Prostate cancer induced bone pain: pathobiology, current treatments and pain responses from recent clinical trials

Abstract Purpose Metastatic spread of prostate cancer to the skeleton may result in debilitating bone pain. In this review, we address mechanisms underpinning the pathobiology of metastatic prostate cancer induced bone pain (PCIBP) that include sensitization and sprouting of primary afferent sensory...

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Main Authors: A. E. Smith, A. Muralidharan, M. T. Smith
Format: Article
Language:English
Published: Springer 2022-10-01
Series:Discover Oncology
Subjects:
Online Access:https://doi.org/10.1007/s12672-022-00569-z
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author A. E. Smith
A. Muralidharan
M. T. Smith
author_facet A. E. Smith
A. Muralidharan
M. T. Smith
author_sort A. E. Smith
collection DOAJ
description Abstract Purpose Metastatic spread of prostate cancer to the skeleton may result in debilitating bone pain. In this review, we address mechanisms underpinning the pathobiology of metastatic prostate cancer induced bone pain (PCIBP) that include sensitization and sprouting of primary afferent sensory nerve fibres in bone. We also review current treatments and pain responses evoked by various treatment modalities in clinical trials in this patient population. Methods We reviewed the literature using PubMed to identify research on the pathobiology of PCIBP. Additionally, we reviewed clinical trials of various treatment modalities in patients with PCIBP with pain response outcomes published in the past 7 years. Results Recent clinical trials show that radionuclides, given either alone or in combination with chemotherapy, evoked favourable pain responses in many patients and a single fraction of local external beam radiation therapy was as effective as multiple fractions. However, treatment with chemotherapy, small molecule inhibitors and/or immunotherapy agents, produced variable pain responses but pain response was the primary endpoint in only one of these trials. Additionally, there were no published trials of potentially novel analgesic agents in patients with PCIBP. Conclusion There is a knowledge gap for clinical trials of chemotherapy, small molecule inhibitors and/or immunotherapy in patients with PCIBP where pain response is the primary endpoint. Also, there are no novel analgesic agents on the horizon for the relief of PCIBP and this is an area of large unmet medical need that warrants concerted research attention.
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spelling doaj.art-19f1f600843041ae916017cf971aab3e2022-12-22T04:06:24ZengSpringerDiscover Oncology2730-60112022-10-0113112310.1007/s12672-022-00569-zProstate cancer induced bone pain: pathobiology, current treatments and pain responses from recent clinical trialsA. E. Smith0A. Muralidharan1M. T. Smith2St Vincent’s HospitalNeurobiology of Chronic Pain, The Charles Perkins Centre, Faculty of Science, The University of SydneyCentre for Integrated Preclinical Drug Development, School of Biomedical Sciences, Faculty of Medicine, The University of QueenslandAbstract Purpose Metastatic spread of prostate cancer to the skeleton may result in debilitating bone pain. In this review, we address mechanisms underpinning the pathobiology of metastatic prostate cancer induced bone pain (PCIBP) that include sensitization and sprouting of primary afferent sensory nerve fibres in bone. We also review current treatments and pain responses evoked by various treatment modalities in clinical trials in this patient population. Methods We reviewed the literature using PubMed to identify research on the pathobiology of PCIBP. Additionally, we reviewed clinical trials of various treatment modalities in patients with PCIBP with pain response outcomes published in the past 7 years. Results Recent clinical trials show that radionuclides, given either alone or in combination with chemotherapy, evoked favourable pain responses in many patients and a single fraction of local external beam radiation therapy was as effective as multiple fractions. However, treatment with chemotherapy, small molecule inhibitors and/or immunotherapy agents, produced variable pain responses but pain response was the primary endpoint in only one of these trials. Additionally, there were no published trials of potentially novel analgesic agents in patients with PCIBP. Conclusion There is a knowledge gap for clinical trials of chemotherapy, small molecule inhibitors and/or immunotherapy in patients with PCIBP where pain response is the primary endpoint. Also, there are no novel analgesic agents on the horizon for the relief of PCIBP and this is an area of large unmet medical need that warrants concerted research attention.https://doi.org/10.1007/s12672-022-00569-zProstate cancer induced bone pain (PCIBP)Metastatic castrate-resistant prostate cancer (mCRPC)AnalgesicsNSAIDsOpioidsMorphine
spellingShingle A. E. Smith
A. Muralidharan
M. T. Smith
Prostate cancer induced bone pain: pathobiology, current treatments and pain responses from recent clinical trials
Discover Oncology
Prostate cancer induced bone pain (PCIBP)
Metastatic castrate-resistant prostate cancer (mCRPC)
Analgesics
NSAIDs
Opioids
Morphine
title Prostate cancer induced bone pain: pathobiology, current treatments and pain responses from recent clinical trials
title_full Prostate cancer induced bone pain: pathobiology, current treatments and pain responses from recent clinical trials
title_fullStr Prostate cancer induced bone pain: pathobiology, current treatments and pain responses from recent clinical trials
title_full_unstemmed Prostate cancer induced bone pain: pathobiology, current treatments and pain responses from recent clinical trials
title_short Prostate cancer induced bone pain: pathobiology, current treatments and pain responses from recent clinical trials
title_sort prostate cancer induced bone pain pathobiology current treatments and pain responses from recent clinical trials
topic Prostate cancer induced bone pain (PCIBP)
Metastatic castrate-resistant prostate cancer (mCRPC)
Analgesics
NSAIDs
Opioids
Morphine
url https://doi.org/10.1007/s12672-022-00569-z
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