scholarly journals Adverse Events Associated With Radium-223 in Metastatic Prostate Cancer: Disproportionality Analysis of FDA Data Reflecting Worldwide Utilization

2020 ◽  
Vol 18 (3) ◽  
pp. 192-200.e2 ◽  
Author(s):  
Minh-Phuong Huynh-Le ◽  
Randall C. Shults ◽  
Michael J. Connor ◽  
Jona A. Hattangadi-Gluth
2019 ◽  
Vol 133 ◽  
pp. S855
Author(s):  
R. Pearson ◽  
X. Jiang ◽  
S. Atkinson ◽  
S. Cumming ◽  
A. Burns ◽  
...  

2019 ◽  
Vol 20 (5) ◽  
pp. e228 ◽  
Author(s):  
Maria Concetta Cursano ◽  
Daniele Santini ◽  
Michele Iuliani ◽  
Giovanni Paganelli ◽  
Ugo De Giorgi

2016 ◽  
Vol 34 (15_suppl) ◽  
pp. e16521-e16521
Author(s):  
Eric Anderson ◽  
William Wong ◽  
Homan Mohammadi ◽  
Thomas Backus Daniels ◽  
Katherine S. Tzou ◽  
...  

2018 ◽  
Vol 36 (15_suppl) ◽  
pp. e17037-e17037
Author(s):  
Norma Sidek ◽  
Gail Buchanan ◽  
David Dodds ◽  
J. Martin Russell ◽  
Gerry Gillen ◽  
...  

2018 ◽  
Vol 36 (15_suppl) ◽  
pp. e17023-e17023 ◽  
Author(s):  
Pedro Henrique Isaacsson Velho ◽  
Fahad Qazi ◽  
Sayeedul Hasan ◽  
Michael Anthony Carducci ◽  
Mario A. Eisenberger ◽  
...  

2018 ◽  
Vol 36 (6_suppl) ◽  
pp. 376-376
Author(s):  
Renato Patrizio Costa ◽  
Fabio Raiti ◽  
Sebastiano Bordonaro ◽  
Vincenzo Tripoli ◽  
Alessandra Murabito ◽  
...  

376 Background: Prostate cancer is the most common cancer among adult men. Bones are the main metastatic site of prostate cancer. Radium-223 is indicated to treat metastatic castrate-resistant prostate cancer ( mCRPC) with symptomatic skeletal metastases. We evaluate the tolerability of Ra223 treatment in real life setting. Methods: We reported the cases of 38 consecutive non-selected patients with mCRPC symptomatic bone metastases treated in two Italian hospital cancer center from August 2016 to October 2017. The cause of Ra 223 treatment discontinuation in elderly prostate cancer patients were evaluated. Results: due bones metastases, 38 patients were treated with Radium-223; 20 were ≥75 years old (range 75-85 yrs). Patients characteristics and main toxicity are reported (Table). Regarding the elderly patients, hematologic toxicity were the most common adverse events reported. Anemia G2-G3 was observed in 10 pts (50%), thrombocytopoenia G3 in 2 patients (10%) and neutropenia G3 in 4 patients (20%); 12/20 patients interrupted the treatment, of which 10 were ECOG PS2. The number of patients who discontinued the drug because of hematologic adverse events was higher than ALSYMPCA clinical trial. Fatigue G1-G2 incidence was 32%. Unexpectedly we did not record any cases of gastrointestinal toxicity (diarrhea, nausea or constipation). Conclusions: In patients ≥75 years old, anemia G2-G3 was more frequent than data reported in literature, while diarrhea is not found. The data of this experience suggest that elderly vulnerable patients are more exposed to hematologic toxicity that may compromise the outcome of the treatment. For these patients surveillance for early supportive care is relevant. Characteristics of patients with ≥75y. [Table: see text]


2017 ◽  
Vol 13 (02) ◽  
pp. 112
Author(s):  
Alan J Koletsky ◽  

Over the past several years a number of novel and diverse agents have provided a significant clinical benefit for patients with metastatic castration-resistant prostate cancer including abiraterone, enzalutamide, sipuleucel-T, cabazitaxel, and radium-223. The early use of docetaxel or abiraterone at initiation of standard androgen deprivation therapy in patients with metastatic hormone-sensitive prostate cancer has also led to substantial improvements in overall survival. The identification of a truncating mutation in the androgen receptor (ARV7), a biomarker of resistance, may help clarify a more optimal sequencing of hormonal and chemotherapy-based therapies for patients with metastatic disease. The genomic landscape of both primary and metastatic prostate cancer has been an important focal point of translational research. The most widely studied pathways that affect tumorigenesis are the phosphoinositide 3-kinase (PI3K)/phosphatase and tensin homolog (PTEN)/protein kinase B (AKT) and poly ADP ribose polymerase (PARP) and DNA repair pathways. This review will highlight recent clinical trials which have had a major impact on the management of patients with metastatic disease with an emphasis on treatments driven by common genomic aberrations present in advanced prostate cancer.


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