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髓样肉瘤的特征和移植结果:单中心研究。

Characteristics and transplant outcome of myeloid sarcoma: a single-institute study.

机构信息

Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Jiangsu Institute of Hematology, National Clinical Research Center for Hematologic Diseases, The First Affiliated Hospital of Soochow University, Soochow University, 188 Shizi Street, Suzhou, 215006, Jiangsu Province, People's Republic of China.

出版信息

Int J Hematol. 2021 May;113(5):682-692. doi: 10.1007/s12185-021-03081-2. Epub 2021 Jan 28.

Abstract

We performed a retrospective study describing the characteristics of myeloid sarcoma (MS) and evaluated the outcome of hematopoietic stem cell transplantation (HSCT) in patients with MS. There were 27 patients with de novo isolated MS, 34 with de novo leukemic MS and 13 with secondary leukemic MS in our study. Sixty-three patients received induction chemotherapy. Following induction therapy, 35 patients underwent HSCT, including 10 autogenous HSCT (auto-HSCT) and 25 allogeneic HSCT (allo-HSCT) cases. Compared with intensive chemotherapy only as consolidation treatment, HSCT (auto-/allo-HSCT) significantly improved the overall survival (OS) of MS patients (p < 0.05), while allo-HSCT also improved progression-free survival (PFS, p = 0.032). According to multivariate analysis, poorer prognosis in terms of OS was observed in older patients (p = 0.024, HR = 1.030, 95% CI 1.004-1.057), while HSCT (auto/allo-HSCT) had a favorable impact on OS for patients with MS (auto-HSCT, p = 0.044, HR = 0.201, 95% CI 0.042-0.959; allo-HSCT, p = 0.038, HR = 0.341, 95% CI 0.124-0.943). Extramedullary disease without complete remission (CR) after induction therapy was the sole variable independent of high OS and PFS (p = 0.049, HR = 2.243, 95% CI: 1.005-5.005; p = 0.017, HR = 2.535, 95% CI 1.180-5.448, respectively). The data indicate that HSCT is an effective treatment for patients with MS who have achieved CR of extramedullary disease after induction therapy.

摘要

我们进行了一项回顾性研究,描述了骨髓肉瘤(MS)的特征,并评估了 MS 患者造血干细胞移植(HSCT)的结果。在我们的研究中,有 27 例初发孤立性 MS、34 例初发白血病性 MS 和 13 例继发性白血病性 MS。63 例患者接受诱导化疗。诱导治疗后,35 例患者接受 HSCT,包括 10 例自体 HSCT(auto-HSCT)和 25 例异基因 HSCT(allo-HSCT)。与强化化疗作为巩固治疗相比,HSCT(自体/异基因)显著改善了 MS 患者的总生存率(OS)(p<0.05),而异基因 HSCT 也改善了无进展生存率(PFS,p=0.032)。根据多因素分析,OS 较差的预后见于年龄较大的患者(p=0.024,HR=1.030,95%CI 1.004-1.057),而 HSCT(自体/异基因)对 MS 患者的 OS 有有利影响(自体 HSCT,p=0.044,HR=0.201,95%CI 0.042-0.959;异基因 HSCT,p=0.038,HR=0.341,95%CI 0.124-0.943)。诱导治疗后无完全缓解(CR)的髓外疾病是唯一独立于高 OS 和 PFS 的变量(p=0.049,HR=2.243,95%CI:1.005-5.005;p=0.017,HR=2.535,95%CI 1.180-5.448)。数据表明,HSCT 是诱导治疗后髓外疾病达到 CR 的 MS 患者的有效治疗方法。

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