Pathologically complete remission to combination of invariant NK T cells and anti-CD20 antibody in a refractory HIV plus diffuse large B-cell lymphoma patient

被引:3
作者
Wang, Jing [1 ]
Zhang, Renfang [1 ]
Ding, Xiangqing [1 ]
Jin, Yanling [1 ]
Qin, Ran [1 ]
Xia, Bili [1 ]
Liao, Qibin [1 ]
Hu, Huiliang [1 ]
Song, Wei [1 ]
Wang, Zhenyan [1 ]
Zhang, Xiaoyan [2 ,3 ]
Xu, Jianqing [2 ,3 ]
机构
[1] Fudan Univ, Shanghai Publ Hlth Clin Ctr, Shanghai 201508, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Shanghai 201508, Peoples R China
[3] Fudan Univ, Inst Biomed Sci, Shanghai 201508, Peoples R China
基金
国家重点研发计划;
关键词
anti-CD20; antibody; chemo-immunotherapy; DLBCL; HIV plus; iNKT; pathologically complete regression; relapsed; refractory; rituximab; THERAPY; RITUXIMAB; RESPONSES; CULTURE; CHOP;
D O I
10.2217/imt-2021-0247
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although there is a high curability rate with rituximab chemotherapy, approximately 40% of patients with diffuse large B-cell lymphoma (DLBCL) develop disease relapse or primary-refractory lymphoma. The prognosis of HIV+ DLBCL patients is even worse with limited therapeutic options. The case is presented of a 28-year-old man who was diagnosed with HIV-DLBCL, refractory to rituximab-based chemo-immunotherapies and radiotherapy before and maintained a pathologically complete regression with the infusion of haplotype-matched invariant NK T cells and anti-CD20 antibody. His abdominal mass kept shrinking during the period of follow-up without relapse to date. A combination of haplotype-matched invariant NK T cells was likely to reinvigorate the efficacy of anti-CD20 antibody and may offer a viable treatment option for refractory DLBCL patients. Plain language summary Diffuse large B-cell lymphoma (DLBCL) is one of the most frequent types of lymphoid cancer. The prognosis of relapsed/refractory DLBCL patients has been dismal with resistance to rituximab-based chemo-immunotherapy. The combination of effective cells with rituximab might improve clinical response by enhancing antibody-dependent cytotoxicity. The authors reported the case of a 28-year-old man diagnosed with HIV-DLBCL, refractory to 3 lines of rituximab-based chemo-immunotherapies and radiotherapy before, and who received 6 experimental infusions of haplotype-matched invariant NK T cells combined with anti-CD20 antibody. The lesion on radiological examination was partially regressed after cycle 3 and cycle 6. The pathological examination, performed 4 weeks after cycle 6, suggested pathologically complete regression. The mass was completely regressed on CT scanning without relapse to date. A combination of invariant NK T cells and anti-CD20 antibody may offer a viable treatment option for relapsed/refractory DLBCL patients for whom rituximab chemotherapy was not effective.
引用
收藏
页码:599 / 607
页数:9
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