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Clinical utility of (188)Rhenium-hydroxyethylidene-1,1-diphosphonate as a bone pain palliative in multiple malignancies

(188)Rhenium-hydroxyethylidene-1,1-diphosphonate ((188)Re-HEDP) is a clinically established radiopharmaceutical for bone pain palliation of patients with metastatic bone cancer. Herein, the effectiveness of (188)Re-HEDP for the palliation of painful bone metastases was investigated in an uncontrolle...

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Autores principales: Shinto, Ajit S., Mallia, Madhava B., Kameswaran, Mythili, Kamaleshwaran, K. K., Joseph, Jephy, Radhakrishnan, E. R., Upadhyay, Indira V., Subramaniam, R., Sairam, Madhu, Banerjee, Sharmila, Dash, Ashutosh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6216741/
https://www.ncbi.nlm.nih.gov/pubmed/30505219
http://dx.doi.org/10.4103/wjnm.WJNM_68_17
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author Shinto, Ajit S.
Mallia, Madhava B.
Kameswaran, Mythili
Kamaleshwaran, K. K.
Joseph, Jephy
Radhakrishnan, E. R.
Upadhyay, Indira V.
Subramaniam, R.
Sairam, Madhu
Banerjee, Sharmila
Dash, Ashutosh
author_facet Shinto, Ajit S.
Mallia, Madhava B.
Kameswaran, Mythili
Kamaleshwaran, K. K.
Joseph, Jephy
Radhakrishnan, E. R.
Upadhyay, Indira V.
Subramaniam, R.
Sairam, Madhu
Banerjee, Sharmila
Dash, Ashutosh
author_sort Shinto, Ajit S.
collection PubMed
description (188)Rhenium-hydroxyethylidene-1,1-diphosphonate ((188)Re-HEDP) is a clinically established radiopharmaceutical for bone pain palliation of patients with metastatic bone cancer. Herein, the effectiveness of (188)Re-HEDP for the palliation of painful bone metastases was investigated in an uncontrolled initial trial in 48 patients with different types of advanced cancers. A group of 48 patients with painful bone metastases of lung, prostate, breast, renal, and bladder cancer was treated with 2.96–4.44 GBq of (188)Re-HEDP. The overall response rate in this group of patients was 89.5%, and their mean visual analog scale score showed a reduction from 9.1 to 5.3 (P < 0.003) after 1 week posttherapy. The patients did not report serious adverse effects either during intravenous administration or within 24 h postadministration of (188)Re-HEDP. Flare reaction was observed in 54.2% of patients between day 1 and day 3. There was no correlation between flare reaction and response to therapy (P < 0.05). Although bone marrow suppression was observed in patients receiving higher doses of (188)Re-HEDP, it did not result in any significant clinical problems. The present study confirmed the clinical utility and cost-effectiveness of (188)Re-HEDP for palliation of painful bone metastases from various types of cancer in developing countries.
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spelling pubmed-62167412018-11-30 Clinical utility of (188)Rhenium-hydroxyethylidene-1,1-diphosphonate as a bone pain palliative in multiple malignancies Shinto, Ajit S. Mallia, Madhava B. Kameswaran, Mythili Kamaleshwaran, K. K. Joseph, Jephy Radhakrishnan, E. R. Upadhyay, Indira V. Subramaniam, R. Sairam, Madhu Banerjee, Sharmila Dash, Ashutosh World J Nucl Med Original Article (188)Rhenium-hydroxyethylidene-1,1-diphosphonate ((188)Re-HEDP) is a clinically established radiopharmaceutical for bone pain palliation of patients with metastatic bone cancer. Herein, the effectiveness of (188)Re-HEDP for the palliation of painful bone metastases was investigated in an uncontrolled initial trial in 48 patients with different types of advanced cancers. A group of 48 patients with painful bone metastases of lung, prostate, breast, renal, and bladder cancer was treated with 2.96–4.44 GBq of (188)Re-HEDP. The overall response rate in this group of patients was 89.5%, and their mean visual analog scale score showed a reduction from 9.1 to 5.3 (P < 0.003) after 1 week posttherapy. The patients did not report serious adverse effects either during intravenous administration or within 24 h postadministration of (188)Re-HEDP. Flare reaction was observed in 54.2% of patients between day 1 and day 3. There was no correlation between flare reaction and response to therapy (P < 0.05). Although bone marrow suppression was observed in patients receiving higher doses of (188)Re-HEDP, it did not result in any significant clinical problems. The present study confirmed the clinical utility and cost-effectiveness of (188)Re-HEDP for palliation of painful bone metastases from various types of cancer in developing countries. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6216741/ /pubmed/30505219 http://dx.doi.org/10.4103/wjnm.WJNM_68_17 Text en Copyright: © 2018 World Journal of Nuclear Medicine http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Shinto, Ajit S.
Mallia, Madhava B.
Kameswaran, Mythili
Kamaleshwaran, K. K.
Joseph, Jephy
Radhakrishnan, E. R.
Upadhyay, Indira V.
Subramaniam, R.
Sairam, Madhu
Banerjee, Sharmila
Dash, Ashutosh
Clinical utility of (188)Rhenium-hydroxyethylidene-1,1-diphosphonate as a bone pain palliative in multiple malignancies
title Clinical utility of (188)Rhenium-hydroxyethylidene-1,1-diphosphonate as a bone pain palliative in multiple malignancies
title_full Clinical utility of (188)Rhenium-hydroxyethylidene-1,1-diphosphonate as a bone pain palliative in multiple malignancies
title_fullStr Clinical utility of (188)Rhenium-hydroxyethylidene-1,1-diphosphonate as a bone pain palliative in multiple malignancies
title_full_unstemmed Clinical utility of (188)Rhenium-hydroxyethylidene-1,1-diphosphonate as a bone pain palliative in multiple malignancies
title_short Clinical utility of (188)Rhenium-hydroxyethylidene-1,1-diphosphonate as a bone pain palliative in multiple malignancies
title_sort clinical utility of (188)rhenium-hydroxyethylidene-1,1-diphosphonate as a bone pain palliative in multiple malignancies
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6216741/
https://www.ncbi.nlm.nih.gov/pubmed/30505219
http://dx.doi.org/10.4103/wjnm.WJNM_68_17
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