Combination Therapy With Asciminib and Ponatinib as a Bridge to Brexucabtagene Autoleucel and Maintenance in a Patient With Relapsed Refractory Philadelphia Positive B-Cell Acute Lymphoblastic Leukemia.

Journal of medical cases Pub Date : 2024-10-01 Epub Date: 2024-09-20 DOI:10.14740/jmc4287
Alina Amin Muhammad, Erum Mir Ghazi, Amir Ali, Eric Tam, Karrune Woan, Preet Chaudhary, George Yaghmour, Abdullah Ladha
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Abstract

Tyrosine kinase inhibitors (TKIs) have changed the prognosis of Philadelphia-positive B-cell acute lymphoblastic leukemia (ALL); however, relapsed and refractory disease after multiple TKIs continues to be a clinical challenge. Brexucabtagene autoleucel (brexu-cel) is a novel FDA-approved therapy for relapsed and refractory ALL. Given the lengthy manufacturing time, bridging therapy is commonly employed prior to brexu-cel. Here we describe a case of a 75-year-old Hispanic male patient with relapsed/refractory Philadelphia-positive B-cell ALL with extramedullary disease involving abdominal lymph nodes and skin. He was initially treated with chemotherapy in combination with imatinib, and later received dasatinib and subsequently blinatumomab and nilotinib. As the patient progressed, he received ponatinib with low-dose salvage chemotherapy and did not show kinase domain mutation. In a final effort, a novel combination of ponatinib with asciminib was used as a bridge therapy before brexu-cel and later as maintenance therapy after brexu-cel. This novel combination was able to control disease prior to brexu-cel for 2 months and maintained remission for at least 10 months. This report shows that the novel combination of ponatinib and asciminib is tolerable and effective as a bridge and maintenance therapy after brexu-cel.

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将阿西米尼和泊纳替尼联合疗法作为一名复发难治性费城阳性B细胞急性淋巴细胞白血病患者通往布雷克巴肽自体白血病和维持治疗的桥梁
酪氨酸激酶抑制剂(TKIs)改变了费城阳性B细胞急性淋巴细胞白血病(ALL)的预后;然而,使用多种TKIs后复发和难治性疾病仍然是临床难题。Brexucabtagene autoleucel(brexu-cel)是美国食品药品管理局批准的一种新型疗法,用于治疗复发和难治性 ALL。由于生产时间较长,在使用brexu-cel之前通常会采用桥接疗法。这里我们描述了一例75岁的西班牙裔男性患者,他患有复发/难治性费城阳性B细胞ALL,髓外疾病累及腹部淋巴结和皮肤。他最初接受了伊马替尼联合化疗,后来又接受了达沙替尼,随后又接受了blinatumomab和尼洛替尼。随着病情的发展,他接受了泊纳替尼联合小剂量挽救性化疗,但没有出现激酶域突变。最后,在布雷克舒赛前,患者接受了泊纳替尼与阿西米尼的新型联合疗法作为桥接疗法,之后又接受了布雷克舒赛后的维持疗法。这种新型组合能够在brexu-cel治疗前控制病情2个月,并维持缓解至少10个月。该报告表明,作为brexu-cel治疗后的过渡和维持疗法,波纳替尼和阿西米尼的新型组合具有耐受性和有效性。
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