ICU sedation, delirium & recovery

Features and outcomes of patients admitted to the intensive care unit (ICU) for chimeric antigen receptor T cell-related toxicity: a French multicentre cohort

Ann Intensive CarePublished Retrospective cohort study

Authors' conclusion

ICU admission is common after CAR-T therapy and is usually performed to manage specific toxicities. Our experience is encouraging, with low ICU mortality despite a high rate of grade 3-4 toxicities, and half of patients being alive and in complete remission at one year.

Study context

Population
Adults admitted to either of two French ICUs in 2018–2022 within 3 months after CAR-T therapy for refractory haematological malignanciesof 238 given CAR-T
Participants
84 adults
Outcome
Clinical features and outcomes of ICU-admitted patients after CAR-T therapy
Methodological detailsobservational, multicentre (two French ICUs), consecutive adults
  • Observational
  • Multicentre (two French ICUs)
  • Consecutive adults

Main finding

As reported in the abstract

Clinical features and outcomes
ICU admission among patients given CAR-T
84 (35.3%)
Time from CAR-T infusion to ICU admission, median [range] days
5 [0-7]
SOFA score, median
3 [2-6]
SAPSII score, median
39 [30-48]
Cytokine release syndrome
80/84 (95.2%)
Cytokine release syndrome grade 3-4
18/80 (22.5%)
ICANS
46/84 (54.8%)
ICANS grade 3-4
29/46 (63%)
Haemophagocytic lymphohistiocytosis
15/84 (17.9%)
Tocilizumab use
73/84 (86.9%)
Tocilizumab doses, median
2 [1-4]
Steroids
55/84 (65.5%)
High-dose pulse steroids
21/55 (38.2%)
Vasopressors
23/84 (27.4%)
Invasive mechanical ventilation
12/84 (14.3%)
Dialysis
4/84 (4.8%)
ICU deaths (incl. 2 after ICU readmission)
4.8%

Observational data: associations, not effects.

Further findings

Status 1 year after CAR-T therapy

Alive and in complete remission
41/84 (48.9%)
Alive and in relapse
14/84 (16.7%)
Died
29/84 (34.5%)
Outcomes similar to patients never admitted to the ICU

Safety

Bacterial infections
23/84 (27.4%)
Fungal infections (1 invasive pulmonary aspergillosis, 2 Mucorales)
3/84 (3.6%)
Cytomegalovirus infection
2 (2.4%)

Original publication

Features and outcomes of patients admitted to the ICU for chimeric antigen receptor T cell-related toxicity: a French multicentre cohort. Ann Intensive Care. Published 31 January 2024. doi:10.1186/s13613-024-01247-9

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