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filingDate 2018-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4cfc35cad5695bb9dfbf8c00498a6c6
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publicationDate 2020-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-3652338-A1
titleOfInvention Method for predicting responsiveness to immunotherapy
abstract The present invention relates to the field of cancer diagnosis and therapy. In particular, the invention relates to a method for predicting sensitivity to immunotherapy in a subject having a neoplastic disease, the method comprising: (A) determining the level of methylation of a gene or fragment thereof; selected from the group consisting of interoxin neuronal intermediate filament protein alpha (ΓΝΑ), protein tyrosine phosphatase, type C receptor-associated protein (PTPRCAP), semaphorin 3B (SEMA3B), a member of the kelch- like 6 (KLHL6), and a member of the Ras 1 association domain family (RASSF1) in a sample from the subject, hypomethylation of the gene or fragment thereof in the sample indicating that the subject will be sensitive to immunotherapy; or hypermethylation of the gene or fragment thereof in the sample indicating that the subject will not be susceptible to immunotherapy; or (B) (i) determining a methylation profile of at least two genes or fragments thereof selected from the group consisting of IN A, PTPRCAP, SEMA3B, KLHL6, and RASSF1 in the sample from topic ; (ii) comparing the methylation profile as determined in (i) with a reference methylation pattern, said reference methylation pattern representing a known sensitivity to immunotherapy; (iii) detecting a deviation or gap between the methylation profile as determined in (i) and said reference methylation profile; and (iv) attributing said finding of deviation or non-deviation to a particular prediction of the subject's sensitivity to immunotherapy.
priorityDate 2017-07-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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