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Francis Giles

Researcher at University of Texas MD Anderson Cancer Center

Publications -  18
Citations -  1599

Francis Giles is an academic researcher from University of Texas MD Anderson Cancer Center. The author has contributed to research in topics: Imatinib mesylate & Imatinib. The author has an hindex of 18, co-authored 18 publications receiving 1515 citations.

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Results of intensive chemotherapy in 998 patients age 65 years or older with acute myeloid leukemia or high-risk myelodysplastic syndrome: predictive prognostic models for outcome.

TL;DR: The aim was to develop prognostic models for complete response (CR), induction (8‐week) mortality, and survival rates in elderly AML, which would be used to advise oncologists and patients of expectations with standard AML type therapy, and to establish baseline therapy results against which novel strategies would be evaluated.
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The significance of myelosuppression during therapy with imatinib mesylate in patients with chronic myelogenous leukemia in chronic phase.

TL;DR: During therapy with imatinib, up to 45% of patients with CML reportedly experience myelosuppression ≥ Grade 3, requiring interruption of therapy and/or dose reductions.
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Results of imatinib mesylate therapy in patients with refractory or recurrent acute myeloid leukemia, high-risk myelodysplastic syndrome, and myeloproliferative disorders†

TL;DR: Imatinib mesylate is a selective tyrosine kinase inhibitor of c‐abl, bcr/abl, c‐kit, and platelet‐derived growth factor‐receptor (PDGF‐R) that is implicated in the pathogenesis of myeloproliferative disorders (MPD).
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Long-term follow-up results of the combination of topotecan and cytarabine and other intensive chemotherapy regimens in myelodysplastic syndrome.

TL;DR: The aim of this study was to analyze the long‐term results with topotecan‐cytarabine versus other intensive chemotherapy regimens in higher‐risk MDS.
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Effects of age on prognosis with imatinib mesylate therapy for patients with Philadelphia chromosome-positive chronic myelogenous leukemia.

TL;DR: The availability of imatinib mesylate, a selective, Bcr‐Abl‐targeted therapy that is administered orally with minimal side effects, may clarify whether older age would remain an adverse factor (thus, implying a different age‐related CML biology).