Is a higher boost dose of radiation necessary after breast-conserving therapy for patients with breast cancer with final close or positive margins?

To determine rates of loco-regional recurrence (LRR), distant failure and overall survival for patients with breast cancer treated with breast-conserving therapy (BCT) with a close or positive surgical margin (C/PM) treated with standard dose boost radiation compared with a higher boost of radiation...

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Veröffentlicht in:Breast cancer research and treatment 2015-11, Vol.154 (1), p.71-79
Hauptverfasser: Sadek, Betro T., Homayounfar, Gelareh, Abi Raad, Rita F., Niemierko, Andrzej, Shenouda, Mina N., Keruakous, Amany R., Specht, Michelle C., Taghian, Alphonse G.
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container_issue 1
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container_title Breast cancer research and treatment
container_volume 154
creator Sadek, Betro T.
Homayounfar, Gelareh
Abi Raad, Rita F.
Niemierko, Andrzej
Shenouda, Mina N.
Keruakous, Amany R.
Specht, Michelle C.
Taghian, Alphonse G.
description To determine rates of loco-regional recurrence (LRR), distant failure and overall survival for patients with breast cancer treated with breast-conserving therapy (BCT) with a close or positive surgical margin (C/PM) treated with standard dose boost radiation compared with a higher boost of radiation. We retrospectively studied 1476 patients with T1–T3 invasive breast cancer treated with BCT between 1992 and 2009. Median age was 57 years. Patients were divided into three groups: Group I included 1197 patients (81 %) with negative margins who received a standard boost (median 60 Gy) total dose to the lumpectomy cavity; Group II included 116 patients (8 %) with C/PM who received a standard boost (median 60 Gy); and Group III included 163 patients (11 %) with C/PM who received a higher boost (median 68 Gy). Biological subtypes (e.g., ER, PR, HER2/neu) were available for 858 patients (58 %) and were also assessed for any relationship to LRR rate. The Kaplan–Meier, Cox-regression, and log-rank tests were used to estimate rates of LRR and the significance of risk factors. Median follow-up was 8.6 years. The overall 5- and 10-year cumulative incidences of LRR were 2.1 % (95 % CI 0.8–2.1 %) and 4.5 % (95 % CI 3.4–6.0 %), respectively. The 5- and 10-year cumulative incidences of LRR for Group I (negative margins + standard boost) were 1.9 and 4.4 %; for Group II (C/PM + standard boost) were 3.9 and 7.0 %; and for Group III (C/PM + higher boost) were 2.9 and 3.8 %, respectively. No statistically significant differences in LRR rates were found among the three groups ( p  = 0.4). Similar results were obtained for distant failure ( p  = 0.3) and overall survival ( p  = 0.4). On multivariate analysis, tumor grade ( p  = 0.03), systemic-therapy ( p  = 0.005), node positivity ( p  = 0.05), young age ( p  = 0.001), and biological subtype ( p  = 0.04) were statistically significantly associated with higher LRR. Higher boost dose and margin positivity were not significant. Our data suggest that the 10-year risk of local recurrence for patients with close or positive margins receiving a standard boost was 7 % compared to 3.8 % for those receiving a higher boost; however, this difference was not significant. A higher boost dose did not significantly improve local control, nor did margins impact LRR risk in our cohort of patients.
doi_str_mv 10.1007/s10549-015-3579-9
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We retrospectively studied 1476 patients with T1–T3 invasive breast cancer treated with BCT between 1992 and 2009. Median age was 57 years. Patients were divided into three groups: Group I included 1197 patients (81 %) with negative margins who received a standard boost (median 60 Gy) total dose to the lumpectomy cavity; Group II included 116 patients (8 %) with C/PM who received a standard boost (median 60 Gy); and Group III included 163 patients (11 %) with C/PM who received a higher boost (median 68 Gy). Biological subtypes (e.g., ER, PR, HER2/neu) were available for 858 patients (58 %) and were also assessed for any relationship to LRR rate. The Kaplan–Meier, Cox-regression, and log-rank tests were used to estimate rates of LRR and the significance of risk factors. Median follow-up was 8.6 years. The overall 5- and 10-year cumulative incidences of LRR were 2.1 % (95 % CI 0.8–2.1 %) and 4.5 % (95 % CI 3.4–6.0 %), respectively. The 5- and 10-year cumulative incidences of LRR for Group I (negative margins + standard boost) were 1.9 and 4.4 %; for Group II (C/PM + standard boost) were 3.9 and 7.0 %; and for Group III (C/PM + higher boost) were 2.9 and 3.8 %, respectively. No statistically significant differences in LRR rates were found among the three groups ( p  = 0.4). Similar results were obtained for distant failure ( p  = 0.3) and overall survival ( p  = 0.4). On multivariate analysis, tumor grade ( p  = 0.03), systemic-therapy ( p  = 0.005), node positivity ( p  = 0.05), young age ( p  = 0.001), and biological subtype ( p  = 0.04) were statistically significantly associated with higher LRR. Higher boost dose and margin positivity were not significant. Our data suggest that the 10-year risk of local recurrence for patients with close or positive margins receiving a standard boost was 7 % compared to 3.8 % for those receiving a higher boost; however, this difference was not significant. 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The 5- and 10-year cumulative incidences of LRR for Group I (negative margins + standard boost) were 1.9 and 4.4 %; for Group II (C/PM + standard boost) were 3.9 and 7.0 %; and for Group III (C/PM + higher boost) were 2.9 and 3.8 %, respectively. No statistically significant differences in LRR rates were found among the three groups ( p  = 0.4). Similar results were obtained for distant failure ( p  = 0.3) and overall survival ( p  = 0.4). On multivariate analysis, tumor grade ( p  = 0.03), systemic-therapy ( p  = 0.005), node positivity ( p  = 0.05), young age ( p  = 0.001), and biological subtype ( p  = 0.04) were statistically significantly associated with higher LRR. Higher boost dose and margin positivity were not significant. Our data suggest that the 10-year risk of local recurrence for patients with close or positive margins receiving a standard boost was 7 % compared to 3.8 % for those receiving a higher boost; however, this difference was not significant. 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We retrospectively studied 1476 patients with T1–T3 invasive breast cancer treated with BCT between 1992 and 2009. Median age was 57 years. Patients were divided into three groups: Group I included 1197 patients (81 %) with negative margins who received a standard boost (median 60 Gy) total dose to the lumpectomy cavity; Group II included 116 patients (8 %) with C/PM who received a standard boost (median 60 Gy); and Group III included 163 patients (11 %) with C/PM who received a higher boost (median 68 Gy). Biological subtypes (e.g., ER, PR, HER2/neu) were available for 858 patients (58 %) and were also assessed for any relationship to LRR rate. The Kaplan–Meier, Cox-regression, and log-rank tests were used to estimate rates of LRR and the significance of risk factors. Median follow-up was 8.6 years. The overall 5- and 10-year cumulative incidences of LRR were 2.1 % (95 % CI 0.8–2.1 %) and 4.5 % (95 % CI 3.4–6.0 %), respectively. The 5- and 10-year cumulative incidences of LRR for Group I (negative margins + standard boost) were 1.9 and 4.4 %; for Group II (C/PM + standard boost) were 3.9 and 7.0 %; and for Group III (C/PM + higher boost) were 2.9 and 3.8 %, respectively. No statistically significant differences in LRR rates were found among the three groups ( p  = 0.4). Similar results were obtained for distant failure ( p  = 0.3) and overall survival ( p  = 0.4). On multivariate analysis, tumor grade ( p  = 0.03), systemic-therapy ( p  = 0.005), node positivity ( p  = 0.05), young age ( p  = 0.001), and biological subtype ( p  = 0.04) were statistically significantly associated with higher LRR. Higher boost dose and margin positivity were not significant. Our data suggest that the 10-year risk of local recurrence for patients with close or positive margins receiving a standard boost was 7 % compared to 3.8 % for those receiving a higher boost; however, this difference was not significant. A higher boost dose did not significantly improve local control, nor did margins impact LRR risk in our cohort of patients.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>26420403</pmid><doi>10.1007/s10549-015-3579-9</doi><tpages>9</tpages></addata></record>
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source MEDLINE; Springer Nature - Complete Springer Journals
subjects Adult
Aged
Aged, 80 and over
Breast cancer
Breast Neoplasms - pathology
Breast Neoplasms - radiotherapy
Breast Neoplasms - surgery
Cancer patients
Cancer research
Cancer therapies
Care and treatment
Clinical Trial
Comparative analysis
Disease-Free Survival
Female
Humans
Kaplan-Meier Estimate
Lumpectomy
Mastectomy, Segmental
Medicine
Medicine & Public Health
Middle Aged
Neoplasm Recurrence, Local - pathology
Neoplasm Recurrence, Local - radiotherapy
Neoplasm Recurrence, Local - surgery
Neoplasm Staging
Neoplasm, Residual - pathology
Neoplasm, Residual - radiotherapy
Neoplasm, Residual - surgery
Oncology
Patients
Radiation (Physics)
Radiation therapy
Receptor, ErbB-2 - genetics
title Is a higher boost dose of radiation necessary after breast-conserving therapy for patients with breast cancer with final close or positive margins?
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