Search

Summary: Radium-223 (Ra-223) has been used to treat metastatic bone disease in prostate cancer, improving overall survival and quality of life. Breast cancer often presents bone metastasis too, but it is often associated with other sites of disease. In such cases, the addition of Ra-223 to the standard of care (SC) may be beneficial. Therefore, our objective is to determine if the use of Radium-223 plus SC is beneficial for metastatic bone breast cancer patients through a systematic review and meta-analysis. A comprehensive search was conducted across MEDLINE, EMBASE, and CENTRAL databases. The search strategy included the following terms: “Breast cancer” AND “Radium-223”. The selection criteria encompassed both single-arm and randomized controlled trials (RCT). MedCalc® Statistical Software was used. Hazard ratios (HR) were preferred. Odds ratios (OR) or Relative risk (RR) were used when HR was not disponible. For single-arm studies, a proportion meta-analysis was performed. Random-effects methods were used. The initial search yielded 349 articles, 28 articles were reviewed with full-text, and 5 were considered eligible (3 RCT and 2 single-arm studies). SC therapy included: capecitabine, paclitaxel, exemestane plus everolimus and hormonal therapy. Overall, the group submitted to Ra-223 showed a trend to have better symptomatic skeletal event-free survival – SSEFS - (HR: 0.855, CI: 0.643-1.138) and pain improvement (OR: 1.308. CI: 0.780-2.196), but without statistical significance. The pooled analysis showed no difference between arms for serious adverse effects (RR: 0.836. CI: 0.331-2.112). The proportion of SAE in patients submitted to Ra-223 plus SC was 20.1% (CI: 3.6-45.3%). Conclusão: Ra-223 plus SC in bone metastatic breast cancer patients showed a trend to better SSEFS and pain improvement. However, the low number of RCT studies and the high heterogeneity of SC are great limitations. Results from ongoing RCT (everolimus and avelumab) can change this scenario.

Craniopharyngioma is a rare embryonic malformation, usually benign, of the sellar or parasellar regions. In this study, an uncommon case of third ventricle craniopharyngioma and a succinct review of its prevalence are presented. Even with low mortality rates, these injuries involve a high degree of endocrinological, visual and neuropsychological morbidities, which have a huge impact on the patient's quality of life. Thus, surgical resection is the preferred therapy for tumors that compromise the flow of cerebrospinal fluid. However, due to the location of the craniopharyngioma, surgical management is accompanied by the risk of injury to important adjacent areas with postoperative repercussions. Therefore, the neurosurgeon's experience and the choice of the best surgical approach, are crucial for increasing prognosis.