Ponatinib vs. Imatinib as Frontline Treatment for Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia: A Matching Adjusted Indirect Comparison

医学 帕纳替尼 伊马替尼 内科学 肿瘤科 长春新碱 危险系数 人口 化疗 环磷酰胺 置信区间 达沙替尼 髓系白血病 环境卫生
作者
Josep‐María Ribera,Thibaud Prawitz,Andreas Freitag,Anuj Sharma,Balázs Dobi,Federica Rizzo,Lorenzo Sabatelli,Petros Patos
出处
期刊:Advances in Therapy [Adis, Springer Healthcare]
卷期号:40 (7): 3087-3103 被引量:4
标识
DOI:10.1007/s12325-023-02497-y
摘要

Efficacy of ponatinib-based treatment for patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph + ALL) has not been compared to imatinib-based treatments in head-to-head clinical trials. We evaluated its efficacy versus imatinib-based regimens using a matching adjusted indirect comparison. Two ponatinib studies were used: the phase 2 MDACC study of ponatinib + hyper-CVAD (cyclophosphamide, vincristine, doxorubicin, and dexamethasone) in adult patients and the phase 2 GIMEMA LAL1811 study of ponatinib + steroids in patients > 60 years/unfit for intensive chemotherapy and stem cell transplant. Studies on imatinib as first-line treatment in adults with Ph + ALL were identified using a systematic literature search. Population adjustment was based on the prognostic factors and effect modifiers identified by clinical experts. Hazard ratios (HRs) were calculated for overall survival (OS) and odds ratios (ORs) for complete molecular response (CMR). The systematic literature search identified two studies (GRAAPH-2005 and NCT00038610) reporting the efficacy of first-line imatinib + hyper-CVAD and one study reporting the efficacy of first-line imatinib monotherapy induction + imatinib-based consolidation (CSI57ADE10). Ponatinib + hyper-CVAD prolonged OS and gave a higher CMR rate than imatinib + hyper-CVAD. The adjusted HR [95% confidence interval (CI)] for OS was 0.35 (0.17–0.74) for MDACC vs. GRAAPH-2005 and 0.35 (0.18–0.70) for MDACC vs. NCT00038610; the adjusted OR (95% CI) for CMR was 12.11 (3.77–38.87) for MDACC vs. GRAAPH-2005 and 5.65 (2.02–15.76) for MDACC vs. NCT00038610. Ponatinib + steroids prolonged OS and gave a higher CMR rate than imatinib monotherapy induction + imatinib-containing consolidation. The adjusted HR (95% CI) for OS was 0.24 (0.09–0.64) and the adjusted OR (95% CI) for CMR was 6.20 (1.60–24.00) for GIMEMA LAL1811 vs. CSI57ADE10. In adults with newly diagnosed Ph + ALL, first-line treatment with ponatinib was associated with better outcomes than first-line treatment with imatinib.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
夜白完成签到,获得积分0
1秒前
anan完成签到 ,获得积分10
6秒前
小陈完成签到,获得积分10
7秒前
噼里啪啦完成签到,获得积分10
11秒前
博林大师完成签到,获得积分0
21秒前
ming完成签到,获得积分10
35秒前
hongt05完成签到 ,获得积分10
40秒前
40秒前
李健应助霸气的以冬采纳,获得10
46秒前
jun完成签到 ,获得积分10
46秒前
GSQ发布了新的文献求助10
47秒前
47秒前
48秒前
49秒前
zyp应助科研通管家采纳,获得10
49秒前
zyp应助科研通管家采纳,获得10
49秒前
hadfunsix完成签到 ,获得积分10
51秒前
52秒前
yyx发布了新的文献求助20
52秒前
xiaobai发布了新的文献求助10
53秒前
林好人发布了新的文献求助10
57秒前
duonicola完成签到,获得积分10
58秒前
twang93完成签到,获得积分10
1分钟前
舒克完成签到,获得积分10
1分钟前
ni完成签到 ,获得积分10
1分钟前
时生111完成签到 ,获得积分10
1分钟前
居学尉完成签到,获得积分0
1分钟前
jjq完成签到,获得积分10
1分钟前
1分钟前
whh123完成签到 ,获得积分10
1分钟前
芝麻汤圆完成签到,获得积分10
1分钟前
听寒完成签到,获得积分10
1分钟前
自然之水完成签到,获得积分10
1分钟前
qq158014169完成签到 ,获得积分10
1分钟前
1分钟前
earthai完成签到,获得积分10
1分钟前
半颗橙子完成签到 ,获得积分10
1分钟前
研时友完成签到,获得积分10
1分钟前
li完成签到 ,获得积分10
1分钟前
杨怂怂完成签到 ,获得积分10
1分钟前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
Mindfulness and Character Strengths: A Practitioner's Guide to MBSP 380
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3776037
求助须知:如何正确求助?哪些是违规求助? 3321608
关于积分的说明 10206370
捐赠科研通 3036673
什么是DOI,文献DOI怎么找? 1666435
邀请新用户注册赠送积分活动 797439
科研通“疑难数据库(出版商)”最低求助积分说明 757839