Chalandon Yves, Passweg Jakob R, Guglielmi Cesare, Iacobelli Simona, Apperley Jane, Schaap Nicolaas P M, Finke Jürgen, Robin Marie, Fedele Roberta, Bron Dominique, Yakoub-Agha Ibrahim, van Biezen Anja, de Witte Theo, Kröger Nicolaus, Olavarria Eduardo
Division of Hematology, Department of Medical Specialties, University Hospital, Geneva, Switzerland
Hematology Division, University Hospital, Basel, Switzerland.
Haematologica. 2014 Sep;99(9):1492-8. doi: 10.3324/haematol.2013.100198. Epub 2014 Jul 4.
Patients with chronic myeloid leukemia relapsing after allogeneic hematopoietic stem cell transplantation may be treated by tyrosine kinase inhibitors and/or by donor lymphocyte infusions. The best strategies and timing of administration of lymphocytes are unclear. We analyzed 155 patients who relapsed after allogeneic stem cell transplantation with disease detectable only by molecular methods and who subsequently received lymphocytes. Transplants were performed in first chronic phase (n=125) or in advanced disease (n=29) from identical siblings (n=84) or unrelated donors (n=71) between 1986 and 2003. They received lymphocytes either during molecular relapse (n=85) or upon progression to more advanced disease (1993 to 2004). The median interval from relapse to lymphocyte infusion was 210 (0-1673) days. The median follow up after it was 46 (3-135) months. Overall survival was 76±4% at five years after lymphocyte infusions (89±8% with sibling donors and 63±13% with unrelated donors (P=0.003)). Survival was 69±14% when lymphocytes were given within six months of the detection of molecular relapse and 81±10% (P=0.061) when given later; 81±11% if given at molecular relapse versus 71±12% (P=0.26) with more advanced disease. In multivariate analysis survival was worse if the donor was unrelated (HR 2.54 (95% CI: 1.15-5.53), P=0.021) and better with lymphocyte infusions beyond six months from molecular relapse (HR 0.4 (95%CI: 0.19-0.84), P=0.018). These data confirm the remarkable efficacy of lymphocyte infusions for this disease. There appears to be no advantage from administering it early upon detection of molecular relapse in patients who received allogeneic stem cell transplantation for chronic myeloid leukemia.
异基因造血干细胞移植后复发的慢性髓性白血病患者可采用酪氨酸激酶抑制剂和/或供体淋巴细胞输注进行治疗。淋巴细胞给药的最佳策略和时机尚不清楚。我们分析了155例异基因干细胞移植后复发的患者,这些患者的疾病仅通过分子方法可检测到,随后接受了淋巴细胞治疗。移植于1986年至2003年间在第一慢性期(n = 125)或晚期疾病(n = 29)时进行,供者为同卵同胞(n = 84)或无关供者(n = 71)。他们在分子复发期间(n = 85)或疾病进展至更晚期时(1993年至2004年)接受淋巴细胞输注。从复发到淋巴细胞输注的中位间隔时间为210(0 - 1673)天。输注后中位随访时间为46(3 - 135)个月。淋巴细胞输注后五年总生存率为76±4%(同胞供者为89±8%,无关供者为63±13%,P = 0.003)。在分子复发检测后六个月内给予淋巴细胞时生存率为69±14%,之后给予时生存率为81±10%(P = 0.061);分子复发时给予为81±11%,疾病更晚期时给予为71±12%(P = 0.26)。多因素分析显示,如果供者为无关供者,生存率更差(风险比2.54(95%置信区间:1.15 - 5.53),P = 0.021),而在分子复发六个月后给予淋巴细胞输注生存率更好(风险比0.4(95%置信区间:0.19 - 0.84),P = 0.018)。这些数据证实了淋巴细胞输注对该疾病具有显著疗效。对于接受异基因干细胞移植治疗慢性髓性白血病的患者,在检测到分子复发后早期给予淋巴细胞输注似乎并无优势。