发明名称 DIAGNOSTIC METHODS FOR DETERMINING PROGNOSIS OF NON-SMALL CELL LUNG CANCER
摘要 The invention provides methods for identifying early stage non-small cell lung cancer (NSCLC) patients who will have a favorable prognosis for the recurrence of lung cancer after surgical resection. The invention is based on the discovery that assessment of chromosomal copy number abnormalities at two or more of chromosome 5p15, 7p12, 8q24 and centromere 6 can be used for prognostic classification. The invention preferably uses fluorescence in situ hybridization with fluorescently labeled nucleic acid probes to hybridize to patient samples to quantify the chromosomal copy number of the these genetic loci. Assessment of the copy number abnormality patterns using four classifiers produced statistically significant prognostic classification for NSCLC: (i) the Range3 pattern of cells showing a difference on a cell by cell basis, of at least three FISH probe signals between the FISH signals at the chromosomal locus with the largest number of FISH signals minus the FISH signals at the chromosomal locus with the lowest number of FISH signals; (ii) the MYC/EGFR % loss pattern assessing the percentage of cells showing fewer MYC FISH probe signals than EGFR FISH probe signals; (iii) a combination of the Range3 pattern and the MYC/CEP6 ratio pattern of a percentage of cells showing a relative loss of MYC FISH probe signals to the FISH probe signal for CEP6; (iv) the combination of the MYC/5p15 ratio pattern showing the relative ratio of MYC and 5p15 locus signals of 0.80 and the 5p15/CEP6 ratio pattern assessing percentage of cells having a relative ratio of 5p15 FISH probe signals to CEP6 FISH probe signals ≧1.1 versus MYC/5p15 ratio of <0.80 or 5p15/CEP6 <1.1; and (v) a combination of the average range of probe signal differences of equal to or greater than about 2.5 with the Range3 pattern in a percentage of the cells. The invention can be used to identify those early stage NSCLC patients at higher risk of recurrence who should be treated with neoadjuvant chemotherapy before surgery or with adjuvant chemotherapy after surgery.
申请公布号 US2015167102(A1) 申请公布日期 2015.06.18
申请号 US201414584788 申请日期 2014.12.29
申请人 Abbott Laboratories 发明人 Morrison Larry E.;Coon John
分类号 C12Q1/68 主分类号 C12Q1/68
代理机构 代理人
主权项 1. A method of determining prognosis of lung cancer in a human patient, the method comprising: (a) obtaining a biological sample from a human patient classified as having early stage non-small cell lung cancer; (b) contacting the biological sample with a set of chromosomal probes comprising at least two probes selected from a group consisting of a chromosome 5p15 locus specific probe, a chromosome 804 locus specific probe, a chromosome 6 enumeration probe, and a chromosome 7p12 locus specific probe under conditions sufficient to enable hybridization of probes in the set to chromosomes in the sample, if any; (c) identifying a hybridization pattern of the set of chromosomal probes to the biological sample; and (d) determining prognosis of lung cancer in the subject based upon the hybridization pattern identified in step (c).
地址 Abbott Park IL US