CAR T in patients with large B‐cell lymphoma not fit for autologous transplant

Author:

Kuhnl A.1ORCID,Kirkwood A. A.2,Roddie C.34ORCID,Menne T.5ORCID,Tholouli E.6,Bloor A.7ORCID,Besley C.8,Chaganti S.9,Osborne W.5,Norman J.6,Gibb A.7,Sharplin K.8,Cuadrado M.1,Correia de Farias M.1,Cheok K.3,Neill L.3,Latif A. L.10,González Arias C.11,Uttenthal B.12,Jones C.13,Johnson R.14ORCID,McMillan A.15,Sanderson R.1ORCID,Townsend W.3

Affiliation:

1. Department of Haematology King's College Hospital London UK

2. Cancer Research UK & UCL Cancer Trials Centre UCL Cancer Institute, University College London London UK

3. Department of Haematology University College London Hospitals London UK

4. UCL Cancer Institute University College London London UK

5. Department of Haematology Freeman Hospital Newcastle UK

6. Department of Haematology Manchester Royal Infirmary Manchester UK

7. Department of Haematology The Christie Hospital Manchester UK

8. Department of Haematology University Hospitals Bristol and Weston Bristol UK

9. Department of Haematology Queen Elizabeth Hospital Birmingham UK

10. Department of Haematology Queen Elizabeth II Hospital Glasgow UK

11. Department of Haematology Royal Marsden Hospital London UK

12. Department of Haematology Addenbrooke's Hospital Cambridge UK

13. Department of Haematology University Hospital of Wales Cardiff UK

14. Department of Haematology St. James's Hospital Leeds UK

15. Department of Haematology Nottingham University Hospitals Nottingham UK

Abstract

SummaryLarge B‐cell lymphoma (LBCL) patients with comorbidities and/or advanced age are increasingly considered for treatment with CD19 CAR T, but data on the clinical benefit of CAR T in the less fit patient population are still limited. We analysed outcomes of consecutive patients approved for treatment with axicabtagene ciloleucel (axi‐cel) or tisagenlecleucel (tisa‐cel) by the UK National CAR T Clinical Panel, according to fitness for autologous stem cell transplant (ASCT). 81/404 (20%) of approved patients were deemed unfit for ASCT. Unfit patients were more likely to receive tisa‐cel versus axi‐cel (52% vs. 48%) compared to 20% versus 80% in ASCT‐fit patients; p < 0.0001. The drop‐out rate from approval to infusion was significantly higher in the ASCT‐unfit group (34.6% vs. 23.5%; p = 0.042). Among infused patients, response rate, progression‐free and overall survival were similar in both cohorts. CAR T was well‐tolerated in ASCT‐unfit patients with an incidence of grade ≥3 cytokine release syndrome and neurotoxicity of 2% and 11%, respectively. Results from this multicentre real‐world cohort demonstrate that CD19 CAR T can be safely delivered in carefully selected older patients and patients with comorbidities who are not deemed suitable for transplant.

Publisher

Wiley

Subject

Hematology

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