Personalizing initial therapy in acute myeloid leukemia: incorporating novel agents into clinical practice. [Review] (Record no. 4)

MARC details
000 -LEADER
fixed length control field 01918nam a22003497a 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 221213s20182018 xxu||||| |||| 00| 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 2040-6207
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code 10.1177_2040620718761778 [pii]
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code 10.1177/2040620718761778 [doi]
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code PMC5900827 [pmc]
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 29713444
245 ## - TITLE STATEMENT
Title Personalizing initial therapy in acute myeloid leukemia: incorporating novel agents into clinical practice. [Review]
251 ## - Source
Source Therapeutic Advances in Hematology. 9(5):109-121, 2018 May.
252 ## - Abbreviated Source
Abbreviated source Ther Adv Hematol. 9(5):109-121, 2018 May.
253 ## - Journal Name
Journal name Therapeutic advances in hematology
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Year 2018
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Manufacturer FY2018
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Publication date 2018 May
265 ## - SOURCE FOR ACQUISITION/SUBSCRIPTION ADDRESS [OBSOLETE]
Publication status ppublish
265 ## - SOURCE FOR ACQUISITION/SUBSCRIPTION ADDRESS [OBSOLETE]
Medline status PubMed-not-MEDLINE
266 ## - Date added to catalog
Date added to catalog 2022-12-13
520 ## - SUMMARY, ETC.
Abstract While the past decade has seen a revolution in understanding of the genetic and molecular etiology of the disease, in clinical practice, initial therapy for acute myeloid leukemia (AML) patients has been a relatively straightforward choice between intensive combination cytotoxic induction therapy as used for decades or less-intensive hypomethylating therapy. The year 2017, however, witnessed US Food and Drug Administration approvals of midostaurin, enasidenib, gemtuzumab ozogamicin and CPX-351 for AML patients, with many other promising agents currently in clinical trials. This review discusses these options, highlights unanswered questions regarding optimal combinations and proposes some suggested approaches for the personalization of initial therapy for AML patients.
546 ## - LANGUAGE NOTE
Language note English
651 ## - SUBJECT ADDED ENTRY--GEOGRAPHIC NAME
Institution Washington Cancer Institute
657 ## - INDEX TERM--FUNCTION
Medline publication type Journal Article
657 ## - INDEX TERM--FUNCTION
Medline publication type Review
700 ## - ADDED ENTRY--PERSONAL NAME
Local Authors DeStefano, Christin B
790 ## - Authors
All authors DeStefano CB, Hourigan CS
856 ## - ELECTRONIC LOCATION AND ACCESS
DOI <a href="https://dx.doi.org/10.1177/2040620718761778">https://dx.doi.org/10.1177/2040620718761778</a>
Public note https://dx.doi.org/10.1177/2040620718761778
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
Item type description Article
Holdings
Withdrawn status Lost status Damaged status Not for loan Collection Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
          MedStar Authors Catalog MedStar Authors Catalog 12/13/2022   29713444 29713444 12/13/2022 12/13/2022 Journal Article

Powered by Koha