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Effects of low-dose capecitabine on Samarium-153-EDTMP therapy for painful bone metastases

INTRODUCTION: Samarium-153 (Sm-153)-EDTMP is routinely used for pain palliation in skeletal metastasis, however most patients report partial response. Many strategies have been contemplated to make radiation therapy for pain more effective, one of them being the use of radiosensitizers. Capecitabine...

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Autores principales: Barai, Sukanta, Gambhir, Sanjay, Rastogi, Neeraj, Mandani, Anil, Siddegowda, Murthy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379668/
https://www.ncbi.nlm.nih.gov/pubmed/25829727
http://dx.doi.org/10.4103/0972-3919.152955
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author Barai, Sukanta
Gambhir, Sanjay
Rastogi, Neeraj
Mandani, Anil
Siddegowda, Murthy
author_facet Barai, Sukanta
Gambhir, Sanjay
Rastogi, Neeraj
Mandani, Anil
Siddegowda, Murthy
author_sort Barai, Sukanta
collection PubMed
description INTRODUCTION: Samarium-153 (Sm-153)-EDTMP is routinely used for pain palliation in skeletal metastasis, however most patients report partial response. Many strategies have been contemplated to make radiation therapy for pain more effective, one of them being the use of radiosensitizers. Capecitabine is a chemotherapeutic drug and is routinely combined with external beam radiation to make the target more radio-sensitive. Aim of the study was to evaluate whether combining capecitabine in radiosensitizing dose with Sm-153-EDTMP produces superior analgesia compared to Sm alone. MATERIALS AND METHODS: Forty-four patients with skeletal metastases from various primaries were randomized into two groups: The study group received 1 mCi/kg Sm-153-EDTMP plus capecitabine (1,650 mg/m(2)) orally for 8 days (equivalent to four t(½) of (153)Sm-EDTMP) and the control arm received 1 mCi/kg Sm-153-EDTMP plus placebo for the 8 days. After treatment, the patients were followed up for 12 weeks to evaluate the degree and duration of pain palliation and hematologic toxicity. RESULTS: All 44 patients reported different degrees of pain relief with none reporting complete pain relief for the entire duration of 12 weeks posttherapy observation period. However the level of pain relief obtained in study arm was significantly better than the control arm with mean posttherapy pain score being 1.29 ± 1.05 and 3.59 ± 2.77 respectively with P of 0.001. Transient and mild hematologic toxicity, as determined by World Health Organization criteria, was apparent in both arms without significant differences. CONCLUSION: The addition of a low-dose of capecitabine significantly enhances the analgesic effect of Sm-153 without any additional side effects.
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spelling pubmed-43796682015-04-01 Effects of low-dose capecitabine on Samarium-153-EDTMP therapy for painful bone metastases Barai, Sukanta Gambhir, Sanjay Rastogi, Neeraj Mandani, Anil Siddegowda, Murthy Indian J Nucl Med Original Article INTRODUCTION: Samarium-153 (Sm-153)-EDTMP is routinely used for pain palliation in skeletal metastasis, however most patients report partial response. Many strategies have been contemplated to make radiation therapy for pain more effective, one of them being the use of radiosensitizers. Capecitabine is a chemotherapeutic drug and is routinely combined with external beam radiation to make the target more radio-sensitive. Aim of the study was to evaluate whether combining capecitabine in radiosensitizing dose with Sm-153-EDTMP produces superior analgesia compared to Sm alone. MATERIALS AND METHODS: Forty-four patients with skeletal metastases from various primaries were randomized into two groups: The study group received 1 mCi/kg Sm-153-EDTMP plus capecitabine (1,650 mg/m(2)) orally for 8 days (equivalent to four t(½) of (153)Sm-EDTMP) and the control arm received 1 mCi/kg Sm-153-EDTMP plus placebo for the 8 days. After treatment, the patients were followed up for 12 weeks to evaluate the degree and duration of pain palliation and hematologic toxicity. RESULTS: All 44 patients reported different degrees of pain relief with none reporting complete pain relief for the entire duration of 12 weeks posttherapy observation period. However the level of pain relief obtained in study arm was significantly better than the control arm with mean posttherapy pain score being 1.29 ± 1.05 and 3.59 ± 2.77 respectively with P of 0.001. Transient and mild hematologic toxicity, as determined by World Health Organization criteria, was apparent in both arms without significant differences. CONCLUSION: The addition of a low-dose of capecitabine significantly enhances the analgesic effect of Sm-153 without any additional side effects. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4379668/ /pubmed/25829727 http://dx.doi.org/10.4103/0972-3919.152955 Text en Copyright: © Indian Journal of Nuclear Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Barai, Sukanta
Gambhir, Sanjay
Rastogi, Neeraj
Mandani, Anil
Siddegowda, Murthy
Effects of low-dose capecitabine on Samarium-153-EDTMP therapy for painful bone metastases
title Effects of low-dose capecitabine on Samarium-153-EDTMP therapy for painful bone metastases
title_full Effects of low-dose capecitabine on Samarium-153-EDTMP therapy for painful bone metastases
title_fullStr Effects of low-dose capecitabine on Samarium-153-EDTMP therapy for painful bone metastases
title_full_unstemmed Effects of low-dose capecitabine on Samarium-153-EDTMP therapy for painful bone metastases
title_short Effects of low-dose capecitabine on Samarium-153-EDTMP therapy for painful bone metastases
title_sort effects of low-dose capecitabine on samarium-153-edtmp therapy for painful bone metastases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4379668/
https://www.ncbi.nlm.nih.gov/pubmed/25829727
http://dx.doi.org/10.4103/0972-3919.152955
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