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Human T-cell leukemia virus type I Tax genotype analysis in Okinawa, the southernmost and remotest islands of Japan: Different distributions compared with mainland Japan and the potential value for the prognosis of aggressive adult T-cell leukemia/lymphoma
•The HTLV-1 genotype distributions in Okinawa differs from that in mainland Japan.•The prognosis of aggressive ATL patients with taxA is poorer than those with taxB.•HTLV-1 Tax genotype has potential value as a prognostic factor for aggressive ATL. Okinawa, comprising remote islands off the mainland...
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Published in: | Leukemia research 2017-10, Vol.61, p.18-24 |
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creator | Sakihama, Shugo Saito, Mineki Kuba-Miyara, Megumi Tomoyose, Takeaki Taira, Naoya Miyagi, Takashi Hayashi, Masaki Kinjo, Shigeko Nakachi, Sawako Tedokon, Iori Nishi, Yukiko Tamaki, Keita Morichika, Kazuho Uchihara, Jun-nosuke Morishima, Satoko Karube, Ken-nosuke Tanaka, Yuetsu Masuzaki, Hiroaki Fukushima, Takuya |
description | •The HTLV-1 genotype distributions in Okinawa differs from that in mainland Japan.•The prognosis of aggressive ATL patients with taxA is poorer than those with taxB.•HTLV-1 Tax genotype has potential value as a prognostic factor for aggressive ATL.
Okinawa, comprising remote islands off the mainland of Japan, is an endemic area of human T-cell leukemia virus type I (HTLV-1), the causative virus of adult T-cell leukemia-lymphoma (ATL) and HTLV-1-associated myelopathy (HAM). We investigated the tax genotype of HTLV-1 among 29 HTLV-1 carriers, 74 ATL patients, and 33 HAM patients in Okinawa. The genotype distribution—60 (44%) taxA cases and 76 (56%) taxB cases—differed from that of a previous report from Kagoshima Prefecture in mainland Japan (taxA, 10%; taxB, 90%). A comparison of the clinical outcomes of 45 patients (taxA, 14; taxB, 31) with aggressive ATL revealed that the overall response and 1-year overall survival rates for taxA (50% and 35%, respectively) were lower than those for taxB (71% and 49%, respectively). In a multivariate analysis of two prognostic indices for aggressive ATL, Japan Clinical Oncology Group-Prognostic Index and Prognostic Index for acute and lymphoma ATL, with respect to age, performance status, corrected calcium, soluble interleukin-2 receptor, and tax genotype, the estimated hazard ratio of taxA compared with taxB was 2.68 (95% confidence interval, 0.87–8.25; P=0.086). Our results suggest that the tax genotype has clinical value as a prognostic factor for aggressive ATL. |
doi_str_mv | 10.1016/j.leukres.2017.08.006 |
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Okinawa, comprising remote islands off the mainland of Japan, is an endemic area of human T-cell leukemia virus type I (HTLV-1), the causative virus of adult T-cell leukemia-lymphoma (ATL) and HTLV-1-associated myelopathy (HAM). We investigated the tax genotype of HTLV-1 among 29 HTLV-1 carriers, 74 ATL patients, and 33 HAM patients in Okinawa. The genotype distribution—60 (44%) taxA cases and 76 (56%) taxB cases—differed from that of a previous report from Kagoshima Prefecture in mainland Japan (taxA, 10%; taxB, 90%). A comparison of the clinical outcomes of 45 patients (taxA, 14; taxB, 31) with aggressive ATL revealed that the overall response and 1-year overall survival rates for taxA (50% and 35%, respectively) were lower than those for taxB (71% and 49%, respectively). In a multivariate analysis of two prognostic indices for aggressive ATL, Japan Clinical Oncology Group-Prognostic Index and Prognostic Index for acute and lymphoma ATL, with respect to age, performance status, corrected calcium, soluble interleukin-2 receptor, and tax genotype, the estimated hazard ratio of taxA compared with taxB was 2.68 (95% confidence interval, 0.87–8.25; P=0.086). Our results suggest that the tax genotype has clinical value as a prognostic factor for aggressive ATL.</description><identifier>ISSN: 0145-2126</identifier><identifier>EISSN: 1873-5835</identifier><identifier>DOI: 10.1016/j.leukres.2017.08.006</identifier><identifier>PMID: 28866351</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Aggressive ATL ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Female ; Gene Products, tax - genetics ; Genotype ; HTLV-1 ; HTLV-I Infections - drug therapy ; HTLV-I Infections - mortality ; HTLV-I Infections - pathology ; Human T-lymphotropic virus 1 - genetics ; Humans ; Japan ; Kaplan-Meier Estimate ; Leukemia-Lymphoma, Adult T-Cell - mortality ; Leukemia-Lymphoma, Adult T-Cell - pathology ; Leukemia-Lymphoma, Adult T-Cell - virology ; Male ; Middle Aged ; Okinawa ; Polymerase Chain Reaction ; Polymorphism, Restriction Fragment Length ; Prognosis ; Prognostic factor ; tax Genotype</subject><ispartof>Leukemia research, 2017-10, Vol.61, p.18-24</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-b79c278a034cf035bfa652803633eb856e5e4edc35caa5da6cf305d96c02d61a3</citedby><cites>FETCH-LOGICAL-c365t-b79c278a034cf035bfa652803633eb856e5e4edc35caa5da6cf305d96c02d61a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28866351$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sakihama, Shugo</creatorcontrib><creatorcontrib>Saito, Mineki</creatorcontrib><creatorcontrib>Kuba-Miyara, Megumi</creatorcontrib><creatorcontrib>Tomoyose, Takeaki</creatorcontrib><creatorcontrib>Taira, Naoya</creatorcontrib><creatorcontrib>Miyagi, Takashi</creatorcontrib><creatorcontrib>Hayashi, Masaki</creatorcontrib><creatorcontrib>Kinjo, Shigeko</creatorcontrib><creatorcontrib>Nakachi, Sawako</creatorcontrib><creatorcontrib>Tedokon, Iori</creatorcontrib><creatorcontrib>Nishi, Yukiko</creatorcontrib><creatorcontrib>Tamaki, Keita</creatorcontrib><creatorcontrib>Morichika, Kazuho</creatorcontrib><creatorcontrib>Uchihara, Jun-nosuke</creatorcontrib><creatorcontrib>Morishima, Satoko</creatorcontrib><creatorcontrib>Karube, Ken-nosuke</creatorcontrib><creatorcontrib>Tanaka, Yuetsu</creatorcontrib><creatorcontrib>Masuzaki, Hiroaki</creatorcontrib><creatorcontrib>Fukushima, Takuya</creatorcontrib><title>Human T-cell leukemia virus type I Tax genotype analysis in Okinawa, the southernmost and remotest islands of Japan: Different distributions compared with mainland Japan and the potential value for the prognosis of aggressive adult T-cell leukemia/lymphoma</title><title>Leukemia research</title><addtitle>Leuk Res</addtitle><description>•The HTLV-1 genotype distributions in Okinawa differs from that in mainland Japan.•The prognosis of aggressive ATL patients with taxA is poorer than those with taxB.•HTLV-1 Tax genotype has potential value as a prognostic factor for aggressive ATL.
Okinawa, comprising remote islands off the mainland of Japan, is an endemic area of human T-cell leukemia virus type I (HTLV-1), the causative virus of adult T-cell leukemia-lymphoma (ATL) and HTLV-1-associated myelopathy (HAM). We investigated the tax genotype of HTLV-1 among 29 HTLV-1 carriers, 74 ATL patients, and 33 HAM patients in Okinawa. The genotype distribution—60 (44%) taxA cases and 76 (56%) taxB cases—differed from that of a previous report from Kagoshima Prefecture in mainland Japan (taxA, 10%; taxB, 90%). A comparison of the clinical outcomes of 45 patients (taxA, 14; taxB, 31) with aggressive ATL revealed that the overall response and 1-year overall survival rates for taxA (50% and 35%, respectively) were lower than those for taxB (71% and 49%, respectively). In a multivariate analysis of two prognostic indices for aggressive ATL, Japan Clinical Oncology Group-Prognostic Index and Prognostic Index for acute and lymphoma ATL, with respect to age, performance status, corrected calcium, soluble interleukin-2 receptor, and tax genotype, the estimated hazard ratio of taxA compared with taxB was 2.68 (95% confidence interval, 0.87–8.25; P=0.086). Our results suggest that the tax genotype has clinical value as a prognostic factor for aggressive ATL.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aggressive ATL</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Female</subject><subject>Gene Products, tax - genetics</subject><subject>Genotype</subject><subject>HTLV-1</subject><subject>HTLV-I Infections - drug therapy</subject><subject>HTLV-I Infections - mortality</subject><subject>HTLV-I Infections - pathology</subject><subject>Human T-lymphotropic virus 1 - genetics</subject><subject>Humans</subject><subject>Japan</subject><subject>Kaplan-Meier Estimate</subject><subject>Leukemia-Lymphoma, Adult T-Cell - mortality</subject><subject>Leukemia-Lymphoma, Adult T-Cell - pathology</subject><subject>Leukemia-Lymphoma, Adult T-Cell - virology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Okinawa</subject><subject>Polymerase Chain Reaction</subject><subject>Polymorphism, Restriction Fragment Length</subject><subject>Prognosis</subject><subject>Prognostic factor</subject><subject>tax Genotype</subject><issn>0145-2126</issn><issn>1873-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFUc9v0zAUDgjEyuBPAPnIgXR2XLsJF4TGYEOTdiln69V5ad3FdrCdjv73c9bCgQsn61nfr_e-onjH6JxRJi928x7H-4BxXlG2nNN6Tql8XsxYveSlqLl4UcwoW4iyYpU8K17HuKOUioY1r4qzqq6l5ILNnhXXowVHVqXGvieTJFoDZG_CGEk6DEhuyAp-kw06_zSCg_4QTSTGkbt74-ABPpK0RRL9mJ_grI8po1oS0PqEeTCxz3MkviM_YAD3iXw1XYcBXSKtiSmY9ZiMd5FobwcI2JIHk7bEgnET88h60pyMhqzqkoGe7KEfkXQ-HP-D3zg_RctGsNnk20Szz4nbsU__bnjRH-yw9RbeFC876CO-Pb3nxc9vV6vL6_L27vvN5ZfbUnMpUrleNrpa1kD5QneUi3UHUlQ15ZJzXNdCosAFtpoLDSBakLrjVLSN1LRqJQN-Xnw46uaYv8Z8FmVNnCKBQz9GxRoueN0sFnWGiiNUBx9jwE4NwVgIB8WomspXO3UqX03lK1qrXH7mvT9ZjGuL7V_Wn7Yz4PMRgHnRvcGgojboNLYmoE6q9eY_Fo-l3soH</recordid><startdate>201710</startdate><enddate>201710</enddate><creator>Sakihama, Shugo</creator><creator>Saito, Mineki</creator><creator>Kuba-Miyara, Megumi</creator><creator>Tomoyose, Takeaki</creator><creator>Taira, Naoya</creator><creator>Miyagi, Takashi</creator><creator>Hayashi, Masaki</creator><creator>Kinjo, Shigeko</creator><creator>Nakachi, Sawako</creator><creator>Tedokon, Iori</creator><creator>Nishi, Yukiko</creator><creator>Tamaki, Keita</creator><creator>Morichika, Kazuho</creator><creator>Uchihara, Jun-nosuke</creator><creator>Morishima, Satoko</creator><creator>Karube, Ken-nosuke</creator><creator>Tanaka, Yuetsu</creator><creator>Masuzaki, Hiroaki</creator><creator>Fukushima, Takuya</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201710</creationdate><title>Human T-cell leukemia virus type I Tax genotype analysis in Okinawa, the southernmost and remotest islands of Japan: Different distributions compared with mainland Japan and the potential value for the prognosis of aggressive adult T-cell leukemia/lymphoma</title><author>Sakihama, Shugo ; Saito, Mineki ; Kuba-Miyara, Megumi ; Tomoyose, Takeaki ; Taira, Naoya ; Miyagi, Takashi ; Hayashi, Masaki ; Kinjo, Shigeko ; Nakachi, Sawako ; Tedokon, Iori ; Nishi, Yukiko ; Tamaki, Keita ; Morichika, Kazuho ; Uchihara, Jun-nosuke ; Morishima, Satoko ; Karube, Ken-nosuke ; Tanaka, Yuetsu ; Masuzaki, Hiroaki ; Fukushima, Takuya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-b79c278a034cf035bfa652803633eb856e5e4edc35caa5da6cf305d96c02d61a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aggressive ATL</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Female</topic><topic>Gene Products, tax - genetics</topic><topic>Genotype</topic><topic>HTLV-1</topic><topic>HTLV-I Infections - drug therapy</topic><topic>HTLV-I Infections - mortality</topic><topic>HTLV-I Infections - pathology</topic><topic>Human T-lymphotropic virus 1 - genetics</topic><topic>Humans</topic><topic>Japan</topic><topic>Kaplan-Meier Estimate</topic><topic>Leukemia-Lymphoma, Adult T-Cell - mortality</topic><topic>Leukemia-Lymphoma, Adult T-Cell - pathology</topic><topic>Leukemia-Lymphoma, Adult T-Cell - virology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Okinawa</topic><topic>Polymerase Chain Reaction</topic><topic>Polymorphism, Restriction Fragment Length</topic><topic>Prognosis</topic><topic>Prognostic factor</topic><topic>tax Genotype</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sakihama, Shugo</creatorcontrib><creatorcontrib>Saito, Mineki</creatorcontrib><creatorcontrib>Kuba-Miyara, Megumi</creatorcontrib><creatorcontrib>Tomoyose, Takeaki</creatorcontrib><creatorcontrib>Taira, Naoya</creatorcontrib><creatorcontrib>Miyagi, Takashi</creatorcontrib><creatorcontrib>Hayashi, Masaki</creatorcontrib><creatorcontrib>Kinjo, Shigeko</creatorcontrib><creatorcontrib>Nakachi, Sawako</creatorcontrib><creatorcontrib>Tedokon, Iori</creatorcontrib><creatorcontrib>Nishi, Yukiko</creatorcontrib><creatorcontrib>Tamaki, Keita</creatorcontrib><creatorcontrib>Morichika, Kazuho</creatorcontrib><creatorcontrib>Uchihara, Jun-nosuke</creatorcontrib><creatorcontrib>Morishima, Satoko</creatorcontrib><creatorcontrib>Karube, Ken-nosuke</creatorcontrib><creatorcontrib>Tanaka, Yuetsu</creatorcontrib><creatorcontrib>Masuzaki, Hiroaki</creatorcontrib><creatorcontrib>Fukushima, Takuya</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>Leukemia research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sakihama, Shugo</au><au>Saito, Mineki</au><au>Kuba-Miyara, Megumi</au><au>Tomoyose, Takeaki</au><au>Taira, Naoya</au><au>Miyagi, Takashi</au><au>Hayashi, Masaki</au><au>Kinjo, Shigeko</au><au>Nakachi, Sawako</au><au>Tedokon, Iori</au><au>Nishi, Yukiko</au><au>Tamaki, Keita</au><au>Morichika, Kazuho</au><au>Uchihara, Jun-nosuke</au><au>Morishima, Satoko</au><au>Karube, Ken-nosuke</au><au>Tanaka, Yuetsu</au><au>Masuzaki, Hiroaki</au><au>Fukushima, Takuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human T-cell leukemia virus type I Tax genotype analysis in Okinawa, the southernmost and remotest islands of Japan: Different distributions compared with mainland Japan and the potential value for the prognosis of aggressive adult T-cell leukemia/lymphoma</atitle><jtitle>Leukemia research</jtitle><addtitle>Leuk Res</addtitle><date>2017-10</date><risdate>2017</risdate><volume>61</volume><spage>18</spage><epage>24</epage><pages>18-24</pages><issn>0145-2126</issn><eissn>1873-5835</eissn><abstract>•The HTLV-1 genotype distributions in Okinawa differs from that in mainland Japan.•The prognosis of aggressive ATL patients with taxA is poorer than those with taxB.•HTLV-1 Tax genotype has potential value as a prognostic factor for aggressive ATL.
Okinawa, comprising remote islands off the mainland of Japan, is an endemic area of human T-cell leukemia virus type I (HTLV-1), the causative virus of adult T-cell leukemia-lymphoma (ATL) and HTLV-1-associated myelopathy (HAM). We investigated the tax genotype of HTLV-1 among 29 HTLV-1 carriers, 74 ATL patients, and 33 HAM patients in Okinawa. The genotype distribution—60 (44%) taxA cases and 76 (56%) taxB cases—differed from that of a previous report from Kagoshima Prefecture in mainland Japan (taxA, 10%; taxB, 90%). A comparison of the clinical outcomes of 45 patients (taxA, 14; taxB, 31) with aggressive ATL revealed that the overall response and 1-year overall survival rates for taxA (50% and 35%, respectively) were lower than those for taxB (71% and 49%, respectively). In a multivariate analysis of two prognostic indices for aggressive ATL, Japan Clinical Oncology Group-Prognostic Index and Prognostic Index for acute and lymphoma ATL, with respect to age, performance status, corrected calcium, soluble interleukin-2 receptor, and tax genotype, the estimated hazard ratio of taxA compared with taxB was 2.68 (95% confidence interval, 0.87–8.25; P=0.086). Our results suggest that the tax genotype has clinical value as a prognostic factor for aggressive ATL.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28866351</pmid><doi>10.1016/j.leukres.2017.08.006</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Aggressive ATL Antineoplastic Combined Chemotherapy Protocols - therapeutic use Female Gene Products, tax - genetics Genotype HTLV-1 HTLV-I Infections - drug therapy HTLV-I Infections - mortality HTLV-I Infections - pathology Human T-lymphotropic virus 1 - genetics Humans Japan Kaplan-Meier Estimate Leukemia-Lymphoma, Adult T-Cell - mortality Leukemia-Lymphoma, Adult T-Cell - pathology Leukemia-Lymphoma, Adult T-Cell - virology Male Middle Aged Okinawa Polymerase Chain Reaction Polymorphism, Restriction Fragment Length Prognosis Prognostic factor tax Genotype |
title | Human T-cell leukemia virus type I Tax genotype analysis in Okinawa, the southernmost and remotest islands of Japan: Different distributions compared with mainland Japan and the potential value for the prognosis of aggressive adult T-cell leukemia/lymphoma |
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