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4/2024
vol. 99 abstract:
Original paper
Incidence of secondary malignancies in Polish children treated for acute lymphoblastic leukemia according to the ALL-IC BFM 2002 protocol
Kamila Wypyszczak
1
,
Agata Pastorczak
2
,
Jerzy Kowalczyk
3
,
Tomasz Szczepański
4
,
Monika Lejman
5
,
Walentyna Balwierz
6
,
Bernarda Kazanowska
7
,
Katarzyna Derwich
8
,
Elżbieta Adamkiewicz-Drożyńska
9
,
Joanna Trelińska
10
,
Andrzej Kołtan
11
,
Maryna Krawczuk-Rybak
12
,
Tomasz Ociepa
13
,
Tomasz Urasiński
13
,
Grażyna Sobol-Milejska
14
,
Grażyna Karolczyk
15
,
Paweł Łaguna
16
,
Jan Styczyński
11
,
Jacek Wachowiak
8
,
Wojciech Młynarski
17
Pediatr Pol 2024; 99 (4): 291-296
Online publish date: 2024/12/30
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Introduction:
Acute lymphoblastic leukemia (ALL) is the most commonly diagnosed childhood cancer, with a peak incidence around 5 years of age. Aim of the study was to assess the incidence, type, and outcome of secondary malignancies in children who were primarily treated for ALL. Material and methods: We enrolled in the analysis 1868 children uniformly treated for ALL between 2 October 2002 and 22 December 2012 according to the protocol ALL-IC BFM 2002. In this study group, we assessed the incidence and type of secondary cancer and outcome. Results: We identified 12 patients (0.64%) who developed secondary malignancies after the median time of 1.72 years from the primary diagnosis of ALL (range: 11.5 months to 18 years). The most frequently diagnosed second neoplasms were hematological malignancies (8 out of 12; 66.7%) including acute myeloid leukemia (AML) (n = 4), non-Hodgkin lymphoma (NHL) (n = 2), chronic myeloid leukemia (CML) (n = 1), and leukemia of unknown immunophenotype (n = 1). In total, four children developed subsequent solid tumors: Ewing sarcoma (n = 1), primitive neuroectodermal tumor (n = 1), myeloid sarcoma (n = 1), and solid tumors of unknown origin (n = 1). Children diagnosed with second cancer were non-significantly older at primary ALL diagnosis in comparison with patients without second cancer (12.083 [3.4–14.0] vs. 5.25 [3.2–10.2]; p = 0.063). The risk group distribution differed between patients with and without a second cancer: 2 (16.67%) vs. 606 (32.65%) children were assigned to the standard risk (SR) group, 5 (41.67%) vs. 894 (48.17%) in the intermediate risk (IR) group, and 5 (41.67%) vs. 356 (19.18%) in the high risk (HR) group. Patients with secondary malignancies showed a significantly lower probability of 5-year overall survival as compared to children without subsequent tumors: 26.5% vs. 85.7%; p < 10–5; HR = 5.9; 95% CI: 2.91–11.96. Conclusions: Blood cancers are the most frequently observed malignancies in children treated for ALL during the first 3 years after treatment completion. Diagnosis of secondary tumor after being treated for ALL is related to poor outcome. keywords:
pediatric acute lymphoblastic leukemia, secondary neoplasm, ALL-IC BFM 2002 |