Evidence map›Paper›PMID 41676895›Full record

ArticleHaematologica2026

ICANS mitigation in high-risk elderly patients treated with CD28 co-stimulatory anti-CD19 CAR-T cells using a standardization protocol: a pilot study.

Gil Fridberg, Odelia Amit, Yehonathan Sherf, Chava Perry, Yair Herishanu, Erel Joffe, Tamir Shragai, Roy Vitkon, Meir Preis, Shoshan Perk and 6 more

Abstract read
In one paragraph

Article in Haematologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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

16 authors.

Gil FridbergBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center; Gray Faculty of Medical and Health Sciences, Aviv University, Aviv. gilfr@tlvmc.gov.il.
Odelia AmitBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center; Gray Faculty of Medical and Health Sciences, Aviv University, Aviv.
Yehonathan SherfHematology Department, Soroka University Medical Center, Affiliated with Ben Gurion University of the Negev, Beer Sheva.
Chava PerryBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center; Gray Faculty of Medical and Health Sciences, Aviv University, Aviv.
Yair HerishanuBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center; Gray Faculty of Medical and Health Sciences, Aviv University, Aviv.
Erel JoffeBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center; Gray Faculty of Medical and Health Sciences, Aviv University, Aviv.
Tamir ShragaiBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center; Gray Faculty of Medical and Health Sciences, Aviv University, Aviv.
Roy VitkonBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center; Gray Faculty of Medical and Health Sciences, Aviv University, Aviv.
Meir PreisInstitute of Hematology, Lady Davis Carmel Medical Center, Haifa.
Shoshan PerkInstitute of Hematology, Lady Davis Carmel Medical Center, Haifa.
Nadav SaridDepartment of Hematology, The Edith Wolfson Medical Center, Holon, Israel; Gray Faculty of Medical and Health Sciences, Aviv University, Aviv.
Sharon Ben BarouchInstitute of Hematology, Assuta Ashdod Medical Center.
Ronit GoldBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center.
Chen Glait-SantarBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center.
Irit AviviBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center; Gray Faculty of Medical and Health Sciences, Aviv University, Aviv.
Ron RamBMT and Cellular Therapy Unit, Hematology Division, Aviv Sourasky Medical Center; Gray Faculty of Medical and Health Sciences, Aviv University, Aviv.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T-cell therapy (CAR-T) has transformed the treatment of relapsed/refractory large B-cell lymphoma (LBCL), with CD28-based products yielding rapid responses but higher rates of immune effector cell-associated neurotoxicity syndrome (ICANS). With axicabtagene-ciloleucel and brexucabtagene-autoleucel, overall and severe ICANS reach 78% and 35%, respectively. Older adults are vulnerable, yet mitigation strategies are still lacking. To address this critical gap, we aimed to develop and implement a standardized ICANS mitigation protocol for older adults receiving CD28-based anti- CD19 CAR-T. We conducted a single-arm prospective pilot study in patients ≥75 or ≥65 years with additional risk factor receiving CD28-based CAR-T. The protocol included levetiracetam and thiamine prophylaxis, early grade-based corticosteroids and anakinra for grade ≥3 and refractory ICANS, which was defined as no improvement within 24 hours. Endpoints were ICANS duration, refractoriness, response, and toxicity. Forty-five patients met eligibility criteria. Median age was 75 years (range: 65-86 years); 78% had Eastern Cooperative Oncology Group (ECOG) ≥2 and 42% had neurologic comorbidity. Grade ≥3 and refractory ICANS developed in 67% overall, with grade ≥3 in 31%, and refractory ICANS in 20%. Median ICANS duration was four days, which was shorter than previous cohorts. Disease and patients' characteristics did not predict ICANS metrics, excluding lactate dehydrogenase which showed a trend for severe ICANS (P=0.07). modified Endothelial Activation and Stress Index (mEASIX) and ICANS-Prognostic Scoring System (PSS) scores were not predictive and expansion was not compromised. Cumulative steroids associated with infections (P=0.002) and non-relapse mortality (P<0.0001). Sixmonth progression-free survival and overall survival were 46% and 59%, respectively. In this high-risk cohort, the ICANS mitigation protocol using anakinra in a graded approach (vs. prophylaxis or salvage therapy) and a pragmatic definition of refractory disease was associated with shorter ICANS duration, despite severe event rates. Steroid-related toxicity remains a concern, and future efforts should focus on steroid-sparing mitigation to optimize outcomes in older adults undergoing CAR-T.

Indexed as

Antigens, CD19Immunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseNeurotoxicity SyndromesReceptors, Chimeric AntigenAgedAged, 80 and overFemaleHumansMalePilot ProjectsProspective StudiesTreatment OutcomeAntigens, CD19Receptors, Chimeric Antigen

Identifiers

PMID41676895
PMCPMC13482263

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.