Tracey DiSipio

Dr. Tracey DiSipio

orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2013 in The Lancet Oncology
Verified
Journal Article
Closed access
TDTracey DiSipio
Tracey DiSipio
SRSheree Rye
Sheree Rye
BNBeth Newman
Beth Newman
SHSandra C Hayes
Sandra C Hayes

9 November 2012 in Breast Cancer Research and Treatment
Verified
Journal Article
Closed access
PDF file
SHSandra C Hayes
Sandra C Hayes
SRSheree Rye
Sheree Rye
TDTracey DiSipio
Tracey DiSipio
PYPatsy Yates
Patsy Yates
JBJohn Bashford
John Bashford
EEElizabeth Eakin
Elizabeth Eakin

6 April 2012 in Cancer
Verified
Journal Article
Closed access
PDF file
KSKathryn H. H Schmitz
Kathryn H. H Schmitz
RSRebecca M. Speck
Rebecca M. Speck
SRSheree A. Rye
Sheree A. Rye
TDTracey DiSipio
Tracey DiSipio
SHSandra C Hayes
Sandra C Hayes

1 January 2010 in Health and Quality of Life Outcomes
Verified
Journal Article
Open access
PDF file
SHSandra C Hayes
Sandra C Hayes
SRSheree Rye
Sheree Rye
DBDiana Battistutta
Diana Battistutta
TDTracey DiSipio
Tracey DiSipio
BNBeth Newman
Beth Newman
Impairments in upper-body function (UBF) are common following breast cancer. However, the relationship between arm morbidity and quality of life (QoL) remains unclear. This investigation uses longitudinal data to describe UBF in a population-based sample of women with breast cancer and examines its relationship with QoL.

1 September 2011 in Lymphatic Research and Biology
Verified
Journal Article
Open access
SHSandra C Hayes
Sandra C Hayes
TDTracey DiSipio
Tracey DiSipio
SRSheree Rye
Sheree Rye
JLJ. Alejandro López
J. Alejandro López
CSChristobel Saunders
Christobel Saunders
BNBeth Newman
Beth Newman
Background: The adverse consequences of lymphedema following breast cancer in relation to physical function and quality of life are clear; however, its potential relationship with survival has not been investigated. Our purpose was to determine the prevalence of lymphedema and associated upper-body symptoms at 6 years following breast cancer and to examine the prognostic significance of lymphedema with respect to overall 6-year survival (OS). Methods and Results: A population-based sample of Australian women ( n =287) diagnosed with invasive, unilateral breast cancer was followed for a median of 6.6 years and prospectively assessed for lymphedema (using bioimpedance spectroscopy [BIS], sum of arm circumferences [SOAC], and self-reported arm swelling), a range of upper-body symptoms, and vital status. OS was measured from date of diagnosis to date of death or last follow-up. Kaplan-Meier methods were used to calculate OS and Cox proportional hazards models quantified the risk associated with lymphedema. Approximately 45% of women had reported at least one moderate to extreme symptom at 6.6 years postdiagnosis, while 34% had shown clinical evidence of lymphedema, and 48% reported arm swelling at least once since baseline assessment. A total of 27 (9.4%) women died during the follow-up period, and lymphedema, diagnosed by BIS or SOAC between 6–18 months postdiagnosis, predicted mortality (BIS: HR=2.5; 95% CI: 0.9, 6.8, p =0.08; SOAC: 3.0; 95% CI: 1.1, 8.7, p =0.04). There was no association (HR=1.2; 95% CI: 0.5, 2.6, p =0.68) between self-reported arm swelling and OS. Conclusions: These findings suggest that lymphedema may influence survival following breast cancer treatment and warrant further investigation in other cancer cohorts and explication of a potential underlying biology.

31 January 2015 in BMC Cancer
Verified
Journal Article
Open access
PDF file
VDVagenas Dimitrios
Vagenas Dimitrios
TDTracey DiSipio
Tracey DiSipio
DBDiana Battistutta
Diana Battistutta
WDWendy Demark-Wahnefried
Wendy Demark-Wahnefried
SRSheree Rye
Sheree Rye
SHSandra C Hayes
Sandra C Hayes
While weight gain following breast cancer is considered common, results supporting these findings are dated. This work describes changes in body weight following breast cancer over 72 months, compares weight with normative data and explores whether weight changes over time are associated with personal, diagnostic, treatment or behavioral characteristics. A population-based sample of 287 Australian women diagnosed with early-stage invasive breast cancer was assessed prospectively at six, 12, 18 and 72 months post-surgery. Weight was clinically measured and linear mixed models were used to explore associations between weight and participant characteristics (collected via self-administered questionnaire). Those with BMI changes of one or more units were considered to have experienced clinically significant changes in weight. More than half (57%) of participants were overweight or obese at 6 months post-surgery, and by 72 months post-surgery 68% of women were overweight or obese. Among those who gained more weight than age-matched norms, clinically significant weight gain between 6 and 18 months and 6 and 72 months post-surgery was observed in 24% and 39% of participants, respectively (median [range] weight gain: 3.9 kg [2.0-11.3 kg] and 5.2 kg [0.6-28.7], respectively). Clinically-significant weight losses were observed in up to 24% of the sample (median [range] weight loss between 6 and 72 months post-surgery: −6.4 kg [−1.9--24.6 kg]). More extensive lymph node removal, being treated on the non-dominant side, receiving radiation therapy and lower physical activity levels at 6 months was associated with higher body weights post-breast cancer (group differences >3 kg; all p < 0.05). While average weight gain among breast cancer survivors in the long-term is small, subgroups of women experience greater gains linked with adverse health and above that experienced by age-matched counterparts. Weight change post-breast cancer is a contemporary public health issue and the integration of healthy weight education and support into standard breast cancer care has potential to significantly improve the length and quality of cancer survivorship.