Cytogenetic and pathologic characterization of MYC-rearranged B-cell lymphomas in pediatric and young adult patients
© 2024. The Author(s)..
MYC-rearranged B-cell lymphoma (BCL) in the pediatric/young adult (YA) age group differs substantially in disease composition from adult cohorts. However, data regarding the partner genes, concurrent rearrangements, and ultimate diagnoses in these patients is scarce compared to that in adult cohorts. We aimed to characterize the spectrum of MYC-rearranged (MYC-R) mature, aggressive BCL in the pediatric/YA population. A retrospective study of morphologic, immunophenotypic, and fluorescence in situ hybridization (FISH) results of patients age ≤ 30 years with suspected Burkitt lymphoma (BL), diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBCL), and a MYC-R by FISH between 2013-2022 was performed. Two-hundred fifty-eight cases (129 (50%) pediatric (< 18 years) and 129 (50%) YA (18-30 years)) were included. Most MYC-R BCL in pediatric (89%) and YA (66%) cases were BL. While double-hit (DH) cytogenetics (MYC with BCL2 and/or BCL6-R, HGBCL-DH) was rare in the pediatric population (2/129, 2%), HGBCL-DH increased with age and was identified in 17/129 (13%) of YA cases. Most HGBCL-DH had MYC and BCL6-R, while BCL2-R were rare in both groups (3/258, 1%). MYC-R without an IG partner was more common in the YA group (14/116 (12%) vs 2/128 (2%), p = 0.001). The pediatric to YA transition is characterized by decreasing frequency in BL and increasing genetic heterogeneity of MYC-R BCL, with emergence of DH-BCL with MYC and BCL6-R. FISH to evaluate for BCL2 and BCL6 rearrangements is likely not warranted in the pediatric population but should continue to be applied in YA BCL.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - year:2024 |
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| Enthalten in: |
Journal of hematopathology - (2024) vom: 02. Apr. |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Gagnon, Marie-France [VerfasserIn] |
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| Links: |
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| Themen: |
B-cell lymphoma |
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| Anmerkungen: |
Date Revised 01.04.2024 published: Print-Electronic Citation Status Publisher |
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| doi: |
10.1007/s12308-024-00579-6 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM370509633 |
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| 100 | 1 | |a Gagnon, Marie-France |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Cytogenetic and pathologic characterization of MYC-rearranged B-cell lymphomas in pediatric and young adult patients |
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| 520 | |a © 2024. The Author(s). | ||
| 520 | |a MYC-rearranged B-cell lymphoma (BCL) in the pediatric/young adult (YA) age group differs substantially in disease composition from adult cohorts. However, data regarding the partner genes, concurrent rearrangements, and ultimate diagnoses in these patients is scarce compared to that in adult cohorts. We aimed to characterize the spectrum of MYC-rearranged (MYC-R) mature, aggressive BCL in the pediatric/YA population. A retrospective study of morphologic, immunophenotypic, and fluorescence in situ hybridization (FISH) results of patients age ≤ 30 years with suspected Burkitt lymphoma (BL), diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBCL), and a MYC-R by FISH between 2013-2022 was performed. Two-hundred fifty-eight cases (129 (50%) pediatric (< 18 years) and 129 (50%) YA (18-30 years)) were included. Most MYC-R BCL in pediatric (89%) and YA (66%) cases were BL. While double-hit (DH) cytogenetics (MYC with BCL2 and/or BCL6-R, HGBCL-DH) was rare in the pediatric population (2/129, 2%), HGBCL-DH increased with age and was identified in 17/129 (13%) of YA cases. Most HGBCL-DH had MYC and BCL6-R, while BCL2-R were rare in both groups (3/258, 1%). MYC-R without an IG partner was more common in the YA group (14/116 (12%) vs 2/128 (2%), p = 0.001). The pediatric to YA transition is characterized by decreasing frequency in BL and increasing genetic heterogeneity of MYC-R BCL, with emergence of DH-BCL with MYC and BCL6-R. FISH to evaluate for BCL2 and BCL6 rearrangements is likely not warranted in the pediatric population but should continue to be applied in YA BCL | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a B-cell lymphoma | |
| 650 | 4 | |a Burkitt lymphoma | |
| 650 | 4 | |a Double-hit cytogenetics | |
| 650 | 4 | |a FISH | |
| 650 | 4 | |a High-grade B-cell lymphoma | |
| 650 | 4 | |a MYC rearrangement | |
| 650 | 4 | |a Pediatric B-cell lymphoma | |
| 650 | 4 | |a Young adult B-cell lymphoma | |
| 700 | 1 | |a Bruehl, Frido K |e verfasserin |4 aut | |
| 700 | 1 | |a Sill, Daniel R |e verfasserin |4 aut | |
| 700 | 1 | |a Meyer, Reid G |e verfasserin |4 aut | |
| 700 | 1 | |a Greipp, Patricia T |e verfasserin |4 aut | |
| 700 | 1 | |a Hoppman, Nicole L |e verfasserin |4 aut | |
| 700 | 1 | |a Xu, Xinjie |e verfasserin |4 aut | |
| 700 | 1 | |a Baughn, Linda B |e verfasserin |4 aut | |
| 700 | 1 | |a Peterson, Jess F |e verfasserin |4 aut | |
| 700 | 1 | |a McPhail, Ellen D |e verfasserin |4 aut | |
| 700 | 1 | |a Ketterling, Rhett P |e verfasserin |4 aut | |
| 700 | 1 | |a King, Rebecca L |e verfasserin |4 aut | |
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