Gagelmann Nico, Wolschke Christine, Badbaran Anita, Janson Dietlinde, Berger Carolina, Klyuchnikov Evgeny, Ayuk Francis, Fehse Boris, Kröger Nicolaus
Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Hemasphere. 2023 Jun 30;7(7):e921. doi: 10.1097/HS9.0000000000000921. eCollection 2023 Jul.
Hematopoietic cell transplantation (HCT) is a curative approach for myelofibrosis patients, but relapse is a major cause of treatment failure. We investigated the effect of donor lymphocyte infusion (DLI) in 37 patients with molecular (n = 17) or hematological relapse (n = 20) after HCT. Patients received median of 2 (range, 1-5) cumulative DLI (total of 91 infusions). Median starting dose was 1 × 10 cells/kg, escalated by half-log ≥6 weeks if no response nor graft-versus-host disease (GvHD) occurred. Median time to first DLI was 40 weeks for molecular relapse versus 145 weeks for hematological relapse. Overall molecular complete response (mCR) at any time was 73% (n = 27) and was significantly higher for initial molecular relapse (88%) versus hematological relapse (60%; = 0.05). The 6-year overall survival was 77% versus 32% ( = 0.03). Acute GvHD 2-4 occurred in 22% and half of the patients achieved mCR without any GvHD. All patients who relapsed from mCR achieved after first DLI could be salvaged with subsequent DLI, showing long-term survival. No second HCT was needed for molecular relapse versus 6 for hematological relapse. This comprehensive and largest study to date suggests molecular monitoring together with DLI as standard of care and a crucial approach to achieve excellent outcomes in relapsed myelofibrosis.
造血细胞移植(HCT)是治疗骨髓纤维化患者的一种治愈性方法,但复发是治疗失败的主要原因。我们调查了供体淋巴细胞输注(DLI)对37例HCT后出现分子学(n = 17)或血液学复发(n = 20)患者的影响。患者接受的DLI累积中位数为2次(范围1 - 5次)(共91次输注)。起始剂量中位数为1×10⁶细胞/kg,如果没有反应或发生移植物抗宿主病(GvHD),则在≥6周时以半对数递增。分子学复发患者首次DLI的中位时间为40周,而血液学复发患者为145周。任何时间的总体分子完全缓解(mCR)率为73%(n = 27),初始分子学复发患者的mCR率(88%)显著高于血液学复发患者(60%;P = 0.05)。6年总生存率分别为77%和32%(P = 0.03)。2 - 4级急性GvHD发生率为22%,一半的患者在未发生任何GvHD的情况下实现了mCR。所有首次DLI后从mCR复发的患者均可通过后续DLI挽救,显示出长期生存。分子学复发患者无需进行第二次HCT,而血液学复发患者有6例需要。这项迄今为止全面且规模最大的研究表明,分子监测与DLI联合作为复发性骨髓纤维化的标准治疗方法以及实现良好预后的关键途径。