A real-world study assessing the use of bone-targeted agents and their impact on bone metastases in patients with prostate cancer treated in clinical practice in Europe.

AAP, abiraterone acetate with prednisone/prednisolone AQA, Analgesic Quantification Algorithm BMs, bone metastases BPI, Brief Pain Inventory BTA, bone-targeted agent Bone metastases Bone pain Bone-targeted agents DSP, Disease Specific Programme EQ-5D-3L, 5-dimension 3-level EuroQol questionnaire EU5, France, Germany, Italy, Spain and the UK FACT-P, Functional Assessment of Cancer Therapy – Prostate questionnaire ONJ, osteonecrosis of the jaw PRF, Patient Record Form PRO, patient-reported outcome PSCF, Patient Self-Completion Form QoL, quality of life SRE, skeletal-related event mCRPC, metastatic castration-resistant prostate cancer

Journal

Journal of bone oncology
ISSN: 2212-1366
Titre abrégé: J Bone Oncol
Pays: Netherlands
ID NLM: 101610292

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 09 08 2018
revised: 10 12 2018
accepted: 14 12 2018
entrez: 11 1 2019
pubmed: 11 1 2019
medline: 11 1 2019
Statut: epublish

Résumé

Bone metastases (BMs) are common in patients with prostate cancer and can lead to skeletal-related events (SREs), which are associated with increased pain and reduced quality of life (QoL). Bone-targeted agents (BTAs), such as zoledronic acid and denosumab, reduce the incidence of SREs and delay progression of bone pain. We evaluated the management of BMs and pain in six European countries (Belgium, France, Germany, Italy, Spain and the UK) using the Adelphi Prostate Cancer Disease Specific Programme. Patient-reported outcomes (PROs) were used to assess the impact of BMs on pain and QoL. In total, 358 physicians completed Patient Record Forms, of whom 246 were oncologists and 112 were urologists. Data were collected on 3667 patients with prostate cancer, including 1971 with BMs and 551 with metastases at sites other than bone (non-BMs). PROs were assessed in 573 patients with BMs and 220 with non-BMs. Most patients with BMs (74%) received a BTA and 53% received treatment within 3 months of BM diagnosis. Patients treated by oncologists were more likely than those treated by urologists to receive a BTA (78% vs. 60%) and to have treatment initiated within 3 months of BM diagnosis (56% vs. 43%). For patients who did not receive a BTA, the main reasons for not treating were very recent BM diagnosis and a perceived low risk of bone complications. Data collected by physicians showed that most patients with BMs (97%) were taking analgesics, with 30% receiving strong opioids. Despite this, 70% were currently experiencing bone pain and 28% were experiencing moderate to severe pain. PRO pain measures showed that 70% of patients with BMs were experiencing moderate to extreme pain, suggesting a disparity between pain levels reported by physicians and by patients. Although most patients with BMs receive a BTA, there remain a proportion of patients who are not receiving adequate treatment to prevent SREs or manage pain. Oncologists are more likely to adhere to clinical guidelines than urologists for the prescription of BTAs. Bone pain is common and undertreated. Increasing awareness of SRE prevention and bone pain management might improve patient care.

Sections du résumé

BACKGROUND BACKGROUND
Bone metastases (BMs) are common in patients with prostate cancer and can lead to skeletal-related events (SREs), which are associated with increased pain and reduced quality of life (QoL). Bone-targeted agents (BTAs), such as zoledronic acid and denosumab, reduce the incidence of SREs and delay progression of bone pain.
METHODS METHODS
We evaluated the management of BMs and pain in six European countries (Belgium, France, Germany, Italy, Spain and the UK) using the Adelphi Prostate Cancer Disease Specific Programme. Patient-reported outcomes (PROs) were used to assess the impact of BMs on pain and QoL.
RESULTS RESULTS
In total, 358 physicians completed Patient Record Forms, of whom 246 were oncologists and 112 were urologists. Data were collected on 3667 patients with prostate cancer, including 1971 with BMs and 551 with metastases at sites other than bone (non-BMs). PROs were assessed in 573 patients with BMs and 220 with non-BMs. Most patients with BMs (74%) received a BTA and 53% received treatment within 3 months of BM diagnosis. Patients treated by oncologists were more likely than those treated by urologists to receive a BTA (78% vs. 60%) and to have treatment initiated within 3 months of BM diagnosis (56% vs. 43%). For patients who did not receive a BTA, the main reasons for not treating were very recent BM diagnosis and a perceived low risk of bone complications. Data collected by physicians showed that most patients with BMs (97%) were taking analgesics, with 30% receiving strong opioids. Despite this, 70% were currently experiencing bone pain and 28% were experiencing moderate to severe pain. PRO pain measures showed that 70% of patients with BMs were experiencing moderate to extreme pain, suggesting a disparity between pain levels reported by physicians and by patients.
CONCLUSIONS CONCLUSIONS
Although most patients with BMs receive a BTA, there remain a proportion of patients who are not receiving adequate treatment to prevent SREs or manage pain. Oncologists are more likely to adhere to clinical guidelines than urologists for the prescription of BTAs. Bone pain is common and undertreated. Increasing awareness of SRE prevention and bone pain management might improve patient care.

Identifiants

pubmed: 30627511
doi: 10.1016/j.jbo.2018.100212
pii: S2212-1374(18)30115-5
pii: 100212
pmc: PMC6319023
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100212

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Auteurs

Jean-Jacques Body (JJ)

Department of Medicine, CHU Brugmann, Université Libre de Bruxelles, Brussels, Belgium.

Roger von Moos (R)

Kantonsspital Graubünden, Chur, Switzerland.

Alex Rider (A)

Adelphi Real World, Bollington, UK.

Pamela Hallworth (P)

Adelphi Real World, Bollington, UK.

Debajyoti Bhowmik (D)

Amgen Inc., Thousand Oaks, CA, USA.

Francesca Gatta (F)

Amgen (Europe) GmbH, Risch-Rotkreuz, Switzerland.

Guy Hechmati (G)

Amgen Inc., Thousand Oaks, CA, USA.

Yi Qian (Y)

Amgen Inc., Thousand Oaks, CA, USA.

Classifications MeSH