Evidence map›Paper›PMID 35196370›Full record

ArticleBlood2022

Fixed-duration ibrutinib plus venetoclax for first-line treatment of CLL: primary analysis of the CAPTIVATE FD cohort.

Constantine S Tam, John N Allan, Tanya Siddiqi, Thomas J Kipps, Ryan Jacobs, Stephen Opat, Paul M Barr, Alessandra Tedeschi, Livio Trentin, Rajat Bannerji and 10 more

2 registry-linked trialsOpen access · hybridAbstract read
In one paragraph

Article in Blood, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 140 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 1 pooled it
31.1field-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.

NCT02910583 phase2completednot on this map

Phase 2 Study of the Combination of Ibrutinib Plus Venetoclax in Subjects With Treatment-naïve Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

TypeinterventionalSponsorPharmacyclics LLC.Ran2016 to 2024Enrolled323ConditionsLeukemia, Chronic Lymphocytic Leukemia, Small Lymphocytic LymphomaArmsibrutinib, venetoclax, Placebo
NCT07682415 phase2not yet recruitingnot on this mapstarted 2026, after this paper: background citation

A Single-arm, Multicenter, Prospective Phase II Clinical Trial of Delayed Fixed-duration Combination With Sotoraclax Following Zanubrutinib Induction in Patients With CLL/SLL: Stop Trial 2.0

TypeinterventionalSponsorYi ShuhuaRan2026 to 2034Enrolled60ConditionsCLL / SLLArms12 cycles of zanubrutinib followed by 12 cycles of zanubrutinib in combination with sonrotoclax, zanubrutinib maintenance until disease progression
3 · Its place in the literature

Who cites it

140 citing papers in PubMed, 1 synthesis or guideline pooled it, 223 citations in OpenAlex.

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  10. Protein Profiles Predict Treatment Responses to the PI3K Inhibitor Umbralisib in Patients with Chronic Lymphocytic Leukemia.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
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80 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 16 institutions in 5 countries.

Constantine S TamPeter MacCallum Cancer Center, Melbourne, VIC, Australia.ORCID 0000-0002-9759-5017
John N AllanWeill Cornell Medicine, New York, NY.ORCID 0000-0002-2088-0899
Tanya SiddiqiCity of Hope National Medical Center, Duarte, CA.ORCID 0000-0001-5292-8298
Thomas J KippsMoores Cancer Center, University of California San Diego, San Diego, CA.
Ryan JacobsLevine Cancer Institute, Charlotte, NC.
Stephen OpatMonash University, Clayton, VIC, Australia.
Paul M BarrWilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY.ORCID 0000-0002-9733-401X
Alessandra TedeschiASST Grande Ospedale Metropolitano Niguarda, Milan, Italy.
Livio TrentinUniversity of Padova, Padova, Italy.ORCID 0000-0003-1222-6149
Rajat BannerjiRutgers Cancer Institute of New Jersey, New Brunswick, NJ.
Sharon JacksonMiddlemore Hospital, Auckland, New Zealand.ORCID 0000-0003-3584-8872
Bryone J KussFlinders University and Medical Center, Bedford Park, SA, Australia.
Carol MorenoHospital de la Santa Creu i Sant Pau, Autonomous University of Barcelona, Barcelona, Spain.
Edith Szafer-GlusmanPharmacyclics LLC, an AbbVie Company, Sunnyvale, CA.
Kristin RussellPharmacyclics LLC, an AbbVie Company, Sunnyvale, CA.
Cathy ZhouPharmacyclics LLC, an AbbVie Company, Sunnyvale, CA.
Joi NinomotoPharmacyclics LLC, an AbbVie Company, Sunnyvale, CA.
James P DeanPharmacyclics LLC, an AbbVie Company, Sunnyvale, CA.
William G WierdaDepartment of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX.
Paolo GhiaUniversità Vita-Salute San Raffaele, Milan, Italy; and.ORCID 0000-0003-3750-7342
AbbVie (United States) · USAzienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · ITCity Of Hope National Medical Center · USCornell University · USFlinders University · AULevine Cancer Institute · USMiddlemore Hospital · NZMonash University · AURutgers, The State University of New Jersey · USThe University of Melbourne · AUThe University of Texas MD Anderson Cancer Center · USUniversitat Autònoma de Barcelona · ESUniversity of California San Diego · USUniversity of Padua · ITUniversity of Rochester Medical Center · USVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CAPTIVATE (NCT02910583) is an international phase 2 study in patients aged ≤70 years with previously untreated chronic lymphocytic leukemia (CLL). Results from the cohort investigating fixed-duration (FD) treatment with ibrutinib plus venetoclax are reported. Patients received 3 cycles of ibrutinib lead-in then 12 cycles of ibrutinib plus venetoclax (oral ibrutinib [420 mg/d]; oral venetoclax [5-week ramp-up to 400 mg/d]). The primary endpoint was complete response (CR) rate. Hypothesis testing was performed for patients without del(17p) with prespecified analyses in all treated patients. Secondary endpoints included undetectable minimal residual disease (uMRD) rates, progression-free survival (PFS), overall survival (OS), and safety. Of the 159 patients enrolled and treated, 136 were without del(17p). The median time on study was 27.9 months, and 92% of patients completed all planned treatment. The primary endpoint was met, with a CR rate of 56% (95% confidence interval [CI], 48-64) in patients without del(17p), significantly higher than the prespecified 37% minimum rate (P < .0001). In the all-treated population, CR rate was 55% (95% CI, 48-63); best uMRD rates were 77% (peripheral blood [PB]) and 60% (bone marrow [BM]); 24-month PFS and OS rates were 95% and 98%, respectively. At baseline, 21% of patients were in the high tumor burden category for tumor lysis syndrome (TLS) risk; after ibrutinib lead-in, only 1% remained in this category. The most common grade ≥3 adverse events (AEs) were neutropenia (33%) and hypertension (6%). First-line ibrutinib plus venetoclax represents the first all-oral, once-daily, chemotherapy-free FD regimen for patients with CLL. FD ibrutinib plus venetoclax achieved deep, durable responses and promising PFS, including in patients with high-risk features.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellAdenineAntineoplastic Combined Chemotherapy ProtocolsBridged Bicyclo Compounds, HeterocyclicHumansNeoplasm, ResidualPiperidinesSulfonamidesAdenineBridged Bicyclo Compounds, HeterocyclicibrutinibPiperidinesSulfonamidesvenetoclax

Identifiers

PMID35196370
PMCPMC11022982
OpenAlexW4213453359

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.