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View the Table of Contents for the June 1 issue of Clinical Cancer Research.
Guo et al. Page 3344
Guo et al. offer a computational model system that may accurately predict clinical outcomes of individual lung adenocarcinoma patients based on gene expression profiles. The prediction accuracy of good prognosis and poor prognosis patients is 0.96 (p < 1E-7) using the identified 37-gene survival signature. The correct classification of stage I and stage III lung adenocarcinoma is 94.2% (p < 2.9E-20) using the 12-gene stage predictors. These results show that the gene expression-based models comprising a small number of markers may accurately predict patient outcome for lung adenocarcinoma.
Van Laere et al. Page 3249
Inflammatory breast cancer (IBC) is an aggressive form of locally advanced breast cancer. At time of diagnosis, most patients have lymph node involvement and one third patients have metastases in distant organs. Van Laere et al. demonstrated that NF-κB, an important mediator of several inflammatory and oncological processes, is activated in IBC. NF-κB target genes were significantly overexpressed in IBC compared with non-IBC by both cDNA microarray and qRT-PCR. By means of protein co-expression analysis, a significantly elevated amount of transcriptionally active NF-κB dimers was present in IBC. The increased activation of the NF-κB transcription factor offers an explanation for several hallmarks of the disease, including increased angiogenic capacity resistance to treatment and high metastatic potential, and supports NF-κB as a potential therapeutic target to treat patients with IBC.
Page 3525
Iversen et al. document the efficacy of a fatty acid analogue (TTA) in treating rats with acute leukemia. TTA treatment resulted in a profound reduction in the number of leukemic cells, a substantial decrease in metastatic potential, and a marked improvement in survival among leukemic rats fed TTA. The fact that TTA was supplied to the animals as part of their diet makes the handling and administration of this drug particularly attractive. The current study provides important new evidence for a putative anti-leukemic drug in animal models.
Page 3243
Despite the growing scientific opportunities and significant investment, the output of new cancer therapies reaching the public as FDA-approved products is insufficient to meet the needs of patients. There are now indications that this issue has registered with the FDA and the NCI and that changes, such as the Critical Path initiative, are being planned to provide a more responsive development and regulatory environment. This process, however, may take years to implement. In this review, Schein et al. state the problem and provide recommendations for a more timely response to the urgent need for reform.