Intention-to-treat outcomes utilising a stringent event definition in children and young people treated with tisagenlecleucel for r/r ALL through a national access scheme.
Macarena Oporto EspuelasSaskia BurridgeAmy A KirkwoodDenise BonneyKelly WattsGeoff ShentonKatarzyna A JalowiecMaeve A O'ReillyClaire RoddieAnna CastletonKatherine CleshamEmma NicholsonRajesh AlajangiShilpa PrabhuLindsay GeorgeBen UttenthalMaria GabelliLorna NeillCaroline BesleySridhar ChagantiRobert F WynnJack BartramRobert ChiesaGiovanna LucchiniVesna PavasovicAnupama RaoKanchan RaoJuliana SilvaSujith SamarasingheAjay VoraPeter ClarkMichelle CumminsDavid I MarksPersis AmroliaRachael HoughSara GhorashianPublished in: Blood cancer journal (2024)
CAR T-cell therapy has transformed relapsed/refractory (r/r) B-cell precursor acute lymphoblastic leukaemia (B-ALL) management and outcomes, but following CAR T infusion, interventions are often needed. In a UK multicentre study, we retrospectively evaluated tisagenlecleucel outcomes in all eligible patients, analysing overall survival (OS) and event-free survival (EFS) with standard and stringent definitions, the latter including measurable residual disease (MRD) emergence and further anti-leukaemic therapy. Both intention-to-treat and infused cohorts were considered. We collected data on feasibility of delivery, manufacture, toxicity, cause of therapy failure and followed patients until death from any cause. Of 142 eligible patients, 125 received tisagenlecleucel, 115/125 (92%) achieved complete remission (CR/CRi). Severe cytokine release syndrome and neurotoxicity occurred in 16/123 (13%) and 10/123 (8.1%), procedural mortality was 3/126 (2.4%). The 2-year intent to treat OS and EFS were 65.2% (95%CI 57.2-74.2%) and 46.5% (95%CI 37.6-57.6%), 2-year intent to treat stringent EFS was 35.6% (95%CI 28.1-44.9%). Median OS was not reached. Sixty-two responding patients experienced CAR T failure by the stringent event definition. Post failure, 1-year OS and standard EFS were 61.2% (95%CI 49.3-75.8) and 55.3% (95%CI 43.6-70.2). Investigation of CAR T-cell therapy for B-ALL delivered on a country-wide basis, including following patients beyond therapy failure, provides clinicians with robust outcome measures. Previously, outcomes post CAR T-cell therapy failure were under-reported. Our data show that patients can be successfully salvaged in this context with good short-term survival.
Keyphrases
- end stage renal disease
- newly diagnosed
- ejection fraction
- cell therapy
- chronic kidney disease
- prognostic factors
- stem cells
- type diabetes
- mesenchymal stem cells
- patient reported outcomes
- low dose
- intensive care unit
- diffuse large b cell lymphoma
- acute myeloid leukemia
- metabolic syndrome
- young adults
- oxidative stress
- coronary artery disease
- hepatitis b virus
- rheumatoid arthritis
- systemic lupus erythematosus
- case report
- cross sectional
- replacement therapy