Pitchaya Thongkhao, et al: Effects of Regular Bra-wearing on Acute Skin Toxicity in Breast-conserving RadiotherapyBreast cancer is the most common cancer in Thai women with the annual Age-Standardized Rate (ASR) per 100,000 being 31.4 in 2015 [1]. According to breast cancer treatments, breast conserving therapy is one of the loco-regional treatment options. Radiotherapy after wide local excision reduces the locoregional recurrence rate as well as the risk of breast cancer death [2][3][4]. Conventional radiotherapy regimens, after breast conservation surgery, deliver a total dose of 46-50 Gy in 23-25 daily fractions over 5 weeks [3][4][5][6][7]. A boost to the tumor bed is recommended in patients with a higher risk of recurrences with the typical boost doses being 10-16 Gy in 4-8 fractions [5-7-12].Acute skin toxicity is the most common side effect of Abstract Purpose: To evaluate the effects of regular bra-wearing during radiotherapy on acute skin toxicity (AST) and the Quality of Life (QOL) in women with breast conserving therapy (BCT). Methods: A prospective study of 99 patients with any stage of breast cancer who underwent BCT. Patients were instructed to wear an appropriate bra then they were classified by total hours of wearing a bra during the radiotherapy treatment course into Non-Bra-Wearing (NBW) (0 hr.) and Bra-Wearing (BW) groups (>0 hr.). The AST was assessed weekly and one week after treatment end by CTCAE v 4.03. The QOL was assessed before and one week after treatment end by The Functional Assessment of Cancer Therapy-Breast Cancer (FACT-B) Thai version 4. Results: 66 patients were in the BW group and 33 patients were in the NBW group. The rate of ≥ G2 AST was lower in the BW group compared to the NBW group (16.7% vs. 54.5%, p<0.001, respectively). In the multivariate analysis, the statistically significant factors that were associated with increased the risk of ≥ G2 AST were NBW (0 hr.) (p<0.001), high body mass index (p=0.001), and the high percentage of maximum dose (p=0.043). There were no differences in all parts of after treatment FACT-B between the two groups (118.4 vs. 114.7, p=0.256, respectively). Conclusions: Regular BW during radiotherapy is not associated with an increased risk of ≥ G2 acute skin toxicity and does not affect the QOL compared to NBW.
This article has been peer reviewed and published immediately upon acceptance.It is an open access article, which means that it can be downloaded, printed, and distributed freely, provided the work is properly cited.
Introduction To investigate the association between chemotherapy (CMT) cycles and oncological outcomes in elders with locally advanced cervical cancer (LACC) who treated with concurrent chemoradiotherapy (CCRT). Methods We retrospective studied 498 elders with LACC who treated with radiotherapy (RT) or CCRT between 2002 and 2018. Patients were divided into three groups: RT, CCRT with 1–4 and CCRT with 5–6 cycles of CMT. We compared progression‐free survival (PFS) and overall survival (OS) among the three groups and explored survival prognostic factors via multivariate analysis and time‐varying analysis effect. Results There were 453 eligible patients; 222, 119 and 112 patients who received RT, CCRT with 1–4 and CCRT with 5–6 cycles of CMT, respectively. Patients in the RT group had older age, poorer performance status, more treatment with conventional RT technique and earlier treatment year comparing with both CCRT groups. Patients who received 5–6 cycles of CMT were less to have underweight, comorbidities and anaemia compared with the RT group. There were patients with lower FIGO stage in 5–6 cycles than in 1–4 cycles of CMT and RT groups. The 5‐year PFS and OS between RT, CCRT with 1–4 and CCRT with 5–6 cycles of the CMT group were significantly different. Performance status, comorbidity, histology, FIGO stage and total received 5–6 CMT cycles were significant prognostic factors of PFS and OS. However, the benefits of receiving 5–6 CMT cycles were evidenced only within the first 2.5 years. Conclusion Elders with LACC who received 5–6 cycles of CMT concurrently with RT can improve PFS and OS, but the benefit persisted only within the first 2.5 years.
Introduction. This study aimed to compare clinicopathological factors between late-recurrence and early-recurrence patients (using late recurrence at ≥ 3 years and 5 years as cut-off points) in locally advanced cervical cancer (LACC) treated with concurrent chemoradiotherapy (CCRT). This study also identified independent risk factors for late recurrence.Material and methods. We analyzed data from LACC patients treated at Songklanagarind Hospital between 2002 and 2016, who had received definitive CCRT. A total of 1231 patients were retrospectively reviewed.Results. The median follow-up was 4.6 years, and the total recurrence rate was 28.7% (353 of 1231 patients). The late recurrence rates were 7.4% and 2.2% for ≥ 3 and 5 years after CCRT, respectively. When comparing the risk factors of late recurrence at ≥ 3 years with early recurrence, we found that anemia and thrombocytosis were found less frequently in late recurrence (26.2% vs. 46.9% and 9.8% vs. 23.6%, respectively). At ≥ 5 years, no differences in risk factors between the recurrent groups were found. When including only patients that remained tumor-free after 3 years, stage III-IVA was the only independent risk factor associated with late recurrence at ≥ 3 years (p = 0.042).Univariate analysis showed no significant associated factor for late recurrence after 5 years.Conclusions. Late recurrence at ≥ 3 years was not rare. Even though we could not find any significant association between clinicopathologic factors and late recurrence after 5 years, 2.2% of patients still had late recurrence.Long-term follow-up should be considered, especially for more advanced stages (stage III-IVA).
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.