2019
DOI: 10.1053/j.seminoncol.2019.07.001
|View full text |Cite
|
Sign up to set email alerts
|

PET/CT in radiation oncology

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4

Citation Types

0
65
0
3

Year Published

2020
2020
2024
2024

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 75 publications
(68 citation statements)
references
References 94 publications
0
65
0
3
Order By: Relevance
“…There are two directions for using predictive biomarkers for individualized treatment, to choose the treatment offered to a patient (e.g., intensifying and choosing a multimodal therapy for a hypoxic tumor with radiation and chemotherapy resistance factors or de-escalating treatment for tumors with radiosensitivity-associated factors such as HPV viral etiology for head and neck cancers). The modulation of the treatment by altered therapeutic and fractional associations (hypo-and hyperfractionation) aims to obtain a higher TCP with the limitation of NTCP of the tissues from the vicinity of target volumes, avoiding the risk of toxicity [2,24,26,27].…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…There are two directions for using predictive biomarkers for individualized treatment, to choose the treatment offered to a patient (e.g., intensifying and choosing a multimodal therapy for a hypoxic tumor with radiation and chemotherapy resistance factors or de-escalating treatment for tumors with radiosensitivity-associated factors such as HPV viral etiology for head and neck cancers). The modulation of the treatment by altered therapeutic and fractional associations (hypo-and hyperfractionation) aims to obtain a higher TCP with the limitation of NTCP of the tissues from the vicinity of target volumes, avoiding the risk of toxicity [2,24,26,27].…”
Section: Introductionmentioning
confidence: 99%
“…Adaptive risk optimization uses a biological objective function instead of an objective function based on dose-volume constraints, maximizing TCP for different regions of the tumor with recurrent risk while also minimizing NTCP for risk organs [2,26,35].…”
Section: Introductionmentioning
confidence: 99%
“…Integration of functional positron emission tomography (PET) images and anatomical computed tomography (CT) images provides the most comprehensive tool for oncological imaging 1,2 due to significant advantages in the detection and characterization of various lesions and in staging cancer and metastatic disease. 1,[3][4][5] Consequently, the volume of radiotracer imaging with the labeled glucose analog fluorodeoxyglucose F-18 (FDG) reached new heights in 2019, with an estimate of over 1.8 million scans and an annual growth rate of about 6% since 2013 in the U.S. alone. 6 Positron emission tomography/CT enables accurately coregistered dual-modality images that provide improved anatomical localization of tracer uptake, 7 which lead to a significant shift in the ratio of CT-coupled to noncoupled PET imaging systems, 6 from 2% in 2001 to 96% in 2018.…”
Section: Introductionmentioning
confidence: 99%
“…Integration of functional positron emission tomography (PET) images and anatomical computed tomography (CT) images provides the most comprehensive tool for oncological imaging 1,2 due to significant advantages in the detection and characterization of various lesions and in staging cancer and metastatic disease 1,3–5 . Consequently, the volume of radiotracer imaging with the labeled glucose analog fluorodeoxyglucose F‐18 (FDG) reached new heights in 2019, with an estimate of over 1.8 million scans and an annual growth rate of about 6% since 2013 in the U.S. alone 6 .…”
Section: Introductionmentioning
confidence: 99%
“…7 Fluorine-18 labeled deoxyglucose ( 18 FDG) imaging has been the backbone of molecular imaging and is in extensive clinical use for diagnosing and staging of solid cancers and in evaluating response to therapy in patients with various malignancies. 8 18 FDG imaging has also provided an interesting insight into the tumor microenvironment: a highly hypoxic and acidic milieu, primarily dependent upon anerobic glycolysis for meeting its energy demand. This requires a profound increase in glucose uptake, facilitated by an upregulation of cell membrane GLUT transporters and an upgraded system for clearance of lactic acid and other waste metabolites in the cancer cells.…”
mentioning
confidence: 99%