Evidence map›Paper›PMID 32198151›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

Assessment of the Efficacy of Therapies Following Venetoclax Discontinuation in CLL Reveals BTK Inhibition as an Effective Strategy.

Anthony R Mato, Lindsey E Roeker, Ryan Jacobs, Brian T Hill, Nicole Lamanna, Danielle Brander, Mazyar Shadman, Chaitra S Ujjani, Maryam Sarraf Yazdy, Guilherme Fleury Perini and 44 more

Open access · bronzeAbstract readComment
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
10.4field-weighted citation impact, top 1% 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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 113 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Adding Umbralisib and Ublituximab (U2) to Ibrutinib in Patients with CLL: A Phase II Study of an MRD-Driven Approach.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Trial
  5. Venetoclax in Previously Treated Waldenström Macroglobulinemia.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Trial
  6. Trial
  7. Trial
  8. Article
  9. Review
  10. Management of Relapsed and/or Refractory Chronic Lymphocytic Leukemia.Hematology/oncology clinics of North America · 2025
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

54 authors at 20 institutions in 3 countries.

Anthony R Mato *Memorial Sloan Kettering Cancer Center, New York, New York. matoa@mskcc.org.
Lindsey E Roeker *Memorial Sloan Kettering Cancer Center, New York, New York.
Ryan JacobsDepartment of Hematology, Lymphoma Division, Levine Cancer Institute, Charlotte, North Carolina.
Brian T HillDepartment of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic Foundation, Cleveland, Ohio.
Nicole LamannaHerbert Irving Comprehensive Cancer Center (New York-Presbyterian Columbia University Medical Center), New York, New York.
Danielle BranderDuke University Medical Center, Durham, North Carolina.
Mazyar ShadmanFred Hutchinson Cancer Research Center, Seattle, Washington.
Chaitra S UjjaniSeattle Cancer Care Alliance/Fred Hutchinson Cancer Research Center, Seattle, Washington.
Maryam Sarraf YazdyGeorgetown University Hospital Lombardi Comprehensive Cancer Center, Washington D.C.ORCID 0000-0003-2787-3867
Guilherme Fleury PeriniHospital Israelita Albert Einstein, Sao Paulo, Pará, Brazil.
Javier A Pinilla-IbarzDivision of Malignant Hematology, Moffitt Cancer Center, Tampa, Florida.
Jacqueline BarrientosNorth Shore University Hospital, Northwell Health, Manhasset, New York.
Alan P SkarbnikNovant Health, Charlotte, North Carolina.
Pallawi TorkaDepartment of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0002-1681-5883
Jeffrey J PuSUNY Upstate Medical University, Syracuse, New York.ORCID 0000-0001-7498-3159
John M PagelCenter for Blood Disorders and Stem Cell Transplantation, Swedish Cancer Institute, Seattle, Washington.ORCID 0000-0002-2088-0899
Satyen GohilUniversity College London, London, United Kingdom.
Bita FakhriDepartment of Medicine, Division of Hematology/Oncology, University of California San Francisco, San Francisco, California.ORCID 0000-0002-2124-7243
Michael ChoiMoores Cancer Center, University of California San Diego, La Jolla, California.
Catherine C CoombsLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.
Joanna RhodesDivision of Hematology and Oncology, Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-5068-9040
Paul M BarrDivision of Hematology/Oncology, Wilmot Cancer Institute, University of Rochester, Rochester, New York.ORCID 0000-0002-9733-401X
Craig A PortellDivision of Hematology and Oncology, University of Virginia, Charlottesville, Virginia.ORCID 0000-0002-9487-8345
Helen ParryInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.ORCID 0000-0002-9707-8167
Christine A GarciaHillman Cancer Pavilion, Division of Hematology and Oncology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
Kate J WhitakerMemorial Sloan Kettering Cancer Center, New York, New York.
Allison M WinterDepartment of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.
Andrea SitlingerHematologic Malignancies and Cellular Therapy, Duke University Medical Center, Durham, North Carolina.ORCID 0000-0002-2231-5527
Sirin KhajavianFred Hutchinson Cancer Research Center, Seattle, Washington.
Ariel F Grajales-CruzDivision of Malignant Hematology, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0003-0999-1771
Krista M IsaacDivision of Hematology and Oncology, University of Virginia, Charlottesville, Virginia.
Pratik ShahNorthwell Health, New York, New York.
Othman S AkhtarRoswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0003-1673-9670
Rachael PocockUniversity of College of London, London, United Kingdom.ORCID 0000-0002-0051-1965
Kentson LamMoores Cancer Center, University of California San Diego, La Jolla, California.
Timothy J VoorheesLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, North Carolina.ORCID 0000-0001-7603-6454
Stephen J SchusterDivision of Hematology and Oncology, Abramson Cancer Center, University of Pennsylvania, Philadelphia, Pennsylvania.
Thomas D RodgersUniversity of Rochester Medical Center, Rochester, New York.ORCID 0000-0002-8937-8231
Christopher P FoxNottingham University Hospitals NHS Trust, Nottingham, United Kingdom.ORCID 0000-0002-6322-9254
Nicolas Martinez-CalleClinical Haematology Department, Nottingham University Hospitals NHS Trust, Nottingham, England, United Kingdom.ORCID 0000-0002-5184-9464
Talha MunirWeill Cornell Medicine, Long Island City, New York.
Erica B BhavsarDepartment of Haematology, St James's University Hospital, Leeds, United Kingdom.
Neil BaileyCenter for Blood Disorders and Stem Cell Transplantation, Swedish Cancer Institute, Seattle, Washington.ORCID 0000-0002-3809-3236
Jason C LeeHerbert Irving Comprehensive Cancer Center (New York-Presbyterian Columbia University Medical Center), New York, New York.
Hanna B WeissbrotHerbert Irving Comprehensive Cancer Center (New York-Presbyterian Columbia University Medical Center), New York, New York.
Chadi NabhanAptitude Health, Atlanta, Georgia.
Julie M GoodfriendMemorial Sloan Kettering Cancer Center, New York, New York.
Amber C KingClinical Pharmacy Specialist-Leukemia, Memorial Sloan Kettering Cancer Center, New York, New York.
Andrew D ZelenetzDepartment of Medicine, Lymphoma Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Colleen DorseyMemorial Sloan Kettering Cancer Center, New York, New York.
Kayla BigelowMemorial Sloan Kettering Cancer Center, New York, New York.
Bruce D ChesonGeorgetown University Hospital Lombardi Comprehensive Cancer Center, Washington D.C.
John N AllanDepartment of Haematology, St James's University Hospital, Leeds, United Kingdom.ORCID 0000-0002-2088-0899
Toby A EyreDepartment of Haematology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.ORCID 0000-0002-6631-9749
Memorial Sloan Kettering Cancer Center · USColumbia University Irving Medical Center · USCleveland Clinic · USFred Hutch Cancer Center · USGeorgetown University · USMoffitt Cancer Center · USNottingham University Hospitals NHS Trust · GBRoswell Park Comprehensive Cancer Center · USSt James's University Hospital · GBSwedish Medical Center · USThe London College · GBUniversity of California San Diego · USUniversity of North Carolina at Chapel Hill · USUniversity of Pennsylvania · USUniversity of Virginia · USChurchill Hospital · GBCornell University · USDuke Medical Center · USDuke University · USGeorgia Department of Public Health · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
UNC Oncology K12K12CA120780 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WILLIAM Y. KIM · 2007 to 2026
$9.6M
NCI NIH HHS K12 CA120780NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeVenetoclax-based therapy is a standard-of-care option in first-line and relapsed/refractory chronic lymphocytic leukemia (CLL). Patient management following venetoclax discontinuation remains nonstandard and poorly understood. EXPERIMENTAL

designTo address this, we conducted a large international study to identify a cohort of 326 patients who discontinued venetoclax and have been subsequently treated. Coprimary endpoints were overall response rate (ORR) and progression-free survival for the post-venetoclax treatments stratified by treatment type [Bruton's tyrosine kinase inhibitor (BTKi), PI3K inhibitor (PI3Ki), and cellular therapies].

resultsWe identified patients with CLL who discontinued venetoclax in the first-line (4%) and relapsed/refractory settings (96%). Patients received a median of three therapies prior to venetoclax; 40% were BTKi naïve (

conclusionsFor BTKi-naïve patients, selection of covalently binding BTKis results in high ORR and durable remissions. For BTKi-exposed patients, covalent BTK inhibition is not effective in the setting of BTKi resistance. PI3Kis following venetoclax do not appear to result in durable remissions. We conclude that BTKi in naïve or previously responsive patients and cellular therapies following venetoclax may be the most effective strategies.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellBridged Bicyclo Compounds, HeterocyclicHumansPhosphatidylinositol 3-KinasesProtein Kinase InhibitorsPyrazolesPyrimidinesSulfonamidesBridged Bicyclo Compounds, HeterocyclicPhosphatidylinositol 3-KinasesProtein Kinase InhibitorsPyrazolesPyrimidinesSulfonamidesvenetoclax

Identifiers

PMID32198151
PMCPMC8588795
OpenAlexW3012414877

What OpenQuestion holds

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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.