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:Efficacy of chimeric antigen receptor T-cell therapy in testicular relapse of pediatric acute lymphoblastic leukemia: a multicenter retrospective study.
Efficacy of chimeric antigen receptor T-cell therapy in testicular relapse of pediatric acute lymphoblastic leukemia: a multicenter retrospective study.
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睾丸复发通常在初次诊断后约 3 年出现。CAR-T 治疗被证明既安全又有效,其生存期与传统方案相当,并可能在长期生存者中提供保留生活质量的潜在优势。
睾丸复发是儿童急性淋巴细胞白血病(ALL)最常见的髓外复发之一,但其临床管理仍未被充分阐明。
本研究评估了CCCG-ALL-2015研究(ChiCTR-IPR-14005706,http://www.chictr.org.cn)中初始治疗后睾丸复发的患儿的治疗结局和长期生存。共回顾性分析了来自13个医疗中心的66例患者。比较了不同挽救治疗方式的临床特征和生存结局。
从初诊到睾丸复发的中位间隔为37个月。在59例接受复发后治疗的患者中,中位随访33个月后,2年总生存期(OS)率为86.1%。接受CAR-T 细胞治疗的患者2年OS为90.7%,而接受化疗、睾丸切除术或造血干细胞移植等常规方案治疗的患者为81.7%(P > 0.05)。在37例孤立性睾丸复发患儿中,18例接受CAR-T 治疗,10例接受睾丸切除术,2年OS率分别为92.3%和100%(P > 0.05)。
This study assessed treatment outcomes and long-term survival in children with testicular relapse following initial therapy under the CCCG-ALL-2015 study (ChiCTR-IPR-14005706, http://www.chictr.org.cn). In total, 66 patients from 13 medical centers were retrospectively analyzed. Clinical characteristics and survival outcomes were compared across salvage treatment modalities.
The median interval from initial diagnosis to testicular relapse was 37 months. Among 59 patients who received post-relapse therapy, the 2-year overall survival (OS) rate was 86.1% after a median follow-up of 33 months. Patients treated with chimeric antigen receptor T-cell (CAR-T) therapy showed a 2-year OS of 90.7%, compared to 81.7% in those managed with conventional regimens, such as chemotherapy, orchiectomy, or hematopoietic stem-cell transplantation (P > 0.05). Among 37 children with isolated testicular relapse, 18 underwent CAR-T therapy and 10 underwent orchiectomy, achieving 2-year OS rates of 92.3% and 100%, respectively (P > 0.05). DISCUSSION: Testicular relapse typically emerged approximately 3 years after initial diagnosis. CAR-T therapy proved to be both safe and effective, providing survival comparable to conventional regimens and offering potential advantages in preserving life quality among long-term survivors.
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