Association between measurable residual disease kinetics and outcomes of Philadelphia chromosome-positive acute lymphoblastic leukemia
The prognosis of Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) has improved dramatically. Although measurable residual disease (MRD) kinetics during pretransplant treatment has been recently reported to correlate with patient outcomes, it is unclear whether prognosis is be...
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Veröffentlicht in: | Annals of hematology 2021-10, Vol.100 (10), p.2479-2486 |
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creator | Hara, Ryujiro Onizuka, Makoto Kikkawa, Eri Shiraiwa, Sawako Harada, Kaito Aoyama, Yasuyuki Ogiya, Daisuke Toyosaki, Masako Suzuki, Rikio Machida, Sinichiro Ohmachi, Ken Ogawa, Yoshiaki Kawada, Hiroshi Matsushita, Hiromichi Ando, Kiyoshi |
description | The prognosis of Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) has improved dramatically. Although measurable residual disease (MRD) kinetics during pretransplant treatment has been recently reported to correlate with patient outcomes, it is unclear whether prognosis is better if the MRD falls below the detection sensitivity soon after induction therapy. We retrospectively analyzed data of 37 Ph + ALL patients who were treated with autologous or allogeneic stem cell transplantation (auto-SCT, allo-SCT) at our institute from 2003 to 2019. Based on MRD kinetics, patients were divided into three groups: early responders (MRD became negative after induction therapy [
n
= 10, 27.0%]); late responders (MRD remained positive after induction therapy and became negative just before SCT [
n
= 12, 32.4%]); and poor responders (MRD was positive until just before SCT [
n
= 15, 40.5%]). The 5-year disease-free survival (DFS) rates for the three groups were 80.0%, 60.0%, and 29.9%, respectively (
P
= 0.037). The 5-year overall survival rates were not significantly different. The 5-year relapse rates were 0.0%, 31.7%, and 49.5%, respectively (
P
= 0.045). Non-relapse mortality (NRM) rates were similar among the three groups. Subgroup analysis for the cases that received posttransplantation tyrosine kinase inhibitor maintenance therapy revealed that DFS was similarly dependent on MRD kinetics (
P
= 0.022). This study clarified that MRD kinetics was a significant prognosticator for DFS and relapse rate in Ph + ALL. |
doi_str_mv | 10.1007/s00277-021-04587-9 |
format | Article |
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n
= 10, 27.0%]); late responders (MRD remained positive after induction therapy and became negative just before SCT [
n
= 12, 32.4%]); and poor responders (MRD was positive until just before SCT [
n
= 15, 40.5%]). The 5-year disease-free survival (DFS) rates for the three groups were 80.0%, 60.0%, and 29.9%, respectively (
P
= 0.037). The 5-year overall survival rates were not significantly different. The 5-year relapse rates were 0.0%, 31.7%, and 49.5%, respectively (
P
= 0.045). Non-relapse mortality (NRM) rates were similar among the three groups. Subgroup analysis for the cases that received posttransplantation tyrosine kinase inhibitor maintenance therapy revealed that DFS was similarly dependent on MRD kinetics (
P
= 0.022). This study clarified that MRD kinetics was a significant prognosticator for DFS and relapse rate in Ph + ALL.</description><identifier>ISSN: 0939-5555</identifier><identifier>EISSN: 1432-0584</identifier><identifier>DOI: 10.1007/s00277-021-04587-9</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Hematology ; Induction therapy ; Inhibitor drugs ; Leukemia ; Medical prognosis ; Medicine ; Medicine & Public Health ; Oncology ; Original Article ; Targeted cancer therapy</subject><ispartof>Annals of hematology, 2021-10, Vol.100 (10), p.2479-2486</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-a518eb8276a9dbe0b9e3c50a149620d100976308703680d7057dd195f305c583</citedby><cites>FETCH-LOGICAL-c418t-a518eb8276a9dbe0b9e3c50a149620d100976308703680d7057dd195f305c583</cites><orcidid>0000-0002-0324-898X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00277-021-04587-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00277-021-04587-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids></links><search><creatorcontrib>Hara, Ryujiro</creatorcontrib><creatorcontrib>Onizuka, Makoto</creatorcontrib><creatorcontrib>Kikkawa, Eri</creatorcontrib><creatorcontrib>Shiraiwa, Sawako</creatorcontrib><creatorcontrib>Harada, Kaito</creatorcontrib><creatorcontrib>Aoyama, Yasuyuki</creatorcontrib><creatorcontrib>Ogiya, Daisuke</creatorcontrib><creatorcontrib>Toyosaki, Masako</creatorcontrib><creatorcontrib>Suzuki, Rikio</creatorcontrib><creatorcontrib>Machida, Sinichiro</creatorcontrib><creatorcontrib>Ohmachi, Ken</creatorcontrib><creatorcontrib>Ogawa, Yoshiaki</creatorcontrib><creatorcontrib>Kawada, Hiroshi</creatorcontrib><creatorcontrib>Matsushita, Hiromichi</creatorcontrib><creatorcontrib>Ando, Kiyoshi</creatorcontrib><title>Association between measurable residual disease kinetics and outcomes of Philadelphia chromosome-positive acute lymphoblastic leukemia</title><title>Annals of hematology</title><addtitle>Ann Hematol</addtitle><description>The prognosis of Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) has improved dramatically. Although measurable residual disease (MRD) kinetics during pretransplant treatment has been recently reported to correlate with patient outcomes, it is unclear whether prognosis is better if the MRD falls below the detection sensitivity soon after induction therapy. We retrospectively analyzed data of 37 Ph + ALL patients who were treated with autologous or allogeneic stem cell transplantation (auto-SCT, allo-SCT) at our institute from 2003 to 2019. Based on MRD kinetics, patients were divided into three groups: early responders (MRD became negative after induction therapy [
n
= 10, 27.0%]); late responders (MRD remained positive after induction therapy and became negative just before SCT [
n
= 12, 32.4%]); and poor responders (MRD was positive until just before SCT [
n
= 15, 40.5%]). The 5-year disease-free survival (DFS) rates for the three groups were 80.0%, 60.0%, and 29.9%, respectively (
P
= 0.037). The 5-year overall survival rates were not significantly different. The 5-year relapse rates were 0.0%, 31.7%, and 49.5%, respectively (
P
= 0.045). Non-relapse mortality (NRM) rates were similar among the three groups. Subgroup analysis for the cases that received posttransplantation tyrosine kinase inhibitor maintenance therapy revealed that DFS was similarly dependent on MRD kinetics (
P
= 0.022). This study clarified that MRD kinetics was a significant prognosticator for DFS and relapse rate in Ph + ALL.</description><subject>Hematology</subject><subject>Induction therapy</subject><subject>Inhibitor drugs</subject><subject>Leukemia</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Targeted cancer therapy</subject><issn>0939-5555</issn><issn>1432-0584</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kc1q3TAQhU1JoLdpXqArQTfdqB1JlmUtQ-gfBNpF9kKW5_YqkS1XY7fkBfLc0e0tFLrIbAZmvnMY5jTNGwHvBYD5QADSGA5ScGh1b7h90exEqyQH3bdnzQ6sslzXetm8IroDELJv5a55vCLKIfo15pkNuP5GnNmEnrbih4SsIMVx84mNkeoU2X2ccY2BmJ9Hlrc15AmJ5T37fojJj5iWQ_QsHEqeMtUdXzLFNf5C5sO2IksP03LIQ_JUXVjC7R6n6F8353ufCC__9ovm9tPH2-sv_Obb56_XVzc8tKJfudeix6GXpvN2HBAGiypo8KK1nYSxvsKaTkFvQHU9jAa0GUdh9V6BDrpXF827k-1S8s8NaXVTpIAp-RnzRk5qDZ00StuKvv0PvctbmetxlTJSaW3skZInKpRMVHDvlhInXx6cAHdMxp2ScTUZ9ycZdxSpk4gqPP_A8s_6GdUTyzqTKg</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Hara, Ryujiro</creator><creator>Onizuka, Makoto</creator><creator>Kikkawa, Eri</creator><creator>Shiraiwa, Sawako</creator><creator>Harada, Kaito</creator><creator>Aoyama, Yasuyuki</creator><creator>Ogiya, Daisuke</creator><creator>Toyosaki, Masako</creator><creator>Suzuki, Rikio</creator><creator>Machida, Sinichiro</creator><creator>Ohmachi, Ken</creator><creator>Ogawa, Yoshiaki</creator><creator>Kawada, Hiroshi</creator><creator>Matsushita, Hiromichi</creator><creator>Ando, Kiyoshi</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0324-898X</orcidid></search><sort><creationdate>20211001</creationdate><title>Association between measurable residual disease kinetics and outcomes of Philadelphia chromosome-positive acute lymphoblastic leukemia</title><author>Hara, Ryujiro ; Onizuka, Makoto ; Kikkawa, Eri ; Shiraiwa, Sawako ; Harada, Kaito ; Aoyama, Yasuyuki ; Ogiya, Daisuke ; Toyosaki, Masako ; Suzuki, Rikio ; Machida, Sinichiro ; Ohmachi, Ken ; Ogawa, Yoshiaki ; Kawada, Hiroshi ; Matsushita, Hiromichi ; Ando, Kiyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-a518eb8276a9dbe0b9e3c50a149620d100976308703680d7057dd195f305c583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Hematology</topic><topic>Induction therapy</topic><topic>Inhibitor drugs</topic><topic>Leukemia</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Targeted cancer therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hara, Ryujiro</creatorcontrib><creatorcontrib>Onizuka, Makoto</creatorcontrib><creatorcontrib>Kikkawa, Eri</creatorcontrib><creatorcontrib>Shiraiwa, Sawako</creatorcontrib><creatorcontrib>Harada, Kaito</creatorcontrib><creatorcontrib>Aoyama, Yasuyuki</creatorcontrib><creatorcontrib>Ogiya, Daisuke</creatorcontrib><creatorcontrib>Toyosaki, Masako</creatorcontrib><creatorcontrib>Suzuki, Rikio</creatorcontrib><creatorcontrib>Machida, Sinichiro</creatorcontrib><creatorcontrib>Ohmachi, Ken</creatorcontrib><creatorcontrib>Ogawa, Yoshiaki</creatorcontrib><creatorcontrib>Kawada, Hiroshi</creatorcontrib><creatorcontrib>Matsushita, Hiromichi</creatorcontrib><creatorcontrib>Ando, Kiyoshi</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hara, Ryujiro</au><au>Onizuka, Makoto</au><au>Kikkawa, Eri</au><au>Shiraiwa, Sawako</au><au>Harada, Kaito</au><au>Aoyama, Yasuyuki</au><au>Ogiya, Daisuke</au><au>Toyosaki, Masako</au><au>Suzuki, Rikio</au><au>Machida, Sinichiro</au><au>Ohmachi, Ken</au><au>Ogawa, Yoshiaki</au><au>Kawada, Hiroshi</au><au>Matsushita, Hiromichi</au><au>Ando, Kiyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between measurable residual disease kinetics and outcomes of Philadelphia chromosome-positive acute lymphoblastic leukemia</atitle><jtitle>Annals of hematology</jtitle><stitle>Ann Hematol</stitle><date>2021-10-01</date><risdate>2021</risdate><volume>100</volume><issue>10</issue><spage>2479</spage><epage>2486</epage><pages>2479-2486</pages><issn>0939-5555</issn><eissn>1432-0584</eissn><abstract>The prognosis of Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) has improved dramatically. Although measurable residual disease (MRD) kinetics during pretransplant treatment has been recently reported to correlate with patient outcomes, it is unclear whether prognosis is better if the MRD falls below the detection sensitivity soon after induction therapy. We retrospectively analyzed data of 37 Ph + ALL patients who were treated with autologous or allogeneic stem cell transplantation (auto-SCT, allo-SCT) at our institute from 2003 to 2019. Based on MRD kinetics, patients were divided into three groups: early responders (MRD became negative after induction therapy [
n
= 10, 27.0%]); late responders (MRD remained positive after induction therapy and became negative just before SCT [
n
= 12, 32.4%]); and poor responders (MRD was positive until just before SCT [
n
= 15, 40.5%]). The 5-year disease-free survival (DFS) rates for the three groups were 80.0%, 60.0%, and 29.9%, respectively (
P
= 0.037). The 5-year overall survival rates were not significantly different. The 5-year relapse rates were 0.0%, 31.7%, and 49.5%, respectively (
P
= 0.045). Non-relapse mortality (NRM) rates were similar among the three groups. Subgroup analysis for the cases that received posttransplantation tyrosine kinase inhibitor maintenance therapy revealed that DFS was similarly dependent on MRD kinetics (
P
= 0.022). This study clarified that MRD kinetics was a significant prognosticator for DFS and relapse rate in Ph + ALL.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00277-021-04587-9</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-0324-898X</orcidid></addata></record> |
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subjects | Hematology Induction therapy Inhibitor drugs Leukemia Medical prognosis Medicine Medicine & Public Health Oncology Original Article Targeted cancer therapy |
title | Association between measurable residual disease kinetics and outcomes of Philadelphia chromosome-positive acute lymphoblastic leukemia |
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