Hematopoietic cell transplantation comorbidity index (HCT-CI) is predictive of adverse events and overall survival in older allogeneic transplant recipients

Abstract Objectives Our goal was to evaluate the ability of the hematopoietic cell transplantation comorbidity index (HCT-CI) to predict outcomes after allogeneic stem cell transplant (SCT) within the context of an older patient population, where multiple comorbidities are common. Materials and Meth...

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Veröffentlicht in:Journal of geriatric oncology 2014-07, Vol.5 (3), p.238-244
Hauptverfasser: Keller, Jesse W, Andreadis, Charalambos, Damon, Lloyd E, Kaplan, Lawrence D, Martin, Thomas G, Wolf, Jeffrey L, Ai, Weiyun Z, Venstrom, Jeffrey M, Smith, Catherine C, Gaensler, Karin M.L, Hwang, Jimmy, Olin, Rebecca L
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container_end_page 244
container_issue 3
container_start_page 238
container_title Journal of geriatric oncology
container_volume 5
creator Keller, Jesse W
Andreadis, Charalambos
Damon, Lloyd E
Kaplan, Lawrence D
Martin, Thomas G
Wolf, Jeffrey L
Ai, Weiyun Z
Venstrom, Jeffrey M
Smith, Catherine C
Gaensler, Karin M.L
Hwang, Jimmy
Olin, Rebecca L
description Abstract Objectives Our goal was to evaluate the ability of the hematopoietic cell transplantation comorbidity index (HCT-CI) to predict outcomes after allogeneic stem cell transplant (SCT) within the context of an older patient population, where multiple comorbidities are common. Materials and Methods We performed a retrospective cohort study of SCT patients ≥ 50 years of age at our institution, identifying 59 patients with complete HCT-CI data collected prospectively. Results HCT-CI category distribution in our sample was disproportionate, with almost half of patients having scores ≥ 3. High HCT-CI score (≥ 3 vs < 3) was associated with significantly inferior OS (median OS not reached for HCT-CI < 3 vs 14 months for HCT-CI ≥ 3; hazard ratio (HR) 2.2, p = 0.02). HCT-CI score was a better predictor of OS than age, performance status or conditioning intensity. When adjusted for disease relapse risk, HCT-CI score conferred a worse prognosis in the low risk group (HR 1.43, p = 0.03) but not in the intermediate/high risk group (HR 1.08, p = 0.65). NRM was low in the total sample (6% at one year) and was not associated with HCT-CI score. Grade 3–4 non-hematologic adverse events within the first 100 days after SCT were significantly more common in the higher HCT-CI groups (p = 0.02). Conclusions In our older patient cohort with a high incidence of multiple comorbidities, HCT-CI score ≥ 3 was significantly associated with OS, particularly in the subset of patients with a low disease relapse risk.
doi_str_mv 10.1016/j.jgo.2014.04.003
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Materials and Methods We performed a retrospective cohort study of SCT patients ≥ 50 years of age at our institution, identifying 59 patients with complete HCT-CI data collected prospectively. Results HCT-CI category distribution in our sample was disproportionate, with almost half of patients having scores ≥ 3. High HCT-CI score (≥ 3 vs &lt; 3) was associated with significantly inferior OS (median OS not reached for HCT-CI &lt; 3 vs 14 months for HCT-CI ≥ 3; hazard ratio (HR) 2.2, p = 0.02). HCT-CI score was a better predictor of OS than age, performance status or conditioning intensity. When adjusted for disease relapse risk, HCT-CI score conferred a worse prognosis in the low risk group (HR 1.43, p = 0.03) but not in the intermediate/high risk group (HR 1.08, p = 0.65). NRM was low in the total sample (6% at one year) and was not associated with HCT-CI score. Grade 3–4 non-hematologic adverse events within the first 100 days after SCT were significantly more common in the higher HCT-CI groups (p = 0.02). Conclusions In our older patient cohort with a high incidence of multiple comorbidities, HCT-CI score ≥ 3 was significantly associated with OS, particularly in the subset of patients with a low disease relapse risk.</description><identifier>ISSN: 1879-4068</identifier><identifier>EISSN: 1879-4076</identifier><identifier>DOI: 10.1016/j.jgo.2014.04.003</identifier><identifier>PMID: 24894413</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Aged ; Allogeneic ; Comorbidity ; Elderly ; Female ; Hematologic Diseases - mortality ; Hematologic Diseases - therapy ; Hematology, Oncology and Palliative Medicine ; Hematopoietic stem cell transplantation ; Hematopoietic Stem Cell Transplantation - adverse effects ; Hematopoietic Stem Cell Transplantation - mortality ; Humans ; Internal Medicine ; Kaplan-Meier Estimate ; Length of Stay ; Male ; Middle Aged ; Myeloablative Agonists - therapeutic use ; Prospective Studies ; Retrospective Studies ; Severity of Illness Index ; Transplant Recipients - statistics &amp; numerical data ; Transplantation, Homologous - adverse effects ; Transplantation, Homologous - mortality ; Treatment Outcome</subject><ispartof>Journal of geriatric oncology, 2014-07, Vol.5 (3), p.238-244</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c544t-7438fb7e10f0d4a2a5a4e8274e772bec23c2890a7701288c101542ab86c3493d3</citedby><cites>FETCH-LOGICAL-c544t-7438fb7e10f0d4a2a5a4e8274e772bec23c2890a7701288c101542ab86c3493d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1879406814000666$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24894413$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Keller, Jesse W</creatorcontrib><creatorcontrib>Andreadis, Charalambos</creatorcontrib><creatorcontrib>Damon, Lloyd E</creatorcontrib><creatorcontrib>Kaplan, Lawrence D</creatorcontrib><creatorcontrib>Martin, Thomas G</creatorcontrib><creatorcontrib>Wolf, Jeffrey L</creatorcontrib><creatorcontrib>Ai, Weiyun Z</creatorcontrib><creatorcontrib>Venstrom, Jeffrey M</creatorcontrib><creatorcontrib>Smith, Catherine C</creatorcontrib><creatorcontrib>Gaensler, Karin M.L</creatorcontrib><creatorcontrib>Hwang, Jimmy</creatorcontrib><creatorcontrib>Olin, Rebecca L</creatorcontrib><title>Hematopoietic cell transplantation comorbidity index (HCT-CI) is predictive of adverse events and overall survival in older allogeneic transplant recipients</title><title>Journal of geriatric oncology</title><addtitle>J Geriatr Oncol</addtitle><description>Abstract Objectives Our goal was to evaluate the ability of the hematopoietic cell transplantation comorbidity index (HCT-CI) to predict outcomes after allogeneic stem cell transplant (SCT) within the context of an older patient population, where multiple comorbidities are common. Materials and Methods We performed a retrospective cohort study of SCT patients ≥ 50 years of age at our institution, identifying 59 patients with complete HCT-CI data collected prospectively. Results HCT-CI category distribution in our sample was disproportionate, with almost half of patients having scores ≥ 3. High HCT-CI score (≥ 3 vs &lt; 3) was associated with significantly inferior OS (median OS not reached for HCT-CI &lt; 3 vs 14 months for HCT-CI ≥ 3; hazard ratio (HR) 2.2, p = 0.02). HCT-CI score was a better predictor of OS than age, performance status or conditioning intensity. When adjusted for disease relapse risk, HCT-CI score conferred a worse prognosis in the low risk group (HR 1.43, p = 0.03) but not in the intermediate/high risk group (HR 1.08, p = 0.65). NRM was low in the total sample (6% at one year) and was not associated with HCT-CI score. Grade 3–4 non-hematologic adverse events within the first 100 days after SCT were significantly more common in the higher HCT-CI groups (p = 0.02). 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Andreadis, Charalambos ; Damon, Lloyd E ; Kaplan, Lawrence D ; Martin, Thomas G ; Wolf, Jeffrey L ; Ai, Weiyun Z ; Venstrom, Jeffrey M ; Smith, Catherine C ; Gaensler, Karin M.L ; Hwang, Jimmy ; Olin, Rebecca L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c544t-7438fb7e10f0d4a2a5a4e8274e772bec23c2890a7701288c101542ab86c3493d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Allogeneic</topic><topic>Comorbidity</topic><topic>Elderly</topic><topic>Female</topic><topic>Hematologic Diseases - mortality</topic><topic>Hematologic Diseases - therapy</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Hematopoietic stem cell transplantation</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>Hematopoietic Stem Cell Transplantation - mortality</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Kaplan-Meier Estimate</topic><topic>Length of Stay</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Myeloablative Agonists - therapeutic use</topic><topic>Prospective Studies</topic><topic>Retrospective Studies</topic><topic>Severity of Illness Index</topic><topic>Transplant Recipients - statistics &amp; numerical data</topic><topic>Transplantation, Homologous - adverse effects</topic><topic>Transplantation, Homologous - mortality</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Keller, Jesse W</creatorcontrib><creatorcontrib>Andreadis, Charalambos</creatorcontrib><creatorcontrib>Damon, Lloyd E</creatorcontrib><creatorcontrib>Kaplan, Lawrence D</creatorcontrib><creatorcontrib>Martin, Thomas G</creatorcontrib><creatorcontrib>Wolf, Jeffrey L</creatorcontrib><creatorcontrib>Ai, Weiyun Z</creatorcontrib><creatorcontrib>Venstrom, Jeffrey M</creatorcontrib><creatorcontrib>Smith, Catherine C</creatorcontrib><creatorcontrib>Gaensler, Karin M.L</creatorcontrib><creatorcontrib>Hwang, Jimmy</creatorcontrib><creatorcontrib>Olin, Rebecca L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of geriatric oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Keller, Jesse W</au><au>Andreadis, Charalambos</au><au>Damon, Lloyd E</au><au>Kaplan, Lawrence D</au><au>Martin, Thomas G</au><au>Wolf, Jeffrey L</au><au>Ai, Weiyun Z</au><au>Venstrom, Jeffrey M</au><au>Smith, Catherine C</au><au>Gaensler, Karin M.L</au><au>Hwang, Jimmy</au><au>Olin, Rebecca L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hematopoietic cell transplantation comorbidity index (HCT-CI) is predictive of adverse events and overall survival in older allogeneic transplant recipients</atitle><jtitle>Journal of geriatric oncology</jtitle><addtitle>J Geriatr Oncol</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>5</volume><issue>3</issue><spage>238</spage><epage>244</epage><pages>238-244</pages><issn>1879-4068</issn><eissn>1879-4076</eissn><abstract>Abstract Objectives Our goal was to evaluate the ability of the hematopoietic cell transplantation comorbidity index (HCT-CI) to predict outcomes after allogeneic stem cell transplant (SCT) within the context of an older patient population, where multiple comorbidities are common. Materials and Methods We performed a retrospective cohort study of SCT patients ≥ 50 years of age at our institution, identifying 59 patients with complete HCT-CI data collected prospectively. Results HCT-CI category distribution in our sample was disproportionate, with almost half of patients having scores ≥ 3. High HCT-CI score (≥ 3 vs &lt; 3) was associated with significantly inferior OS (median OS not reached for HCT-CI &lt; 3 vs 14 months for HCT-CI ≥ 3; hazard ratio (HR) 2.2, p = 0.02). HCT-CI score was a better predictor of OS than age, performance status or conditioning intensity. When adjusted for disease relapse risk, HCT-CI score conferred a worse prognosis in the low risk group (HR 1.43, p = 0.03) but not in the intermediate/high risk group (HR 1.08, p = 0.65). NRM was low in the total sample (6% at one year) and was not associated with HCT-CI score. Grade 3–4 non-hematologic adverse events within the first 100 days after SCT were significantly more common in the higher HCT-CI groups (p = 0.02). Conclusions In our older patient cohort with a high incidence of multiple comorbidities, HCT-CI score ≥ 3 was significantly associated with OS, particularly in the subset of patients with a low disease relapse risk.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>24894413</pmid><doi>10.1016/j.jgo.2014.04.003</doi><tpages>7</tpages></addata></record>
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subjects Aged
Allogeneic
Comorbidity
Elderly
Female
Hematologic Diseases - mortality
Hematologic Diseases - therapy
Hematology, Oncology and Palliative Medicine
Hematopoietic stem cell transplantation
Hematopoietic Stem Cell Transplantation - adverse effects
Hematopoietic Stem Cell Transplantation - mortality
Humans
Internal Medicine
Kaplan-Meier Estimate
Length of Stay
Male
Middle Aged
Myeloablative Agonists - therapeutic use
Prospective Studies
Retrospective Studies
Severity of Illness Index
Transplant Recipients - statistics & numerical data
Transplantation, Homologous - adverse effects
Transplantation, Homologous - mortality
Treatment Outcome
title Hematopoietic cell transplantation comorbidity index (HCT-CI) is predictive of adverse events and overall survival in older allogeneic transplant recipients
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