Literature DB >> 30190863

The potential complementary role of targeted alpha therapy in the management of metastatic melanoma.

Michael P Brown1,2,3,1,2,3, Eva Bezak4,5,6,4,5,6, Barry J Allen7,7.   

Abstract

Standard treatments for metastatic melanoma have recently extended survival although many patients still succumb. Targeted alpha therapy (TAT) is a new therapeutic approach in which a cancer-targeting vector is labeled with an alpha-emitting radioisotope. Alpha-particles have the shortest range and highest energy transfer, and produce localized, high-density and lethal ionization damage to DNA. Thus, the targeted radiation can kill isolated cancer cells circulating in blood and lymphatic vessels, regress metastatic cancer cell clusters, and disrupt the vasculature of solid tumors. Preclinical and clinical studies of TAT for metastatic melanoma demonstrate its safety and anti-tumor activity. We recommend ways in which TAT can be used to treat small-volume disease sometimes in conjunction with cytoreductive anti-melanoma therapies.

Entities:  

Keywords:  Bi-213 alpha emitter; Phase I clinical trials; complementary therapies; immunotherapy; intralesional; kinase inhibitors; metastatic melanoma; radioisotopes; systemic; targeted alpha therapy

Year:  2015        PMID: 30190863      PMCID: PMC6094593          DOI: 10.2217/mmt.15.26

Source DB:  PubMed          Journal:  Melanoma Manag        ISSN: 2045-0885


  92 in total

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Authors:  Ugur Ozerdem; Edward Monosov; William B Stallcup
Journal:  Microvasc Res       Date:  2002-01       Impact factor: 3.514

Review 2.  Treatment options in melanoma in situ: topical and radiation therapy, excision and Mohs surgery.

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Journal:  Int J Dermatol       Date:  2010-05       Impact factor: 2.736

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Journal:  J Invest Dermatol       Date:  2006-01       Impact factor: 8.551

Review 4.  Targeted therapy of cancer with radiolabeled antibodies.

Authors:  David M Goldenberg
Journal:  J Nucl Med       Date:  2002-05       Impact factor: 10.057

5.  Accuracy of the non-sentinel node risk score (N-SNORE) in patients with cutaneous melanoma and positive sentinel lymph nodes: a retrospective study.

Authors:  R Feldmann; A M Fink; W Jurecka; K Rappersberger; A Steiner
Journal:  Eur J Surg Oncol       Date:  2013-09-12       Impact factor: 4.424

6.  Differential expression of markers for endothelial cells, pericytes, and basal lamina in the microvasculature of tumors and granulation tissue.

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Journal:  Am J Pathol       Date:  1991-06       Impact factor: 4.307

7.  In vivo localisation of radiolabelled monoclonal antibody in human gliomas.

Authors:  J Behnke; J P Mach; F Buchegger; S Carrel; B Delaloye; N De Tribolet
Journal:  Br J Neurosurg       Date:  1988       Impact factor: 1.596

8.  MAP kinase pathway alterations in BRAF-mutant melanoma patients with acquired resistance to combined RAF/MEK inhibition.

Authors:  Nikhil Wagle; Eliezer M Van Allen; Daniel J Treacy; Dennie T Frederick; Zachary A Cooper; Amaro Taylor-Weiner; Mara Rosenberg; Eva M Goetz; Ryan J Sullivan; Deborah N Farlow; Dennis C Friedrich; Kristin Anderka; Danielle Perrin; Cory M Johannessen; Aaron McKenna; Kristian Cibulskis; Gregory Kryukov; Eran Hodis; Donald P Lawrence; Sheila Fisher; Gad Getz; Stacey B Gabriel; Scott L Carter; Keith T Flaherty; Jennifer A Wargo; Levi A Garraway
Journal:  Cancer Discov       Date:  2013-11-21       Impact factor: 39.397

Review 9.  Yttrium-90 labelled resin microspheres for treatment of primary and secondary malignant liver tumors.

Authors:  C Van De Wiele; L Defreyne; M Peeters; B Lambert
Journal:  Q J Nucl Med Mol Imaging       Date:  2009-06       Impact factor: 2.346

10.  Do BRAF inhibitors select for populations with different disease progression kinetics?

Authors:  Paolo Antonio Ascierto; Ester Simeone; Antonio Maria Grimaldi; Marcello Curvietto; Assunta Esposito; Giuseppe Palmieri; Nicola Mozzillo
Journal:  J Transl Med       Date:  2013-03-08       Impact factor: 5.531

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