Outcome and feasibility of radiotherapy bridging in large B‐cell lymphoma patients receiving CD19 CAR T in the UK

Author:

Kuhnl A.1ORCID,Roddie C.23ORCID,Kirkwood A. A.4,Chaganti S.5,Norman J.6,Lugthart S.7,Osborne W.89,Gibb A.10,Gonzalez Arias C.11,Latif A.12,Uttenthal B.13,Seymour F.14ORCID,Jones C.15,Springell D.2,Brady J. L.16,Illidge T.17,Stevens A.5,Alexander E.11,Hawley L.7,O'Rourke N.12,Bedi C.18,Prestwich R.14ORCID,Frew J.8,Burns D.5,O'Reilly M.2ORCID,Sanderson R.1ORCID,Sivabalasingham S.2,Mikhaeel N. G.16ORCID

Affiliation:

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

2. University College London Hospitals London UK

3. UCL Cancer Institute University College London London UK

4. Cancer Research UK & UCL Cancer Trials Centre UCL Cancer Institute, UCL London UK

5. Queen Elizabeth Hospital Birmingham UK

6. Department of Haematology Manchester Royal Infirmary Manchester UK

7. University Hospitals Bristol and Weston Bristol UK

8. Freeman Hospital Newcastle UK

9. Newcastle University Newcastle UK

10. Department of Medical Oncology The Christie Hospital Manchester UK

11. Royal Marsden Hospital London UK

12. Queen Elizabeth University Hospital Glasgow UK

13. Department of Haematology Addenbrooke's Hospital Cambridge UK

14. St. James's Hospital Leeds UK

15. Department of Haematology University Hospital of Wales Cardiff UK

16. Guy's and St Thomas' NHS Foundation Trust London UK

17. Cancer Sciences University of Manchester Christie NHS Trust, Manchester NIHR BRC Manchester UK

18. Western General Hospital Edinburgh UK

Abstract

SummaryRadiotherapy (RT) has potential synergistic effects with chimeric antigen receptor (CAR) T but is not widely used as bridging therapy due to logistical challenges and lack of standardised protocols. We analysed RT bridging in a multicentre national cohort of large B‐cell lymphoma patients approved for 3L axicabtagene ciloleucel or tisagenlecleucel across 12 UK centres. Of 763 approved patients, 722 were leukapheresed, 717 had data available on bridging therapy. 169/717 (24%) received RT bridging, 129 as single modality and 40 as combined modality treatment (CMT). Of 169 patients, 65.7% had advanced stage, 36.9% bulky disease, 86.5% elevated LDH, 41.7% international prognostic index (IPI) ≥3 and 15.2% double/triple hit at the time of approval. Use of RT bridging varied from 11% to 32% between centres and increased over time. Vein‐to‐vein time and infusion rate did not differ between bridging modalities. RT‐bridged patients had favourable outcomes with 1‐year progression‐free survival (PFS) of 56% for single modality and 47% for CMT (1‐year PFS 43% for systemic bridging). This is the largest cohort of LBCL patients receiving RT bridging prior to CAR T reported to date. Our results show that RT bridging can be safely and effectively used even in advanced stage and high‐risk disease, with low dropout rates and excellent outcomes.

Publisher

Wiley

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