Impact of Synchronous Multiple Primary Malignant Tumors on Newly Diagnosed Hematological Malignancies

The existence of synchronous multiple primary malignant tumors was not a significant risk factor for patients with newly diagnosed hematological malignancies. It is important to provide adequate treatment to both hematological malignancies and solid tumors appropriately. Hematological malignancies a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Clinical lymphoma, myeloma and leukemia myeloma and leukemia, 2017-12, Vol.17 (12), p.e79-e85
Hauptverfasser: Nishiwaki, Satoshi, Okuno, Shingo, Suzuki, Kotaro, Kurahashi, Shingo, Sugiura, Isamu
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e85
container_issue 12
container_start_page e79
container_title Clinical lymphoma, myeloma and leukemia
container_volume 17
creator Nishiwaki, Satoshi
Okuno, Shingo
Suzuki, Kotaro
Kurahashi, Shingo
Sugiura, Isamu
description The existence of synchronous multiple primary malignant tumors was not a significant risk factor for patients with newly diagnosed hematological malignancies. It is important to provide adequate treatment to both hematological malignancies and solid tumors appropriately. Hematological malignancies are occasionally observed with synchronous multiple primary malignant tumors (sMPMTs) at diagnosis. We aimed to clarify the impact of sMPMTs on newly diagnosed hematological malignancies and determine the optimal treatment strategies. We analyzed the outcomes of 649 patients with hematological malignancies, including 19 patients with sMPMTs (2.9%), and compared the outcomes between patients with and without sMPMTs. The overall survival (OS) and disease-free survival (DFS) rates for patients with sMPMTs were 77% and 70%, respectively, at 2 years; these rates were not statistically different from those for patients without sMPMTs (P = .17 and P = .64, respectively). Multivariate analysis showed that the presence of sMPMTs was not a significant prognostic factor for OS, DFS, or relapse (hazard ratio [HR] 1.48, 95% confidence interval [CI] 0.65-3.38, P = .35; HR 0.97, 95% CI 0.46-2.10, P = .97; and HR 0.79, 95% CI 0.29-2.14, P = .65). In patients with sMPMTs, the order of treatment was not a significant prognostic factor. However, discontinuation of treatment was a marginally favorable factor and might reflect a selection bias. The presence of sMPMTs was not a significant risk factor for patients with newly diagnosed hematological malignancies. It is important to provide adequate treatment for both hematological malignancies and solid tumors at the physician's discretion.
doi_str_mv 10.1016/j.clml.2017.09.006
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1951569479</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2152265017314040</els_id><sourcerecordid>1951569479</sourcerecordid><originalsourceid>FETCH-LOGICAL-c422t-4218fb3c1c2382258c507c45cfbeffc42d61b35a06cab6db03659398c7d9fa993</originalsourceid><addsrcrecordid>eNp9kE1v1DAURS1ERT_oH2CBvGQz4dkeO2OJDWqhrdQWJNq15by8DB458WAnoPn3ZDRllqzeW5x7pXsYeyegEiDMx02FsY-VBFFXYCsA84qdSaHlQhpjXx9_DafsvJQNQA0g7Bt2Ki0opQDOGN31W48jTx3_sRvwZ05Dmgp_mOIYtpH49xx6n3f8wcewHvww8qepT7nwNPBH-hN3_Dr49ZAKtfyWej-mmNYBfTwmMFB5y046HwtdvtwL9vz1y9PV7eL-283d1ef7BS6lHBdLKVZdo1CgVCsp9Qo11LjU2DXUdTPTGtEo7cGgb0zbgDLaKrvCurWdt1ZdsA-H3m1OvyYqo-tDQYrRDzTPcsJqoY1d1ntUHlDMqZRMndsepjoBbq_Xbdxer9vrdWDdrHcOvX_pn5qe2mPkn88Z-HQAaF75O1B2Zd4_ILUhE46uTeF__X8BDpaM_A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1951569479</pqid></control><display><type>article</type><title>Impact of Synchronous Multiple Primary Malignant Tumors on Newly Diagnosed Hematological Malignancies</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Nishiwaki, Satoshi ; Okuno, Shingo ; Suzuki, Kotaro ; Kurahashi, Shingo ; Sugiura, Isamu</creator><creatorcontrib>Nishiwaki, Satoshi ; Okuno, Shingo ; Suzuki, Kotaro ; Kurahashi, Shingo ; Sugiura, Isamu</creatorcontrib><description>The existence of synchronous multiple primary malignant tumors was not a significant risk factor for patients with newly diagnosed hematological malignancies. It is important to provide adequate treatment to both hematological malignancies and solid tumors appropriately. Hematological malignancies are occasionally observed with synchronous multiple primary malignant tumors (sMPMTs) at diagnosis. We aimed to clarify the impact of sMPMTs on newly diagnosed hematological malignancies and determine the optimal treatment strategies. We analyzed the outcomes of 649 patients with hematological malignancies, including 19 patients with sMPMTs (2.9%), and compared the outcomes between patients with and without sMPMTs. The overall survival (OS) and disease-free survival (DFS) rates for patients with sMPMTs were 77% and 70%, respectively, at 2 years; these rates were not statistically different from those for patients without sMPMTs (P = .17 and P = .64, respectively). Multivariate analysis showed that the presence of sMPMTs was not a significant prognostic factor for OS, DFS, or relapse (hazard ratio [HR] 1.48, 95% confidence interval [CI] 0.65-3.38, P = .35; HR 0.97, 95% CI 0.46-2.10, P = .97; and HR 0.79, 95% CI 0.29-2.14, P = .65). In patients with sMPMTs, the order of treatment was not a significant prognostic factor. However, discontinuation of treatment was a marginally favorable factor and might reflect a selection bias. The presence of sMPMTs was not a significant risk factor for patients with newly diagnosed hematological malignancies. It is important to provide adequate treatment for both hematological malignancies and solid tumors at the physician's discretion.</description><identifier>ISSN: 2152-2650</identifier><identifier>EISSN: 2152-2669</identifier><identifier>DOI: 10.1016/j.clml.2017.09.006</identifier><identifier>PMID: 29033300</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Hematological malignancies ; Order of treatment ; Solid tumors ; Synchronous multiple primary malignant tumors ; Treatment discontinuation</subject><ispartof>Clinical lymphoma, myeloma and leukemia, 2017-12, Vol.17 (12), p.e79-e85</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-4218fb3c1c2382258c507c45cfbeffc42d61b35a06cab6db03659398c7d9fa993</citedby><cites>FETCH-LOGICAL-c422t-4218fb3c1c2382258c507c45cfbeffc42d61b35a06cab6db03659398c7d9fa993</cites><orcidid>0000-0002-6430-8958</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2152265017314040$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29033300$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nishiwaki, Satoshi</creatorcontrib><creatorcontrib>Okuno, Shingo</creatorcontrib><creatorcontrib>Suzuki, Kotaro</creatorcontrib><creatorcontrib>Kurahashi, Shingo</creatorcontrib><creatorcontrib>Sugiura, Isamu</creatorcontrib><title>Impact of Synchronous Multiple Primary Malignant Tumors on Newly Diagnosed Hematological Malignancies</title><title>Clinical lymphoma, myeloma and leukemia</title><addtitle>Clin Lymphoma Myeloma Leuk</addtitle><description>The existence of synchronous multiple primary malignant tumors was not a significant risk factor for patients with newly diagnosed hematological malignancies. It is important to provide adequate treatment to both hematological malignancies and solid tumors appropriately. Hematological malignancies are occasionally observed with synchronous multiple primary malignant tumors (sMPMTs) at diagnosis. We aimed to clarify the impact of sMPMTs on newly diagnosed hematological malignancies and determine the optimal treatment strategies. We analyzed the outcomes of 649 patients with hematological malignancies, including 19 patients with sMPMTs (2.9%), and compared the outcomes between patients with and without sMPMTs. The overall survival (OS) and disease-free survival (DFS) rates for patients with sMPMTs were 77% and 70%, respectively, at 2 years; these rates were not statistically different from those for patients without sMPMTs (P = .17 and P = .64, respectively). Multivariate analysis showed that the presence of sMPMTs was not a significant prognostic factor for OS, DFS, or relapse (hazard ratio [HR] 1.48, 95% confidence interval [CI] 0.65-3.38, P = .35; HR 0.97, 95% CI 0.46-2.10, P = .97; and HR 0.79, 95% CI 0.29-2.14, P = .65). In patients with sMPMTs, the order of treatment was not a significant prognostic factor. However, discontinuation of treatment was a marginally favorable factor and might reflect a selection bias. The presence of sMPMTs was not a significant risk factor for patients with newly diagnosed hematological malignancies. It is important to provide adequate treatment for both hematological malignancies and solid tumors at the physician's discretion.</description><subject>Hematological malignancies</subject><subject>Order of treatment</subject><subject>Solid tumors</subject><subject>Synchronous multiple primary malignant tumors</subject><subject>Treatment discontinuation</subject><issn>2152-2650</issn><issn>2152-2669</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kE1v1DAURS1ERT_oH2CBvGQz4dkeO2OJDWqhrdQWJNq15by8DB458WAnoPn3ZDRllqzeW5x7pXsYeyegEiDMx02FsY-VBFFXYCsA84qdSaHlQhpjXx9_DafsvJQNQA0g7Bt2Ki0opQDOGN31W48jTx3_sRvwZ05Dmgp_mOIYtpH49xx6n3f8wcewHvww8qepT7nwNPBH-hN3_Dr49ZAKtfyWej-mmNYBfTwmMFB5y046HwtdvtwL9vz1y9PV7eL-283d1ef7BS6lHBdLKVZdo1CgVCsp9Qo11LjU2DXUdTPTGtEo7cGgb0zbgDLaKrvCurWdt1ZdsA-H3m1OvyYqo-tDQYrRDzTPcsJqoY1d1ntUHlDMqZRMndsepjoBbq_Xbdxer9vrdWDdrHcOvX_pn5qe2mPkn88Z-HQAaF75O1B2Zd4_ILUhE46uTeF__X8BDpaM_A</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Nishiwaki, Satoshi</creator><creator>Okuno, Shingo</creator><creator>Suzuki, Kotaro</creator><creator>Kurahashi, Shingo</creator><creator>Sugiura, Isamu</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6430-8958</orcidid></search><sort><creationdate>201712</creationdate><title>Impact of Synchronous Multiple Primary Malignant Tumors on Newly Diagnosed Hematological Malignancies</title><author>Nishiwaki, Satoshi ; Okuno, Shingo ; Suzuki, Kotaro ; Kurahashi, Shingo ; Sugiura, Isamu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-4218fb3c1c2382258c507c45cfbeffc42d61b35a06cab6db03659398c7d9fa993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Hematological malignancies</topic><topic>Order of treatment</topic><topic>Solid tumors</topic><topic>Synchronous multiple primary malignant tumors</topic><topic>Treatment discontinuation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nishiwaki, Satoshi</creatorcontrib><creatorcontrib>Okuno, Shingo</creatorcontrib><creatorcontrib>Suzuki, Kotaro</creatorcontrib><creatorcontrib>Kurahashi, Shingo</creatorcontrib><creatorcontrib>Sugiura, Isamu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical lymphoma, myeloma and leukemia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nishiwaki, Satoshi</au><au>Okuno, Shingo</au><au>Suzuki, Kotaro</au><au>Kurahashi, Shingo</au><au>Sugiura, Isamu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Synchronous Multiple Primary Malignant Tumors on Newly Diagnosed Hematological Malignancies</atitle><jtitle>Clinical lymphoma, myeloma and leukemia</jtitle><addtitle>Clin Lymphoma Myeloma Leuk</addtitle><date>2017-12</date><risdate>2017</risdate><volume>17</volume><issue>12</issue><spage>e79</spage><epage>e85</epage><pages>e79-e85</pages><issn>2152-2650</issn><eissn>2152-2669</eissn><abstract>The existence of synchronous multiple primary malignant tumors was not a significant risk factor for patients with newly diagnosed hematological malignancies. It is important to provide adequate treatment to both hematological malignancies and solid tumors appropriately. Hematological malignancies are occasionally observed with synchronous multiple primary malignant tumors (sMPMTs) at diagnosis. We aimed to clarify the impact of sMPMTs on newly diagnosed hematological malignancies and determine the optimal treatment strategies. We analyzed the outcomes of 649 patients with hematological malignancies, including 19 patients with sMPMTs (2.9%), and compared the outcomes between patients with and without sMPMTs. The overall survival (OS) and disease-free survival (DFS) rates for patients with sMPMTs were 77% and 70%, respectively, at 2 years; these rates were not statistically different from those for patients without sMPMTs (P = .17 and P = .64, respectively). Multivariate analysis showed that the presence of sMPMTs was not a significant prognostic factor for OS, DFS, or relapse (hazard ratio [HR] 1.48, 95% confidence interval [CI] 0.65-3.38, P = .35; HR 0.97, 95% CI 0.46-2.10, P = .97; and HR 0.79, 95% CI 0.29-2.14, P = .65). In patients with sMPMTs, the order of treatment was not a significant prognostic factor. However, discontinuation of treatment was a marginally favorable factor and might reflect a selection bias. The presence of sMPMTs was not a significant risk factor for patients with newly diagnosed hematological malignancies. It is important to provide adequate treatment for both hematological malignancies and solid tumors at the physician's discretion.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>29033300</pmid><doi>10.1016/j.clml.2017.09.006</doi><orcidid>https://orcid.org/0000-0002-6430-8958</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 2152-2650
ispartof Clinical lymphoma, myeloma and leukemia, 2017-12, Vol.17 (12), p.e79-e85
issn 2152-2650
2152-2669
language eng
recordid cdi_proquest_miscellaneous_1951569479
source Elsevier ScienceDirect Journals Complete
subjects Hematological malignancies
Order of treatment
Solid tumors
Synchronous multiple primary malignant tumors
Treatment discontinuation
title Impact of Synchronous Multiple Primary Malignant Tumors on Newly Diagnosed Hematological Malignancies
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T19%3A24%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Impact%20of%20Synchronous%20Multiple%20Primary%20Malignant%20Tumors%20on%20Newly%20Diagnosed%20Hematological%20Malignancies&rft.jtitle=Clinical%20lymphoma,%20myeloma%20and%20leukemia&rft.au=Nishiwaki,%20Satoshi&rft.date=2017-12&rft.volume=17&rft.issue=12&rft.spage=e79&rft.epage=e85&rft.pages=e79-e85&rft.issn=2152-2650&rft.eissn=2152-2669&rft_id=info:doi/10.1016/j.clml.2017.09.006&rft_dat=%3Cproquest_cross%3E1951569479%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1951569479&rft_id=info:pmid/29033300&rft_els_id=S2152265017314040&rfr_iscdi=true