Literature DB >> 22282307

KRAS genotyping in rectal adenocarcinoma specimens with low tumor cellularity after neoadjuvant treatment.

Florence Boissière-Michot1, Evelyne Lopez-Crapez, Hélène Frugier, Marie-Laurence Berthe, Alexandre Ho-Pun-Cheung, Eric Assenat, Thierry Maudelonde, Pierre-Jean Lamy, Frédéric Bibeau.   

Abstract

KRAS status assessment is mandatory in patients with metastatic colorectal cancer before therapy with anti-epidermal growth factor receptor monoclonal antibodies, as KRAS mutations are associated with resistance to this treatment. However, KRAS genotyping may be very challenging in case of poor tumor cellularity, particularly when major tumor regression is achieved in locally advanced rectal adenocarcinomas after radiochemotherapy. We aimed at identifying the most reliable strategy to detect KRAS mutations in such samples. DNA was extracted from 31 surgical specimens with major tumor regression, following manual dissection, and from paired pre-treatment biopsies and analyzed by high-resolution melting. DNA samples displaying altered melting curve shapes were then sequenced. Samples with unmodified melting curves or wild-type sequence were further investigated by using an allele-specific PCR assay (TheraScreen) and laser microdissection (followed by high-resolution melting and sequencing analyses). In the 31 post-radiochemotherapy surgical specimens, seven KRAS mutations were identified by high-resolution melting analysis/sequencing. One additional mutation was detected by the TheraScreen assay and two mutations, including the one identified by the TheraScreen assay, were detected following laser microdissection. Altogether, 9/31 surgical specimens (29%) presented KRAS mutations. In the manually dissected pre-treatment biopsies, 12 mutations (39%) were identified by high-resolution melting analysis and sequencing. No additional mutations were found by using the TheraScreen assay or laser microdissection. These results indicate that, in the case of post-radiochemotherapy surgical specimens of colorectal cancer with low tumor cellularity, pre-treatment biopsies might represent the most cost-effective option for reliable KRAS genotyping. The use of more sensitive assays, such as allele-specific PCR or laser microdissection, can be envisaged but with higher costs and longer delays.

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Year:  2012        PMID: 22282307     DOI: 10.1038/modpathol.2011.210

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  15 in total

1.  Circulating DNA Demonstrates Convergent Evolution and Common Resistance Mechanisms during Treatment of Colorectal Cancer.

Authors:  Alain R Thierry; Brice Pastor; Zhi-Qin Jiang; Anastasia D Katsiampoura; Christine Parseghian; Jonathan M Loree; Michael J Overman; Cynthia Sanchez; Safia El Messaoudi; Marc Ychou; Scott Kopetz
Journal:  Clin Cancer Res       Date:  2017-04-11       Impact factor: 12.531

2.  Clinical validation of the detection of KRAS and BRAF mutations from circulating tumor DNA.

Authors:  Alain R Thierry; Florent Mouliere; Safia El Messaoudi; Caroline Mollevi; Evelyne Lopez-Crapez; Fanny Rolet; Brigitte Gillet; Celine Gongora; Pierre Dechelotte; Bruno Robert; Maguy Del Rio; Pierre-Jean Lamy; Frederic Bibeau; Michelle Nouaille; Virginie Loriot; Anne-Sophie Jarrousse; Franck Molina; Muriel Mathonnet; Denis Pezet; Marc Ychou
Journal:  Nat Med       Date:  2014-03-23       Impact factor: 53.440

3.  [Association of RAS mutations in circulating cell-free DNA in the plasma with clinicopathological features of colorectal cancer].

Authors:  Jing Wu; Li-Rong Zhao; Xiu-Qiang Lin; Fen Feng; Yong-Chang Chen; Wei-Ying Deng; Yan-Ming Deng; Wei Wang
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2017-07-20

4.  The gene mutational discrepancies between primary and paired metastatic colorectal carcinoma detected by next-generation sequencing.

Authors:  Shuang-Mei Zou; Wei-Hua Li; Wen-Miao Wang; Wen-Bin Li; Su-Sheng Shi; Jian-Ming Ying; Ning Lyu
Journal:  J Cancer Res Clin Oncol       Date:  2018-08-31       Impact factor: 4.553

5.  Tumor cellularity as a quality assurance measure for accurate clinical detection of BRAF mutations in melanoma.

Authors:  Jonathan C Dudley; Grzegorz T Gurda; Li-Hui Tseng; Derek A Anderson; Guoli Chen; Janis M Taube; Christopher D Gocke; James R Eshleman; Ming-Tseh Lin
Journal:  Mol Diagn Ther       Date:  2014-08       Impact factor: 4.074

6.  Mutational and clinical predictors of pathologic complete response in the treatment of locally advanced rectal cancer.

Authors:  Andrea L Russo; David P Ryan; Darrell R Borger; Jennifer Y Wo; Jackie Szymonifka; Wen-Yih Liang; Eunice L Kwak; Lawrence S Blaszkowsky; Jeffrey W Clark; Jill N Allen; Andrew X Zhu; David L Berger; James C Cusack; Harvey J Mamon; Kevin M Haigis; Theodore S Hong
Journal:  J Gastrointest Cancer       Date:  2014-03

7.  The non-crosslinking fixative RCL2®-CS100 is compatible with both pathology diagnosis and molecular analyses.

Authors:  Florence Boissière-Michot; Amélie Denouël; Nathalie Boulle; Carole Guillaume; Béatrice Orsetti; Evelyne Lopez-Crapez; Marie-Christine Chateau; Frédéric Bibeau
Journal:  Pathol Oncol Res       Date:  2012-08-15       Impact factor: 3.201

8.  Low percentage of KRAS mutations revealed by locked nucleic acid polymerase chain reaction: implications for treatment of metastatic colorectal cancer.

Authors:  Mariella Dono; Carlotta Massucco; Silvana Chiara; Claudia Sonaglio; Marco Mora; Anna Truini; Giannamaria Cerruti; Gabriele Zoppoli; Alberto Ballestrero; Mauro Truini; Manlio Ferrarini; Simona Zupo
Journal:  Mol Med       Date:  2013-02-08       Impact factor: 6.354

9.  Immunohistochemical staining for p16 and BRAFV600E is useful to distinguish between sporadic and hereditary (Lynch syndrome-related) microsatellite instable colorectal carcinomas.

Authors:  Florence Boissière-Michot; Hélène Frugier; Alexandre Ho-Pun-Cheung; Evelyne Lopez-Crapez; Jacqueline Duffour; Frédéric Bibeau
Journal:  Virchows Arch       Date:  2016-05-25       Impact factor: 4.064

10.  KRAS mutation status is highly homogeneous between areas of the primary tumor and the corresponding metastasis of colorectal adenocarcinomas: one less problem in patient care.

Authors:  Mariana Petaccia de Macedo; Fernanda M Melo; Heber Salvador C Ribeiro; Marcio C Marques; Luciane T Kagohara; Maria Dirlei Begnami; Julio C Neto; Júlia S Ribeiro; Fernando A Soares; Dirce M Carraro; Isabela W Cunha
Journal:  Am J Cancer Res       Date:  2017-09-01       Impact factor: 6.166

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