PIK3CA mutation is associated with increased local failure in lung stereotactic body radiation therapy (SBRT)

Autor: E. Gelb, T. Jonathan Yang, Andreas Rimner, David Barron, Abraham J. Wu, Weiji Shi, Ellen Yorke, Zhigang Zhang, Daphna Y. Gelblum, Natalie A. Lockney
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
Oncology
medicine.medical_specialty
Pathology
Radiation resistance
GTV
gross tumor volume

R895-920
BED
biologically effective dose

AKT1
SBRT
stereotactic body radiation therapy

ITV
internal target volume

AKT
protein kinase B

Article
Lesion
03 medical and health sciences
Medical physics. Medical radiology. Nuclear medicine
0302 clinical medicine
Internal medicine
Radioresistance
medicine
Radiology
Nuclear Medicine and imaging

neoplasms
CTV
clinical target volume

PI3K/AKT/mTOR pathway
RC254-282
Univariate analysis
Lung
business.industry
PIP2
phosphatidylinositol-4
5-biphosphate

Neoplasms. Tumors. Oncology. Including cancer and carcinogens
PIK3CA
medicine.disease
PIP3
phosphatidylinositol-3
4
5-triphosphate

Primary tumor
CT
computed tomography

3. Good health
PI3K
phosphatidylinositol-3-kinases

030104 developmental biology
medicine.anatomical_structure
Lung stereotactic body radiation therapy (SBRT)
030220 oncology & carcinogenesis
Mutation (genetic algorithm)
medicine.symptom
LF
local failure

Local failure
business
PTV
planning target volume
Zdroj: Clinical and Translational Radiation Oncology, Vol 7, Iss, Pp 91-93 (2017)
Clinical and Translational Radiation Oncology
ISSN: 2405-6308
Popis: Highlights • An examination of mutations in PIK3CA signaling pathways and radioresistance. • PIK3CA mutation was found to be associated with local failure after lung SBRT. • This is a small study and there is need for further validation.
Objectives Hyperactivation of the phosphatidylinositol-3-kinase (PI3K) pathway has been associated with radioresistance. It is unclear whether such mutations confer suboptimal local control for patients who receive lung stereotactic body radiation therapy (SBRT). Our objective was to examine whether mutations in the EGFR/AKT/PIK3CA signaling pathway are associated with local failure (LF) after lung SBRT. Methods We retrospectively reviewed 166 patients who underwent SBRT to primary or metastatic lung lesions from 2007 to 2015 for whom genetic testing data was available for EGFR, AKT, and PIK3CA genes. Association between clinical factors, including molecular mutation status, and LF was evaluated. Results Six patients (4%) had PIK3CA mutation, 36 patients (22%) had EGFR mutation, and one patient (0.6%) had AKT1 mutation. Median lesion size was 2.0 cm (range, 0.6–5.6 cm); median dose was 48 Gy in 4 fractions (range, 30–70 Gy in 3–10 fractions). Median follow-up for survivors was 27.3 months (range, 3.8–66.7 months). LF occurred in 16 patients (10%). On univariate analysis, PIK3CA mutation was associated with LF (HR 10.44 [95% CI 2.16–50.46], p = .003), while tumor histology, tumor size, primary tumor site, BED and EGFR mutation were not. At one year, probability of LF in lesions with PIK3CA mutation was 20.0% vs. 2.9% in lesions without mutation (p
Databáze: OpenAIRE