18F‐fluorodeoxyglucose uptake predicts pathological complete response after neoadjuvant chemotherapy for breast cancer: A retrospective cohort study1. Issue 2 (4th September 2012)
- Record Type:
- Journal Article
- Title:
- 18F‐fluorodeoxyglucose uptake predicts pathological complete response after neoadjuvant chemotherapy for breast cancer: A retrospective cohort study1. Issue 2 (4th September 2012)
- Main Title:
- 18F‐fluorodeoxyglucose uptake predicts pathological complete response after neoadjuvant chemotherapy for breast cancer: A retrospective cohort study1
- Authors:
- Jin, Soyoung
Kim, Sung‐Bae
Ahn, Jin‐Hee
Jung, Kyung Hae
Ahn, Sei Hyun
Son, Byung Ho
Lee, Jong Won
Gong, Gyungyub
Kim, Hye Ok
Moon, Dae Hyuk - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="abs1-1" sec-type="section"> <title>Background and Objectives</title> <p> <sup>18</sup>F‐fluorodeoxyglucose (<sup>18</sup>F‐FDG) uptake may identify poorly differentiated tumors with a high proliferation rate that are more responsive to neoadjuvant chemotherapy.</p> </sec> <sec id="abs1-2" sec-type="section"> <title>Methods</title> <p>We retrospectively evaluated 273 patients (mean age, 44.2 years; range 23–78 years) newly diagnosed with stage II or III invasive ductal breast cancer between 2006 and 2010. All patients were treated with neoadjuvant chemotherapy followed by surgery. The ability of parameters to predict pathological complete response (pCR), was assessed by multivariate analysis.</p> </sec> <sec id="abs1-3" sec-type="section"> <title>Results</title> <p>Of the 273 breast cancer patients, 30 (11.0%) achieved pCR. Univariate analysis revealed that higher histologic grade (<italic>P</italic> &lt; 0.001), lack of estrogen receptor (ER, <italic>P</italic> &lt; 0.001); and a higher maximal standardized uptake value (SUVmax, <italic>P</italic> &lt; 0.001) were associated with pCR, whereas HER2/neu amplification and Ki‐67 expression were not (<italic>P</italic> &gt; 0.05 for each comparison). Multivariate analysis showed that negative ER (odds ratio [OR] = 9.98; 95% confidence interval [CI], 2.88–34.52, <italic>P</italic> &lt; 0.001) and the SUVmax of <sup>18</sup>F‐FDG uptake (OR per one unit<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="abs1-1" sec-type="section"> <title>Background and Objectives</title> <p> <sup>18</sup>F‐fluorodeoxyglucose (<sup>18</sup>F‐FDG) uptake may identify poorly differentiated tumors with a high proliferation rate that are more responsive to neoadjuvant chemotherapy.</p> </sec> <sec id="abs1-2" sec-type="section"> <title>Methods</title> <p>We retrospectively evaluated 273 patients (mean age, 44.2 years; range 23–78 years) newly diagnosed with stage II or III invasive ductal breast cancer between 2006 and 2010. All patients were treated with neoadjuvant chemotherapy followed by surgery. The ability of parameters to predict pathological complete response (pCR), was assessed by multivariate analysis.</p> </sec> <sec id="abs1-3" sec-type="section"> <title>Results</title> <p>Of the 273 breast cancer patients, 30 (11.0%) achieved pCR. Univariate analysis revealed that higher histologic grade (<italic>P</italic> &lt; 0.001), lack of estrogen receptor (ER, <italic>P</italic> &lt; 0.001); and a higher maximal standardized uptake value (SUVmax, <italic>P</italic> &lt; 0.001) were associated with pCR, whereas HER2/neu amplification and Ki‐67 expression were not (<italic>P</italic> &gt; 0.05 for each comparison). Multivariate analysis showed that negative ER (odds ratio [OR] = 9.98; 95% confidence interval [CI], 2.88–34.52, <italic>P</italic> &lt; 0.001) and the SUVmax of <sup>18</sup>F‐FDG uptake (OR per one unit increase in SUVmax = 1.09; 95% CI, 1.02–1.16, <italic>P</italic> = 0.008) were independent predictors of pCR.</p> </sec> <sec id="abs1-4" sec-type="section"> <title>Conclusions</title> <p>ER status and <sup>18</sup>F‐FDG uptake are independent predictors of pCR after neoadjuvant chemotherapy for breast cancer. J. Surg. Oncol. 2013;107:180–187. © 2012 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of surgical oncology. Volume 107:Issue 2(2013:Feb. 01)
- Journal:
- Journal of surgical oncology
- Issue:
- Volume 107:Issue 2(2013:Feb. 01)
- Issue Display:
- Volume 107, Issue 2 (2013)
- Year:
- 2013
- Volume:
- 107
- Issue:
- 2
- Issue Sort Value:
- 2013-0107-0002-0000
- Page Start:
- 180
- Page End:
- 187
- Publication Date:
- 2012-09-04
- Subjects:
- Cancer -- Surgery -- Periodicals
Neoplasms -- Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1096-9098 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jso.23255 ↗
- Languages:
- English
- ISSNs:
- 0022-4790
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5067.380000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3670.xml