共 50 条
Children's Oncology Group blueprint for research: Acute lymphoblastic leukemia
被引:4
|作者:
Raetz, Elizabeth A.
[1
]
Bhojwani, Deepa
[2
,3
]
Devidas, Meenakshi
[4
,5
]
Gore, Lia
[6
]
Rabin, Karen R.
[7
]
Tasian, Sarah K.
[8
]
Teachey, David T.
[8
]
Loh, Mignon L.
[9
,10
]
机构:
[1] New York Univ Langone Hlth, Perlmutter Canc Ctr, Dept Pediat, New York, NY USA
[2] Univ Southern Calif, Childrens Hosp Los Angeles, Norris Comprehens Canc Ctr, Dept Pediat, Los Angeles, CA USA
[3] Univ Southern Calif, Childrens Hosp Los Angeles, Keck Sch Med, Dept Pediat, Los Angeles, CA USA
[4] St Jude Childrens Res Hosp, Dept Biostat, Memphis, TN USA
[5] St Jude Childrens Res Hosp, Dept Global Med, Memphis, TN USA
[6] Univ Colorado, Childrens Hosp Colorado, Ctr Canc & Blood Disorders, Dept Pediat,Sch Med, Aurora, CO USA
[7] Baylor Coll Med, Texas Childrens Canc Ctr, Div Pediat Hematol Oncol, Houston, TX USA
[8] Univ Penn, Childrens Hosp Philadelphia, Ctr Childhood Canc Res, Div Oncol,Sch Med, Philadelphia, PA USA
[9] Seattle Childrens Res Inst, Ben Towne Ctr Childhood Canc Res, Seattle, WA 98101 USA
[10] Univ Washington, Seattle Childrens Hosp, Dept Pediat, Seattle, WA 98195 USA
关键词:
clinical trials;
lymphoblastic leukemia;
precision medicine;
MINIMAL RESIDUAL DISEASE;
HIGH-RISK;
INOTUZUMAB OZOGAMICIN;
1ST RELAPSE;
CHEMOTHERAPY;
ADOLESCENTS;
SURVIVAL;
TRIAL;
BLINATUMOMAB;
LANDSCAPE;
D O I:
10.1002/pbc.30585
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Cure rates for acute lymphoblastic leukemia (ALL), the most common childhood cancer have steadily improved over the past five decades. This is due to intensifying systemic therapy, recognizing and treating the central nervous system as a sanctuary site, and implementing modern risk stratification to deliver varying intensities of therapy based on age, presenting white blood count, sentinel somatic genetics, and therapy response. Recently, numerous Children's Oncology Group trials have demonstrated the lack of benefit of intensifying traditional chemotherapy, providing evidence that new approaches are needed to cure the patients for whom cure has been elusive. Distinguishing those who require intensive or novel therapeutic approaches from others who will be cured with minimal therapy is key for future trials. Incorporating new genomic biomarkers and more sensitive measures of minimal/measurable residual disease provide opportunities to achieve these goals.
引用
收藏
页数:10
相关论文