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异基因 SCT 与 tisagenlecleucel 在具有不良预后因素的 R/R LBCL 患者中的结局比较

英文原题:Outcomes of allogeneic SCT versus tisagenlecleucel in patients with R/R LBCL and poor prognostic factors.

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Outcomes of allogeneic SCT versus tisagenlecleucel in patients with R/R LBCL and poor prognostic factors.

PubMed 2024/12/16(内容时间) Int J Hematol Q3 · IF 1.9(JCR 2025)

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中文摘要

本研究评估替沙格列赛(tisa-cel)及异基因造血干细胞移植(allo-SCT)治疗伴有不良预后因素的复发和/或难治性(r/r)大B细胞淋巴瘤(LBCL)患者的疗效;不良预后因素包括体能状态(PS)2、多处结外病灶(EN)、化疗难治性疾病或乳酸脱氢酶(LDH)升高。

总体而言,allo-SCT组无进展生存期(PFS)较差、非复发死亡率较高,而复发/进展率相近。值得注意的是,在化疗难治性患者中,tisa-cel组PFS优于allo-SCT组(3.2对2.0个月,p=0.092);在LDH升高患者中也更优(4.0对2.0个月,p=0.018)。

然而,PS为2或多处EN患者中,两种细胞疗法的PFS相近。伴有不良预后因素患者接受细胞治疗后复发时,allo-SCT组和tisa-cel组生存时间分别为1.6和4.6个月。倾向评分匹配队列验证了这些结果。

总之,tisa-cel治疗不良预后因素患者的生存优于allo-SCT;但无论采用何种疗法,细胞治疗后复发患者结局均极差。仍需进一步制定策略以改善此类患者结局。

展开英文摘要原文

This study investigated the efficacy of tisagenlecleucel (tisa-cel) and allogeneic hematopoietic stem cell transplantation (allo-SCT) for patients with relapsed and/or refractory (r/r) large B-cell lymphoma (LBCL) with poor prognostic factors, defined as performance status (PS) 2, multiple extranodal lesions (EN), chemorefractory disease, or higher lactate dehydrogenase (LDH).

Overall, the allo-SCT group demonstrated worse progression-free survival (PFS), higher non-relapse mortality, and a similar relapse/progression rate.

Notably, the tisa-cel group showed better PFS than the allo-SCT group among patients with chemorefractory disease (3. 2 vs. 2. 0 months, p = 0. 092) or higher LDH (4. 0 vs. 2. 0 months, p = 0. 018), whereas PFS in the two cellular therapy groups was similar among those with PS 2 or multiple EN. Survival time after relapse post-cellular therapy in patients with poor prognostic factors was 1. 6 with allo-SCT and 4. 6 months with tisa-cel.

These findings were confirmed in a propensity score matching cohort.

In conclusion, tisa-cel resulted in better survival than allo-SCT in patients with poor prognostic factors.

However, patients who relapsed post-cellular therapy had dismal outcomes regardless of therapy.

Further strategies are warranted to improve outcomes in these patients.

论文信息

作者
Hayashino K、Terao T、Nishimori H、Kitamura W、Kobayashi H、Kamoi C、Seike K、Fujiwara H
第一作者单位
Department of Hematology and Oncology, Okayama University Hospital, Okayama University, 2-5-1 Shikata-cho, Kita-ku, Okayama-shi, Okayama, 700-8558, Japan.Japan
通讯作者单位
Department of Hematology and Oncology, Okayama University Hospital, Okayama University, 2-5-1 Shikata-cho, Kita-ku, Okayama-shi, Okayama, 700-8558, Japan. tarao.toshiki.0127@gmail.com.Japan
文献类型
对照研究
期刊
International journal of hematology2025 Feb
原文标识
PubMed 39680351 · DOI 10.1007/s12185-024-03888-9