Kochenderfer James N, Somerville Robert P T, Lu Tangying, Shi Victoria, Bot Adrian, Rossi John, Xue Allen, Goff Stephanie L, Yang James C, Sherry Richard M, Klebanoff Christopher A, Kammula Udai S, Sherman Marika, Perez Arianne, Yuan Constance M, Feldman Tatyana, Friedberg Jonathan W, Roschewski Mark J, Feldman Steven A, McIntyre Lori, Toomey Mary Ann, Rosenberg Steven A
James N. Kochenderfer, Robert P.T. Somerville, Tangying Lu, Victoria Shi, Stephanie L. Goff, James C. Yang, Richard M. Sherry, Christopher A. Klebanoff, Udai S. Kammula, Constance M. Yuan, Mark J. Roschewski, Steven A. Feldman, Lori McIntyre, Mary Ann Toomey, and Steven A. Rosenberg, National Cancer Institute, National Institutes of Health, Bethesda, MD; Adrian Bot, John Rossi, Allen Xue, Marika Sherman, and Arianne Perez, Kite Pharma, Santa Monica, CA; Tatyana Feldman, John Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ; and Jonathan W. Friedberg, University of Rochester School of Medicine, Rochester, NY.
J Clin Oncol. 2017 Jun 1;35(16):1803-1813. doi: 10.1200/JCO.2016.71.3024. Epub 2017 Mar 14.
Purpose T 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 Methods We 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. Results The 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/μL and those who did not achieve a remission had a median peak blood CAR cell level of 15/μL ( P = .027). High serum IL-15 levels were associated with high peak blood CAR cell levels ( P = .001) and remissions of lymphoma ( P < .001). Conclusion CAR-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.
目的 经基因改造以表达靶向CD19的嵌合抗原受体(CAR)的T细胞(CAR-19)对急性淋巴细胞白血病具有强大活性,但支持用CAR-19 T细胞治疗淋巴瘤的结果报道较少。自体干细胞移植后化疗难治或复发的淋巴瘤患者预后严峻,显然需要针对这些患者的新治疗方法。已证明在过继性T细胞转移前给予化疗可增强过继性转移T细胞的抗恶性活性。
患者和方法 我们在一项CAR-19 T细胞临床试验中,对22例晚期淋巴瘤患者先给予低剂量化疗,然后进行治疗。19例患者患有弥漫性大B细胞淋巴瘤,2例患者患有滤泡性淋巴瘤,1例患者患有套细胞淋巴瘤。患者在接受环磷酰胺加氟达拉滨的低剂量化疗预处理方案2天后接受单剂量CAR-19 T细胞。
结果 总缓解率为73%,其中55%为完全缓解,18%为部分缓解。12例完全缓解中有11例仍在持续。55%的患者出现3级或4级神经毒性,但均完全缓解。低剂量化疗预处理方案使血液淋巴细胞减少,并使血清白细胞介素-15(IL-15)升高。缓解的患者血液中CAR细胞峰值水平中位数为98/μL,未缓解的患者血液中CAR细胞峰值水平中位数为15/μL(P = 0.027)。高血清IL-15水平与血液中CAR细胞峰值高水平相关(P = 0.001),也与淋巴瘤缓解相关(P < 0.001)。
结论 低剂量化疗后给予CAR-19 T细胞可诱导晚期淋巴瘤缓解,高血清IL-15水平与该治疗方案的有效性相关。CAR-19 T细胞可能会成为复发淋巴瘤患者的重要治疗方法。