Nadia Di Muzio

Prof. Dr. Nadia Di Muzio


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

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1 November 2018 in International Journal of Radiation Oncology, Biology, Physics
Verified
Journal Article
Closed access
Nicola DinapoliNicola Dinapoli
Nicola Dinapoli
BBBrunella Barbaro
Brunella Barbaro
RGRoberto Gatta
Roberto Gatta
GCGiuditta Chiloiro
Giuditta Chiloiro
Calogero CasàCalogero Casà
Calogero Casà
VVVincenzo Valentini
Vincenzo Valentini

1 June 2009 in International Journal of Radiation Oncology, Biology, Physics
Verified
Journal Article
Closed access
NMNadia Di Muzio
Nadia Di Muzio
Claudio FiorinoClaudio Fiorino
Claudio Fiorino
CCCesare Cozzarini
Cesare Cozzarini
Filippo AlongiFilippo Alongi
Filippo Alongi
SBSara Broggi
Sara Broggi
FFFerruccio Fazio
Ferruccio Fazio


31 October 2009 in Radiotherapy and Oncology
Verified
Journal Article
Closed access
LPLucia Perna
Lucia Perna
Claudio FiorinoClaudio Fiorino
Claudio Fiorino
CCCesare Cozzarini
Cesare Cozzarini
SBSara Broggi
Sara Broggi
GCGiovanni Mauro Cattaneo
Giovanni Mauro Cattaneo
RCRiccardo Calandrino
Riccardo Calandrino

1 September 2016 in British Journal of Radiology
Verified
Journal Article
Closed access
GFGiovanni Fellin
Giovanni Fellin
MMMaria A Mirri
Maria A Mirri
LSLuigi Santoro
Luigi Santoro
BJBarbara Alicja Jereczek-Fossa
Barbara Alicja Jereczek-Fossa
CDClaudio Divan
Claudio Divan
RORoberto Orecchia
Roberto Orecchia
Objective:Low Dose Rate Brachytherapy (LDR-BT) in localized prostate cancer is available since 15 years in Italy. We realized the first national multicentre and multidisciplinary data collection to evaluate LDR-BT practice, given as monotherapy, and outcome in terms of biochemical failure.Methods:Between 5/1998 and 12/2011, 2237 early stage prostate cancer patients from 11 Italian Community and Academic Hospitals were treated with Iodine-125 (125I) or Palladium-103 (103Pd) LDR-BT as monotherapy and followed-up for at least two years. 125I seeds were implanted in 97.7% of the patients: the mean dose received by 90% of target volume (D90) was 145 Gy; the mean V100 (target volume receiving 100% of prescribed dose) equals 91.1%. Biochemical failure free survival (BFFS), Disease specific survival (DSS) and Overall Survival (OS) were estimated using Kaplan-Meier method. Log-Rank test and multivariable Cox regression were used to evaluate relationship of covariates with outcomes.Results:Median follow-up time was...

31 January 2020 in British Journal of Radiology
Verified
Journal Article
Closed access
CDChiara Lucrezia Deantoni
Chiara Lucrezia Deantoni
AFAndrei Fodor
Andrei Fodor
CCCesare Cozzarini
Cesare Cozzarini
Claudio FiorinoClaudio Fiorino
Claudio Fiorino
CBChiara Brombin
Chiara Brombin
NMNadia Di Muzio
Nadia Di Muzio
Objective: To evaluate toxicity and clinical outcome in synchronous bone only oligometastatic (≤2 lesions) prostate cancer patients, simultaneously irradiated to prostate/prostatic bed, lymph nodes and bone metastases. Methods: From 2/2009 to 6/2015, 39 bone only prostate cancer patients underwent radiotherapy (RT) at “radical” doses to bone metastases (median 2 Gy equivalent dose, EQD2>40Gy, α/β = 1,5), nodes, and prostate/prostatic bed, within the same RT course, in association with androgen deprivation therapy (ADT). Biochemical relapse-free survival, clinical relapse-free survival, freedom from distant metastases and overall survival were evaluated. Results: After a median follow-up of 46.5 (1.2–103.6) months, 5 patients died from disease progression, 10 experienced biochemical relapse, 19, still in ADT, presented undetectable prostate-specific antigen (PSA) at the last follow-up. Five patients who discontinued ADT after a median of 34 months (5.8–41) are free from biochemical relapse. The 4 year Kaplan–Meier estimates of biochemical relapse-free survival, clinical relapse-free survival, freedom from distant metastases and overall survival were 53.3%, 65.7%, 73.4% and 82.4% respectively. No Grade > 2 acute events and only two severe late urinary events were recorded, not due to the concomitant treatment of primary and metastatic disease. Conclusion: Our results suggest that “radical” and synchronous irradiation of primitive tumor and metastatic disease may be a valid approach in synchronous bone only prostate cancer patients, showing mild toxicity profile and promising survival results. Advances in knowledge: To the best of our knowledge, this is the first analysis of clinical outcome in synchronous bone-only metastasis (neither nodal nor visceral) patients at diagnosis, treated with radical RT to all disease, associated to ADT.