Evidence map›Paper›PMID 36672456›Full record

ArticleCancers2023

Characteristics and Clinical Outcomes of Patients with Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Receiving Ibrutinib for ≥5 Years in the RESONATE-2 Study.

Jennifer A Woyach, Paul M Barr, Thomas J Kipps, Jacqueline C Barrientos, Inhye E Ahn, Paolo Ghia, Vincent Girardi, Emily Hsu, Mandy Jermain, Jan A Burger

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  5. Back from (BTKi) holiday.Blood advances · 2025
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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

10 authors at 8 institutions in 2 countries.

Jennifer A WoyachOhio State University Comprehensive Cancer Center, Columbus, OH 43210, USA.ORCID 0000-0002-3403-9144
Paul M BarrWilmot Cancer Institute, University of Rochester, Rochester, NY 14642, USA.
Thomas J KippsUniversity of California San Diego Moores Cancer Center, San Diego, CA 92037, USA.ORCID 0000-0002-0064-4549
Jacqueline C BarrientosMount Sinai Comprehensive Cancer Center, Miami Beach, FL 33140, USA.
Inhye E AhnLaboratory of Lymphoid Malignancies, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20814, USA.
Paolo GhiaUniversità Vita-Salute San Raffaele and IRCCS Ospedale San Raffaele, 20132 Milan, Italy.
Vincent GirardiPharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
Emily HsuPharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
Mandy JermainPharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
Jan A BurgerUniversity of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
AbbVie (United States) · USMount Sinai Medical Center · USNational Institutes of Health · USThe Ohio State University · USThe University of Texas MD Anderson Cancer Center · USUniversity of California San Diego · USUniversity of Rochester · USVita-Salute San Raffaele University · IT

Funding

Pharmacyclics, an AbbVie Company NA
6 · The paper itself

Abstract

Primary results from the phase 3 RESONATE-2 study demonstrated superior efficacy and tolerability with ibrutinib versus chlorambucil in patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). Here, we describe characteristics and outcomes of patients who received ibrutinib treatment for ≥5 years in RESONATE-2. Patients aged ≥65 years with previously untreated CLL/SLL, without del(17p), were randomly assigned 1:1 to once-daily ibrutinib 420 mg until disease progression/unacceptable toxicity (n = 136) or chlorambucil 0.5−0.8 mg/kg for ≤12 cycles (n = 133). Baseline characteristics in ibrutinib-randomized patients (n = 136) were generally similar between patients on ibrutinib treatment for ≥5 years (n = 79) versus those on treatment for <5 years (n = 57). In patients on ibrutinib treatment for ≥5 years, complete response rates improved over time, reaching 42% by 5 years. Estimated 7-year progression-free survival and overall survival rates were 82% and 94%, respectively. Adverse events (AEs) led to dose reductions in 16/79 patients (20%); these AEs were resolved for 13/16 patients (81%). AEs led to dose holds (≥7 days) in 45/79 patients (57%); these AEs were resolved for 43/45 patients (96%). More than half (58%) of ibrutinib-randomized patients benefitted from ibrutinib treatment for ≥5 years regardless of baseline characteristics. Dose modification resolved AEs for most patients, thereby facilitating continued treatment.

Indexed as

chronic lymphocytic leukemiaibrutiniblong-term outcomes

Identifiers

PMID36672456
PMCPMC9857192
OpenAlexW4316467843

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.