Long term outcome of a patient with relapsed refractory early thymic precursor acute lymphoblastic leukemia treated with daratumumab.

American journal of blood research Pub Date : 2021-10-15 eCollection Date: 2021-01-01
Sachin Punatar, Anant Gokarn, Lingaraj Nayak, Avinash Bonda, Akanksha Chichra, Sumeet Mirgh, Bhausaheb Bagal, Prashant Tembhare, Papagudi Subramanian, Navin Khattry
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引用次数: 0

Abstract

The prognosis of patients with relapsed Early Thymic Precursor acute lymphoblastic leukemia (ETP-ALL) remains poor. Unlike B cell Precursor-ALL (BCP-ALL), there are no approved targeted therapies for ETP-ALL. Recent studies have identified a consistent expression of CD38 on the blasts of patients with T-ALL (both ETP-ALL and non ETP-ALL). Pre-clinical studies indicate that CD38 expression persists on the blasts of T-ALL even after receipt of conventional chemotherapy. These findings make CD38 an attractive targetable surface protein for patients with relapsed refractory T-ALL. We were the first to describe the clinical use of daratumumab in a patient of ETP-ALL, with relapsed disease post allogeneic transplant. We describe here the long term outcome of this patient more than 3 years after starting single agent daratumumab.

Abstract Image

Abstract Image

用达拉单抗治疗复发的难治性早期胸腺前体急性淋巴细胞白血病患者的长期预后
早期胸腺前体急性淋巴细胞白血病(ETP-ALL)复发患者的预后仍然很差。与B细胞前体all (BCP-ALL)不同,ETP-ALL还没有被批准的靶向治疗方法。最近的研究发现CD38在T-ALL(包括ETP-ALL和非ETP-ALL)患者的细胞中一致表达。临床前研究表明,即使在接受常规化疗后,T-ALL细胞的CD38表达仍然存在。这些发现使CD38成为复发性难治性T-ALL患者的一个有吸引力的靶向表面蛋白。我们首次描述了在异基因移植后疾病复发的ETP-ALL患者中使用达拉单抗的临床应用。我们在这里描述了该患者在单药达拉单抗开始治疗3年以上的长期结果。
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American journal of blood research
American journal of blood research MEDICINE, RESEARCH & EXPERIMENTAL-
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