Evidence map›Paper›PMID 38826396›Full record

ArticlebioRxiv : the preprint server for biology2024

Timing antigenic escape in multiple myeloma treated with T-cell redirecting immunotherapies.

Marios Papadimitriou, Sungwoo Ahn, Benjamin Diamond, Holly Lee, John McIntyre, Marietta Truger, Michael Durante, Bachisio Ziccheddu, Ola Landgren, Leo Rasche and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Marios PapadimitriouMyeloma Division, University of Miami, Sylvester Comprehensive Cancer Center, Miami, FL, USA.
Sungwoo AhnArnie Charbonneau Cancer Institute, University of Calgary, Calgary, Alberta, Canada.
Benjamin DiamondMyeloma Division, University of Miami, Sylvester Comprehensive Cancer Center, Miami, FL, USA.
Holly LeeArnie Charbonneau Cancer Institute, University of Calgary, Calgary, Alberta, Canada.
John McIntyrePrecision Oncology Hub Laboratory, Tom Baker Cancer Centre, Calgary, Alberta, Canada.
Marietta TrugerMLL Munich Leukemia Laboratory, Munich, German.
Michael DuranteMyeloma Division, University of Miami, Sylvester Comprehensive Cancer Center, Miami, FL, USA.
Bachisio ZicchedduMyeloma Division, University of Miami, Sylvester Comprehensive Cancer Center, Miami, FL, USA.
Ola LandgrenMyeloma Division, University of Miami, Sylvester Comprehensive Cancer Center, Miami, FL, USA.
Leo RascheDepartment of Internal Medicine, University Hospital of Wu rzburg, Wu rzburg, Germany.
Nizar J BahlisArnie Charbonneau Cancer Institute, University of Calgary, Calgary, Alberta, Canada.
Paola NeriArnie Charbonneau Cancer Institute, University of Calgary, Calgary, Alberta, Canada.
Francesco MauraMyeloma Division, University of Miami, Sylvester Comprehensive Cancer Center, Miami, FL, USA.

Funding

Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Stephen D. Nimer · 2019 to 2026
$24.1M
NCI NIH HHS P30 CA240139
6 · The paper itself

Abstract

Recent data highlight genomic events driving antigen escape as a recurring cause of chimeric antigen receptor T-cell (CAR-T) and bispecific T-cell engager (TCE) resistance in multiple myeloma (MM). Yet, it remains unclear if these events, leading to clonal dominance at progression, result from acquisition under treatment selection or selection of pre-existing undetectable clones. This differentiation gains importance as these immunotherapies progress to earlier lines of treatment, prompting the need for innovative diagnostic testing to detect these events early on. By reconstructing phylogenetic trees and exploring chemotherapy mutational signatures as temporal barcodes in 11 relapsed refractory MM patients with available whole genome sequencing data before and after CART/TCE treatment, we demonstrated that somatic antigen escape mechanisms for BCMA- and GPRC5D-targeting therapies are acquired post-diagnosis, likely during CART/TCE treatment. Longitudinal tracking of these mutations using digital PCR in 4 patients consistently showed that genomic events promoting antigen escape were not detectable during the initial months of therapy but began to emerge nearly 1 year post therapy initiation. This finding reduces the necessity for a diagnostic panel to identify these events before CART/TCE. Instead, it underscores the importance of surveillance and identifying patients at higher risk of acquiring these events.

Indexed as

BCMAbispecific T cell engagerchimeric antigen receptor T-cellgenomicsGPRC5Dimmunotherapymultiple myeloma

Identifiers

PMID38826396
PMCPMC11142165

What OpenQuestion holds

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Registered trials

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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.