Optimal sequencing of ibrutinib, idelalisib, and venetoclax in chronic lymphocytic leukemia: results from a multicenter study of 683 patients. (Record no. 3202)

MARC details
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fixed length control field 04233nam a22005657a 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 170508s20172017 xxu||||| |||| 00| 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0923-7534
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 28453705
245 ## - TITLE STATEMENT
Title Optimal sequencing of ibrutinib, idelalisib, and venetoclax in chronic lymphocytic leukemia: results from a multicenter study of 683 patients.
251 ## - Source
Source Annals of Oncology. 28(5):1050-1056, 2017 May 01
252 ## - Abbreviated Source
Abbreviated source Ann Oncol. 28(5):1050-1056, 2017 May 01
253 ## - Journal Name
Journal name Annals of oncology : official journal of the European Society for Medical Oncology
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Year 2017
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Manufacturer FY2017
266 ## - Date added to catalog
Date added to catalog 2017-05-08
520 ## - SUMMARY, ETC.
Abstract Background: Ibrutinib, idelalisib, and venetoclax are approved for treating CLL patients in the United States. However, there is no guidance as to their optimal sequence.
520 ## - SUMMARY, ETC.
Abstract Conclusions: In the largest real-world experience of novel agents in CLL, ibrutinib appears superior to idelalisib as first KI. Furthermore, in the setting of KI failure, alternate KI or venetoclax therapy appear superior to chemoimmunotherapy combinations. The use of venetoclax upon ibrutinib failure might be superior to idelalisib. These data support the need for trials testing sequencing strategies to optimize treatment algorithms.
520 ## - SUMMARY, ETC.
Abstract Patients and methods: We conducted a multicenter, retrospective analysis of CLL patients treated with kinase inhibitors (KIs) or venetoclax. We examined demographics, discontinuation reasons, overall response rates (ORR), survival, and post-KI salvage strategies. Primary endpoint was progression-free survival (PFS).
520 ## - SUMMARY, ETC.
Abstract Results: A total of 683 patients were identified. Baseline characteristics were similar in the ibrutinib and idelalisib groups. ORR to ibrutinib and idelalisib as first KI was 69% and 81%, respectively. With a median follow-up of 17 months (range 1-60), median PFS and OS for the entire cohort were 35 months and not reached. Patients treated with ibrutinib (versus idelalisib) as first KI had a significantly better PFS in all settings; front-line [hazard ratios (HR) 2.8, CI 1.3-6.3, P = 0.01], relapsed-refractory (HR 2.8, CI 1.9-4.1, P < 0.001), del17p (HR 2.0, CI 1.2-3.4, P = 0.008), and complex karyotype (HR 2.5, CI 1.2-5.2, P = 0.02). At the time of initial KI failure, use of an alternate KI or venetoclax had a superior PFS when compared with chemoimmunotherapy. Furthermore, patients who discontinued ibrutinib due to progression or toxicity had marginally improved outcomes if they received venetoclax (ORR 79%) versus idelalisib (ORR 46%) (PFS HR .6, CI.3-1.0, P = 0.06).
546 ## - LANGUAGE NOTE
Language note English
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Topical term or geographic name entry element *Antineoplastic Combined Chemotherapy Protocols/tu [Therapeutic Use]
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Topical term or geographic name entry element *Leukemia, Lymphocytic, Chronic, B-Cell/dt [Drug Therapy]
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Topical term or geographic name entry element Adult
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Topical term or geographic name entry element Aged
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Topical term or geographic name entry element Aged, 80 and over
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Topical term or geographic name entry element Bridged Bicyclo Compounds, Heterocyclic/ad [Administration & Dosage]
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Topical term or geographic name entry element Disease-Free Survival
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Topical term or geographic name entry element Drug Administration Schedule
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Topical term or geographic name entry element Humans
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Topical term or geographic name entry element Kaplan-Meier Estimate
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Topical term or geographic name entry element Leukemia, Lymphocytic, Chronic, B-Cell/mo [Mortality]
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Topical term or geographic name entry element Middle Aged
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Topical term or geographic name entry element Proportional Hazards Models
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Topical term or geographic name entry element Purines/ad [Administration & Dosage]
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Topical term or geographic name entry element Pyrazoles/ad [Administration & Dosage]
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Topical term or geographic name entry element Pyrimidines/ad [Administration & Dosage]
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Topical term or geographic name entry element Quinazolinones/ad [Administration & Dosage]
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Retrospective Studies
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Topical term or geographic name entry element Sulfonamides/ad [Administration & Dosage]
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Treatment Outcome
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Young Adult
651 ## - SUBJECT ADDED ENTRY--GEOGRAPHIC NAME
Institution MedStar Washington Hospital Center
656 ## - INDEX TERM--OCCUPATION
Department Hematology/Oncology
657 ## - INDEX TERM--FUNCTION
Medline publication type Journal Article
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Local Authors Cruz, Allan-Louie
790 ## - Authors
All authors Barr PM, Brander DM, Cheson BD, Claxton DF, Cruz AL, Daniel C, Fanning M, Foon K, Gashonia L, Goy A, Henick Bachow S, Hill BT, Howlett C, Isaac K, Kennard KH, Kiselev P, Lamanna N, Lenhart J, Mato AR, Nabhan C, Pu JJ, Schuster SJ, Skarbnik AP, Svoboda J, Timlin C, Ujjani CS, Winter AM, Yacur M, Zent CS
856 ## - ELECTRONIC LOCATION AND ACCESS
DOI <a href="https://dx.doi.org/10.1093/annonc/mdx031">https://dx.doi.org/10.1093/annonc/mdx031</a>
Public note https://dx.doi.org/10.1093/annonc/mdx031
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 05/08/2017   28453705 28453705 05/08/2017 05/08/2017 Journal Article

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