Rousselot Philippe, Coudé Marie Magdelaine, Gokbuget Nicola, Gambacorti Passerini Carlo, Hayette Sandrine, Cayuela Jean-Michel, Huguet Françoise, Leguay Thibaut, Chevallier Patrice, Salanoubat Celia, Bonmati Caroline, Alexis Magda, Hunault Mathilde, Glaisner Sylvie, Agape Philippe, Berthou Christian, Jourdan Eric, Fernandes José, Sutton Laurent, Banos Anne, Reman Oumedaly, Lioure Bruno, Thomas Xavier, Ifrah Norbert, Lafage-Pochitaloff Marina, Bornand Anne, Morisset Laure, Robin Valérie, Pfeifer Heike, Delannoy Andre, Ribera Josep, Bassan Renato, Delord Marc, Hoelzer Dieter, Dombret Herve, Ottmann Oliver G
Hemato-Oncology Unit, Centre Hospitalier de Versailles, Le Chesnay, France; Université Versailles Saint Quentin en Yvelines, EA4340, Université Paris-Saclay, Communauté Paris-Saclay, France;
Laboratory of Hematology, University Hospital Saint-Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France; EA3518, University Paris Diderot, Paris, France;
Blood. 2016 Aug 11;128(6):774-82. doi: 10.1182/blood-2016-02-700153. Epub 2016 Apr 27.
Prognosis of Philadelphia-positive (Ph(+)) acute lymphoblastic leukemia (ALL) in the elderly has improved during the imatinib era. We investigated dasatinib, another potent tyrosine kinase inhibitor, in combination with low-intensity chemotherapy. Patients older than age 55 years were included in the European Working Group on Adult ALL (EWALL) study number 01 for Ph(+) ALL (EWALL-PH-01 international study) and were treated with dasatinib 140 mg/day (100 mg/day over 70 years) with intrathecal chemotherapy, vincristine, and dexamethasone during induction. Patients in complete remission continued consolidation with dasatinib, sequentially with cytarabine, asparaginase, and methotrexate for 6 months. Maintenance therapy was dasatinib and vincristine/dexamethasone reinductions for 18 months followed by dasatinib until relapse or death. Seventy-one patients with a median age of 69 years were enrolled; 77% had a high comorbidity score. Complete remission rate was 96% and 65% of patients achieved a 3-log reduction in BCR-ABL1 transcript levels during consolidation. Only 7 patients underwent allogeneic hematopoietic stem cell transplantation. At 5 years, overall survival was 36% and up to 45% taking into account deaths unrelated to disease or treatment as competitors. Thirty-six patients relapsed, 24 were tested for mutation by Sanger sequencing, and 75% were T315I-positive. BCR-ABL1(T315I) was tested by allele-specific oligonucleotide reverse transcription-quantitative polymerase chain reaction in 43 patients and detection was associated with short-term relapses. Ten patients (23%) were positive before any therapy and 8 relapsed, all with this mutation. In conclusion, dasatinib combined with low-intensity chemotherapy was well-tolerated and gave long-term survival in 36% of elderly patients with Ph(+) ALL. Monitoring of BCR-ABL1(T315I) from diagnosis identified patients with at high risk of early relapse and may help to personalize therapy.
在伊马替尼时代,老年费城染色体阳性(Ph(+))急性淋巴细胞白血病(ALL)的预后有所改善。我们研究了另一种强效酪氨酸激酶抑制剂达沙替尼与低强度化疗联合使用的情况。年龄超过55岁的患者被纳入欧洲成人ALL工作组(EWALL)的Ph(+) ALL研究编号01(EWALL-PH-01国际研究),在诱导期接受140 mg/天的达沙替尼治疗(70岁以上为100 mg/天),并联合鞘内化疗、长春新碱和地塞米松。完全缓解的患者继续使用达沙替尼巩固治疗,随后依次使用阿糖胞苷、天冬酰胺酶和甲氨蝶呤,为期6个月。维持治疗为达沙替尼和长春新碱/地塞米松再诱导治疗18个月,之后使用达沙替尼直至复发或死亡。共纳入71例患者,中位年龄为69岁;77%的患者合并症评分较高。完全缓解率为96%,65%的患者在巩固治疗期间BCR-ABL1转录水平降低了3个对数。只有7例患者接受了异基因造血干细胞移植。5年时,总生存率为36%,若将与疾病或治疗无关的死亡作为竞争因素考虑,总生存率可达45%。36例患者复发,24例通过桑格测序检测突变,75%为T315I阳性。对43例患者采用等位基因特异性寡核苷酸逆转录定量聚合酶链反应检测BCR-ABL1(T315I),检测结果与短期复发相关。10例患者(23%)在任何治疗前即为阳性,8例复发,均携带此突变。总之,达沙替尼联合低强度化疗耐受性良好,36%的老年Ph(+) ALL患者获得了长期生存。从诊断开始监测BCR-ABL1(T315I)可识别早期复发高危患者,并可能有助于实现个体化治疗。