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Clinical Implications of Minimal Residual Disease Detection in Infants With KMT2A-Rearranged Acute Lymphoblastic Leukemia Treated on the Interfant-06 Protocol

Authors :
Tomasz Szczepański
Claus Meyer
Maria Grazia Valsecchi
Jan Stary
Birgitte Lausen
Alina Ferster
Gabriele Escherich
Inge M. van der Sluis
Martin Schrappe
Myriam Campbell
Vincent H.J. van der Velden
Giovanni Cazzaniga
Rishi S. Kotecha
Luca Lo Nigro
Julia Alten
Andishe Attarbaschi
Franco Locatelli
Andrea Biondi
Ajay Vora
Rolf Marschalek
Chi Kong Li
Jan Zuna
Benoit Brethon
Rob Pieters
Paola De Lorenzo
Philip Ancliffe
Janine Stutterheim
Stutterheim, J
van der Sluis, I
de Lorenzo, P
Alten, J
Ancliffe, P
Attarbaschi, A
Brethon, B
Biondi, A
Campbell, M
Cazzaniga, G
Escherich, G
Ferster, A
Kotecha, R
Lausen, B
Li, C
Lo Nigro, L
Locatelli, F
Marschalek, R
Meyer, C
Schrappe, M
Stary, J
Vora, A
Zuna, J
van der Velden, V
Szczepanski, T
Valsecchi, M
Pieters, R
Immunology
Source :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 39(6), 652-662. American Society of Clinical Oncology
Publication Year :
2021

Abstract

PURPOSE Infant acute lymphoblastic leukemia (ALL) is characterized by a high incidence of KMT2A gene rearrangements and poor outcome. We evaluated the value of minimal residual disease (MRD) in infants with KMT2A-rearranged ALL treated within the Interfant-06 protocol, which compared lymphoid-style consolidation (protocol IB) versus myeloid-style consolidation (araC, daunorubicin, etoposide/mitoxantrone, araC, etoposide). MATERIALS AND METHODS MRD was measured in 249 infants by DNA-based polymerase chain reaction of rearranged KMT2A, immunoglobulin, and/or T-cell receptor genes, at the end of induction (EOI) and end of consolidation (EOC). MRD results were classified as negative, intermediate (< 5 × 10−4), and high (≥ 5 × 10−4). RESULTS EOI MRD levels predicted outcome with 6-year disease-free survival (DFS) of 60.2% (95% CI, 43.2 to 73.6), 45.0% (95% CI, 28.3 to 53.1), and 33.8% (95% CI, 23.8 to 44.1) for infants with negative, intermediate, and high EOI MRD levels, respectively ( P = .0039). EOC MRD levels were also predictive of outcome, with 6-year DFS of 68.2% (95% CI, 55.2 to 78.1), 40.1% (95% CI, 28.1 to 51.9), and 11.9% (95% CI, 2.6 to 29.1) for infants with negative, intermediate, and high EOC MRD levels, respectively ( P < .0001). Analysis of EOI MRD according to the type of consolidation treatment showed that infants treated with lymphoid-style consolidation had 6-year DFS of 78.2% (95% CI, 51.4 to 91.3), 47.2% (95% CI, 33.0 to 60.1), and 23.2% (95% CI, 12.1 to 36.4) for negative, intermediate, and high MRD levels, respectively ( P < .0001), while for myeloid-style–treated patients the corresponding figures were 45.0% (95% CI, 23.9 to 64.1), 41.3% (95% CI, 23.2 to 58.5), and 45.9% (95% CI, 29.4 to 60.9). CONCLUSION This study provides support for the idea that induction therapy selects patients for subsequent therapy; infants with high EOI MRD may benefit from AML-like consolidation (DFS 45.9% v 23.2%), whereas patients with low EOI MRD may benefit from ALL-like consolidation (DFS 78.2% v 45.0%). Patients with positive EOC MRD had dismal outcomes. These findings will be used for treatment interventions in the next Interfant protocol.

Details

Language :
English
ISSN :
0732183X
Volume :
39
Issue :
6
Database :
OpenAIRE
Journal :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Accession number :
edsair.doi.dedup.....ff6e805aa4f36865f5de5258990e88b0