Evidence map›Paper›PMID 34619768›Full record

ReviewBlood advances2021

Infectious complications of CAR T-cell therapy across novel antigen targets in the first 30 days.

Lekha Mikkilineni, Bonnie Yates, Seth M Steinberg, Shilpa A Shahani, John C Molina, Tara Palmore, Daniel W Lee, Rosandra N Kaplan, Crystal L Mackall, Terry J Fry and 5 more

Open access · goldAbstract readReview
In one paragraph

Review in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
3.9field-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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 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

15 authors at 4 institutions in 3 countries.

Lekha MikkilineniSurgery Branch, National Cancer Institute.
Bonnie YatesPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute.
Seth M SteinbergBiostatistics and Data Management Section, Office of the Clinical Director, Center for Cancer Research, National Cancer Institute, and.
Shilpa A ShahaniPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute.
John C MolinaPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute.ORCID 0000-0003-3142-516X
Tara PalmoreLaboratory of Clinical Immunology and Microbiology Infectious Disease, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
Daniel W LeePediatric Oncology Branch, Center for Cancer Research, National Cancer Institute.ORCID 0000-0002-3249-9796
Rosandra N KaplanPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute.ORCID 0000-0002-8580-0001
Crystal L MackallPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute.ORCID 0000-0003-0359-9023
Terry J FryPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute.ORCID 0000-0001-8044-5226
Juan Gea-BanaclocheDivision of Clinical Research, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD; and.
Theresa JerussiNational Institutes of Health Clinical Center, Bethesda, MD.
Veronique NussenblattLaboratory of Clinical Immunology and Microbiology Infectious Disease, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
James N KochenderferSurgery Branch, National Cancer Institute.
Nirali N ShahPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute.ORCID 0000-0002-8474-9080
Cancer Institute (WIA) · INNational Institutes of Health · USNational Cancer Institute · MYNational Institutes of Health Clinical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infections are a known complication of chimeric antigen receptor (CAR) T-cell therapy with data largely emerging from CD19 CAR T-cell targeting. As CAR T-cell therapy continues to evolve, infection risks and management thereof will become increasingly important to optimize outcomes across the spectrum of antigens and disease targeted. We retrospectively characterized infectious complications occurring in 162 children and adults treated among 5 phase 1 CAR T-cell clinical trials. Trials included targeting of CD19, CD22, disialoganglioside (GD2) or B-cell maturation antigen (BCMA). Fifty-three patients (32.7%) had 76 infections between lymphocyte depleting (LD) chemotherapy and day 30 (D30); with the majority of infections (61, 80.3%) occurring between day 0 (D0) and D30. By trial, the highest proportion of infections was seen with CD22 CAR T cells (n = 23/53; 43.4%), followed by BCMA CAR T cells (n = 9/24; 37.5%). By disease, patients with multiple myeloma had the highest proportion of infections (9/24; 37.5%) followed by acute lymphoblastic leukemia (36/102; 35.3%). Grade 4 infections were rare (n = 4; 2.5%). Between D0 and D30, bacteremia and bacterial site infections were the most common infection type. In univariate analysis, increasing prior lines of therapy, recent infection within 100 days of LD chemotherapy, corticosteroid or tocilizumab use, and fever and neutropenia were associated with a higher risk of infection. In a multivariable analysis, only prior lines of therapy and recent infection were associated with higher risk of infection. In conclusion, we provide a broad overview of infection risk within the first 30 days post infusion across a host of multiple targets and diseases, elucidating both unique characteristics and commonalities highlighting aspects important to improving patient outcomes.

Indexed as

Immunotherapy, AdoptiveMultiple MyelomaAntigens, CD19HumansRetrospective StudiesT-LymphocytesAntigens, CD19

Identifiers

PMID34619768
PMCPMC9153053
OpenAlexW3204393409

What OpenQuestion holds

Textmetadata
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.