Novel CAD-ALK gene rearrangement is drugable by entrectinib in colorectal cancer
Background: Activated anaplastic lymphoma kinase ( ALK ) gene fusions are recurrent events in a small fraction of colorectal cancers (CRCs), although these events have not yet been exploited as in other malignancies. Methods: We detected ALK protein expression by immunohistochemistry and gene rearra...
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Veröffentlicht in: | British journal of cancer 2015-12, Vol.113 (12), p.1730-1734 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background:
Activated anaplastic lymphoma kinase (
ALK
) gene fusions are recurrent events in a small fraction of colorectal cancers (CRCs), although these events have not yet been exploited as in other malignancies.
Methods:
We detected ALK protein expression by immunohistochemistry and gene rearrangements by fluorescence
in situ
hybridisation in the ALKA-372-001 phase I study of the pan-Trk, ROS1, and ALK inhibitor entrectinib. One out of 487 CRCs showed ALK positivity with a peculiar pattern that prompted further characterisation by targeted sequencing using anchored multiplex PCR.
Results:
A novel ALK fusion with the carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase (
CAD
) gene (
CAD
-
ALK
fusion gene) was identified. It resulted from inversion within chromosome 2 and the fusion of exons 1–35 of
CAD
with exons 20–29 of
ALK
. After failure of previous standard therapies, treatment of this patient with the ALK inhibitor entrectinib resulted in a durable objective tumour response.
Conclusions:
We describe the novel
CAD-ALK
rearrangement as an oncogene and provide the first evidence of its drugability as a new molecular target in CRC. |
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ISSN: | 0007-0920 1532-1827 |
DOI: | 10.1038/bjc.2015.401 |