Evidence map›Paper›PMID 28077600›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Ibrutinib Therapy Increases T Cell Repertoire Diversity in Patients with Chronic Lymphocytic Leukemia.

Qingsong Yin, Mariela Sivina, Harlan Robins, Erik Yusko, Marissa Vignali, Susan O'Brien, Michael J Keating, Alessandra Ferrajoli, Zeev Estrov, Nitin Jain and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
7.2field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

76 citing papers in PubMed, 109 citations in OpenAlex.

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  6. Phase II Study of Combination Obinutuzumab, Ibrutinib, and Venetoclax in Treatment-Naïve and Relapsed or Refractory Chronic Lymphocytic Leukemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020
    Trial
  7. Trial
  8. Article
  9. Review
  10. Expanded CD16Scientific reports · 2025
    Article
  11. Article
  12. Review
  13. Article
  14. Deciphering tuberculosis: lysosome-centric insights into pathogenesis and therapies.Frontiers in cellular and infection microbiology · 2025
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

16 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Qingsong YinDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77230.
Mariela SivinaDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77230.
Harlan RobinsAdaptive Biotechnologies, Seattle, WA 98102; and.
Erik YuskoAdaptive Biotechnologies, Seattle, WA 98102; and.
Marissa VignaliAdaptive Biotechnologies, Seattle, WA 98102; and.
Susan O'BrienDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77230.
Michael J KeatingDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77230.ORCID 0000-0002-9121-6450
Alessandra FerrajoliDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77230.
Zeev EstrovDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77230.
Nitin JainDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77230.
William G WierdaDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77230.
Jan A BurgerDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77230; jaburger@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USAdaptive Biotechnologies (United States) · USFred Hutch Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Tissue CoreP01CA081534 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KIPPS, THOMAS J · 2000 to 2016
$59.5M
NCI NIH HHS P01 CA081534NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

The Bruton's tyrosine kinase inhibitor ibrutinib is a highly effective, new targeted therapy for chronic lymphocytic leukemia (CLL) that thwarts leukemia cell survival, growth, and tissue homing. The effects of ibrutinib treatment on the T cell compartment, which is clonally expanded and thought to support the growth of malignant B cells in CLL, are not fully characterized. Using next-generation sequencing technology, we characterized the diversity of TCRβ-chains in peripheral blood T cells from 15 CLL patients before and after 1 y of ibrutinib therapy. We noted elevated CD4

Indexed as

AdenineAgedB-LymphocytesCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCytokinesHigh-Throughput Nucleotide SequencingHumansLeukemia, Lymphocytic, Chronic, B-CellPiperidinesProtein-Tyrosine KinasesPyrazolesPyrimidinesAdenineCytokinesibrutinibPiperidinesProtein-Tyrosine KinasesPyrazolesPyrimidines

Identifiers

PMID28077600
PMCPMC5296363
OpenAlexW2580312756

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.