Outcomes in patients with ETV6::RUNX1 or high-hyperdiploid B-ALL treated in the St. Jude Total Therapy XV/XVI studies

被引:1
|
作者
Purvis, Katelyn [1 ]
Zhou, Yinmei [2 ]
Karol, Seth E. [1 ]
Rubnitz, Jeffrey E. [1 ]
Ribeiro, Raul C. [1 ]
Lee, Shawn [3 ,4 ,5 ]
Yang, Jun J. [3 ]
Bowman, W. Paul [6 ]
Wang, Lu [7 ]
Dixon, Stephanie B. [1 ]
Roberts, Kathryn G. [7 ]
Gao, Qingsong [7 ]
Cheng, Cheng [2 ]
Mullighan, Charles G. [7 ]
Jeha, Sima [1 ,8 ]
Pui, Ching-Hon [1 ,8 ]
Inaba, Hiroto [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Oncol, 262 Danny Thomas Pl, Mail Stop 260, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Biostat, Memphis, TN USA
[3] St Jude Childrens Res Hosp, Dept Pharm & Pharmaceut Sci, Memphis, TN USA
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Paediat, Singapore, Singapore
[5] Natl Univ Hlth Syst, Khoo Teck Puat Natl Univ Childrens Med Inst, Singapore, Singapore
[6] Cook Childrens Med Ctr, Dept Pediat, Ft Worth, TX USA
[7] St Jude Childrens Res Hosp, Dept Pathol, Memphis, TN USA
[8] St Jude Childrens Res Hosp, Dept Global Pediat Med, Memphis, TN USA
基金
美国国家卫生研究院;
关键词
ACUTE LYMPHOBLASTIC-LEUKEMIA; LOW-RISK; CHILDHOOD; INTENSIFICATION; SENSITIVITY; ETV6-RUNX1; REDUCTION; CHILDREN; PROTOCOL; FAILURE;
D O I
10.1182/blood.2024024936
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Children with ETV6::RUNX1 or high-hyperdiploid B-cell acute lymphoblastic leukemia (B-ALL) have favorable outcomes. The St. Jude (SJ) classification considers these patients low risk, regardless of their National Cancer Institute (NCI) risk classification, except when there is slow minimal residual disease (MRD) response or central nervous system/testicular involvement. We analyzed outcomes in children (aged 1-18.99 years) with these genotypes in the SJ Total XV/XVI studies (2000-2017). Patients with ETV6::RUNX1 (n = 222) or high-hyperdiploid (n = 296) B-ALL had 5-year event-free survival (EFS) of 97.7% +/- 1.1% and 94.7% +/- 1.4%, respectively. For ETV6::RUNX1, EFS was comparable between NCI standard-risk and high-risk patients and between SJ low-risk and standard-risk patients. Of the 40 NCI high-risk patients, 37 who received SJ low-risk therapy had excellent EFS (97.3% +/- 2.8%). For high-hyperdiploid B-ALL, NCI high-risk patients had worse EFS than standard-risk patients (87.6% +/- 4.5% vs 96.4%+/- 1.3%; P = .016). EFS was similar for NCI standard-risk and high-risk patients classified as SJ low risk (96.0% +/- 1.5% and 96.9% +/- 3.2%; P = .719). However, EFS was worse for NCI high-risk patients than for NCI standard-risk patients receiving SJ standard/high-risk therapy (77.4% +/- 8.2% vs 98.0% +/- 2.2%; P = .004). NCI high-risk patients with ETV6::RUNX1 or high-hyperdiploid B-ALL who received SJ low-risk therapy had lower incidences of thrombosis (P = .013) and pancreatitis (P = .011) than those who received SJ standard/high-risk therapy. MRD-directed therapy yielded excellent outcomes, except for NCI high-risk high-hyperdiploid B-ALL patients with slow MRD response, who require new treatment approaches. Among NCI high-risk patients, 93% with ETV6::RUNX1 and 54% with highhyperdiploid B-ALL experienced excellent outcomes with a low-intensity regimen. These trials were registered at www.clinicaltrials.gov as #NCT00137111 and #NCT00549848.
引用
收藏
页码:190 / 201
页数:12
相关论文
共 8 条
  • [1] OUTCOMES OF PATIENTS WITH ETV6-RUNX1 AND HYPERDIPLOID B-ACUTE LYMPHOBLASTIC LEUKEMIA TREATED IN THE ST. JUDE TOTAL 15 AND 16 STUDIES
    Purvis, Katelyn
    Zhou, Yinmei
    Karol, Seth
    Rubnitz, Jeffrey
    Ribeiro, Raul
    Lee, Shawn
    Yang, Jun
    Cheng, Cheng
    Mullighan, Charles
    Jeha, Sima
    Pui, Ching-Hon
    Inaba, Hiroto
    PEDIATRIC BLOOD & CANCER, 2022, 69
  • [2] Response Adapted Therapy in ETV6/RUNX1-Positive Childhood Acute Lymphoblastic Leukemia Treated per Modified St Jude Total XV Study
    Abu Shanap, Mayada
    Sultan, Iyad
    Abu-Ghosh, Amal
    Hashem, Hasan
    Tbakhi, Abdelghani
    Rihani, Rawad
    BLOOD, 2020, 136
  • [3] Recurrent Focal Mkks-SLX4IP Deletion in ETV6::RUNX1 and Ph/Ph-like B-ALL
    Zhang, Yang
    Liu, Ming
    Ma, Xiaoli
    Fang, Jiancheng
    Wang, Fang
    Chen, Xue
    Liu, Hongxing
    BLOOD, 2024, 144 : 1467 - 1468
  • [4] Analysis of ETV6/RUNX1 fusions for evaluating the late effects of cancer therapy in ALL (acute lymphoblastic leukemia) cured patients
    Brassesco, MS
    Camparoto, ML
    Tone, LG
    Sakamoto-Hojo, ET
    CYTOGENETIC AND GENOME RESEARCH, 2004, 104 (1-4) : 346 - 351
  • [5] CLINICAL CHARACTERISTICS AND THERAPY OUTCOMES OF PATIENTS WITH ETV6/RUNX1 POSITIVE B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA, TREATED ACCORDING TO RUSSIAN MB-2008 PROTOCOL
    Kazakova, A. N.
    Matveeva, E. A.
    Timofeeva, N. M.
    Chekmeneva, J. J.
    Lagoiko, S. N.
    Rumyantceva, J. V.
    Bydanov, O. I.
    Tsaur, G. A.
    Nasedkina, T. V.
    Alenikova, O. V.
    Olshanskaya, Y. V.
    Karachunskiy, A. I.
    PEDIATRIC BLOOD & CANCER, 2013, 60 : 63 - 63
  • [6] Apparent coexistence of ETV6::RUNX1 and KMT2A::MLLT3 fusions due to a nonproductive KMT2A rearrangement in B-ALL
    Gagnon, Marie-France
    Smadbeck, James B.
    Sharma, Neeraj
    Blackburn, Patrick R.
    Demasi Benevides, Jonna
    Akkari, Yassmine M. N.
    Jaroscak, Jennifer J.
    Znoyko, Iya
    Wolff, Daynna J.
    Schandl, Cynthia A.
    Meyer, Reid
    Greipp, Patricia T.
    Xu, Xinjie
    Hoppman, Nicole L.
    Ketterling, Rhett P.
    Peterson, Jess F.
    Baughn, Linda B.
    LEUKEMIA & LYMPHOMA, 2022, 63 (09) : 2243 - 2246
  • [7] FISH信号类型和染色体核型分析在ETV6/RUNX1阳性B-ALL患儿中的诊疗价值评估
    高雨晴
    徐鸥
    胡绍燕
    临床与实验病理学杂志, 2024, 40 (01) : 40 - 43
  • [8] Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol
    Barbany, Gisela
    Andersen, Mette K.
    Autio, Kirsti
    Borgstrom, Georg
    Franco, Lucia Cavalier
    Golovleva, Irina
    Heim, Sverre
    Heinonen, Kristina
    Hovland, Randi
    Johansson, Bertil
    Johannsson, Johann H.
    Kjeldsen, Eigil
    Nordgren, Ann
    Palmqvist, Lars
    Forestier, Erik
    LEUKEMIA RESEARCH, 2012, 36 (07) : 936 - 938