David E. Wazer
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
David E. Wazer has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
Neenad M. Shah
Department of Radiation Oncology, Tufts-New England Medical Center/Tufts University School of Medicine, Boston, MA 02111, USA
2 shared publicationsSeth Kaufman
2 shared publicationsThomas DiPetrillo
2 shared publicationsBruce Bornstein
Tufts Medical Center
1 shared publicationDouglas Arthur
Department of Radiation Oncology, Medical College of Virginia of Virginia Commonwealth University Health System, Richmond, Virginia
1 shared publicationDouglas W. Arthur
1 shared publication
Latest Publications
- 1 January 2007
- Published by Taylor & Francis in The Women's Oncology Review
- Vol. 6 (1) , 75-77
Long term toxicity following interstitial breast brachytherapy: results from RTOG 95-17
- 1 January 2007
- Published by Taylor & Francis in The Women's Oncology Review
- Vol. 6 (1) , 75-77
Long term toxicity following interstitial breast brachytherapy: results from RTOG 95-17
- 1 February 2006
- Published by Elsevier in International Journal of Radiation Oncology - Biology - Physics (IJROBP)
- Vol. 64 (2) , 489-495
Accelerated partial breast irradiation: An analysis of variables associated with late toxicity and long-term cosmetic outcome after high-dose-rate interstitial brachytherapy
- 1 February 2006
- Published by Elsevier in International Journal of Radiation Oncology - Biology - Physics (IJROBP)
- Vol. 64 (2) , 489-495
Accelerated partial breast irradiation: An analysis of variables associated with late toxicity and long-term cosmetic outcome after high-dose-rate interstitial brachytherapy
- 30 March 2005
- Published by Elsevier in Seminars in Radiation Oncology
- Vol. 15 (2) , 100-107
The MammoSite balloon brachytherapy catheter for accelerated partial breast irradiation
- 30 March 2005
- Published by Elsevier in Seminars in Radiation Oncology
- Vol. 15 (2) , 100-107
The MammoSite balloon brachytherapy catheter for accelerated partial breast irradiation
- Open Access
MammoSite and interstitial brachytherapy for accelerated partial breast irradiation
BACKGROUND In interstitial brachytherapy (IB), cosmesis and toxicity correlate with volume of tissue irradiated, dose homogeneity index (DHI), and adjuvant doxorubicin/cyclophosphamide based chemotherapy (ACCT). MammoSite brachytherapy (MSB) irradiates smaller volumes than IB, and lower dose homogeneity does not appear to affect toxicity. However, clinical experience suggests that other factors may also play an important role in cosmesis and toxicity with MSB. We reviewed our prospectively maintained data base of women who underwent accelerated partial breast irradiation (APBI) to assess this issue. METHODS Beginning in September 1995, 115 women were enrolled in a trial evaluating APBI as monotherapy after lumpectomy. The first 75 eligible patients received IB, and the most recent 28 eligible patients received MSB. All patients received 34 gray (Gy) in 10 twice-daily fractions through high-dose rate iridium-192 brachytherapy; 19% of patients in the IB group and 0% of patients in the MSB group received ACCT. RESULTS At 1 year after treatment, MSB caused significantly less Grade 2–4 subcutaneous fibrosis (as graded by a radiation oncologist according to the Radiation Therapy Oncology Group/Eastern Cooperative Oncology Group system) compared with IB (10.7% vs. 32%; P = 0.04). However, when only ACCT-naïve patients in the IB group were compared with patients in the MSB group, this finding became nonsignificant. Among the patients who received MSB, significantly smaller volumes were irradiated, and the DHI was lower. CONCLUSIONS Current studies suggest an improved toxicity profile with MSB compared with IB that is attributed to lower irradiated volumes with MSB. When only chemotherapy-naïve patients were compared, however, toxicity and cosmesis were found to be similar between MSB and IB, suggesting a more complex interplay between irradiated volumes, DHI, and chemotherapy. The relation of ACCT to toxicity in this scenario is intriguing and warrants further investigation. Cancer 2004. © 2004 American Cancer Society.
Open AccessMammoSite and interstitial brachytherapy for accelerated partial breast irradiation
BACKGROUND In interstitial brachytherapy (IB), cosmesis and toxicity correlate with volume of tissue irradiated, dose homogeneity index (DHI), and adjuvant doxorubicin/cyclophosphamide based chemotherapy (ACCT). MammoSite brachytherapy (MSB) irradiates smaller volumes than IB, and lower dose homogeneity does not appear to affect toxicity. However, clinical experience suggests that other factors may also play an important role in cosmesis and toxicity with MSB. We reviewed our prospectively maintained data base of women who underwent accelerated partial breast irradiation (APBI) to assess this issue. METHODS Beginning in September 1995, 115 women were enrolled in a trial evaluating APBI as monotherapy after lumpectomy. The first 75 eligible patients received IB, and the most recent 28 eligible patients received MSB. All patients received 34 gray (Gy) in 10 twice-daily fractions through high-dose rate iridium-192 brachytherapy; 19% of patients in the IB group and 0% of patients in the MSB group received ACCT. RESULTS At 1 year after treatment, MSB caused significantly less Grade 2–4 subcutaneous fibrosis (as graded by a radiation oncologist according to the Radiation Therapy Oncology Group/Eastern Cooperative Oncology Group system) compared with IB (10.7% vs. 32%; P = 0.04). However, when only ACCT-naïve patients in the IB group were compared with patients in the MSB group, this finding became nonsignificant. Among the patients who received MSB, significantly smaller volumes were irradiated, and the DHI was lower. CONCLUSIONS Current studies suggest an improved toxicity profile with MSB compared with IB that is attributed to lower irradiated volumes with MSB. When only chemotherapy-naïve patients were compared, however, toxicity and cosmesis were found to be similar between MSB and IB, suggesting a more complex interplay between irradiated volumes, DHI, and chemotherapy. The relation of ACCT to toxicity in this scenario is intriguing and warrants further investigation. Cancer 2004. © 2004 American Cancer Society.
- 1 October 1993
- Published by Elsevier in International Journal of Radiation Oncology - Biology - Physics (IJROBP)
- Vol. 27 (3) , 757-758
Reply to Dr. Abraham Recht's editorial
- 1 October 1993
- Published by Elsevier in International Journal of Radiation Oncology - Biology - Physics (IJROBP)
- Vol. 27 (3) , 757-758
Reply to Dr. Abraham Recht's editorial