Evidence map›Paper›PMID 37626420›Full record

ReviewJournal of hematology & oncology2023

Beyond Bruton's tyrosine kinase inhibitors in mantle cell lymphoma: bispecific antibodies, antibody-drug conjugates, CAR T-cells, and novel agents.

Neeraj Jain, Mukesh Mamgain, Sayan Mullick Chowdhury, Udita Jindal, Isha Sharma, Lalit Sehgal, Narendranath Epperla

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

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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

7 authors at 5 institutions in 2 countries.

Neeraj JainDivision of Cancer Biology, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh, India.
Mukesh MamgainDepartment of Medical Oncology and Hematology, All India Institute of Medical Sciences, Rishikesh, India.
Sayan Mullick ChowdhuryDivision of Hematology, Department of Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH, USA.
Udita JindalDivision of Cancer Biology, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh, India.
Isha SharmaDivision of Cancer Biology, CSIR-Central Drug Research Institute, Lucknow, Uttar Pradesh, India.
Lalit SehgalDivision of Hematology, Department of Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH, USA.
Narendranath EpperlaThe Ohio State University Comprehensive Cancer Center, Suite 7198, 2121 Kenny Rd, Columbus, OH, 43221, USA. Narendranath.Epperla@osumc.edu.
Central Drug Research Institute · INThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USAcademy of Scientific and Innovative Research · INAll India Institute of Medical Sciences Rishikesh · INThe Ohio State University · US

Funding

Developing novel therapy to improve outcomes in MCLR01CA282483 · NCI · OHIO STATE UNIVERSITY · PI Lalit Sehgal · 2023 to 2026
$1.6M
NCI NIH HHS R01 CA282483
6 · The paper itself

Abstract

Mantle cell lymphoma is a B cell non-Hodgkin lymphoma (NHL), representing 2-6% of all NHLs and characterized by overexpression of cyclin D1. The last decade has seen the development of many novel treatment approaches in MCL, most notably the class of Bruton's tyrosine kinase inhibitors (BTKi). BTKi has shown excellent outcomes for patients with relapsed or refractory MCL and is now being studied in the first-line setting. However, patients eventually progress on BTKi due to the development of resistance. Additionally, there is an alteration in the tumor microenvironment in these patients with varying biological and therapeutic implications. Hence, it is necessary to explore novel therapeutic strategies that can be effective in those who progressed on BTKi or potentially circumvent resistance. In this review, we provide a brief overview of BTKi, then discuss the various mechanisms of BTK resistance including the role of genetic alteration, cancer stem cells, tumor microenvironment, and adaptive reprogramming bypassing the effect of BTK inhibition, and then provide a comprehensive review of current and emerging therapeutic options beyond BTKi including novel agents, CAR T cells, bispecific antibodies, and antibody-drug conjugates.

Indexed as

Antibodies, BispecificImmunoconjugatesLymphoma, Mantle-CellAdultHumansT-LymphocytesTumor MicroenvironmentTyrosine Kinase InhibitorsAntibodies, BispecificImmunoconjugatesTyrosine Kinase InhibitorsAntibody–drug conjugatesBispecific antibodiesBTK inhibitor resistanceCAR T cell therapiesMantle cell lymphoma

Identifiers

PMID37626420
PMCPMC10463717
OpenAlexW4386167518

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.