Clinical anti-lymphoma effect of T cells expressing an anti-CD19 chimeric antigen receptor in synthetic biology optimizing system.

2020 ◽  
Vol 38 (15_suppl) ◽  
pp. e20021-e20021
Author(s):  
Hong-jiu Dai ◽  
Yanyun Li ◽  
Lan Shi ◽  
Hui Dai ◽  
Yan Li ◽  
...  

e20021 Background: Anti-CD19 chimeric antigen receptor (CAR) T cells for relapse/refractory B-cell malignancies has been remarkably effective in previous clinical trials. However, most of subjects has severe adverse effect even though the infusion of CAR T cells is at the low dose. Herein, we investigated the safety of administering CAR T cells which express the anti-CD19 chimeric antigen receptor in synthetic biology optimizing system. Methods: We designed an anti-CD19 CAR with FMC63 Scfv (KD-019). This CAR has a CD8 hinge and transmembrane domains and a 4-1BB costimulatory domain; T cells expresses CAR in synthetic biology optimizing system. A phase I dose-escalation trial was conducted to investigate the safety of KD-019 CAR T cells and to assess efficacy for patients with previously treated B-cell lymphoma. The patient at the 76 years old received Flu/Cy chemotherapy to enhance CAR T cells activity. Two days after the completion of chemotherapy, about 3 million KD-019 CAR T cells were infused. Results: The patient who has chemotherapy-refractory lymphoma has received KD-019 CAR T cells infusion. Post infusion KD-019 CAR T cells expansion were observed; peak CAR T cells level occurred between Day 3 and 10, and CAR T cells were still detected on Day 243. In addition, we found that CD3+CD8+ T cells level peaked on Day 15. Moreover, after infusion of CAR-T cells, the right peripheral pulmonary lymphaden and visible nodules were respectively shrunk by 53% and 85% on Day 28; and some peripheral pulmonary nodules were obviously reduced and nearly disappeared. We also found that pelvic effusion was significantly reduced, and pain symptoms of the left hip and leg were reduced by 50%. Exhilaratingly, our KD-019 CAR therapy has no obvious cytokine release syndrome (CRS) and central nervous system toxicity. Conclusions: KD-019 CAR T cells express an anti-CD19 chimeric antigen receptor in synthetic biology optimizing system. this innovative KD-019 product can offer significant clinical benefit for NHL patients at the low dose without fever and neurotoxicity. Clinical trial information: NCT03854994. Clinical trial information: NCT03854994 .

2020 ◽  
Vol 12 (567) ◽  
pp. eabf2636
Author(s):  
Bence György

Bispecific CD19/CD20 chimeric antigen receptor T cells show high efficacy in B cell malignancies.


2017 ◽  
Vol 35 (15_suppl) ◽  
pp. TPS7568-TPS7568 ◽  
Author(s):  
Jae Hong Park ◽  
Isabelle Riviere ◽  
Xiuyan Wang ◽  
Brigitte Senechal ◽  
Yvette Bernal ◽  
...  

TPS7568 Background: Despite the recent progress in the therapy of CLL with BTK, PI3Kδ, and BCL2 inhibitors, CLL remains incurable and patients with high-risk disease features (i.e. del17p, complex karyotype) and patients whose disease progress after treatment with the above targeted agents continue to have extremely poor prognosis. CD19-specific chimeric antigen receptor (CAR) T cell therapy with various 2nd generation CARs (19-28z or 19-41BBz) have demonstrated anti-tumor efficacy in CLL but the complete response (CR) rates in CLL have been suboptimal (20-45%) compared to CR rates in ALL (80-90%). The suboptimal activity of the current 2nd generation CAR T cells can be due to the inhibitory tumor microenvironment (TM) of CLL. We believe one approach to over the hostile TM is through the use of CD19-CAR T cells further modified to express a second costimulatory ligand, 4-1BBL. A binding of 4-1BBL to its cognate receptor enhances T cell proliferation, IL-2 secretion, and survival and cytolytic activity of the T cells compared to 19-28z. 19-41BBz and 1928BBz (Zhao Z et al. Cancer Cell 2015;28:415-428). Methods: This phase I dose escalating trial is a single-center clinical trial (MSKCC) to study the safety and efficacy of autologous EGFRt/19-28z/4-1BBL+ CAR T cells in patients with relapsed CLL. Given the concern for potential systemic toxicity the vector includes a "safety switch" in the form of a gene for the expression of truncated form of human epidermal growth factor receptor (EGFRt). Patients with relapsed CLL are eligible for the trial. Patients will receive conditioning chemotherapy of cyclophosphamide followed by escalating doses of CAR T cells (1x105 – 3x106 CAR T cells/kg). The primary endpoint is safety and maximum tolerated doses of the CAR T ells. Secondary objectives include response assessment by iwCLL criteria. The comprehensive treatment algorithms for CRS and neurotoxicity are based on our CAR T cell experience in other studies. The study will begin enrollment in February 2017 and enroll up to 30 patients. Clinical trial information: Pending.


Blood ◽  
2015 ◽  
Vol 126 (23) ◽  
pp. 264-264 ◽  
Author(s):  
Lung-Ji Chang ◽  
Lujia Dong ◽  
Jun Zhu ◽  
Zhitao Ying ◽  
Hao-Hsian Kuo ◽  
...  

Abstract Background: Chemo-resistant, advanced B cell lymphomas with bulky tumor are difficult to treat and often fatal. Recent studies have shown that CD19 chimeric antigen receptor-engineered T (CAR-T) cells can effectively treat B-cell malignancies. However, CAR-T therapy-associated adverse systemic responses including fever, tachycardia, profound hypotension, and respiratory distress, can be life-threatening. The toxicities of CAR-T infusion are directly correlated with tumor burden, disease sites and other complications during treatment. Therefore, highly individualized CAR-T therapy regimen is key to the success of such innovative treatment. Patients and Methods: In this phase I/II multi-center CAR-T therapy trial, we have evaluated 13 patients (pts) with chemo-resistant B cell lymphomas, including 12 advanced diffuse large B cell lymphomas (DLBCL) and 1 Burkitt's lymphoma, average age 37 (range 9-61), stage IIIA/IVB. Twelve of them had bulky tumor and met the criteria of high-risk by the second-line age-adjusted international prognostic index (sAAIPI) and were associated with the following co-morbidities: Aspergillus invasive fungal infection (IFI) pneumonia (2), drug-induced liver injury (2), pleural pericardial cavity effusion (2), hepatitis B (2), diabetes mellitus (1), gastrointestinal hemorrhage (1), deep venous thrombosis (1), and lung tumor argon-helium cryoablation surgery (1). Autologous T cells were apheresis collected and lentivirally transduced with a 4th generation, apoptosis-inducible, safety-engineered CAR: CD19- scFv/CD28/CD137/CD27/CD3ζ-iCasp9 (4SCAR19). All pts received conditioning regimen of cyclophosphamide 250 mg/m2/d x3d, and fludarabine 30 mg/m2/d x3d, followed by 1 to 3 infusions of CAR-T cells in a dose range of 0.45- 4.59 x106 cells/kg per infusion. Results: The lentiviral 4SCAR19 transduction efficiencies were in the range of 5-100%. Patient response did not always correlate with CAR gene transfer efficiencies, but instead, correlated better with the condition of the T cells. Eight pts have achieved complete tumor regression (CR) for 3 to 10 months, with stable CAR DNA copies of 0.1-0.4% in the blood. Three pts achieved dramatic tumor reduction but died from various causes including: intracranial hemorrhage due to low platelet count, pre-existing ureteral obstruction/acute renal failure and cardiopulmonary complications, with or without severe cytokine release syndrome (CRS) at day 29, 28 and 66 after CAR-T infusion, respectively. Two pts died from progressive diseases. Treatment toxicities included CRS with fever over 39o C (9/13), massive hemorrhage of the alimentary tract (1/13) and severe myelo-suppression (3/13), which were correlated with increased plasma cytokines including IL-6 and IFN-γ. The 120 day disease-free survival (DFS) rate is 53% (CI, 36-69%), and the 10 month overall survival probability is 55% (CI, 39-74%). Conclusion and discussion: While 4SCAR19 T cells can relieve severe disease symptoms and obtain dramatic tumor control even in late-stage, highly chemo-resistant, bulky tumor-bearing pts, our studies suggest that in order to obtain favorable and durable clinical outcomes in the late-stage pts, the optimal timing for CAR-T engagement, a highly individualized chemo-regimen, and better clinical management for CRS and pre-existing health conditions are critical. While long-term follow-up and better understanding of the tumor genotype and immunobiology are needed, our study indicates that a highly experienced clinical management team is key to the success of CAR-T therapy for advanced B cell lymphomas. Disclosures Dong: America Yuva Biomed: Consultancy. Kuo:America Yuva Biomed: Employment. Liu:America Yuva Biomed: Employment.


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