CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Is there still a place for autologous salvage transplantation in relapsed/refractory multiple myeloma in the era of novel therapies?
Is there still a place for autologous salvage transplantation in relapsed/refractory multiple myeloma in the era of novel therapies?
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对于既往接受过自体造血细胞移植(AHCT)后复发/难治性多发性骨髓瘤(RRMM)患者(pts),新型药物、细胞和免疫治疗日益可及。二线治疗选择主要包括基于蛋白酶体抑制剂、免疫调节药物和抗CD38单克隆抗体的三联方案,近期也包括CAR-T 细胞。近年来,由于众多新治疗选择的出现,自体挽救性移植(再移植,Re-AHCT)的重要性已显著下降。
因此,我们对2002年至2021年间接受Re-AHCT的171例RRMM患者病例进行了回顾性分析。中位随访74.7个月,5年无进展生存期(PFS)率和总生存期(OS)率分别为18%(中位20.6个月)和57%(中位65.0个月),100天死亡率为4%。多因素分析确定R-ISS分期和既往缓解持续时间(DoR)是PFS和OS的独立预后因素。所揭示的高危人群(R-ISS II/III期,DoR 24个月)与显著更差的PFS(HR 2.728)和OS(HR 3.129)相关,而低危组(R-ISS I期,DoR > 24个月)的中位PFS和OS分别达到45.0个月和80.2个月。
因此,即使在新型治疗时代,Re-AHCT仍可作为此类预后良好的RRMM患者的一种选择,尤其是在无法获得更强效治疗方式时。
For patients (pts) with relapsed or refractory multiple myeloma (RRMM) after previous autologous hematopoietic cell transplantation (AHCT), novel agents, cellular and immunotherapies are increasingly available.
Options for second-line treatment mostly include triplet regimens based on proteasome inhibitors, immunomodulatory drugs and anti-CD38 monoclonal antibodies and since recently also CAR T cells. The importance of autologous salvage transplantation (retransplantation, Re-AHCT) has significantly decreased in recent years due to the availability of many new treatment options.
Therefore, we performed a retrospective analysis of 171 pts cases with RRMM who received Re-AHCT between 2002 and 2021. With a median follow-up of 74. 7 months, the 5-year rates of progression-free survival (PFS) and overall survival (OS) were 18% (median 20. 6 months) and 57% (median 65. 0 months), respectively, the 100-day mortality rate was 4%.
Multivariate analysis identified R-ISS stage and duration of previous response (DoR) as independent prognostic factors for PFS and OS. While the revealed high-risk population (R-ISS stage II/III, DoR 24 months) was associated with a significantly worse PFS (HR 2. 728) and OS (HR 3. 129), the low-risk group (R-ISS I, DoR > 24 months) achieved a median PFS and OS of 45. 0 months and 80. 2 months, respectively.
Therefore, Re-AHCT could remain an option in such prognostically favorable pts with RRMM even in the era of novel therapies especially when more potent treatment modalities are not available.
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