D. Domain
University of Texas MD Anderson Cancer Center
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Featured researches published by D. Domain.
International Journal of Radiation Oncology Biology Physics | 2008
Ian J. Bristol; Wendy A. Woodward; Eric A. Strom; Massimo Cristofanilli; D. Domain; S. Eva Singletary; George H. Perkins; Julia L. Oh; Tse Kuan Yu; Welela Terrefe; Aysegul A. Sahin; Kelly K. Hunt; Gabriel N. Hortobagyi; Thomas A. Buchholz
PURPOSE The aims of this study were to determine outcomes for patients with inflammatory breast cancer (IBC) treated with multimodality therapy, to identify factors associated with locoregional recurrence, and to determine which patients may benefit from radiation dose escalation. METHODS AND MATERIALS We retrospectively reviewed 256 consecutive patients with nonmetastatic IBC treated at our institution between 1977 and 2004. RESULTS The 192 patients who were able to complete the planned course of chemotherapy, mastectomy, and postmastectomy radiation had significantly better outcomes than the 64 patients who did not. The respective 5-year outcome rates were: locoregional control (84% vs. 51%), distant metastasis-free survival (47% vs. 20%), and overall survival (51% vs. 24%) (p < 0.0001 for all comparisons). Univariate factors significantly associated with locoregional control in the patients who completed plan treatment were response to neoadjuvant chemotherapy, surgical margin status, number of involved lymph nodes, and use of taxanes. Increasing the total chest-wall dose of postmastectomy radiation from 60 Gy to 66 Gy significantly improved locoregional control for patients who experienced less than a partial response to chemotherapy, patients with positive, close, or unknown margins, and patients <45 years of age. CONCLUSIONS Patients with IBC who are able to complete treatment with chemotherapy, mastectomy, and postmastectomy radiation have a high probability of locoregional control. Escalation of postmastectomy radiation dose to 66 Gy appears to benefit patients with disease that responds poorly to chemotherapy, those with positive, close, or unknown margin status, and those <45 years of age.
Journal of Clinical Oncology | 2006
Julia L. Oh; Mark J. Dryden; Wendy A. Woodward; Tse Kuan Yu; Welela Tereffe; Eric A. Strom; George H. Perkins; Lavinia P. Middleton; Kelly K. Hunt; Sharon H. Giordano; Mary Jane Oswald; D. Domain; Thomas A. Buchholz
PURPOSE The purpose was to assess whether patients with clinical multifocal or multicentric (MFMC) breast cancer determined by mammogram, ultrasound, or physical examination have inferior outcome compared with patients with clinical unicentric lesions. PATIENTS AND METHODS We retrospectively analyzed 706 consecutive patients with stages I-III breast cancer treated at the M.D. Anderson Cancer Center (Houston, TX) from 1976 to 2003 who received neoadjuvant anthracycline-based chemotherapy followed by breast conservation therapy (BCT), mastectomy alone, or mastectomy plus postmastectomy radiation therapy. RESULTS The mean follow-up was 66 months. At presentation, 97 of 706 patients had clinically MFMC disease (13.7%). The 5-year rate of locoregional failure was 10% for unicentric disease compared with 7% for MFMC disease (P = .78). Subset analyses of patients by treatment groups confirmed no statistical difference in locoregional control regardless of the type of locoregional treatment. Among patients with multifocal disease treated with BCT, there were no in-breast recurrences and one supraclavicular recurrence. Five-year disease-free survival and overall survival was equivalent between patients with MFMC and unicentric breast cancers. CONCLUSION Patients with clinical MFMC breast cancer at the time of diagnosis treated with neoadjuvant chemotherapy followed by locoregional therapy have similar 5-year rates of locoregional control, disease-free survival, and overall survival as those with unicentric disease. Clinically detected MFMC disease did not predict for inferior outcome.
Cancer | 2008
Wendy A. Woodward; Jean Bernard Durand; Susan L. Tucker; Eric A. Strom; George H. Perkins; J.L. Oh; Lisa Arriaga; D. Domain; Thomas A. Buchholz
International Journal of Radiation Oncology Biology Physics | 2006
Thomas A. Buchholz; Eric A. Strom; Mary Jane Oswald; George H. Perkins; J.L. Oh; D. Domain; Tse Kuan Yu; Wendy A. Woodward; Welela Tereffe; S. Eva Singletary; Eva Thomas; Aman U. Buzdar; Gabriel N. Hortobagyi; Marsha D. McNeese
Journal of The National Comprehensive Cancer Network | 2014
Lydia T. Madsen; Deborah A. Kuban; Seungtaek Choi; John W. Davis; Jeri Kim; Andrew K. Lee; D. Domain; Larry B. Levy; Louis L. Pisters; Curtis A. Pettaway; John F. Ward; Christopher J. Logothetis; Karen E. Hoffman
International Journal of Radiation Oncology Biology Physics | 2011
D. Domain; Karen E. Hoffman; Lydia T. Madsen; Curtis A. Pettaway; Jeri Kim; John W. Davis; Andrew K. Lee; Louis L. Pisters; Lawrence B. Levy; Deborah A. Kuban
International Journal of Radiation Oncology Biology Physics | 2011
Karen E. Hoffman; Jeri Kim; John W. Davis; S. Choi; Curtis A. Pettaway; Andrew K. Lee; D. Domain; Lawrence B. Levy; Lydia T. Madsen; Deborah A. Kuban
International Journal of Radiation Oncology Biology Physics | 2006
Ian J. Bristol; Eric A. Strom; D. Domain; Massimo Cristofanilli; George H. Perkins; Wendy A. Woodward; J.L. Oh; T. Yu; Welela Tereffe; Thomas A. Buchholz
International Journal of Radiation Oncology Biology Physics | 2005
Wendy A. Woodward; Jean Bernard Durand; Susan L. Tucker; Eric A. Strom; George H. Perkins; J.L. Oh; Lisa Arriaga; D. Domain; Thomas A. Buchholz
International Journal of Radiation Oncology Biology Physics | 2005
J.L. Oh; Eric A. Strom; George H. Perkins; Mary Jane Oswald; D. Domain; Kelly K. Hunt; Sharon H. Giordano; Thomas A. Buchholz