Breast implant-associated anaplastic large cell lymphoma: two distinct clinicopathological variants with different outcomes.
Détails
ID Serval
serval:BIB_2E032821781D
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Breast implant-associated anaplastic large cell lymphoma: two distinct clinicopathological variants with different outcomes.
Périodique
Annals of oncology : official journal of the European Society for Medical Oncology
ISSN
1569-8041 (Electronic)
ISSN-L
0923-7534
Statut éditorial
Publié
Date de publication
02/2016
Peer-reviewed
Oui
Volume
27
Numéro
2
Pages
306-314
Langue
anglais
Notes
Publication types: Journal ArticlePublication Status: ppublish
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Résumé
ALK-negative anaplastic large cell lymphoma associated with breast implant (i-ALCL) has been recently recognized as a distinct entity. Among 43 830 lymphomas registered in the French Lymphopath network since 2010, 300 breast lymphomas comprising 25 peripheral T-cell lymphomas (PTCL) were reviewed. Among PTCL, ALK-negative ALCL was the most frequent and all of them were associated with breast implants.
Since 2010, all i-ALCL cases were collected from different institutions through Lymphopath. Immuno-morphologic features, molecular data and clinical outcome of 19 i-ALCLs have been retrospectively analyzed.
The median age of the patients was 61 years and the median length between breast implant and i-ALCL was 9 years. Most implants were silicone-filled and textured. Implant removal was performed in 17 out of 19 patients with additional treatment based on mostly CHOP or CHOP-like chemotherapy regimens (n = 10/19) or irradiation (n = 1/19). CHOP alone or ABVD following radiation without implant removal have been given in two patients. The two clinical presentations, i.e. effusion and less frequently tumor mass correlated with distinct histopathologic features: in situ i-ALCL (anaplastic cell proliferation confined to the fibrous capsule) and infiltrative i-ALCL (pleomorphic cells massively infiltrating adjacent tissue with eosinophils and sometimes Reed-Sternberg-like cells mimicking Hodgkin lymphoma). Malignant cells were CD30-positive, showed a variable staining for EMA and were ALK negative. Most cases had a cytotoxic T-cell immunophenotype with variable T-cell antigen loss and pSTAT3 nuclear expression. T-cell receptor genes were clonally rearranged in 13 out of 13 tested cases. After 18 months of median follow-up, the 2-year overall survival for in situ and infiltrative i-ALCL was 100% and 52.5%, respectively.
In situ i-ALCLs have an indolent clinical course and generally remain free of disease after implant removal. However, infiltrative i-ALCLs could have a more aggressive clinical course that might require additional therapy to implant removal.
Since 2010, all i-ALCL cases were collected from different institutions through Lymphopath. Immuno-morphologic features, molecular data and clinical outcome of 19 i-ALCLs have been retrospectively analyzed.
The median age of the patients was 61 years and the median length between breast implant and i-ALCL was 9 years. Most implants were silicone-filled and textured. Implant removal was performed in 17 out of 19 patients with additional treatment based on mostly CHOP or CHOP-like chemotherapy regimens (n = 10/19) or irradiation (n = 1/19). CHOP alone or ABVD following radiation without implant removal have been given in two patients. The two clinical presentations, i.e. effusion and less frequently tumor mass correlated with distinct histopathologic features: in situ i-ALCL (anaplastic cell proliferation confined to the fibrous capsule) and infiltrative i-ALCL (pleomorphic cells massively infiltrating adjacent tissue with eosinophils and sometimes Reed-Sternberg-like cells mimicking Hodgkin lymphoma). Malignant cells were CD30-positive, showed a variable staining for EMA and were ALK negative. Most cases had a cytotoxic T-cell immunophenotype with variable T-cell antigen loss and pSTAT3 nuclear expression. T-cell receptor genes were clonally rearranged in 13 out of 13 tested cases. After 18 months of median follow-up, the 2-year overall survival for in situ and infiltrative i-ALCL was 100% and 52.5%, respectively.
In situ i-ALCLs have an indolent clinical course and generally remain free of disease after implant removal. However, infiltrative i-ALCLs could have a more aggressive clinical course that might require additional therapy to implant removal.
Mots-clé
Adult, Aged, Aged, 80 and over, Antigens, CD30/metabolism, Breast Implants/adverse effects, Female, Hodgkin Disease/pathology, Humans, Immunophenotyping, Lymphoma, Large-Cell, Anaplastic/chemically induced, Lymphoma, Large-Cell, Anaplastic/mortality, Lymphoma, Large-Cell, Anaplastic/pathology, Lymphoma, T-Cell, Peripheral/chemically induced, Lymphoma, T-Cell, Peripheral/mortality, Lymphoma, T-Cell, Peripheral/pathology, Middle Aged, Receptor Protein-Tyrosine Kinases/metabolism, Receptors, Antigen, T-Cell/metabolism, Retrospective Studies, STAT3 Transcription Factor/metabolism, Silicones/adverse effects, T-Lymphocytes, Cytotoxic/immunology
Pubmed
Web of science
Open Access
Oui
Création de la notice
11/03/2016 11:09
Dernière modification de la notice
20/08/2019 13:12