Lymphoma Remissions Caused by Anti-CD19 Chimeric Antigen Receptor T Cells Are Associated With High Serum Interleukin-15 Levels

被引:451
作者
Kochenderfer, James N. [1 ]
Somerville, Robert P. T. [1 ]
Lu, Tangying [1 ]
Shi, Victoria [1 ]
Bot, Adrian [2 ]
Rossi, John [2 ]
Xue, Allen [2 ]
Goff, Stephanie L. [1 ]
Yang, James C. [1 ]
Sherry, Richard M. [1 ]
Klebanoff, Christopher A. [1 ]
Kammula, Udai S. [1 ]
Sherman, Marika [2 ]
Perez, Arianne [2 ]
Yuan, Constance M. [1 ]
Feldman, Tatyana [3 ]
Friedberg, Jonathan W. [4 ]
Roschewski, Mark J. [1 ]
Feldman, Steven A. [1 ]
McIntyre, Lori [1 ]
Toomey, Mary Ann [1 ]
Rosenberg, Steven A. [1 ]
机构
[1] NCI, NIH, Bethesda, MD 20892 USA
[2] Kite Pharma, Santa Monica, CA USA
[3] Hackensack Univ, John Theurer Canc Ctr, Med Ctr, Hackensack, NJ USA
[4] Univ Rochester, Sch Med, Rochester, NY USA
基金
美国国家卫生研究院;
关键词
B-CELL; ADOPTIVE IMMUNOTHERAPY; TRANSPLANTATION; THERAPY; CANCER; CD19; MALIGNANCIES; LYMPHOCYTES; EXPANSION; LEUKEMIA;
D O I
10.1200/JCO.2016.71.3024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeT cells genetically modified to express chimeric antigen receptors (CARs) targeting CD19 (CAR-19) have potent activity against acute lymphoblastic leukemia, but fewer results supporting treatment of lymphoma with CAR-19 T cells have been published. Patients with lymphoma that is chemotherapy refractory or relapsed after autologous stem-cell transplantation have a grim prognosis, and new treatments for these patients are clearly needed. Chemotherapy administered before adoptive T-cell transfer has been shown to enhance the antimalignancy activity of adoptively transferred T cells.Patients and MethodsWe treated 22 patients with advanced-stage lymphoma in a clinical trial of CAR-19 T cells preceded by low-dose chemotherapy. Nineteen patients had diffuse large B-cell lymphoma, two patients had follicular lymphoma, and one patient had mantle cell lymphoma. Patients received a single dose of CAR-19 T cells 2 days after a low-dose chemotherapy conditioning regimen of cyclophosphamide plus fludarabine.ResultsThe overall remission rate was 73% with 55% complete remissions and 18% partial remissions. Eleven of 12 complete remissions are ongoing. Fifty-five percent of patients had grade 3 or 4 neurologic toxicities that completely resolved. The low-dose chemotherapy conditioning regimen depleted blood lymphocytes and increased serum interleukin-15 (IL-15). Patients who achieved a remission had a median peak blood CAR(+) cell level of 98/L and those who did not achieve a remission had a median peak blood CAR(+) cell level of 15/L (P = .027). High serum IL-15 levels were associated with high peak blood CAR(+) cell levels (P = .001) and remissions of lymphoma (P < .001).ConclusionCAR-19 T cells preceded by low-dose chemotherapy induced remission of advanced-stage lymphoma, and high serum IL-15 levels were associated with the effectiveness of this treatment regimen. CAR-19 T cells will likely become an important treatment for patients with relapsed lymphoma.
引用
收藏
页码:1803 / 1813
页数:13
相关论文
共 53 条
[41]   IL-10: Master Switch from Tumor-Promoting Inflammation to Antitumor Immunity [J].
Oft, Martin .
CANCER IMMUNOLOGY RESEARCH, 2014, 2 (03) :194-199
[42]   IL15 and T-cell Stemness in T-cell-Based Cancer Immunotherapy [J].
Pilipow, Karolina ;
Roberto, Alessandra ;
Roederer, Mario ;
Waldmann, Thomas A. ;
Mavilio, Domenico ;
Lugli, Enrico .
CANCER RESEARCH, 2015, 75 (24) :5187-5193
[43]   Chimeric Antigen Receptor-Modified T Cells in Chronic Lymphoid Leukemia [J].
Porter, David L. ;
Levine, Bruce L. ;
Kalos, Michael ;
Bagg, Adam ;
June, Carl H. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (08) :725-733
[44]   Failed adoptive immunotherapy with tumor-specifle T cells: Reversal with low-dose interleukin 15 but not low-dose interleukin 2 [J].
Roychowdhury, S ;
May, KF ;
Tzou, KS ;
Lin, T ;
Bhatt, D ;
Freud, AG ;
Guimond, M ;
Ferketich, AK ;
Liu, Y ;
Caligiuri, MA .
CANCER RESEARCH, 2004, 64 (21) :8062-8067
[45]   CAR therapy: the CD19 paradigm [J].
Sadelain, Michel .
JOURNAL OF CLINICAL INVESTIGATION, 2015, 125 (09) :3392-3400
[46]   Two subsets of memory T lymphocytes with distinct homing potentials and effector functions [J].
Sallusto, F ;
Lenig, D ;
Förster, R ;
Lipp, M ;
Lanzavecchia, A .
NATURE, 1999, 401 (6754) :708-712
[47]   CD28 costimulation improves expansion and persistence of chimeric antigen receptor-modified T cells in lymphoma patients [J].
Savoldo, Barbara ;
Ramos, Carlos Almeida ;
Liu, Enli ;
Mims, Martha P. ;
Keating, Michael J. ;
Carrum, George ;
Kamble, Rammurti T. ;
Bollard, Catherine M. ;
Gee, Adrian P. ;
Mei, Zhuyong ;
Liu, Hao ;
Grilley, Bambi ;
Rooney, Cliona M. ;
Heslop, Helen E. ;
Brenner, Malcolm K. ;
Dotti, Gianpietro .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (05) :1822-1826
[48]   Immunotherapy of non-Hodgkin's lymphoma with a defined ratio of CD8+ and CD4+ CD19-specific chimeric antigen receptor-modified T cells [J].
Turtle, Cameron J. ;
Hanafi, Laila-Aicha ;
Berger, Carolina ;
Hudecek, Michael ;
Pender, Barbara ;
Robinson, Emily ;
Hawkins, Reed ;
Chaney, Colette ;
Cherian, Sindhu ;
Chen, Xueyan ;
Soma, Lorinda ;
Wood, Brent ;
Li, Daniel ;
Heimfeld, Shelly ;
Riddell, Stanley R. ;
Maloney, David G. .
SCIENCE TRANSLATIONAL MEDICINE, 2016, 8 (355)
[49]   CD19 CAR-T cells of defined CD4+: CD8+ composition in adult B cell ALL patients [J].
Turtle, Cameron J. ;
Hanafi, Laila-Aicha ;
Berger, Carolina ;
Gooley, Theodore A. ;
Cherian, Sindhu ;
Hudecek, Michael ;
Sommermeyer, Daniel ;
Melville, Katherine ;
Pender, Barbara ;
Budiarto, Tanya M. ;
Robinson, Emily ;
Steevens, Natalia N. ;
Chaney, Colette ;
Soma, Lorinda ;
Chen, Xueyan ;
Yeung, Cecilia ;
Wood, Brent ;
Li, Daniel ;
Cao, Jianhong ;
Heimfeld, Shelly ;
Jensen, Michael C. ;
Riddell, Stanley R. ;
Maloney, David G. .
JOURNAL OF CLINICAL INVESTIGATION, 2016, 126 (06) :2123-2138
[50]  
VOSE JM, 1992, BLOOD, V80, P2142