Literature DB >> 19496721

Novel therapeutics for melanoma.

Nagashree Seetharamu1, Patrick A Ott, Anna C Pavlick.   

Abstract

Advanced melanoma has the highest per-death loss of years of potential life expectancy except for adult leukemia. Standard therapy with agents such as dacarbazine, temozolomide and IL-2 is associated with notoriously low response rates. The identification of new active agents is, therefore, critical in this disease. In recent years, better understanding of melanoma biology, as well as cancer and immune biology in general has led to the development of a number of new potential therapeutic agents for advanced melanoma. While many of these compounds are being tested in clinical trials, there are more agents in various stages of preclinical development. These novel therapeutics offer hope for this aggressive and so far largely treatment-resistant disease. In this review we will discuss some of the most promising novel therapeutic agents for advanced melanoma.

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Year:  2009        PMID: 19496721     DOI: 10.1586/era.09.40

Source DB:  PubMed          Journal:  Expert Rev Anticancer Ther        ISSN: 1473-7140            Impact factor:   4.512


  9 in total

1.  Additive melanoma suppression with intralesional phospholipid-conjugated TLR7 agonists and systemic IL-2.

Authors:  Tomoko Hayashi; Michael Chan; John T Norton; Christina C N Wu; Shiyin Yao; Howard B Cottam; Rommel I Tawatao; Maripat Corr; Dennis A Carson; Gregory A Daniels
Journal:  Melanoma Res       Date:  2011-02       Impact factor: 3.599

Review 2.  Mucosal melanomas: a case-based review of the literature.

Authors:  Nagashree Seetharamu; Patrick A Ott; Anna C Pavlick
Journal:  Oncologist       Date:  2010-06-22

3.  Analysis of MLN4924 (pevonedistat) as a potential therapeutic agent in malignant melanoma.

Authors:  Gonzalo N Olaverria Salavaggione; Megan C Duggan; William E Carson
Journal:  Melanoma Res       Date:  2018-10       Impact factor: 3.599

4.  Melanoma cells show a heterogeneous range of sensitivity to ionizing radiation and are radiosensitized by inhibition of B-RAF with PLX-4032.

Authors:  Maria J Sambade; Eldon C Peters; Nancy E Thomas; William K Kaufmann; Randall J Kimple; Janiel M Shields
Journal:  Radiother Oncol       Date:  2011-02-04       Impact factor: 6.280

5.  Is GP-led follow-up feasible?

Authors:  A B Francken; J W Hoekstra-Weebers; H J Hoekstra
Journal:  Br J Cancer       Date:  2010-05-11       Impact factor: 7.640

6.  Membrane transport proteins in human melanoma: associations with tumour aggressiveness and metastasis.

Authors:  N Walsh; S Kennedy; A M Larkin; D Tryfonopoulos; A J Eustace; T Mahgoub; C Conway; I Oglesby; D Collins; J Ballot; W S Ooi; G Gullo; M Clynes; J Crown; L O'Driscoll
Journal:  Br J Cancer       Date:  2010-03-16       Impact factor: 7.640

7.  Docosahexaenoic acid, G protein-coupled receptors, and melanoma: is G protein-coupled receptor 40 a potential therapeutic target?

Authors:  Deepika Nehra; Amy H Pan; Hau D Le; Erica M Fallon; Sarah J Carlson; Brian T Kalish; Mark Puder
Journal:  J Surg Res       Date:  2014-01-29       Impact factor: 2.192

8.  A phase II, randomized, double-blind, placebo-controlled multicenter trial of Endostar in patients with metastatic melanoma.

Authors:  Chuanliang Cui; Lili Mao; Zhihong Chi; Lu Si; Xinan Sheng; Yan Kong; Siming Li; Bin Lian; Kangsheng Gu; Min Tao; Xin Song; Tongyu Lin; Xiubao Ren; Shukui Qin; Jun Guo
Journal:  Mol Ther       Date:  2013-05-14       Impact factor: 11.454

Review 9.  Checkpoint inhibitors for renal cell carcinoma: current landscape and future directions.

Authors:  Matthew Zibelman; Pooja Ghatalia; Daniel M Geynisman; Elizabeth R Plimack
Journal:  Immunotherapy       Date:  2016-06       Impact factor: 4.196

  9 in total

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