate_xml | – month: 04 year: 1984 text: 1984-04-01 day: 01 |
PublicationDecade | 1980 |
PublicationTitle | Blood |
PublicationYear | 1984 |
SSID | ssj0014325 |
Score | 1.7754886 |
Snippet | The prognostic significance of disease features recorded at the time of diagnosis was examined among 813 patients with Philadelphia chromosome- positive,... |
SourceID | crossref |
SourceType | Aggregation Database |
StartPage | 789 |
Title | Prognostic discrimination in "good-risk" chronic granulocytic leukemia |
Volume | 63 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3faxQxEB6uFasvoldFrZVQ1AfLnrub3WxCn9p6pQgWoaf4tmSTbDl6vZPTfeh_38mP3duzD1bElyUbyBAyw0yS-TIfwJsCN61VomhEtcyjrBY8qpJERsxoUysWa1nbh8Kn58XZd_5xnI0Hgxbsvur7r5rGPtS1fTn7F9ruhGIHtlHn-EWt4_dOev-yXFjsnK3Dal_cetauFtH4Nk0vLFDdAsqxva98adz9C4xYDYa1aztsZppLczWVa_neWSCVd7cxi0s5Wy_TGeiKx10C50ii0paeMGp14zppHK1RuG_V_vUd72NUWgfKLCmd7zLBZ9oi13Ea951q8FrT_o2B85CFZwwKwbbw7Ei3_Ti3dWEddn_0jdFRNsJxI_cf1prRrBPVL6L9W3DrIIfusMPT0skoUWaZlSigvC1zA-6l6LWs0zz_dNalpDKaejqMsAJb8D7M9MOf59nb9fS2L5PH8CicO8ihN5gnMDDzIWwfomksrq7JO-KQwC7FMoT7R23rwXHLBziErc8BhrENJysjI-tGRqZzsteZ2B4JBkb6BkZaA3sKX0_Gk-PTKBByRApdv4iqOhY1zbWslC6kqPEszzOFm0hZYSwQisd1zESuKokb6VzjyaIyhqpU6DyRsTT0GWzOF3PzHIhONGc25WuLN6FAoSkzSa65MIollXwBB-2ClT983ZXy7ip8-U-jd-DhyvZfweavZWN2YeOnbl47k7gB96CGSQ |
link.rule.ids | 315,782,786,27933,27934 |
linkProvider | Multiple Vendors |
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=Prognostic+discrimination+in+%22good-risk%22+chronic+granulocytic+leukemia&rft.jtitle=Blood&rft.au=Sokal%2C+JE&rft.au=Cox%2C+EB&rft.au=Baccarani%2C+M&rft.au=Tura%2C+S&rft.date=1984-04-01&rft.issn=0006-4971&rft.eissn=1528-0020&rft.volume=63&rft.issue=4&rft.spage=789&rft.epage=799&rft_id=info:doi/10.1182%2Fblood.V63.4.789.bloodjournal634789&rft.externalDBID=n%2Fa&rft.externalDocID=10_1182_blood_V63_4_789_bloodjournal634789 |
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 |