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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Retrospective study on pomalidomide-PACE as a salvage regimen in aggressive relapsed and refractory multiple myeloma.
Retrospective study on pomalidomide-PACE as a salvage regimen in aggressive relapsed and refractory multiple myeloma.
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泊马度胺-PACE 能够在重度预处理、侵袭性 RRMM 中诱导快速缓解,且毒性特征可控,因此提供了一种有效的挽救方案,以及一种潜在的桥接策略,以衔接如 CAR-T 细胞疗法等进一步治疗选择。
尽管多发性骨髓瘤(MM)的治疗选择取得了重大进展,但对主要药物类别难治的患者以及具有侵袭性、尤其是髓外疾病的患者,仍然面临不良结局。对于这些患者,迫切需要有效的治疗选择。
在这项回顾性研究中,我们报告了泊马度胺联合顺铂、多柔比星、环磷酰胺和依托泊苷(Pom-PACE)强化联合方案在复发难治性MM(RRMM)或浆细胞白血病(PCL)患者中的安全性和疗效。研究纳入在两个学术中心连续接受Pom-PACE治疗的20例患者进行分析。所有患者在开始治疗前必须根据国际骨髓瘤工作组标准确认复发,并具有足够的器官功能。数据通过查阅病历收集。对疗效和安全性进行了探索性分析。
患者既往接受过大量治疗,中位既往治疗线数为四线(范围:1-10)。所有患者均暴露于免疫调节剂、蛋白酶体抑制剂和烷化剂,80%为双耐药,40%为三耐药。15例患者(75%)存在髓外MM或PCL。总体缓解率(ORR)为68%,其中31%达到至少非常好的部分缓解。缓解迅速,一个周期后ORR为64%。中位无进展生存期为8.9个月(0.92-未达到[NR]),中位总生存期为11.8个月(3-40.6)。Pom-PACE与显著毒性相关。所有可评估患者均出现4级血液学毒性。然而,未观察到治疗相关死亡。
Despite major advances in treatment options for multiple myeloma (MM), patients refractory to the main drug classes and those with aggressive, especially extramedullary disease, still face a dismal outcome. For these patients, effective therapeutic options are urgently warranted.
In this retrospective study, we report on the safety and efficacy of the intensive combination regimen of pomalidomide plus cisplatin, doxorubicin, cyclophosphamide, and etoposide (Pom-PACE) in patients with relapsed refractory MM (RRMM) or plasma cell leukemia (PCL). A study population of 20 consecutive patients treated with Pom-PACE at two academic centers was included for analysis. All patients had to have a confirmed relapse according to International Myeloma Working Group criteria and adequate organ function prior to the start of therapy. Data were collected by reviewing medical charts. Exploratory analyses were performed with regard to efficacy and safety.
Patients were heavily pretreated with a median number of four prior therapies (range: 1-10). All patients were exposed to immunomodulators, proteasome inhibitors, and alkylating agents, 80% were double-class refractory, 40% were triple-class refractory. Extramedullary MM or PCL were present in 15 patients (75%). Overall response rate (ORR) was 68%, with 31% achieving at least a very good partial response. Responses were achieved rapidly with an ORR of 64% after one cycle. Median progression-free survival was 8.9 months (0.92-not reached [NR]) and median overall survival was 11.8 months (3-40.6). Pom-PACE was associated with significant toxicity. All evaluable patients experienced Grade 4 hematological toxicity. However, no treatment related mortality was observed.
Pomalidomide-PACE was able to induce rapid responses in heavily pretreated, aggressive RRMM with a manageable toxicity profile and therefore offers an effective salvage regimen and a potential bridging strategy to further treatment options such as chimeric antigen receptor T-cell therapy.
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