Prognostic assay for squamous cell lung carcinoma

Patent metadata

Field	Value
Publication number	US-10421994-B2
Application number	US-201815948908-A
Country	US
Kind code	B2
Filing date	Apr 9, 2018
Priority date	Mar 15, 2013
Publication date	Sep 24, 2019
Grant date	Sep 24, 2019

Abstract

Methods for predicting clinical outcome for a human subject diagnosed with squamous cell lung carcinoma using a panel of molecular markers that includes CDKN2A and CCND1. The markers are related to the subject's increased likelihood of a negative clinical outcome.

First claim

What is claimed is:

1. A method of providing a clinical outcome predictor for a human subject diagnosed with early stage squamous cell lung carcinoma comprising:
a) obtaining a biological sample comprising early stage squamous cell lung carcinoma cancer cells from a human subject diagnosed with early stage squamous cell lung carcinoma;
b) detecting whether a loss of function mutation or a deletion of the cyclin-dependent kinase inhibitor 2A (CDKN2A) gene is present in the subject by determining the presence or absence of a loss of function mutation or a deletion in the CDKN2A gene by next generation sequence examination in the biological sample comprising cancer cells; and
c) detecting whether an increase in the copy number of the G1/S-specific cyclin-D1 (CCND1) gene is present in the subject by determining the presence or absence of an increase in the copy number of the CCND1 gene by comparative genomic hybridization examination in the biological sample comprising cancer cells; and
d) combining the detecting result of b) and c) and providing a clinical outcome predictor for the subject,
wherein the presence of a loss of function mutation or deletion in the CDKN2A gene and/or the presence of an increase in the copy number of the CCND1 gene is a predictor of a negative clinical outcome, and wherein the absence of a loss of function mutation or deletion in the CDKN2A gene and the absence of an increase in the copy number of the CCND1 gene is a predictor of a positive clinical outcome.

2. The method of claim 1 , wherein the loss of function mutation in the CDKN2A gene is a missense mutation, nonsense mutation, or frameshift mutation, or any combination thereof.

3. The method of claim 2 , wherein the missense mutation is any of D108G, D108N, D108Y, G125R, P114L mutation, or any combination thereof.

4. The method of claim 1 , wherein the increase in the copy number of the CCDN1 gene is greater than or equal to 4.

5. The method of claim 1 , wherein the next generation sequence examination of a loss of function mutation or deletion in the CDKN2A gene comprises contacting the biological sample with reagents and
a) amplifying the CDKN2A gene or a portion thereof thereby providing an amplification product of the gene or portion thereof, or
b) reverse transcribing a RNA transcript encoded by the CDKN2A gene and amplifying the reverse transcription product thereby providing an amplification product of the gene or portion thereof.

6. The method of claim 5 , wherein the next generation sequencing examination comprises sequencing the entire coding region of the CDKN2A gene.

7. The method of claim 5 , wherein the next generation sequencing examination comprises qPCR.

8. The method of claim 5 , wherein the reagents are oligonucleotides.

9. The method of claim 5 , wherein the reagents are PCR primer sets.

10. The method of claim 5 , wherein the reagents are RT-PCR primer sets.

11. The method of claim 1 , wherein the squamous cell lung carcinoma is stage I.

12. The method of claim 1 , wherein the squamous cell lung carcinoma is stage II.

13. The method of claim 1 , wherein the biological sample is obtained from a surgically resected tumor.

14. The method of claim 1 , wherein the biological sample is obtained from lymph node or a distant metastasis sample.

15. The method of claim 1 , wherein the biological sample is obtained from a blood sample.

16. A method of identifying a negative clinical outcome predictor consisting of a loss of function mutation or deletion in the cyclin-dependent kinase inhibitor 2A (CDKN2A) gene and an increased copy number of the G1/S-specific cyclin-D1 (CCND1) gene in a biological sample of a human subject diagnosed with early stage squamous cell lung carcinoma, the method comprising:
a) obtaining a biological sample comprising early stage squamous cell lung carcinoma cancer cells from a human subject diagnosed with early stage squamous cell lung carcinoma;
b) detecting the presence of a loss of function mutation or a deletion in the CDKN2A gene by next generation sequence examination in the biological sample comprising cancer cells; and
c) detecting whether an increase in the copy number of the CCND1 gene is present in the subject by determining the presence or absence of an increase in the copy number of the CCND1 gene by comparative genomic hybridization examination in the biological sample comprising cancer cells;
wherein detecting the presence of a loss of function mutation or deletion in the CDKN2A gene and the presence of an increase in the copy number of the CCND1 gene identifies the negative clinical outcome predictor.

17. The method of claim 16 , wherein the biological sample is obtained from a surgically resected tumor.

18. The method of claim 16 , wherein the biological sample is obtained from lymph node, a distant metastasis sample, or a blood sample.

19. A method of treating early stage squamous cell lung carcinoma in a patient comprising;
a) obtaining a biological sample from a patient containing early stage squamous cell lung carcinoma cells obtained from surgical resection of a tumor;
b) detecting the presence of a loss of function mutation or a deletion of the cyclin-dependent kinase inhibitor 2A (CDKN2A) gene in the subject by determining the presence of a loss of function mutation or a deletion in the CDKN2A gene in the biological sample by next generation sequence examination; and
c) detecting whether an increase in the copy number of the G1/S-specific cyclin-D1 (CCND1) gene is present in the subject by determining the presence or absence of an increase in the copy number of the CCND1 gene in the biological sample by comparative genomic hybridization examination; and
d) treating the patient having early stage squamous cell lung carcinoma cells comprising a loss of function mutation or a deletion in the CDKN2A gene and an increase in the copy number of the CCDN1 gene with post-surgical adjuvant therapy.

20. The method of claim 19 , wherein the post-surgical adjuvant therapy is chemotherapy, radiation therapy, or a combination thereof.

Assignees

• Life Technologies Corp

Inventors

• Sadis Seth
• Williams Paul

Classifications

• C12Q1/686 Primary

  Polymerase chain reaction [PCR] · CPC title

• C12Q2600/118

  Prognosis of disease development · CPC title

• C12Q2600/156

  Polymorphic or mutational markers · CPC title

• C12Q1/6886 Primary

  for cancer (immunoassay for cancer G01N33/575) · CPC title