scholarly journals Guideline Adherence In Docetaxel Treatment Of Castration Resistant Prostate Cancer (CRPC) Patients In A Real-World Population: The Castration Resistant Prostate Cancer Registry (CAPRI) In The Netherlands

2017 ◽  
Vol 20 (9) ◽  
pp. A471-A472
Author(s):  
H Westgeest ◽  
M Kuppen ◽  
A Van den Eertwegh ◽  
W Gerritsen ◽  
C Uyl-de Groot
2020 ◽  
Vol 15 (3) ◽  
pp. 301-315 ◽  
Author(s):  
Simon Chowdhury ◽  
Anders Bjartell ◽  
Nicolaas Lumen ◽  
Pablo Maroto ◽  
Thomas Paiss ◽  
...  

2019 ◽  
Vol 18 (11) ◽  
pp. e3465-e3466
Author(s):  
A.S. Bjartell ◽  
N. Lumen ◽  
P. Maroto ◽  
T. Paiss ◽  
F. Gomez Veiga ◽  
...  

2020 ◽  
Vol 106 (5) ◽  
pp. 406-412
Author(s):  
Alessandra Raimondi ◽  
Pierangela Sepe ◽  
Melanie Claps ◽  
Marco Maccauro ◽  
Gianluca Aliberti ◽  
...  

Introduction: Therapeutic decision-making in metastatic castration-resistant prostate cancer (mCRPC) represents an open challenge. Radium-223 is approved for patients with symptomatic bone metastases, no visceral involvement, progressing after at least 2 lines of systemic therapy, or ineligible for any other systemic treatment. Methods: We performed a retrospective, observational study on patients with mCRPC treated with radium-223 at our institution outside of clinical trials, to assess the safety and activity in a real-world population. Data regarding baseline patient/disease characteristics and treatment outcomes (number of cycles, treatment-related adverse events [AEs], cause of discontinuation, and best response) were collected. Results: Overall, 41 patients were treated from September 2015 to September 2018. Median age was 73 years; baseline Eastern Cooperative Oncology Group Performance Status (ECOG PS) was 0, 1, or 2 in 15%, 80%, and 5% of cases, respectively; and 3%, 41%, 44%, and 12% of patients had <6, 6–20, >20, and superscan bone lesions, respectively. A median number of 5 cycles (interquartile range 3–6) with median dose 19.52 MBq (interquartile range 12.87–24.83) was received. Treatment schedule was completed in 49% of cases; discontinuations due to AEs, disease-related death, or disease progression occurred in 24%, 33%, and 43% of patients, respectively. Any-grade AEs occurred in 73% and grade 3/4 treatment-related AEs occurred in 29% of patients, mainly anemia, decreased platelet count, and fatigue. No skeletal-related events or treatment-related deaths were recorded. After treatment, 66%, 2%, and 32% of patients had a stable, improved, or deteriorated ECOG PS versus baseline, respectively, and 24%, 61%, and 15% reported a stable, improved, or worsened pain symptom control. Post-treatment versus baseline alkaline phosphatase was reduced or stable in 46% and increased in 54% of patients, whereas prostate-specific antigen was decreased or stable in 83% and increased in 17% of patients. Conclusions: Our study provides clinically useful real-world data on radium-223, highlighting the importance of multidisciplinary patient management to guarantee the best continuum of care for patients with mCRPC.


2018 ◽  
Vol 4 (5) ◽  
pp. 694-701 ◽  
Author(s):  
Hans M. Westgeest ◽  
Carin A. Uyl-de Groot ◽  
Reindert J.A. van Moorselaar ◽  
Ronald de Wit ◽  
Alphonsus C.M. van den Bergh ◽  
...  

2017 ◽  
Vol 35 (15_suppl) ◽  
pp. 5028-5028 ◽  
Author(s):  
Simon Chowdhury ◽  
Alison J. Birtle ◽  
Anders Bjartell ◽  
Luis Costa ◽  
Susan Feyerabend ◽  
...  

5028 Background: The Prostate Cancer Registry is a prospective, international observational study that began in June 2013 and will assess the characteristics and management of > 3000 mCRPC patients (pts) in routine clinical practice for ≤ 3 years. Methods: Data were collected from men with mCRPC irrespective of treatment (tx). This interim analysis reports baseline characteristics, txs and outcomes in pts with ≥ 12-month follow-up receiving second-line mCRPC tx following docetaxel as the only prior mCRPC tx. Results: The most commonly initiated second-line mCPRC txs (n ≥ 50) were abiraterone acetate + prednisone (AAP, n = 177), enzalutamide (ENZ, n = 94), or cabazitaxel (CAB, n = 70). Characteristics and outcomes are shown in the table below. TTP was not significantly different for AAP vs ENZ, AAP vs CAB or ENZ vs CAB (propensity score adjusted p = 0.5954, p = 0.5888 and p= 0.4808, respectively). Conclusions: In this real-world study, clinical outcomes reveal that, in pts receiving second-line mCRPC tx after docetaxel, TTP was similar across tx groups; QoL improved most in AAP and ENZ groups and no deterioration was observed most in AAP and CAB groups. Clinical trial information: NCT02236637. [Table: see text]


2020 ◽  
Vol 18 (3) ◽  
pp. e233-e253
Author(s):  
Malou C.P. Kuppen ◽  
Hans M. Westgeest ◽  
Alphonsus J.M. van den Eertwegh ◽  
Jules L.L.M. Coenen ◽  
Reindert J.A. van Moorselaar ◽  
...  

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