Evidence map›Paper›PMID 42240938›Full record

ArticleDiscover oncology2026

Patterns of relapse and survival outcomes in pediatric ALL from a single center cohort under the CCCG ALL 2015 protocol.

Jianming Fang, Hongyan Liu, Qi Liu, Yingli Zhang, Guoqin Hai, Han Gong, Xin Tian

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Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Jianming Fang *Department of Hematological Solid Oncology, Beijing Jingdu Children's Hospital, Beijing, 102200, China.
Hongyan Liu *Department of Hematological Solid Oncology, Beijing Jingdu Children's Hospital, Beijing, 102200, China.
Qi LiuDepartment of Hematological Solid Oncology, Beijing Jingdu Children's Hospital, Beijing, 102200, China.
Yingli ZhangDepartment of Hematological Solid Oncology, Beijing Jingdu Children's Hospital, Beijing, 102200, China.
Guoqin HaiTranslational Cancer Research Center, Peking University First Hospital, Beijing, China.
Han GongDepartment of Hematological Solid Oncology, Beijing Jingdu Children's Hospital, Beijing, 102200, China.
Xin TianHematology Department, Yunnan Children's Medical Center, No. 288 Qianxing Road, Xishan District, Kunming, 650000, Yunnan, China. 19350303814@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo characterize relapse patterns, identify relapse-related risk factors, and evaluate prognostic determinants of post-relapse outcomes in pediatric acute lymphoblastic leukemia (ALL) patients treated with the Chinese Children's Cancer Group (CCCG)-ALL-2015 protocol.

methodsThis retrospective study included 380 children diagnosed with ALL between 2016 and 2019. We analyzed relapse timing (very early, early, late), relapse sites (bone marrow (BM) vs. extramedullary), early treatment response (morphology and minimal residual disease (MRD)), and post-relapse outcomes. Survival was estimated using Kaplan-Meier methods.

resultsRelapse rate was 11.1% (42/380), predominantly isolated BM (69.0%) and very early timing (47.6%). Relapse varied significantly by risk group (low-risk: 5.9%; intermediate-risk: 10.4%; high-risk: 22.4%; P < 0.001), immunophenotype (B-ALL: 9.8% vs. T-ALL: 23.5%; P = 0.015), Day 19 morphology (M1:9.9% vs. M3:20.0%; P < 0.001), Day 46 morphology (M1:10.5% vs. M3:21.4%; P = 0.025), and Day 46 MRD status (positive:21.4% vs. negative:8.7%; P = 0.002). Fusion gene positivity was significantly associated with earlier relapse timing (P < 0.05). Post-relapse survival differed by relapse timing (very early: 7.2 months; early: 23.2 months; late: 37.8 months; P < 0.001) and initial risk group (low-risk: 38.2 months; high-risk: 18.1 months; P = 0.006).

conclusionsNon-remission on Days 19/46, Day 46 MRD positivity, and high-risk status predict ALL relapse. High-risk patients experience earlier relapses and poorer survival. Fusion gene positivity is associated with earlier relapse timing.

Indexed as

Acute lymphoblastic leukemiaCCCG-ALL-2015PediatricsPrognostic factorsRelapse

Identifiers

PMID42240938
PMCPMC13454078

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.