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March 2013 Volume 10 Number 3 | ||||||||||||||||||||||||||||||||||||||||||||
In this issue Research Highlights News and Views Reviews Perspectives
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NEWS AND VIEWS | Top | |||||||||||||||||||||||||||||||||||||||||||
Breast cancer: Tamoxifen—when more might be better Carlos Caldas & Ian F. Tannock Published online: 05 February 2013 p125 | doi:10.1038/nrclinonc.2013.17 The ATLAS trial demonstrated improved survival for women with oestrogen receptor-positive breast cancer who continued taking tamoxifen for 10 years compared to stopping at 5 years. Women for whom absolute benefit outweighs adverse-effects should be selected based on their risk of recurrence beyond 5 years; support must be provided to maintain compliance. Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||
Prostate cancer: The androgen receptor remains front and centre Philip J. Saylor Published online: 05 February 2013 p126 | doi:10.1038/nrclinonc.2013.14 Abiraterone is an androgen biosynthesis inhibitor that further lowers testosterone in men receiving standard androgen deprivation therapy for metastatic castration-resistant prostate cancer. Previously shown to improve survival in patients after treatment with docetaxel, abiraterone has demonstrated benefits in a new phase III trial in men who are chemotherapy naive. Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||
Breast cancer: Investment biobanking—increased returns from tissue samples Valerie Speirs & Adrienne Morgan Published online: 05 February 2013 p128 | doi:10.1038/nrclinonc.2013.19 Researchers now expect that samples obtained from biobanks are accompanied with well-annotated clinical data. Opened in 2010, the Breast Cancer Campaign Tissue Bank takes this criterion a step further: researchers obtaining tissues are required to return the data they generate from every sample back to the Tissue Bank. Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||
REVIEWS | Top | |||||||||||||||||||||||||||||||||||||||||||
Colorectal cancer screening—optimizing current strategies and new directions Ernst J. Kuipers, Thomas Rösch & Michael Bretthauer Published online: 05 February 2013 p130 | doi:10.1038/nrclinonc.2013.12 Many methods are available for colorectal cancer (CRC) screening, ranging from noninvasive stool tests to endoscopy. In this Review, E. J. Kuipers et al. argue that the strength of any single test must be viewed in the context of a range of factors across the screening programme, including test characteristics, uptake, screenee autonomy, cost, endoscopy performance and long-term follow-up. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||
Development of PI3K inhibitors: lessons learned from early clinical trials Jordi Rodon, Rodrigo Dienstmann, Violeta Serra & Josep Tabernero Published online: 12 February 2013 p143 | doi:10.1038/nrclinonc.2013.10 Agents targeting the PI3K/AKT/mTOR pathway have been shown to be safe and effective in treating a number of tumour types. This Review outlines the background to these inhibitors and discusses the second-generation inhibitors of this pathway. The authors propose that the way forward for the development of inhibitors of the PI3K/AKT/mTOR pathway might be a systems biology approach and biomarker-driven studies. Abstract | Full Text | PDF | Supplementary information | ||||||||||||||||||||||||||||||||||||||||||||
Safety and feasibility of targeted agent combinations in solid tumours Sook Ryun Park, Myrtle Davis, James H. Doroshow & Shivaani Kummar Published online: 29 January 2013 p154 | doi:10.1038/nrclinonc.2012.245 Combination strategies of molecular-targeted agents (MTAs) are being used in the hope of optimizing antitumour efficacy and to minimize the development of resistance, but very little effort is focused on molecular vulnerabilities of normal tissues. This Review discusses the main toxicities and the lack of tolerability of some common MTA combinations, and highlights what steps can be introduced for new preclinical testing paradigms for the assessment of chronic toxicities. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||
PERSPECTIVES | Top | |||||||||||||||||||||||||||||||||||||||||||
OPINION Translating metastasis-related biomarkers to the clinic—progress and pitfalls François-Clément Bidard, Jean-Yves Pierga, Jean-Charles Soria & Jean Paul Thiery Published online: 05 February 2013 p169 | doi:10.1038/nrclinonc.2013.4 The majority of patients with cancer do not die as a result of the primary tumour, rather from the metastases that arise from that tumour. The mechanisms and markers of metastasis have, therefore, been a main focus of both clinical and preclinical research. This Perspectives article discusses the hurdles that need to be overcome to successfully translate the preclinical metastasis research into the clinic. Abstract | Full Text | PDF | ||||||||||||||||||||||||||||||||||||||||||||
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*Journal Citation Reports, Thomson, 2011. Nature Reviews Clinical Oncology was previously published as Nature Clinical Practice Oncology. |
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