Oana Craciunescu

Prof. Oana Craciunescu

Department of Radiation Oncology, Duke University, Durham, NC 27710, USA

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

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

Representative Publications

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2 October 2009 in Medical Physics
Verified
Journal Article
Closed access
OCOana Craciunescu
Oana Craciunescu
PSPaul R. Stauffer
Paul R. Stauffer
BSBrian J. Soher
Brian J. Soher
CWCory R. Wyatt
Cory R. Wyatt
OAOmar Arabe
Omar Arabe
JMJames R. MacFall
James R. MacFall

1 January 2009 in International Journal of Hyperthermia
Verified
Journal Article
Closed access
OCOana Craciunescu
Oana Craciunescu
KBKimberly L. Blackwell
Kimberly L. Blackwell
EJEllen L. Jones
Ellen L. Jones
JMJames R. Macfall
James R. Macfall
DYDaohai Yu
Daohai Yu
MDMark W. Dewhirst
Mark W. Dewhirst
Combined therapies represent a staple of modern medicine. For women treated with neoadjuvant chemotherapy (NA ChT) for locally advanced breast cancer (LABC), early determination of whether the patient will fail to respond can enable the use of alternative, more beneficial therapies. This is even more desirable when the combined therapy includes hyperthermia (HT), an efficient way to improve drug delivery, however, more costly and time consuming. There is data showing that this goal can be achieved using magnetic resonance imaging (MRI) with contrast agent (CA) enhancement. This work for the first time proposes combining the information extracted from pre-treatment MR imaging into a morpho-physiological tumour score (MPTS) with the hypothesis that this score will increase the prognostic efficacy, compared to each of its MR-derived components: morphological (derived from the shape of the tumour enhancement) and physiological (derived from the CA enhancement variance dynamics parameters). The MPTS was correlated with response as determined by both pathologic residual tumour and MRI imaging, and was shown to have potential to predict response. The MPTS was extracted from pre-treatment MRI parameters, so independent of the combined therapy used. Purpose: To use a novel morpho-physiological tumour score (MPTS) generated from dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) to predict response to treatment. Materials and methods: A protocol was designed to acquire DCE-MRI images of 20 locally advanced breast cancer (LABC) patients treated with neoadjuvant chemotherapy (NA ChT) and hyperthermia (HT). Imaging was done over 30 min following bolus injection of gadopentetate-based contrast agent. Parametric maps were generated by fitting the signal intensity to a double exponential curve and were used to derive a morphological characterisation of the lesions. Enhancement-variance dynamics parameters, wash-in and wash-out parameters (WiP, WoP), were extracted. The morphological characterisation and the WiP and WoP were combined into a MPTS with the intent of achieving better prognostic efficacy. The MPTS was correlated with response to NA therapy as determined by pathological residual tumour and MRI imaging. Results: The contrast agent in all tumours typically peaked in the first 1–4 min. The tumours’ WiP and WoP varied considerably. The MPTS was highly correlated with whether the patients had a pathological response. This scoring system has a specificity of 78% and a sensitivity of 91% for predicting response to NA chemotherapy. The kappa was 0.69 with a 95% confidence interval of [0.38, 1] and a p-value of 0.002. Conclusions: This pilot study shows that the MPTS derived using pre-treatment MRI images has the potential to predict response to NA ChT and HT in LABC patients. Further prospective studies are needed to confirm the validity of these results.

1 March 2011 in International Journal of Radiation Oncology - Biology - Physics (IJROBP)
Verified
Journal Article
Closed access
OCOana Craciunescu
Oana Craciunescu
BSBeverly A. Steffey
Beverly A. Steffey
CKChris R. Kelsey
Chris R. Kelsey
NLNicole A. Larrier
Nicole A. Larrier
CPCathy J. Paarz-Largay
Cathy J. Paarz-Largay
KSKeith M. Sullivan
Keith M. Sullivan

4 September 2020 in Brachytherapy
Verified
Journal Article
Open access
SCSabrina N Campelo
Sabrina N Campelo
ESErgys Subashi
Ergys Subashi
SMSheridan G. Meltsner
Sheridan G. Meltsner
ZCZheng Chang
Zheng Chang
JCJunzo Chino
Junzo Chino
OCOana Craciunescu
Oana Craciunescu
As the utilization of brachytherapy procedures continues to decline in clinics, a need for accessible training tools is required to help bridge the gap between resident comfort in brachytherapy training and clinical practice. To improve the quality of intracavitary and interstitial HDR brachytherapy education, a multi-material modular 3D printed pelvic phantom prototype simulating normal and cervix pathological conditions has been developed. Patient anatomy was derived from pelvic CT and MRI scans from 50 representative patients diagnosed with localized cervical cancer. Dimensions measured from patients’ uterine body and uterine canal sizes were used to construct a variety of uteri based off of the averages and standard deviations of the subjects in our study. Soft-tissue anatomy was 3D printed using Agilus blends (shore 30 and 70), and modular components in Vero (shore 85). The kit consists of four uteri, a standard bladder, standard rectum, two embedded GTVs and four clip-on GTV attachments. The three anteverted uteri in the kit are based on the smallest, the average, and the largest dimensions from our patient set while the retroverted uterus assumes average dimensions. This educational HDR gynecological pelvic phantom is an accessible and cost-effective way to improve radiation oncology resident training in intracavitary/interstitial brachytherapy cases. Implementation of this phantom in resident education will allow for more thorough and comprehensive physician training through its ability to transform the patient scenario. It is expected that this tool will help improve confidence and efficiency when performing brachytherapy procedures in patients.

1 March 2012 in International Journal of Radiation Oncology - Biology - Physics (IJROBP)
Verified
Journal Article
Closed access
OCOana Craciunescu
Oana Craciunescu
DYDavid S. Yoo
David S. Yoo
ECEsi Cleland
Esi Cleland
NMNaira Muradyan
Naira Muradyan
MCMadeline D. Carroll
Madeline D. Carroll
DBDavid M. Brizel
David M. Brizel

1 July 2014 in International Journal of Radiation Oncology - Biology - Physics (IJROBP)
Verified
Journal Article
Closed access
JOJennifer D. Onxley
Jennifer D. Onxley
DYDavid S. Yoo
David S. Yoo
NMNaira Muradyan
Naira Muradyan
JMJames R. MacFall
James R. MacFall
DBDavid M. Brizel
David M. Brizel
OCOana Craciunescu
Oana Craciunescu