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异基因造血细胞移植后复发性高危血液系统恶性肿瘤患者的预后

Outcomes among patients with recurrent high-risk hematologic malignancies after allogeneic hematopoietic cell transplantation.

作者信息

Mielcarek Marco, Storer Barry E, Flowers Mary E D, Storb Rainer, Sandmaier Brenda M, Martin Paul J

机构信息

Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.

出版信息

Biol Blood Marrow Transplant. 2007 Oct;13(10):1160-8. doi: 10.1016/j.bbmt.2007.06.007. Epub 2007 Aug 3.

Abstract

We retrospectively analyzed outcomes among 307 consecutive patients who had recurrent or persistent acute leukemia (n = 244), chronic myelogenous leukemia in blast phase (CML; n = 28), or advanced myelodysplastic syndromes (MDS; n = 35) after allogeneic hematopoietic cell transplantation and who received at least 1 relapse-directed intervention: withdrawal of immunosuppression, chemotherapy, or donor lymphocyte infusion (DLI). Transplants were performed at a single institution between 1995 and 2004, and outcomes were analyzed according to time intervals from transplantation to detection of malignancy: "early," <100 days (n = 111); "intermediate," 100-200 days (n = 73); and "late," >200 days (n = 123). The overall remission rate was 30%. Compared to early recurrence, intermediate recurrence and late recurrence were associated with increasing probabilities of remission (hazard ratios, 1.89 and 2.16; P = .05 and .02) and decreasing risks of overall mortality (hazard ratios, 0.73 and 0.33; P = .05 and <.0001). The 2-year overall survival (OS) estimates for patients with early, intermediate, and late recurrence were 3%, 9%, and 19%, respectively. Remission was associated with a median survival prolongation of 9.5 months. Individual types or combinations of these nonrandomly assigned relapse-directed interventions were not associated with higher or lower probabilities of remission or survival. More effective intervention strategies are needed for treatment of recurrent high-risk hematologic malignancies after hematopoietic cell transplantation. In the absence of innovative clinical trials, patients with early recurrence might wish to forego further interventions in favor of palliative care.

摘要

我们回顾性分析了307例接受异基因造血细胞移植后复发或持续存在急性白血病(n = 244)、急变期慢性粒细胞白血病(CML;n = 28)或晚期骨髓增生异常综合征(MDS;n = 35)且至少接受过1次复发导向干预(免疫抑制撤除、化疗或供者淋巴细胞输注[DLI])的连续患者的预后。移植于1995年至2004年在单一机构进行,并根据从移植到检测到恶性肿瘤的时间间隔分析预后:“早期”,<100天(n = 111);“中期”,100 - 200天(n = 73);“晚期”,>200天(n = 123)。总体缓解率为30%。与早期复发相比,中期复发和晚期复发缓解概率增加(风险比分别为1.89和2.16;P = 0.05和0.02),总体死亡率风险降低(风险比分别为0.73和0.33;P = 0.05和<0.0001)。早期、中期和晚期复发患者的2年总生存(OS)估计分别为3%、9%和19%。缓解与中位生存期延长9.5个月相关。这些非随机分配的复发导向干预的个体类型或组合与缓解或生存的较高或较低概率无关。造血细胞移植后复发性高危血液系统恶性肿瘤的治疗需要更有效的干预策略。在缺乏创新性临床试验的情况下,早期复发患者可能希望放弃进一步干预而选择姑息治疗。

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