Artigo Revisado por pares

CD19‐DIRECTED CAR T CELL THERAPY (CTL019) FOR RELAPSED/REFRACTORY DIFFUSE LARGE B‐CELL AND FOLLICULAR LYMPHOMAS: FOUR YEAR OUTCOMES

2019; Wiley; Volume: 37; Issue: S2 Linguagem: Inglês

10.1002/hon.96_2629

ISSN

1099-1069

Autores

Elise A. Chong, Jakub Svoboda, Sunita D. Nasta, Daniel J. Landsburg, Nicole Winchell, Emeline R. Chong, David L. Porter, Bruce L. Levine, Carl H. June, Stephen J. Schuster,

Tópico(s)

CAR-T cell therapy research

Resumo

Introduction: Anti-CD19 chimeric antigen receptor-modified T cell therapy (CAR T) is indicated for diffuse large B-cell, high grade B-cell, transformed follicular and primary mediastinal B-cell lymphomas. To date, the longest reported median follow-up is 19 months (mo) for tisagenlecleucel (Schuster et al., Blood 2018) and 24 mo for axicabtagene ciloleucel (Locke et al., Lancet Oncol 2019). We previously reported two-year follow-up for 28 patients (pts) who received CTL019 (Schuster et al., NEJM 2017). We now report our four-year experience with CAR T (CTL019, now tisagenlecleucel). Methods: We enrolled pts with relapsed/refractory CD19+ diffuse large B cell lymphoma (DLBCL) or follicular lymphoma (FL) from February 2014 to September 2017 on a single institution trial of CTL019. Eligible pts had no curative treatment options, prognosis of <2 years survival, and less than complete response to last therapy. Pts underwent leukapheresis, bridging therapy at the investigator's discretion, then lymphodepleting therapy followed by a single dose of 1e8 to 5e8 CTL019 cells. Outcomes were analyzed as of February 25, 2019. Results: Median follow-up is now 49 mos. 49 pts, 24 with DLBCL and 15 with FL, were enrolled. Median age at enrollment was 56 years (range: 25 – 77) and 41% were women. The median number of prior therapies was 5 (range: 2-10). Median ECOG PS was 1 (range: 0-1). 78% had advanced stage lymphoma at enrollment. 38 pts received the protocol-specified dose of CTL019. 46% of DLBCL pts and 71% of FL pts had a complete response (CR). For DLBCL, median progression free survival (PFS) is 5.8 mo (95%CI: 1.6 mo-NE), median overall survival (OS) 22.2 mo (95%CI: 10.9-45.6mo). For FL, median PFS is 32.4 mo (95%CI: 3.5 mo-NE), median OS was not reached (95%CI: 27.2mo-NE). For responding patients with DLBCL or FL, median response duration (RD) was not reached at 49 mo follow-up (DLBCL RD, 95%CI: 3.2 mo-NE; FL RD, 95%CI: 9.5 mo-NE). The patient with the longest follow-up remains in remission from DLBCL (double-hit) at 60 mo after CTL019. Of 21 pts in CR, only 6 received IVIG for recurrent or severe infections and 2 pts developed late myelodysplasia. Four patients relapsed more than 12 months from CTL019 infusion (PFS: 16.3 mo, 26.2 mo, 32.4 mo, 35.2 mo). At the time of these late relapses, CAR T cells persisted by quantitative PCR and there was no loss of CD19 expression by tumor cells. Keywords: diffuse large B-cell lymphoma (DLBCL); follicular lymphoma (FL); T-cells. Disclosures: Chong, E: Consultant Advisory Role: Novartis. Svoboda, J: Consultant Advisory Role: Kite Pharma; Research Funding: Novartis. Nasta, S: Research Funding: Roche, Incyte, Debiopharm, Rafael, Aileron, Takeda/Millennium. Landsburg, D: Consultant Advisory Role: Curis, Celgene; Research Funding: Curis, Takeda, Triphase; Other Remuneration: Seattle Genetics =. Porter, D: Employment Leadership Position: Genentech; Consultant Advisory Role: Novartis, Kite Pharma, Incyte, Glenmark; Stock Ownership: Genentech; Research Funding: Novartis; Other Remuneration: Novartis. Levine, B: Employment Leadership Position: Tmunity Therapeutics; Consultant Advisory Role: CRC Oncology, Cure Genetics, Novartis, Terumo, Avectas, Brammer Bio, Incysus, Vycellix; Other Remuneration: Novartis. June, C: Consultant Advisory Role: Novartis, Immune Design, Viracta, Carisma; Stock Ownership: Tmunity Therapeutics; Research Funding: Novartis; Other Remuneration: Novartis. Schuster, S: Consultant Advisory Role: Pfizer, Nordic Nanovector, Celgene, Gilead, Merck, Novartis, Pharmacyclics, Loxo Oncology, Acerta, AstraZeneca; Research Funding: Acerta, Celgene, Genentech, Gilead, Merck, Novartis, Pharmacyclics; Other Remuneration: Novartis.

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