Cited by 143Multiple Myeloma Research and TreatmentsPI3K/AKT/mTOR signaling in cancerAcute Myeloid Leukemia Research

The DOI matches its Crossref record; 27 of the 28 references it cites were found in a registry or an index.

The novel AKT inhibitor afuresertib shows favorable safety, pharmacokinetics, and clinical activity in multiple myeloma

Open access

Abstract

Key Points: Afuresertib has a favorable safety profile with manageable side effects and demonstrates single-agent activity against hematologic malignancies. Inhibition of AKT with afuresertib may provide a novel therapeutic strategy for hematologic malignancies, especially for multiple myeloma.

Overview

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Registry

Crossref · 10.1182/blood-2014-03-559963

Cites

27 of 27 references verified0 citation errors · 0 not checkable

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Metadata

Authors
Spencer, A., Yoon, S.-S., Harrison, S. J., Morris, S. R., Smith, D. A., Brigandi, R. A., Gauvin, J., Kumar, R., Opalinska, J. B., & Chen, C.
Affiliations
  • The Alfred Hospital (AU)
  • Seoul National University Hospital (KR)
  • The University of Melbourne (AU)
  • GlaxoSmithKline (United States) (US)
  • Princess Margaret Cancer Centre (CA)
Venue
Blood
Published
2014-10-02
Volume
124
Issue
14
Pages
2190-2195
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W2094611598
Cited by
142
References
28
Citations by year
2026: 5 · 2025: 13 · 2024: 12 · 2023: 7 · 2022: 15 · 2021: 11 · 2020: 9 · 2019: 17 · 2018: 17 · 2017: 11 · 2016: 13 · 2015: 10 · 2014: 2
FWCI
8.75
Type
journal article
Language
en
Open access
Locations
  • Blood (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
GlaxoSmithKline
Topics
  • Health Sciences › Medicine › Hematology › Multiple Myeloma Research and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
  • Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
Keywords
AKT inhibitors, multiple myeloma, PI3K/Akt signaling, hematologic malignancies, maximum tolerated dose, pharmacokinetics, safety, adverse events, non-Hodgkin lymphoma, Langerhans cell histiocytosis, Hodgkin's disease, drug resistance
MeSH terms
Administration, Oral, Adolescent, Adult, Aged, Aged, 80 and over, Dose-Response Relationship, Drug, Female, Humans, Male, Middle Aged, Multiple Myeloma, Pyrazoles, Thiophenes, Time Factors, Hematologic Neoplasms, Maximum Tolerated Dose, Protein Kinase Inhibitors, Proto-Oncogene Proteins c-akt, Young Adult, Patient Safety

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