15 research outputs found

    Genetic changes associated with relapse in favorable histology Wilms tumor: A Children's Oncology Group AREN03B2 study

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    Over the last decade, sequencing of primary tumors has clarified the genetic underpinnings of Wilms tumor but has not affected therapy, outcome, or toxicity. We now sharpen our focus on relapse samples from the umbrella AREN03B2 study. We show that over 40% of relapse samples contain mutations in SIX1 or genes of the MYCN network, drivers of progenitor proliferation. Not previously seen in large studies of primary Wilms tumors, DIS3 and TERT are now identified as recurrently mutated. The analysis of primary-relapse tumor pairs suggests that 11p15 loss of heterozygosity (and other copy number changes) and mutations in WT1 and MLLT1 typically occur early, but mutations in SIX1, MYCN, and WTX are late developments in some individuals. Most strikingly, 75% of relapse samples had gain of 1q, providing strong conceptual support for studying circulating tumor DNA in clinical trials to better detect 1q gain earlier and monitor response

    Patient Selection for Later Delivery Timing With Suspected Previa-accreta

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    Cell Migration along the Basement Membrane during Wound Repair. The Corneal Endothelium as a Model System

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    Income Inequality Across Regions Over Time

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    This paper provides a profile of regional income inequality using a distributional criterion whereby a state\u27s share of total income equals its share of total population. The results for 1929 to 1990 show that inequality persisted among regions with a substantial declining trend up to 1979 and a slight rise thereafter. On the other hand, equality among states within their regions is found to have been the condition since 1929
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