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Pediatric Precursor B-Cell Lymphoblastic Malignancies: From Extramedullary to Medullary Involvement

Kroeze, E. (author)
Padilla, L. A. (author)
Bakker, M. (author)
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Boer, J. M. (author)
Hagleitner, M. M. (author)
Burkhardt, B. (author)
Mori, T. (author)
Attarbaschi, A. (author)
Verdu-Amoros, J. (author)
Pillon, M. (author)
Anderzhanova, L. (author)
Kabickova, E. (author)
Chiang, A. K. S. (author)
Kebudi, R. (author)
Mellgren, Karin, 1962 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics
Lazic, J. (author)
Jazbec, J. (author)
Meijerink, J. P. P. (author)
Beishuizen, A. (author)
Loeffen, J. L. C. (author)
European Intergrp, Childhood (author)
Int Berlin Frankfurt, Munster (author)
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 (creator_code:org_t)
2022-08-12
2022
English.
In: Cancers. - : MDPI AG. - 2072-6694. ; 14:16
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Simple Summary B-cell lymphoblastic lymphoma (BCP-LBL) and B-cell acute lymphoblastic leukemia (BCP-ALL) are both malignancies of immature B-cells. However, BCP-ALL has been extensively studied and treatment protocols have changed over the last decades, whereas BCP-LBL is quite rare, and treatment has stayed roughly the same. In this retrospective study, we compare the clinical characteristics of a cohort of BCP-LBL patients to a cohort BCP-ALL patients. With the comparison of this unique large cohort of immature B-cell malignancies, we aim to contribute to elucidating whether BCP-LBL and BCP-ALL represent two diseases, or different representations of the same disease. Increasing the understanding of BCP-LBL in comparison to BCP-ALL is crucial for improving treatment and prognosis for BCP-LBL. B-cell lymphoblastic lymphoma (BCP-LBL) and B-cell acute lymphoblastic leukemia (BCP-ALL) are the malignant counterparts of immature B-cells. BCP-ALL is the most common hematological malignancy in childhood, while BCP-LBL accounts for only 1% of all hematological malignancies in children. Therefore, BCP-ALL has been well studied and treatment protocols have changed over the last decades, whereas treatment for BCP-LBL has stayed roughly the same. Clinical characteristics of 364 pediatric patients with precursor B-cell malignancies were studied, consisting of BCP-LBL (n = 210) and BCP-ALL (n = 154) patients. Our results indicate that based on the clinical presentation of disease, B-cell malignancies probably represent a spectrum ranging from complete isolated medullary disease to apparent complete extramedullary disease. Hepatosplenomegaly and peripheral blood involvement are the most important discriminators, as both seen in 80% and 95% of the BCP-ALL patients and in 2% of the BCP-LBL patients, respectively. In addition, we show that the overall survival rates in this cohort differ significantly between BCP-LBL and BCP-ALL patients aged 1-18 years (p = 0.0080), and that the outcome for infants (0-1 years) with BCP-LBL is significantly decreased compared to BCP-LBL patients of all other pediatric ages (p < 0.0001).

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

B-cell lymphoblastic lymphoma
BCP-LBL
B-cell acute lymphoblastic
leukemia
BCP-ALL
non-Hodgkin lymphoma
NHL
disease spectrum
leukemia
children
adolescents
infants
disease
reduction
lymphomas
survival
therapy
trial
Oncology

Publication and Content Type

ref (subject category)
art (subject category)

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