Background According to pathologico-clinical features, patients diagnosed with localized prostate cancer (PCa) are stratified into distinct risk groups (low-risk, intermediate-risk or high-risk). Data have demonstrated that 68 Gallium-prostate-specific membrane antigen positron emission tomography ( 68 Ga-PSMA PET/CT) is superior to conventional radiological exams (CT or MRI and bone scintigraphy) in the primary staging of high-risk localized PCa. However, it is still unknown if in a population of high-risk PCa, there would be a subgroup of patients with a higher probability of identifying metastatic disease by the 68 Ga-PSMA PET/CT. Materials and Methods Data from patients with localized PCa who underwent 68 GA-PSMA PET/CT for primary staging from four institutions were retrospectively collected. We selected patients with at least one D'Amico classification risk factor (International Society of Urological Pathology ≥ IV and/or prostate-specific antigen > 20 ng/ml). To detect an association between extent of disease and number of risk factors as well as International Society of Urological Pathology prostate cancer grade, contingency tables were used, and Fisher Exact Test was performed. Results Between 2016 and 2020, 60 patients underwent a 68 GA-PSMA PET/CT for primary staging of high-risk localized PCa. Regarding the number of risk factors, 37 patients (62%) had one risk factor, and 23 (38%) had two risk factors. In the subgroup of patients with metastatic disease (n = 22), those with two risk factors had higher incidence of metastatic disease, and it was statistically significant ( p = 0.011 ). Conclusion This retrospective analysis demonstrated that 68 GA-PSMA PET/CT was able to identify advanced disease in more than one-third of patients with high-risk disease especially those with two adverse risk factors.
No abstract
Objective: Chemotherapy-induced alopecia (CIA) has a major impact on oncological patients and is reported as one of the first concerns among women, being often a condition that causes suffering. CIA is an expected adverse event in paclitaxel, an agent widely used in the treatment of breast cancer. Strategies have been used to minimize this undesirable effect, including the scalp cooling. The objective of our study was to report the frequency of the preservation of hair volu me in women who used a monodrug called “paclitaxel” at a dose of 80 mg/m²/week for 12 weeks, using a hypothermic glycerinbased hydrogel cap in a private institution in the federal district. Methods: This descriptive retrospective study included 92 women with no evidence of alopecia at the beginning of monotherapy treatment with paclitaxel 80 mg/m2 /week for 12 weeks. They used a hypothermic glycerin-based hydrogel cap during the infusion of the drug. The quantification of alopecia was performed using the modified Dean scale and Common Terminology Criteria for Adverse Events version 4 (CTCAEv4). The patient characteristics such as age, type of hair, purpose of treatment, site of primary neoplasm were described. Results: From 2014 to 2018, 86 (93.5%) of the 92 patients who were included in the study had breast cancer. At the end of the 12 weeks of treatment, 83% of patients developed grade 1 alopecia by CTCAEv4. According to the modified Dean scale, 71% of patients were classified as alopecia grade 1, 12% as grade 2, 7.5% as grade 3, and 9.5% as grade 4. Conclusion: More than 80% of women, who were treated with paclitaxel weekly and used the hypothermic glycerin-based hydrogel cap, had at least 50% of their initial hair volume preserved by the two scales. These results suggest the effectiveness of the scalp cooling therapy in preventing CIA, being an important strategy to be considered to minimize the impact on the appearance and emotional damage caused by alopecia in these patients.
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.