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Guillermo Garcia-Manero

Researcher at University of Texas MD Anderson Cancer Center

Publications -  1611
Citations -  52621

Guillermo Garcia-Manero is an academic researcher from University of Texas MD Anderson Cancer Center. The author has contributed to research in topics: Myeloid leukemia & Myelodysplastic syndromes. The author has an hindex of 108, co-authored 1411 publications receiving 43103 citations. Previous affiliations of Guillermo Garcia-Manero include Sapporo Medical University & University of Texas Health Science Center at Houston.

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Presence of 4 or More Driver Mutations Predicts Poor Response to Hypomethylating Agent (HMA) Therapy and Poor Overall Survival in MDS

TL;DR: High-confidence driver mutations in myelodysplastic syndromes patients with untreated MDS were detected in 39 genes by sequencing, and patients who were found to carry 4 or more driver mutations had significantly poor response to HMA therapy compared to patients with less than 4 driver mutations.
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Final Report of a Phase II Trial of Vorinostat, Idarubicin and Cytarabine In Previously Untreated Acute Myelogenous Leukemia (AML) or High Risk Myelodysplastic Syndrome (MDS)

TL;DR: A phase I trial of Vor and Ida demonstrated that doses of vorinostat up to 500 mg po TID daily × 3 are safe in combination with Ida, and a phase II trial to study the safety and activity of the triple combination in patients with AML or higher-risk MDS was developed.
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Development and Validation of a New Prognostic Model for Myelodysplastic Syndrome (MDS) That Accounts for Events Not Considered by the International Prognostic Scoring System (IPSS)

TL;DR: A new prognostic model was developed and validated for MDS, which accounts for all MDS or CMML cases, regardless of prior therapy, which has been validated in an independent test group and was shown to be superior to IPSS.
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Clinical Application of Artificial Intelligence in Patients with Chronic Myeloid Leukemia in Chronic Phase

TL;DR: This study introduces a prototype of AI to predict outcome such as achievement of major molecular response (MMR) within 1 year of the start of tyrosine kinase inhibitor (TKI) in 630 patients with newly diagnosed CML-CP.