Bosi Guilherme Rasia, Fogliatto Laura Maria, Costa Tito Emilio Vanelli, Grokoski Kamila Castro, Pereira Mariana Pinto, Bugs Nathan, Kalil Marco, Fraga Christina, Daudt Liane Esteves, Silla Lucia Mariano da Rocha
Universidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, Brazil.
Universidade Federal do Rio Grande do Sul (UFRS), Porto Alegre, RS, Brazil.
Hematol Transfus Cell Ther. 2019 Jul-Sep;41(3):222-228. doi: 10.1016/j.htct.2018.11.005. Epub 2019 Mar 28.
To assess clinical outcomes of intolerant, relapsed or refractory patients who could not be treated with new tyrosine kinase inhibitors or experimental therapies.
A retrospective cohort of 90 chronic myeloid leukemia patients in all phases of the disease treated with imatinib mesylate as their first TKI therapy, and with dasatinib or nilotinib as the next line of therapy. We evaluated clinical outcomes of these patients, with special focus on the group that needed more than two therapy lines.
Thirty-nine percent of patients were refractory or intolerant to imatinib. An 8-year overall survival rate of the patients who went through three or more lines of treatment was significantly lower, compared to those who were able to maintain imatinib as their first-line therapy (83% and 22%, respectively p<0.01). Decreased overall survival was associated with advanced-phase disease (p<0.01), failure to achieve major molecular response in first-line treatment (p<0.01) and interruption of first-line treatment due to any reason (p=0.023). Failure in achieving complete cytogenetic response and major molecular response and treatment interruption were associated with the progression to the third-line treatment.
The critical outcome observed in relapsed, intolerant or refractory chronic phase CML patients reflects the unmet need for this group of patients without an alternative therapy, such as new drugs or experimental therapies in clinical trials. Broader access to newer treatment possibilities is a crucial asset to improve survival among CML patients, especially those refractory or intolerant to first-line therapies.
评估无法接受新型酪氨酸激酶抑制剂或实验性疗法治疗的不耐受、复发或难治性患者的临床结局。
一项回顾性队列研究,纳入90例处于疾病各阶段的慢性髓性白血病患者,这些患者以甲磺酸伊马替尼作为首个酪氨酸激酶抑制剂(TKI)疗法,随后以达沙替尼或尼罗替尼作为二线疗法。我们评估了这些患者的临床结局,特别关注需要两种以上治疗方案的患者组。
39%的患者对伊马替尼难治或不耐受。与能够将伊马替尼维持作为一线疗法的患者相比,接受三线或更多线治疗的患者8年总生存率显著更低(分别为83%和22%,p<0.01)。总生存率降低与疾病晚期(p<0.01)、一线治疗未达到主要分子反应(p<0.01)以及因任何原因中断一线治疗(p=0.023)相关。未达到完全细胞遗传学反应和主要分子反应以及治疗中断与进展至三线治疗相关。
复发、不耐受或难治的慢性期慢性髓性白血病患者中观察到的关键结局反映了这组患者在没有替代疗法(如临床试验中的新药或实验性疗法)的情况下未满足的需求。更广泛地获得更新的治疗可能性是提高慢性髓性白血病患者生存率的关键资产,尤其是那些对一线疗法难治或不耐受的患者。