Integrated use of minimal residual disease classification and IKZF1 alteration status accurately predicts 79% of relapses in pediatric acute lymphoblastic leukemia

Response to therapy as determined by minimal residual disease (MRD) is currently used for stratification in treatment protocols for pediatric acute lymphoblastic leukemia (ALL). However, the large MRD-based medium risk group (MRD-M; 50–60% of the patients) harbors many relapses. We analyzed MRD in 1...

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Veröffentlicht in:Leukemia 2011-02, Vol.25 (2), p.254-258
Hauptverfasser: Waanders, E, van der Velden, V H J, van der Schoot, C E, van Leeuwen, F N, van Reijmersdal, S V, de Haas, V, Veerman, A J, van Kessel, A Geurts, Hoogerbrugge, P M, Kuiper, R P, van Dongen, J J M
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container_end_page 258
container_issue 2
container_start_page 254
container_title Leukemia
container_volume 25
creator Waanders, E
van der Velden, V H J
van der Schoot, C E
van Leeuwen, F N
van Reijmersdal, S V
de Haas, V
Veerman, A J
van Kessel, A Geurts
Hoogerbrugge, P M
Kuiper, R P
van Dongen, J J M
description Response to therapy as determined by minimal residual disease (MRD) is currently used for stratification in treatment protocols for pediatric acute lymphoblastic leukemia (ALL). However, the large MRD-based medium risk group (MRD-M; 50–60% of the patients) harbors many relapses. We analyzed MRD in 131 uniformly treated precursor-B-ALL patients and evaluated whether combined MRD and IKZF1 (Ikaros zinc finger-1) alteration status can improve risk stratification. We confirmed the strong prognostic significance of MRD classification, which was independent of IKZF1 alterations. Notably, 8 of the 11 relapsed cases in the large MRD-M group ( n =81; 62%) harbored an IKZF1 alteration. Integration of both MRD and IKZF1 status resulted in a favorable outcome group ( n =104; 5 relapses) and a poor outcome group ( n =27; 19 relapses), and showed a stronger prognostic value than each of the established risk factors alone (hazard ratio (95%CI): 24.98 (8.29–75.31)). Importantly, whereas MRD and IKZF1 status alone identified only 46 and 54% of the relapses, respectively, their integrated use allowed prediction of 79% of all the relapses with 93% specificity. Because of the unprecedented sensitivity in upfront relapse prediction, the combined parameters have high potential for future risk stratification, particularly for patients originally classified as non-high risk, such as the large group of MRD-M patients.
doi_str_mv 10.1038/leu.2010.275
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Myelofibrosis ; Leukocytes ; Life sciences ; Lymphatic leukemia ; Medical prognosis ; Medical sciences ; Medicine ; Medicine &amp; Public Health ; Minimal residual disease ; Mutation ; Neoplasm, Residual - pathology ; Oncology ; original-article ; Parameter sensitivity ; Patients ; Pediatrics ; Physiological aspects ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality ; Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology ; Predictive Value of Tests ; Recurrence ; Relapse ; Risk analysis ; Risk Assessment ; Risk factors ; Sensitivity and Specificity ; Zinc finger proteins</subject><ispartof>Leukemia, 2011-02, Vol.25 (2), p.254-258</ispartof><rights>Macmillan Publishers Limited 2011</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2011 Nature Publishing Group</rights><rights>Macmillan Publishers Limited 2011.</rights><rights>Copyright Nature Publishing Group Feb 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c581t-773db1d1fa514b9172d92fd9f274568c1e73dfdef5096a7cb8834b84dbf2cd403</citedby><cites>FETCH-LOGICAL-c581t-773db1d1fa514b9172d92fd9f274568c1e73dfdef5096a7cb8834b84dbf2cd403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/leu.2010.275$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/leu.2010.275$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23955624$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21102428$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Waanders, E</creatorcontrib><creatorcontrib>van der Velden, V H J</creatorcontrib><creatorcontrib>van der Schoot, C E</creatorcontrib><creatorcontrib>van Leeuwen, F N</creatorcontrib><creatorcontrib>van Reijmersdal, S V</creatorcontrib><creatorcontrib>de Haas, V</creatorcontrib><creatorcontrib>Veerman, A J</creatorcontrib><creatorcontrib>van Kessel, A Geurts</creatorcontrib><creatorcontrib>Hoogerbrugge, P M</creatorcontrib><creatorcontrib>Kuiper, R P</creatorcontrib><creatorcontrib>van Dongen, J J M</creatorcontrib><title>Integrated use of minimal residual disease classification and IKZF1 alteration status accurately predicts 79% of relapses in pediatric acute lymphoblastic leukemia</title><title>Leukemia</title><addtitle>Leukemia</addtitle><addtitle>Leukemia</addtitle><description>Response to therapy as determined by minimal residual disease (MRD) is currently used for stratification in treatment protocols for pediatric acute lymphoblastic leukemia (ALL). 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subjects 692/53/2422
692/699/67/1990/283/2125
692/700/1720
Acute lymphoblastic leukemia
Acute lymphocytic leukemia
Analysis
Biological and medical sciences
Blood
Bone marrow
Cancer Research
Child
Classification
Critical Care Medicine
Diseases
DNA binding proteins
Drug therapy
Gene Rearrangement
Genetic aspects
Hematologic and hematopoietic diseases
Hematology
Humans
Ikaros protein
Ikaros Transcription Factor - genetics
Induction therapy
Intensive
Internal Medicine
Kaplan-Meier Estimate
Laboratories
Leukemia
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Leukocytes
Life sciences
Lymphatic leukemia
Medical prognosis
Medical sciences
Medicine
Medicine & Public Health
Minimal residual disease
Mutation
Neoplasm, Residual - pathology
Oncology
original-article
Parameter sensitivity
Patients
Pediatrics
Physiological aspects
Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality
Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology
Predictive Value of Tests
Recurrence
Relapse
Risk analysis
Risk Assessment
Risk factors
Sensitivity and Specificity
Zinc finger proteins
title Integrated use of minimal residual disease classification and IKZF1 alteration status accurately predicts 79% of relapses in pediatric acute lymphoblastic leukemia
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