With the development of molecular biology and precise medical treatment, new challenges have been raised in the diagnosis and treatment of non-Hodgkin lymphoma (NHL) in children. In recent years, the criteria for clinical staging and efficacy evaluation of NHL in children have been updated. Recent clinical studies of COG in the United States and LMB in France have confirmed that molecular biological markers such as Notch1, PTEN and LOH6q are significantly associated with the prognosis of T-lymphoblastic lymphoma (T-LBL). These molecular biological markers should be included in the new risk stratification system. High-intensity treatment of high-risk patients will improve survival. Recent studies have also suggested that PET/CT is helpful in evaluating residual lesions in patients with lymphoma after chemotherapy. In order to keep pace with the times in the diagnosis, clinical staging, risk stratification, efficacy evaluation and treatment of NHL in children. SCCCG-LBL-2017 was formulated by South China Children's Cancer Group of Non-Hodgkin lymphoma, which mainly updated in clinical staging, efficacy evaluation, risk stratification, treatment,etc..
Research purpose: 1. To investigate the efficacy and safety of SCCCG-LBL-2017 in Chinese children with LBL. 2. To explore the feasibility of risk stratification of T-LBL by combining genotyping. 3. To investigate the correlation between MDD and MRD in lymphoblastic lymphoma and prognosis. 4. To investigate the role of PET/CT in the assessment of residual lymphoblastic lymphoma. 5. To explore the effect of reducing HD-MTX dosage and shortening maintenance therapy time on the efficacy and survival of low-risk LBL patients. 6. To explore the effect of prolonging the duration of maintenance therapy on the efficacy and survival of high-risk LBL patients.
Study Type
OBSERVATIONAL
Enrollment
300
Sun Yat-sen University Cancer Center
Guangzhou, Guangdong, China
RECRUITINGEvent-free survival (EFS)
EFS is defined as time from start of treatment/randomization up to event or to date of last contact for patients without event. The following occurrences are defined as an event: non-response, progressive disease or relapse, treatment related death, death of any other cause or diagnosis of secondary malignancies.
Time frame: through study completion, maximal eight years
Overall survival (OS)
OS is defined as time from start of treatment/randomization up to death of any
Time frame: through study completion, maximal eight years
Relapse-free survival (RFS)
RFS is defined as time from start of treatment/randomization up to event or to date of last contact for patients without event. The following occurrences are defined as an event: non-response, progressive disease, or relapse.
Time frame: through study completion, maximal eight years
Response rate (RR)
Complete response, partial remission, objective effect, stable disease or progressive disease
Time frame: on an average 3 weeks after finish of treatment
Adverse event rate
Rate of patients with acute toxicity defined as grade III/IV/V AE
Time frame: through study completion, maximal eight years
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