Treatment of adult ALL patients with third-generation CD19-directed CAR T cells: results of a pivotal trial

被引:14
|
作者
Schubert, Maria-Luisa [1 ]
Schmitt, Anita [1 ]
Hueckelhoven-Krauss, Angela [1 ]
Neuber, Brigitte [1 ]
Kunz, Alexander [1 ]
Waldhoff, Philip [1 ]
Vonficht, Dominik [2 ,3 ,4 ,5 ]
Yousefian, Schayan [6 ,7 ,8 ]
Jopp-Saile, Lea [2 ,3 ,4 ,5 ]
Wang, Lei [1 ]
Korell, Felix [1 ]
Keib, Anna [1 ]
Michels, Birgit [1 ]
Haas, Dominik [1 ]
Sauer, Tim [1 ]
Derigs, Patrick [1 ]
Kulozik, Andreas [9 ]
Kunz, Joachim [9 ]
Pavel, Petra [10 ]
Laier, Sascha [10 ]
Wuchter, Patrick [11 ]
Schmier, Johann [12 ]
Bug, Gesine [13 ]
Lang, Fabian [13 ]
Goekbuget, Nicola [13 ]
Casper, Jochen [14 ]
Goerner, Martin [15 ]
Finke, Juergen [16 ]
Neubauer, Andreas [17 ]
Ringhoffer, Mark [18 ]
Wolleschak, Denise [19 ]
Brueggemann, Monika [20 ]
Haas, Simon [2 ,3 ,4 ,6 ,7 ,8 ,21 ,22 ]
Ho, Anthony D. [1 ,21 ,22 ]
Mueller-Tidow, Carsten [1 ,21 ,22 ]
Dreger, Peter [1 ,21 ,22 ]
Schmitt, Michael [1 ,21 ,22 ]
机构
[1] Univ Hosp Heidelberg, Dept Internal Med 5, Neuenheimer Feld 410, D-69120 Heidelberg, Germany
[2] Heidelberg Inst Stem Cell Technol & Expt Med HI S, Heidelberg, Germany
[3] Deutsch Krebsforschungszentrum DKFZ, Div Stem Cells & Canc, Heidelberg, Germany
[4] DKFZ ZMBH Alliance, Heidelberg, Germany
[5] Heidelberg Univ, Fac Biosci, Heidelberg, Germany
[6] Charite Univ Med Berlin, Berlin Inst Hlth BIH, Berlin, Germany
[7] Max Delbruck Ctr Mol Med Helmholtz Assoc, Berlin Inst Med Syst Biol, Berlin, Germany
[8] Charite, Dept Hematol Oncol & Tumor Immunol, Berlin, Germany
[9] Univ Hosp Heidelberg, Dept Pediat Oncol Hematol & Immunol, Heidelberg, Germany
[10] German Red Cross Blood Serv Baden Wurttemberg Hes, Inst Clin Transfus Med & Cell Therapy IKTZ, Heidelberg, Germany
[11] Heidelberg Univ, Inst Transfus Med & Immunol, Med Fac Mannheim, German Red Cross Blood Serv Baden Wurttemberg Hes, Mannheim, Germany
[12] GRN MVZ Sinsheim, Sinsheim, Germany
[13] Univ Hosp Frankfurt, Dept Internal Med 2, Frankfurt, Germany
[14] Univ Hosp Oldenburg, Dept Hematol & Oncol, Oldenburg, Germany
[15] Hosp Bielefeld, Dept Hematol & Oncol, Bielefeld, Germany
[16] Univ Hosp Freiburg, Dept Internal Med 1, Freiburg, Germany
[17] Univ Hosp Giessen & Marburg, Dept Hematol Oncol & Immunol, Marburg, Germany
[18] Stadtisches Klinikum Karlsruhe, Karlsruhe, Germany
[19] Otto von Guericke Univ, Ctr Internal Med, Dept Hematol & Oncol, Med Ctr, Magdeburg, Germany
[20] Univ Hosp Kiel, Dept Internal Med 2, Kiel, Germany
[21] German Canc Consortium DKTK, Heidelberg, Germany
[22] German Canc Res Ctr, Natl Ctr Tumor Dis NCT, Heidelberg, Germany
关键词
Acute lymphoblastic leukemia (ALL); Third-generation chimeric antigen receptor (CAR) T cells; Investigator-initiated trial (IIT); CART-associated toxicities; Cytokine release syndrome (CRS); Cytopenia; Immune effector cell-associated neurotoxicity syndrome (ICANS); CD39; ACUTE LYMPHOBLASTIC-LEUKEMIA; B-CELL; CD28; COSTIMULATION; RECEPTORS; EFFICACY; SAFETY; CD8(+); 4-1BB; BLINATUMOMAB; PERSISTENCE;
D O I
10.1186/s13045-023-01470-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThird-generation chimeric antigen receptor (CAR)-engineered T cells (CARTs) might improve clinical outcome of patients with B cell malignancies. This is the first report on a third-generation CART dose-escalating, phase-1/2 investigator-initiated trial treating adult patients with refractory and/or relapsed (r/r) acute lymphoblastic leukemia (ALL).MethodsThirteen patients were treated with escalating doses of CD19-directed CARTs between 1 x 106 and 50 x 106 CARTs/m2. Leukapheresis, manufacturing and administration of CARTs were performed in-house.ResultsFor all patients, CART manufacturing was feasible. None of the patients developed any grade of Immune effector cell-associated neurotoxicity syndrome (ICANS) or a higher-grade (>= grade III) catokine release syndrome (CRS). CART expansion and long-term CART persistence were evident in the peripheral blood (PB) of evaluable patients. At end of study on day 90 after CARTs, ten patients were evaluable for response: Eight patients (80%) achieved a complete remission (CR), including five patients (50%) with minimal residual disease (MRD)-negative CR. Response and outcome were associated with the administered CART dose. At 1-year follow-up, median overall survival was not reached and progression-free survival (PFS) was 38%. Median PFS was reached on day 120. Lack of CD39-expression on memory-like T cells was more frequent in CART products of responders when compared to CART products of non-responders. After CART administration, higher CD8 + and gamma delta-T cell frequencies, a physiological pattern of immune cells and lower monocyte counts in the PB were associated with response.ConclusionIn conclusion, third-generation CARTs were associated with promising clinical efficacy and remarkably low procedure-specific toxicity, thereby opening new therapeutic perspectives for patients with r/r ALL.Trial registration This trial was registered at www.clinicaltrials.gov as NCT03676504.ConclusionIn conclusion, third-generation CARTs were associated with promising clinical efficacy and remarkably low procedure-specific toxicity, thereby opening new therapeutic perspectives for patients with r/r ALL.Trial registration This trial was registered at www.clinicaltrials.gov as NCT03676504.
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页数:17
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