Rates of deep molecular response by digital and conventional PCR with frontline nilotinib in newly diagnosed chronic myeloid leukemia: A landmark analysis Journal Article


Authors: Berdeja, J. G.; Heinrich, M. C.; Dakhil, S. R.; Goldberg, S. L.; Wadleigh, M.; Kuriakose, P.; Cortes, J.; Radich, J.; Helton, B.; Rizzieri, D.; Paley, C.; Dautaj, I.; Mauro, M. J.
Article Title: Rates of deep molecular response by digital and conventional PCR with frontline nilotinib in newly diagnosed chronic myeloid leukemia: A landmark analysis
Abstract: ENESTnext (NCT01227577) was a single-arm, multicenter trial evaluating the rate of deep molecular response by 2 years in patients with newly diagnosed (within 6 months) chronic myeloid leukemia in chronic phase (CML-CP) treated with nilotinib 300 mg twice daily. Among 128 enrolled patients, 94 (73%) achieved major molecular response (MMR; BCR-ABL1 ≤ 0.1% on the International Scale [BCR-ABL1IS]) and 34 (27%) achieved confirmed MR4.5 (BCR-ABL1IS ≤0.0032% detectable or undetectable; primary endpoint) by 2 years. Three-month BCR-ABL1 levels were predictive of later responses. In exploratory analyses, digital polymerase chain reaction (PCR) detected BCR-ABL1 in 39.4% of samples from patients with confirmed MR4.5 and identified further decreases in BCR-ABL1 with continued nilotinib. Safety results, including cardiovascular events, were consistent with those in other nilotinib trials. These results further substantiate the molecular response rates associated with frontline nilotinib therapy and demonstrate the feasibility of monitoring very low BCR-ABL1 transcript levels using digital PCR. © 2019, © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor &Francis Group.
Keywords: chronic myeloid leukemia; nilotinib; bcr-abl1; deep molecular response; digital pcr
Journal Title: Leukemia and Lymphoma
Volume: 60
Issue: 10
ISSN: 1042-8194
Publisher: Taylor & Francis Group  
Date Published: 2019-01-01
Start Page: 2384
End Page: 2393
Language: English
DOI: 10.1080/10428194.2019.1590569
PUBMED: 30912699
PROVIDER: scopus
DOI/URL:
Notes: Source: Scopus
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  1. Michael John Mauro
    267 Mauro