The prognostic value of pain in castration-sensitive prostate cancer.


Journal

Prostate cancer and prostatic diseases
ISSN: 1476-5608
Titre abrégé: Prostate Cancer Prostatic Dis
Pays: England
ID NLM: 9815755

Informations de publication

Date de publication:
12 2020
Historique:
received: 29 04 2020
accepted: 02 07 2020
revised: 07 06 2020
pubmed: 12 7 2020
medline: 18 9 2021
entrez: 12 7 2020
Statut: ppublish

Résumé

Cancer-related pain, usually associated with bone metastases, is a frequent and debilitating morbidity in patients with prostate cancer. To date there are only limited data regarding the prognostic role of pain in men with metastatic castration-sensitive prostate cancer (mCSPC). The objective of our analysis was to assess if the presence of pain can be considered an independent prognostic factor in mCSPC patients. A retrospective analysis was performed on patients with mCSPC referring to six oncology centers in Italy. Clinical and pathological features were recorded. Patients were considered to have pain if this was reported within the patient's file or in case of a chronic analgesic therapy was found among the concomitant medications. Survivals were estimated by the Kaplan-Meier method, and compared across groups using the log-rank test. Cox proportional hazard models, stratified according to the baseline characteristics, were used to estimate hazard ratios for overall survival (OS). All the variables were significant if p < 0.05. Data about pain were available for 365 cases and pain was present in 34.8% of patients. Pain was mainly associated with high value of prostate-specific antigen, metastatic bone extension regardless of the site, and lymph node involvement. mCSPC patients with pain had in most of the cases high-volume or Hr disease, and significant shorter OS (27.0 vs. 58.2 months, p < 0.001) and PFS (10.1 vs. 17.4 months, p < 0.001) compared to those without pain. The negative impact of pain on OS remained significant even if adjusted for CHAARTED or LATITUDE classification, and other significant baseline prognostic factors. This analysis supports the poor prognostic role of cancer-related pain in the setting of mCSPC patients. A prospective validation is required.

Sections du résumé

BACKGROUND
Cancer-related pain, usually associated with bone metastases, is a frequent and debilitating morbidity in patients with prostate cancer. To date there are only limited data regarding the prognostic role of pain in men with metastatic castration-sensitive prostate cancer (mCSPC). The objective of our analysis was to assess if the presence of pain can be considered an independent prognostic factor in mCSPC patients.
METHODS
A retrospective analysis was performed on patients with mCSPC referring to six oncology centers in Italy. Clinical and pathological features were recorded. Patients were considered to have pain if this was reported within the patient's file or in case of a chronic analgesic therapy was found among the concomitant medications. Survivals were estimated by the Kaplan-Meier method, and compared across groups using the log-rank test. Cox proportional hazard models, stratified according to the baseline characteristics, were used to estimate hazard ratios for overall survival (OS). All the variables were significant if p < 0.05.
RESULTS
Data about pain were available for 365 cases and pain was present in 34.8% of patients. Pain was mainly associated with high value of prostate-specific antigen, metastatic bone extension regardless of the site, and lymph node involvement. mCSPC patients with pain had in most of the cases high-volume or Hr disease, and significant shorter OS (27.0 vs. 58.2 months, p < 0.001) and PFS (10.1 vs. 17.4 months, p < 0.001) compared to those without pain. The negative impact of pain on OS remained significant even if adjusted for CHAARTED or LATITUDE classification, and other significant baseline prognostic factors.
CONCLUSIONS
This analysis supports the poor prognostic role of cancer-related pain in the setting of mCSPC patients. A prospective validation is required.

Identifiants

pubmed: 32651468
doi: 10.1038/s41391-020-0255-x
pii: 10.1038/s41391-020-0255-x
doi:

Substances chimiques

Androgen Antagonists 0
Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

654-660

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Auteurs

Roberto Iacovelli (R)

Medical Oncology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy. roberto.iacovelli@policlinicogemelli.it.

Chiara Ciccarese (C)

Medical Oncology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Orazio Caffo (O)

Department of Medical Oncology, Santa Chiara Hospital, 38112, Trento, Italy.

Ugo De Giorgi (U)

Department of Medical Oncology, Scientific Institute Romagnolo for the Study and Treatment of Cancer (IRST) IRCCS, Meldola, Italy.

Marcello Tucci (M)

SC Oncologia, Ospedale Cardinal Massaia, Asti, Italy.

Claudia Mosillo (C)

Medical Oncology Unit, Azienda Ospedaliera Santa Maria di Terni, Terni, Italy.

Davide Bimbatti (D)

Medical Oncology Unit 1, Istituto Oncologico Veneto IOV IRCCS, Padua, Italy.

Francesco Pierantoni (F)

Medical Oncology Unit 1, Istituto Oncologico Veneto IOV IRCCS, Padua, Italy.

Francesca Maines (F)

Department of Medical Oncology, Santa Chiara Hospital, 38112, Trento, Italy.

Chiara Casadei (C)

Department of Medical Oncology, Scientific Institute Romagnolo for the Study and Treatment of Cancer (IRST) IRCCS, Meldola, Italy.

Consuelo Buttigliero (C)

Department of Oncology, University of Turin, San Luigi Gonzaga Hospital, Turin, Italy.

Michele Milella (M)

Medical Oncology Unit, Azienda Ospedaliera Universitaria Integrata (AOUI), Verona, Italy.

Giampaolo Tortora (G)

Medical Oncology Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

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