scholarly journals XI. How to treat children and adolescents with relapsed non-Hodgkin lymphoma?

2013 ◽  
Vol 31 (S1) ◽  
pp. 64-68 ◽  
Author(s):  
Wilhelm Woessmann
2019 ◽  
Vol 66 (9) ◽  
Author(s):  
Charlotte Rigaud ◽  
Anne Auperin ◽  
Anne Jourdain ◽  
Stephanie Haouy ◽  
Marie‐Laure Couec ◽  
...  

2018 ◽  
Vol 10 (1) ◽  
pp. e2018020 ◽  
Author(s):  
Paola Angelini ◽  
Laura Rodriguez ◽  
Mohammed Zolaly ◽  
Ahmed Naqvi ◽  
Sheila Weitzman ◽  
...  

Background: The incidence and biology of non-Hodgkin lymphoma (NHL) vary according to age. Some data suggest that the impact of age in pediatric and adolescent NHL patients depends on the histological subtype. Objectives: We aimed to analyze the impact of age at diagnosis on clinical characteristics and treatment-related toxicity in children and adolescents with NHL.Methods: Retrospective review of medical records of children and adolescents diagnosed with NHL at the Hospital for Sick children, Toronto, between January 1995 and December 2008.Results: 164 children were diagnosed with NHL during the study period, with a median age at diagnosis of 10 years. With a median follow-up of 6.2 years, 5-year OS in patients aged <15 and 15-18 years was 89± 2% vs 82% ± 6%, respectively (P = 0.30), and 5-year EFS was 84% ± 3% vs. 77% ± 7%  (P= 0.37). In Burkitts lymphoma (BL) and lymphoblastic lymphoma (LL) there was a trend towards better outcomes in children compared to adolescents, with EFS of  91% ± 4% vs. 75% ± 15%, respectively in BL (P= 0.17),  and 82% ± 7% vs. 51.4% ± 2% respectively in LL (P= 0.16). Late effects occurred in 21 patients (12.8%).Conclusions: Children with NHL aged < 15 years tend to have better survival rates and less long-term toxicity than adolescents aged 15-18 years.


2014 ◽  
Vol 61 (11) ◽  
pp. 2083-2085 ◽  
Author(s):  
Cristiano de Queiroz Mendonca ◽  
Cristiano Prado de Souza ◽  
Paulo Ricardo Saquete Martins-Filho ◽  
Simone Santana Viana ◽  
Bruno Campelo Leal ◽  
...  

2008 ◽  
Vol 143 (3) ◽  
pp. 387-394 ◽  
Author(s):  
Eva Landmann ◽  
Ilske Oschlies ◽  
Martin Zimmermann ◽  
Olga Moser ◽  
Norbert Graf ◽  
...  

Author(s):  
Ana Rosa S. Costa ◽  
Juliana T. Costa ◽  
Carla Nolasco Monteiro Breviglieri ◽  
Lucélia M.P. Melgares ◽  
Patrick R. Godinho ◽  
...  

Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 4413-4413 ◽  
Author(s):  
Roques Gaelle ◽  
Ananth Shankar ◽  
Thierry Leblanc ◽  
Claudine Schmitt ◽  
Janis Hayward ◽  
...  

Abstract Background: Advanced stage nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) in children and adolescents is a very rare entity and therefore few data about their treatment and outcome are available. Aim of the study: To describe the clinical characteristics and evolution of advanced stage NLPHL in children and adolescents Methods:A retrospective analysis of clinical data of patients treated in the SFCE and UK CCLG centers Patients and Results: 32 patients with NLPHL according to the REAL/WHO classification with disease stage ≥ IIB were recorded between 1998 and 2013. Two patients had composite NLPHL and B cell non-Hodgkin lymphoma at diagnosis. Median age was 12 years (range 4-17) and the majority were boys [n=28; 88%]. Stage distribution was: IIB =2 ( 6%), III =25 (71%) & stage IV =5 (15%). Twenty-seven patients had cervical node involvement while mediastinum involvement was seen in 11 (34% ) patients. B symptoms were seen in 2 and eight patients had ESR >30 mm. Sites of extra nodal localisation were bone, bone marrow, liver and lungs.Standard Hodgkin chemotherapy regimens (CT) were used in 26 patients (81%), combined with rituximab (R) in 5 children (3 to 6 doses) and along with 20Gy involved field radiotherapy in 6 children. NHL chemotherapy regimens were used in 5 patients; R-CHOP [n=3], LMB 01 regimen [n=1] and other regimen [n=1]. One patient received rituximab alone (4 doses) and 1 child had no treatment [watch and wait strategy]. Median follow up is 45 months (5 – 162). Outcome: Overall survival is 96% and cumulative incidence of an event is 25%. Eight patients relapsed with a median delay of 15 months (5-73), and 3 had a second relapse 9,11 and 48 months respectively after first relapse. One patient treated with chemotherapy alone developed Ewing's sarcoma and died 2 years later. The only patient treated with rituximab alone relapsed at 22 months. Of note, no relapses were observed in patients who had chemotherapy and rituximab. Conclusion: Our report shows that while advanced stage NLPHL in children and adolescents is rare, their clinical outcome is very good. Additionally, this report may inform the basis of future treatment of advanced stage NLPHL in children and adolescents. Disclosures No relevant conflicts of interest to declare.


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