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Mutational analysis of anal cancers demonstrates frequent PIK3CA mutations associated with poor outcome after salvage abdominoperineal resection
Background: A better understanding of the molecular profile of anal squamous cell carcinomas (ASCCs) is necessary to consider new therapeutic approaches, and the identification of prognostic and predictive factors for response to treatment. Methods: We retrospectively analysed tumours from ASCC pati...
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Published in: | British journal of cancer 2016-06, Vol.114 (12), p.1387-1394 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background:
A better understanding of the molecular profile of anal squamous cell carcinomas (ASCCs) is necessary to consider new therapeutic approaches, and the identification of prognostic and predictive factors for response to treatment.
Methods:
We retrospectively analysed tumours from ASCC patients for mutational analysis of
KRAS
,
NRAS
,
HRAS
,
BRAF
,
PIK3CA
,
MET
,
TP53
and
FBXW7
genes by HRM and Sanger sequencing analysis.
Results:
Specimens from 148 patients were analysed: 96 treatment-naive tumours and 52 recurrences after initial radiotherapy (RT) or chemoradiotherapy (CRT). Mutations of
KRAS
,
PIK3CA
,
FBXW7
and
TP53
genes were present in 3 (2.0%), 30 (20.3%), 9 (6.1%) and 7 tumours (4.7%), respectively. The distribution of the mutations was similar between treatment-naive tumours and recurrences, except for
TP53
mutations being more frequent in recurrences (
P
=0.0005). In patients treated with abdominoperineal resection (APR) after relapse (
n
=38, median follow-up of 18.2 years), overall survival (OS) was significantly correlated with HPV16 status (
P
=0.048), gender (
P
=0.045) and
PIK3CA
mutation (
P
=0.037). The
PIK3CA
status retained its prognostic significance in Cox multivariate regression analysis (
P
=0.025).
Conclusions:
Our study identified
PIK3CA
mutation as an independent prognostic factor in patients who underwent APR for ASCC recurrence, suggesting a potential benefit from adjuvant treatment and the evaluation of targeted therapies with PI3K/Akt/mTor inhibitors in
PIK3CA-
mutated patients. |
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ISSN: | 0007-0920 1532-1827 |
DOI: | 10.1038/bjc.2016.144 |