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Andre Rogatko
Researcher at Cedars-Sinai Medical Center
Publications - 157
Citations - 7533
Andre Rogatko is an academic researcher from Cedars-Sinai Medical Center. The author has contributed to research in topics: Cancer & Survival rate. The author has an hindex of 43, co-authored 146 publications receiving 6826 citations. Previous affiliations of Andre Rogatko include Emory Healthcare & Fox Chase Cancer Center.
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Cancer phase I clinical trials: efficient dose escalation with overdose control
TL;DR: An adaptive dose escalation scheme for use in cancer phase I clinical trials that makes use of all the information available at the time of each dose assignment, and directly addresses the ethical need to control the probability of overdosing is described.
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International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity.
TL;DR: It is concluded that hypersensitivity to the clastogenic effect of DEB is a useful discriminator for FA and a simplified scoring method for classifying patients on the basis of eight clinical manifestations that are the best predictors for FA is presented.
Journal Article
UGT1A7 and UGT1A9 polymorphisms predict response and toxicity in colorectal cancer patients treated with capecitabine/irinotecan.
Leslie E. Carlini,Neal J. Meropol,John Bever,Michael L. Andria,Todd Hill,Philip J. Gold,Andre Rogatko,Hao Wang,Rebecca L. Blanchard +8 more
TL;DR: Patients with genotypes conferring low UGT1A7 activity and/or the UGT 1A9 (dT)(9/9) genotype may be particularly likely to exhibit greater antitumor response with little toxicity in CRC patients treated with capecitabine plus irinotecan.
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Association of the Lewis blood-group phenotype with recurrent urinary tract infections in women
TL;DR: There is an increased frequency of the Lewis blood-group nonsecretor (Le (a+b-] and recessive (Le(a-b-)] phenotypes among women with recurrent urinary tract infections.
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Prognosis of pregnancy-associated breast cancer.
TL;DR: Across stages, patients with PA breast cancer have survival not significantly different from those patients with non‐pregnancy‐associated (non‐PA) breast cancer.