Literature DB >> 21034411

Targeted radiotherapy of bone malignancies.

David R Jansen1, Gerard C Krijger, Zvonimir I Kolar, Bernard A Zonnenberg, Jan Rijn Zeevaart.   

Abstract

The severe pain associated with many disorders affecting bone account for a large proportion of cases of patient morbidity, due to the encumbrance of mobility and therefore, compromised quality of life. Skeletal metastasis is one such condition, which generally complicates the treatment of the primary cancers such as that of the breast, prostate and lung - causing intense pain and eventually even mortality. This paper presents examples of various approaches explored and proposed in the ongoing search to identify better radiopharmaceuticals for the treatment of bone disorders such as metastases. The primary objective of these developments is to alleviate the debilitating pain commonly associated with bone lesions. The efficacy of a radiotherapeutic agent intended for the treatment of diseased bone is particularly dependent on the radiation dose to the tumor cells and on the extent to which suppression of bone marrow or other critical organs can be avoided. Therefore, the design rationale requires careful consideration of the choice radionuclide and especially ensuring that the drug selectively targets the lesion or tumor site. The options pursued include the use of radioisotopes with an intrinsic affinity for bone, such as (89)Sr or (223)Ra, or the design of bone-seeking ligands, such as phosphonates, to selectively deliver the radionuclide to the target, e.g. [(153)Sm]Sm-EDTMP. A combination of the above may too be possible, where the bone seeking ligand facilitates the selective accumulation of a radionuclide, which by itself is also bone homing. In terms of therapeutic application radionuclides with various decay modes are proposed, including beta (-) emitters: (153)Sm, (89)Sr, (186)Re, (188)Re, (32)P, (177)Lu and (170)Tm; alpha (α) emitters: (223)Ra and (225)Ra; and Auger or conversion electron emitter: (117)mSn. From a purely diagnostic perspective, the radioisotopes used for imaging include the well known photon emitting (99)mTc, and positron emitters (18)F and (68)Ga. The current status in the development and application of internal radiotherapy for the palliative treatment of bone pain will be discussed, summarizing the progress made and challenges encountered in the process to realizing an effective drug candidate.

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Year:  2010        PMID: 21034411     DOI: 10.2174/157016310793360675

Source DB:  PubMed          Journal:  Curr Drug Discov Technol        ISSN: 1570-1638


  6 in total

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Authors:  Justin Sturge; Matthew P Caley; Jonathan Waxman
Journal:  Nat Rev Clin Oncol       Date:  2011-05-10       Impact factor: 66.675

Review 2.  Targeted α-particle therapy of bone metastases in prostate cancer.

Authors:  Hossein Jadvar; David I Quinn
Journal:  Clin Nucl Med       Date:  2013-12       Impact factor: 7.794

3.  Sodium iodide symporter for nuclear molecular imaging and gene therapy: from bedside to bench and back.

Authors:  Byeong-Cheol Ahn
Journal:  Theranostics       Date:  2012-04-11       Impact factor: 11.556

4.  [68Ga]/[188Re] Complexed [CDTMP] Trans-1,2-Cyclohexyldinitrilotetraphosphonic Acid As a Theranostic Agent for Skeletal Metastases.

Authors:  Ambika P Jaswal; Virendra K Meena; Surbhi Prakash; Ankita Pandey; Baljinder Singh; Anil K Mishra; Puja P Hazari
Journal:  Front Med (Lausanne)       Date:  2017-06-09

5.  Evaluation of (188)Re-labeled NGR-VEGI protein for radioimaging and radiotherapy in mice bearing human fibrosarcoma HT-1080 xenografts.

Authors:  Wenhui Ma; Yahui Shao; Weidong Yang; Guiyu Li; Yingqi Zhang; Mingru Zhang; Changjing Zuo; Kai Chen; Jing Wang
Journal:  Tumour Biol       Date:  2016-01-14

6.  Influence of internal fixation systems on radiation therapy for spinal tumor.

Authors:  Jingfeng Li; Lei Yan; Jianping Wang; Lin Cai; Dongcai Hu
Journal:  J Appl Clin Med Phys       Date:  2015-07-08       Impact factor: 2.102

  6 in total

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