TY - JOUR
T1 - Integrated use of minimal residual disease classification and IKZF1 alteration status accurately predicts 79% of relapses in pediatric acute lymphoblastic leukemia
AU - Waanders, E
AU - van der Velden, V H J
AU - van der Schoot, C E
AU - van Leeuwen, F N
AU - van Reijmersdal, S V
AU - de Haas, V
AU - Veerman, A J
AU - van Kessel, A Geurts
AU - Hoogerbrugge, P M
AU - Kuiper, R P
AU - van Dongen, J J M
N1 - Funding Information:
We thank Patricia Hoogeveen, Maaike de Bie, Annemarie Wijkhuijs, Phary Hart, Jane Voerman, Christa Homburg, Erik Bus and Rob Dee for performing the MRD analyses, Edwin Sonneveld for help in collecting the clinical data, Eveline Kamping for technical assistance and Paul Span and Peggy Manders for advice regarding the statistical analyses. This work was supported by grants from the Dutch Cancer Society (KUN2009–4298 to RPK, AGvK and PMH; EMCR2006–3547 to VHJvdV; and SNWLK 97–1567 and SNWLK 2000–2268 to JJMvD and CEvdS), KiKa (to FNvL, PMH and RPK) and the Quality of Life Gala Foundation (to PMH, FNvL, AGvK and RPK).
PY - 2011/2
Y1 - 2011/2
N2 - 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.
AB - 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.
KW - Child
KW - Gene Rearrangement
KW - Humans
KW - Ikaros Transcription Factor/genetics
KW - Kaplan-Meier Estimate
KW - Mutation
KW - Neoplasm, Residual/pathology
KW - Precursor Cell Lymphoblastic Leukemia-Lymphoma/mortality
KW - Predictive Value of Tests
KW - Recurrence
KW - Risk Assessment
KW - Sensitivity and Specificity
UR - http://www.scopus.com/inward/record.url?scp=79751538993&partnerID=8YFLogxK
U2 - 10.1038/leu.2010.275
DO - 10.1038/leu.2010.275
M3 - Article
C2 - 21102428
SN - 0887-6924
VL - 25
SP - 254
EP - 258
JO - Leukemia
JF - Leukemia
IS - 2
ER -