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首页> 外文期刊>Leukemia and lymphoma >Long-term survival with allogeneic stem cell transplant and donor lymphocyte infusion following salvage therapy with anti-CD52 monoclonal antibody (Campath) in a patient with alpha/beta hepatosplenic T-cell non-Hodgkin's lymphoma.
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Long-term survival with allogeneic stem cell transplant and donor lymphocyte infusion following salvage therapy with anti-CD52 monoclonal antibody (Campath) in a patient with alpha/beta hepatosplenic T-cell non-Hodgkin's lymphoma.

机译:在患有α/β肝脾性T细胞非霍奇金淋巴瘤的患者中,应用抗CD52单克隆抗体(Campath)进行挽救治疗后,通过同种异体干细胞移植和供体淋巴细胞输注可以长期生存。

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摘要

Hepatosplenic T-cell non-Hodgkin's lymphoma (HSTCL) is a rare, aggressive form of NHL, with a median survival of approximately 8 months. We were able to successfully induce complete remission in a patient with alpha/beta HSTCL who was refractory to multiple prior chemotherapy regimens, using the humanized anti-CD52 monoclonal antibody alemtuzumab (Campath). Once disease was controlled, the patient was able to undergo allogeneic stem cell transplantation (SCT), which resulted in complete remission. Furthermore, upon relapse, we were able to re-induce complete clinical and molecular remission with donor lymphocyte infusions. At Day 655 (post-SCT), the patient remains in complete remission. These data suggest a potential role for alemtuzumab and allogeneic SCT in the treatment of T-cell NHL.
机译:肝脾T细胞非霍奇金淋巴瘤(HSTCL)是一种罕见的侵袭性NHL,中位生存期约为8个月。使用人源化抗CD52单克隆抗体alemtuzumab(Campath),我们能够成功诱导对多种先前化疗方案均无效的alpha / beta HSTCL患者完全缓解。一旦疾病得到控制,患者就可以进行异基因干细胞移植(SCT),从而完全缓解。此外,一旦复发,我们就能够通过输注供体淋巴细胞来重新诱导完全的临床和分子缓解。在第655天(SCT后),患者保持完全缓解。这些数据表明阿仑单抗和同种异体SCT在T细胞NHL的治疗中具有潜在作用。

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