V.M. Diavolitsis
Ohio State University
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Featured researches published by V.M. Diavolitsis.
Laryngoscope | 2018
Rishabh Sethia; Ali Cemal Yumusakhuylu; Isa Ozbay; V.M. Diavolitsis; Nicole V. Brown; Songzhu Zhao; Lai Wei; Matthew Old; Amit Agrawal; Theodoros N. Teknos; Enver Ozer
To compare quality of life (QOL) of patients who underwent transoral robotic surgery (TORS) alone, with adjuvant radiation therapy (RT), or adjuvant chemoradiation therapy (CRT) in the treatment of oropharyngeal squamous cell cancer (OPSCCA).
Journal of Clinical Oncology | 2016
Theodoros Teknos; Matthew Old; John C. Grecula; Amit Agrawal; Enver Ozer; Ricardo Carrau; Stephan Y Kang; James W. Rocco; Dukagjin Blakaj; V.M. Diavolitsis; Robert A. Baiocchi; Bhavna Kumar; P. Savvides
6036Background: Vorinostat (Zolinza) is a potent HDAC inhibitor that sensitizes head and neck squamous cell carcinoma (HNSCC) to cytotoxic therapy while sparing normal epithelium The primary object...
Oral Oncology | 2018
Ramez H. W. Philips; Daniel R. Martin; Antoine Eskander; Jeffrey Schord; Nicole V. Brown; Songzhu Zhao; Guy N. Brock; Bhavna Kumar; Ricardo Carrau; Enver Ozer; Amit Agrawal; Stephen Y. Kang; James W. Rocco; David E. Schuller; Syed Ashraf Ali; Dukagjin Blakaj; A.D. Bhatt; John C. Grecula; Theodoros Teknos; V.M. Diavolitsis; Matthew Old
OBJECTIVES to examine the impact of radiotherapy center volume on overall survival in patients with oral cavity and oropharyngeal squamous cell carcinoma getting adjuvant radiation therapy after receiving surgery at a high-volume center. MATERIALS AND METHODS a retrospective study was conducted on patients with oral cavity squamous cell carcinoma or oropharyngeal squamous cell carcinoma treated surgically at a tertiary institution from 2000 to 2012 who received adjuvant radiotherapy. The outcome variable was overall survival and the independent variable was location of adjuvant radiation therapy: high-volume center (HVC) versus low-volume center (LVC). Cox proportional hazards models were used to assess associations between predictors of death. Variables that were found to be significant at the α = 0.10 were included in a multivariable model. RESULTS 336 patients met inclusion criteria. One-hundred thirty-nine patients received adjuvant radiation therapy at HVC and 197 patients received adjuvant radiation therapy at LVC. A univariate Cox proportional hazards model identified the variables location, age, marital status, subsite, T stage, extracapsular extension, and smoking status to include in a multivariable model. Age, subsite, T stage, and extracapsular extension were independent predictors of overall survival (p < .05). Location (p = .55), marital status (p = .29), and smoking status (p = .22) were not statistically significant predictors of survival. CONCLUSION After surgery at a HVC, the volume of adjuvant radiation therapy center was not significantly associated with overall survival. Significant predictors of survival included age, subsite, T stage, and extracapsular extension.
Oral Oncology | 2018
C. Barney; Steve Walston; Pedro Zamora; Erin H. Healy; Nicole Nolan; V.M. Diavolitsis; Anterpreet Neki; Robert Rupert; Panos Savvides; Amit Agrawal; Matthew Old; Enver Ozer; Ricardo L. Carrau; Stephen Y. Kang; James W. Rocco; Theodoros N. Teknos; John C. Grecula; J.L. Wobb; Darrion Mitchell; Dukagjin Blakaj; A.D. Bhatt
OBJECTIVES Randomized trials evaluating cisplatin versus cetuximab chemoradiation (CRT) for p16+ oropharyngeal cancer (OPC) have yet to report preliminary data. Meanwhile, as a preemptive step toward morbidity reduction, the off-trial use of cetuximab in p16+ patients is increasing, even in those who could potentially tolerate cisplatin. The purpose of this study was to compare the efficacy of cisplatin versus cetuximab CRT in the treatment of p16+ OPC and to identify prognostic factors and predictors of tumor response. MATERIALS AND METHODS Cases of p16+ OPC treated with cisplatin or cetuximab CRT at our institution from 2010 to 2014 were identified. Recursive partitioning analysis (RPA) classification was used to determine low-risk (LR-RPA) and intermediate-risk (IR-RPA) groups. Log-rank/Kaplan-Meier and Cox Regression methods were used to compare groups. RESULTS We identified 205 patients who received cisplatin (n = 137) or cetuximab (n = 68) CRT in the definitive (n = 178) or postoperative (n = 27) setting. Median follow-up was 3 years. Cisplatin improved 3-year locoregional control (LRC) [92.7 vs 65.4%], distant metastasis-free survival (DMFS) [88.3 vs 71.2%], recurrence-free survival (RFS) [86.6 vs 50.6%], and overall survival (OS) [92.6 vs 72.2%] compared to cetuximab [all p < .001]. Concurrent cisplatin improved 3-year OS for LR-RPA (97.1 vs 80.3%, p < .001) and IR-RPA (97.1 vs 80.3%, p < .001) groupings. CONCLUSION When treating p16+ OPC with CRT, the threshold for substitution of cisplatin with cetuximab should be maintained appropriately high in order to prolong survival times and optimize locoregional and distant tumor control. When cetuximab is used in cisplatin-ineligible patients, altered fractionation RT should be considered in an effort to improve LRC.
Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 2017
Eric D. Miller; D. Blakaj; Benjamin Swanson; Weihong Xiao; Maura L. Gillison; Lai Wei; A.D. Bhatt; V.M. Diavolitsis; J.L. Wobb; Stephen Y. Kang; Ricardo L. Carrau; John C. Grecula
The purpose of this study was to review long‐term outcomes of sinonasal adenoid cystic carcinoma (ACC) and to clarify its association with human papillomavirus (HPV).
Current Otorhinolaryngology Reports | 2015
V.M. Diavolitsis; Harry Quon
A subset of oropharyngeal squamous cell carcinomas (OPSCC) has been shown to be related to human papillomavirus (HPV). These cancers have improved prognosis compared to non-HPV-associated OPSCC. The recognition of this favorable prognosis cohort of patients has occurred in the midst of decades of investigations seeking to intensify local-regional therapy to improve tumor control and survival rates. With long-term follow-up, it is now clear that these intensification strategies are associated with significant late toxicities prompting a re-evaluation of the role of intensified local-regional therapy for HPV-associated OPSCC. The de-intensification strategies that have been evaluated or currently under evaluation are reviewed in this article.
International Journal of Radiation Oncology Biology Physics | 2016
E. Allan; C. Barney; S. Baum; T. Kessling; V.M. Diavolitsis; D. Blakaj; John C. Grecula; James W. Rocco; M. Van Putten; A.D. Bhatt
International Journal of Radiation Oncology Biology Physics | 2015
N. Nolan; V.M. Diavolitsis; D. Blakaj; X. Pan; John C. Grecula; P. Savvides; A.D. Bhatt
International Journal of Radiation Oncology Biology Physics | 2018
C. Barney; A. Branstetter; A. Yaney; E. Healy; R. Rupert; A. Neki; Steve Walston; V.M. Diavolitsis; D. Blakaj; J.L. Wobb; D.L. Mitchell; John C. Grecula; P. Savvides; A.D. Bhatt
International Journal of Radiation Oncology Biology Physics | 2017
D. Fabian; Joseph P. McElroy; A.D. Bhatt; D. Blakaj; D.L. Mitchell; John C. Grecula; J.L. Wobb; V.M. Diavolitsis