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Ignacio Garrido-Laguna

Researcher at Huntsman Cancer Institute

Publications -  154
Citations -  7364

Ignacio Garrido-Laguna is an academic researcher from Huntsman Cancer Institute. The author has contributed to research in topics: Cancer & Medicine. The author has an hindex of 28, co-authored 125 publications receiving 4888 citations. Previous affiliations of Ignacio Garrido-Laguna include City of Hope National Medical Center & University of Utah.

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Entrectinib in patients with advanced or metastatic NTRK fusion-positive solid tumours: integrated analysis of three phase 1–2 trials

TL;DR: Results show that entrectinib induced durable and clinically meaningful responses in patients with NTRK fusion-positive solid tumours, and was well tolerated with a manageable safety profile.
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NCCN Guidelines® Insights Colon Cancer, Version 2.2018 Featured Updates to the NCCN Guidelines

TL;DR: The NCCN Colon Cancer Panel discussions for the 2018 update of the guidelines regarding risk stratification and adjuvant treatment for patients with stage III colon cancer, and treatment of BRAF V600E mutation-positive metastatic colorectal cancer with regimens containing vemurafenib are summarized.
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Colon Cancer, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.

Al B. Benson, +38 more
TL;DR: The NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines) for Colon Cancer focuses on systemic therapy options for the treatment of metastatic colorectal cancer (mCRC), because important updates have recently been made to this section as discussed by the authors.
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Pancreatic cancer: From state-of-the-art treatments to promising novel therapies

TL;DR: The state-of-the-art of pancreatic cancer treatment, and the upcoming novel therapeutics that hold promise in this disease are reviewed.
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PI3K/AKT/mTOR Inhibitors in Patients With Breast and Gynecologic Malignancies Harboring PIK3CA Mutations

TL;DR: A subset of patients with ovarian cancer with simultaneous PIK3CA and MAPK mutations responded to PI3K/AKT/mTOR inhibitors, suggesting that not all patients demonstrate resistance when the MAPK pathway is concomitantly activated.