Nachmias Boaz, Shaulov Adir, Gatt Moshe E, Shapira Michael, Gural Alexander
Leukemia Service, Department of Hematology, Hadassah-Hebrew University Medical Center, Jerusalem,
Department of Hematology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Acta Haematol. 2018;140(4):209-214. doi: 10.1159/000493252. Epub 2018 Oct 19.
The treatment of relapsed/refractory acute lymphoblastic leukemia (RR-ALL) presents a true clinical challenge. In 2012, a protocol combining bortezomib, dexamethasone, asparaginase, doxorubicin, and vincristine administered to children with RR-ALL was published with encouraging results. Over the past 5 years, we have implemented this protocol in the adult RR-ALL population (> 18 years) and addressed its feasibility in terms of remission rate and toxicity. Here, we present the results of our experience in 9 patients, all of whom received multiple previous chemotherapy protocols, two of them relapsing after an allogeneic bone marrow transplantation. All of the five B-ALL patients, and two of the four T-ALL achieved complete remission. Of the seven patients achieving complete remission, two patients were referred for allogeneic bone marrow transplantation, two patients were subsequently given blinatumomab, and one patient subsequently received donor lymphocyte infusion followed by blinatumomab. Thus, five out of nine patients treated (55%) were able to proceed to best available therapy in a complete remission. We observed minimal adverse effects, mainly hematological toxicity. We conclude that the bortezomib-based protocol should be evaluated as an effective and well-tolerated treatment option for adult patients either unfit for or failing standard salvage chemotherapy, as a bridge to immunotherapy or allogeneic bone marrow transplantation.
复发/难治性急性淋巴细胞白血病(RR-ALL)的治疗是一项真正的临床挑战。2012年,一项将硼替佐米、地塞米松、天冬酰胺酶、阿霉素和长春新碱联合应用于RR-ALL儿童患者的方案发表,结果令人鼓舞。在过去5年中,我们在成年RR-ALL患者群体(>18岁)中实施了该方案,并从缓解率和毒性方面探讨了其可行性。在此,我们展示了我们对9例患者的治疗结果,所有患者此前均接受过多种化疗方案,其中2例在异基因骨髓移植后复发。5例B-ALL患者全部缓解,4例T-ALL患者中有2例缓解。在7例获得完全缓解的患者中,2例被转诊接受异基因骨髓移植,2例随后接受了博纳吐单抗治疗,1例随后接受了供体淋巴细胞输注,之后又接受了博纳吐单抗治疗。因此,9例接受治疗的患者中有5例(55%)能够在完全缓解的情况下接受最佳可用治疗。我们观察到的不良反应极小,主要是血液学毒性。我们得出结论,对于不适合标准挽救化疗或标准挽救化疗失败的成年患者,基于硼替佐米的方案应作为一种有效且耐受性良好的治疗选择进行评估,作为免疫治疗或异基因骨髓移植的桥梁。