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NOPHO ALL2008 方案治疗 1-45 岁急性淋巴细胞白血病患者的结果。

Results of NOPHO ALL2008 treatment for patients aged 1-45 years with acute lymphoblastic leukemia.

机构信息

Department of Hematology, Herlev University Hospital, University of Copenhagen, Herlev, Denmark.

Department of Hematology, University Hospital Rigshospitalet, Copenhagen, Denmark.

出版信息

Leukemia. 2018 Mar;32(3):606-615. doi: 10.1038/leu.2017.265. Epub 2017 Aug 18.

Abstract

Adults with acute lymphoblastic leukemia (ALL) do worse than children. From 7/2008 to 12/2014, Nordic and Baltic centers treated 1509 consecutive patients aged 1-45 years with Philadelphia chromosome-negative ALL according to the NOPHO ALL2008 without cranial irradiation. Overall, 1022 patients were of age 1-9 years (A), 266 were 10-17 years (B) and 221 were 18-45 years (C). Sixteen patients (three adults) died during induction. All others achieved remission after induction or 1-3 intensive blocks. Subsequently, 45 patients (12 adults) died, 122 patients relapsed (32 adults) with a median time to relapse of 1.6 years and 13 (no adult) developed a second malignancy. Median follow-up time was 4.6 years. Among the three age groups, older patients more often had higher risk ALL due to T-ALL (32%/25%/9%, P<0.001), KMT2A rearrangements (6%/5%/3%, P<0.001) and higher day 29 residual leukemia for B-lineage (P<0.001), but not T-ALL (P=0.53). Event-free survival rates (pEFS) were 89±1% (A), 80±3% (B) and 74±4% (C) with significant differences only for non-high risk groups. Except for thrombosis, pancreatitis and osteonecrosis, the risk of 19 specified toxicities was not enhanced by age above 10 years. In conclusion, a pediatric-based protocol is tolerable and effective for young adults, despite their increased frequency of higher risk features.

摘要

1-45 岁费城染色体阴性急性淋巴细胞白血病患者的治疗结果:北欧和波罗的海协作组儿童肿瘤研究组 NOPHO ALL2008 方案的成人患者报告

从 2008 年 7 月至 2014 年 12 月,北欧和波罗的海协作组儿童肿瘤研究组 NOPHO ALL2008 方案治疗了 1509 例连续的费城染色体阴性急性淋巴细胞白血病患者,这些患者年龄为 1-45 岁,未接受颅脑照射。总体而言,1022 例患者年龄为 1-9 岁(A 组),266 例患者年龄为 10-17 岁(B 组),221 例患者年龄为 18-45 岁(C 组)。16 例患者(3 例为成人)在诱导期死亡。所有其他患者在诱导期或 1-3 个强化治疗后达到缓解。随后,45 例患者(12 例为成人)死亡,122 例患者复发(32 例为成人),中位复发时间为 1.6 年,13 例(无成人)发生第二恶性肿瘤。中位随访时间为 4.6 年。在这三个年龄组中,年龄较大的患者因 T-ALL(32%/25%/9%,P<0.001)、KMT2A 重排(6%/5%/3%,P<0.001)和更高的 B 系残留白血病(P<0.001),而非 T-ALL(P=0.53),更常出现高危 ALL。无事件生存(pEFS)率分别为 89±1%(A 组)、80±3%(B 组)和 74±4%(C 组),仅在非高危组中差异有统计学意义。除血栓形成、胰腺炎和骨坏死外,年龄大于 10 岁并未增加 19 种特定毒性的风险。总之,尽管高危特征的发生率增加,但基于儿科的方案对于年轻成人是可耐受且有效的。

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