B. Dingle
University of Western Ontario
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Featured researches published by B. Dingle.
Clinical Lung Cancer | 2009
Alexander V. Louie; George Rodrigues; Brian Yaremko; Edward Yu; A. Rashid Dar; B. Dingle; Mark Vincent; Michael Sanatani; Jawaid Younus; Richard A. Malthaner; Richard Inculet
BACKGROUND Reports in the medical literature have described cases of extended survival of patients with non-small-cell lung cancer (NSCLC) with solitary metastatic disease who have received aggressive treatment both to the brain metastasis and to the local/regional disease. The objective of this research is to analyze prognostic factors that predict for outcome in this unique patient population. PATIENTS AND METHODS A single-institution, retrospective chart review was performed on 35 patients with NSCLC and a synchronous solitary brain metastasis (SSBM) treated with craniotomy and whole-brain radiation therapy. Eight patients (22.9%) had chest surgery, 24 (68.6%) had chemotherapy, and 14 (40%) had thoracic radiation as part of their local management. Fourteen had stage I/II disease (42.9%), and 20 had stage III disease (57.1%). Mean age at diagnosis was 58.5 years. Eighteen patients (56.25%) had a brain metastasis < 3 cm, and 14 patients (43.75%) had a metastasis > 3 cm. RESULTS Median survival was 7.8 months, and at last follow-up, 3 patients (8.6%) were alive and well, 6 patients (17.1%) were alive and with disease, 24 patients (68.6%) had died of disease, and 2 patients (5.7%) had died of other causes. Univariate analysis demonstrated that lung surgery (P = .0033), primary lung treatment > 8 weeks after brain surgery (P = .0128), and stage I/II disease (P = .0467) were predictive of overall survival. CONCLUSION Survival remains poor for patients with NSCLC with an SSBM. However, patients with thoracic disease amenable to local resection should be considered for such therapy because a survival advantage could exist compared with patients with more locally advanced disease.
Clinical Lung Cancer | 2010
Eugenie Waters; B. Dingle; George Rodrigues; Mark Vincent; R. Ash; R. Dar; Richard Inculet; Walter Kocha; Richard A. Malthaner; Michael Sanatani; Larry Stitt; Brian Yaremko; Jawaid Younus; Edward Yu
BACKGROUND The London Regional Cancer Program (LRCP) uses a unique schedule of induction plus concurrent chemoradiation, termed VCRT (vinblastine, cisplatin, and radiation therapy), for the treatment of a subset of unresectable stage IIIA and IIIB non-small-cell lung cancer (NSCLC). This analysis was conducted to better understand the outcomes in VCRT-treated patients. PATIENTS AND METHODS We report a retrospective analysis of a large cohort of patients who underwent VCRT at the LRCP over a 10-year period, from 1996 to 2006. The analysis focused on OS, toxicities, and the outcomes from completion surgery in a small subset of patients. RESULTS A total of 294 patients were included and 5-year OS, determined using Kaplan-Meier methodology, was 19.8% with a MST of 18.2 months. Reported grade 3-4 toxicities included neutropenia (39%), anemia (10%), pneumonitis (1%), and esophagitis (3%). Significant differences in survival between groups of patients were demonstrated with log-rank tests for completion surgery, use of radiation therapy, and cisplatin dose. Similarly, Univariate Cox regression showed that completion surgery, use of radiation therapy, cisplatin dose, and vinblastine dose were associated with increased survival. CONCLUSION This retrospective analysis of a large cohort of patients reveals an OS for VCRT comparable to that reported in the literature for other current combined chemoradiation protocols. The success of this protocol seems to be dose dependent and the outcomes in those who underwent completion surgery suggests that pathologic complete remission is possible for IIIA and IIIB NSCLC.
Breast Cancer Research and Treatment | 2013
Wendy A. Teft; Inna Y. Gong; B. Dingle; Kylea Potvin; Jawaid Younus; Theodore A. Vandenberg; Muriel Brackstone; Francisco Perera; Yun-Hee Choi; Zou G; Robin M. Legan; Rommel G. Tirona; Richard B. Kim
BMC Cancer | 2014
Douglas A. Hoover; Dante P. I. Capaldi; Khadija Sheikh; David A. Palma; George Rodrigues; A. Rashid Dar; Edward Yu; B. Dingle; Mark Landis; Walter Kocha; Michael Sanatani; Mark Vincent; Jawaid Younus; Sara Kuruvilla; Stewart Gaede; Grace Parraga; Brian Yaremko
Current Oncology | 2010
Edward Yu; Patricia Tai; Richard A. Malthaner; Larry Stitt; George Rodrigues; R. Dar; Brian Yaremko; Jawaid Younus; Michael Sanatani; Mark Vincent; B. Dingle; Dalilah Fortin; Richard Inculet
Current Oncology | 2009
Edward Yu; Patricia Tai; Jawaid Younus; R. Malthaner; P. Truong; Larry Stitt; George Rodrigues; R. Ash; R. Dar; Brian Yaremko; A. Tomiak; B. Dingle; Michael Sanatani; Mark Vincent; W. Kocha; D. Fortin; Richard Inculet
International Journal of Radiation Oncology Biology Physics | 2017
Brian Yaremko; D. Hoover; Dante Capaldi; Khadija Sheikh; A.R. Dar; Edward Yu; George Rodrigues; Alexander V. Louie; Stewart Gaede; J. Chen; A. Erickson; A. Warner; B. Dingle; Mark Landis; Michael Sanatani; Mark Vincent; Jawaid Younus; S. Kuruvilla; David A. Palma; Grace Parraga
Current Oncology | 2018
T.W. Zhang; George Rodrigues; Alexander V. Louie; David A. Palma; A.R. Dar; B. Dingle; W. Kocha; Michael Sanatani; Brian Yaremko; Edward Yu; Jawaid Younus; Mark Vincent
Radiotherapy and Oncology | 2016
Tina W. Zhang; George Rodrigues; Alexander V. Louie; A. Rashid Dar; B. Dingle; Michael Sanatani; David Small; Brian Yaremko; Jawaid Younus; Mark Vincent
International Journal of Radiation Oncology Biology Physics | 2016
T.W. Zhang; George Rodrigues; Alexander V. Louie; A.R. Dar; B. Dingle; Michael Sanatani; D. Small; Brian Yaremko; Jawaid Younus; Mark Vincent