Evidence map›Paper›PMID 37296940›Full record

ArticleCancers2023

Results from a Phase 1b/2 Study of Ibrutinib Combination Therapy in Advanced Urothelial Carcinoma.

Nataliya Mar, Yousef Zakharia, Alejandro Falcon, Rafael Morales-Barrera, Begona Mellado, Ignacio Duran, Do-Youn Oh, Stephen K Williamson, Pablo Gajate, Hendrik-Tobias Arkenau and 9 more

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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

19 authors at 14 institutions in 4 countries.

Nataliya MarDivision of Hematology/Oncology, University of California Irvine, Orange, CA 92868, USA.
Yousef ZakhariaDivision of Hematology/Oncology, University of Iowa Hospitals and Clinics, Iowa City, IA 52242, USA.ORCID 0000-0001-9480-2626
Alejandro FalconHospital Universitario Virgen del Rocío, 41013 Seville, Spain.
Rafael Morales-BarreraVall d'Hebron Institute of Oncology, Vall d'Hebron University Hospital, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.ORCID 0000-0001-7398-0685
Begona MelladoMedical Oncology Department, Hospital Clínic i Provincial de Barcelona, Institut D'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), University of Barcelona, 08036 Barcelona, Spain.ORCID 0000-0002-8088-5966
Ignacio DuranHospital Universitario Marqués de Valdecilla, Instituto de Investigación Valdecilla (IDIVAL), 39011 Santander, Spain.
Do-Youn OhSeoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Seoul National University Graduate School, Seoul 03080, Republic of Korea.
Stephen K WilliamsonUniversity of Kansas Hospital Cancer Center, Kansas City, KS 64114, USA.ORCID 0000-0003-4118-1242
Pablo GajateHospital Universitario Ramón y Cajal, 28034 Madrid, Spain.ORCID 0000-0001-5156-7080
Hendrik-Tobias ArkenauSarah Cannon Research Institute United Kingdom (SCRI-UK) and University College London Cancer Institute, London W1G 6AD, UK.ORCID 0000-0002-2015-1549
Robert J JonesBeatson West of Scotland Cancer Centre, University of Glasgow, Glasgow G12 0YN, UK.ORCID 0000-0002-2904-6980
Min Yuen TeoGenitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0003-2511-6731
Tolga TuranPharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
Robert T McLaughlinPharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
Hillary M PeltierPharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.ORCID 0000-0002-9732-5068
Elizabeth ChongPharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
Harisha AtluriPharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
James P DeanPharmacyclics LLC, an AbbVie Company, South San Francisco, CA 94080, USA.
Daniel CastellanoHospital Universitario 12 de Octubre, 28041 Madrid, Spain.
AbbVie (United States) · USBeatson West of Scotland Cancer Centre · GBConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESHospital Universitario 12 De Octubre · ESHospital Universitario Ramón y Cajal · ESHospital Universitario Virgen del Rocío · ESInstituto de Investigación Marqués de Valdecilla · ESMemorial Sloan Kettering Cancer Center · USSarah Cannon Research Institute · GBSeoul National University Hospital · KRThe University of Kansas Health System · USUniversitat Autònoma de Barcelona · ESUniversity of California, Irvine · USUniversity of Iowa Hospitals and Clinics · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Ibrutinib is a first-in-class Bruton's tyrosine kinase inhibitor approved for the treatment of various B-cell malignancies and chronic graft-versus-host disease. We evaluated the safety and efficacy of ibrutinib, alone or combined with standard-of-care regimens, in adults with advanced urothelial carcinoma (UC). Once-daily ibrutinib was administered orally at 840 mg (single-agent or with paclitaxel) or at 560 mg (with pembrolizumab). Phase 1b determined the recommended phase 2 dose (RP2D) of ibrutinib, and phase 2 assessed progression-free survival (PFS), overall response rate (ORR), and safety. Thirty-five, eighteen, and fifty-nine patients received ibrutinib, ibrutinib plus pembrolizumab, and ibrutinib plus paclitaxel at the RP2D, respectively. Safety profiles were consistent with those of the individual agents. The best-confirmed ORRs were 7% (two partial responses) with single-agent ibrutinib and 36% (five partial responses) with ibrutinib plus pembrolizumab. Median PFS was 4.1 months (range, 1.0-37.4+) with ibrutinib plus paclitaxel. The best-confirmed ORR was 26% (two complete responses). In previously treated patients with UC, ORR was higher with ibrutinib plus pembrolizumab than with either agent alone (historical data in the intent-to-treat population). ORR with ibrutinib plus paclitaxel was greater than historical values for single-agent paclitaxel or ibrutinib. These data warrant further evaluation of ibrutinib combinations in UC.

Indexed as

ibrutinibpaclitaxelpembrolizumaburothelial carcinoma

Identifiers

PMID37296940
PMCPMC10251876
OpenAlexW4378882771

What Socratic 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 Socratic graph.