KLUIN-NELEMANS, H.C., M. JAWHAR, A. REITER, B. VAN ANROOIJ, J. GOTLIB, K. HARTMANN, A. ILLERHAUS, H.N.G.O. ELBERINK, A. GORSKA, M. NIEDOSZYTKO, M. LANGE, L. SCAFFIDI, R. ZANOTTI, P. BONADONNA, C. PERKINS, C. ELENA, L. MALCOVATI, K. SHOUMARIYEH, N. VON BUBNOFF, S. MULLER, M. TRIGGIANI, R. PARENTE, J. SCHWAAB, M. KUNDI, A.B. FORTINA, F. CAROPPO, K. BROCKOW, A. ZINK, D. FUCHS, I. ANGELOVA-FISCHER, A,S. YAVUZ, Michael DOUBEK, M. MATTSSON, H. HAGGLUND, J. PANSE, A. SIMONOWSKI, V. SABATO, T. SCHUG, M. JENTZSCH, C. BREYNAERT, J. VARKONYI, V. KENNEDY, O. HERMINE, J. ROSSIGNOL, M. AROCK, P. VALENT and W.R. SPERR. Cytogenetic and molecular aberrations and worse outcome for male patients in systemic mastocytosis. Theranostics. Lake Haven: Ivyspring International Publisher, 2021, vol. 11, No 1, p. 292-303. ISSN 1838-7640. Available from: https://dx.doi.org/10.7150/thno.51872.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Cytogenetic and molecular aberrations and worse outcome for male patients in systemic mastocytosis
Authors KLUIN-NELEMANS, H.C., M. JAWHAR, A. REITER, B. VAN ANROOIJ, J. GOTLIB, K. HARTMANN, A. ILLERHAUS, H.N.G.O. ELBERINK, A. GORSKA, M. NIEDOSZYTKO, M. LANGE, L. SCAFFIDI, R. ZANOTTI, P. BONADONNA, C. PERKINS, C. ELENA, L. MALCOVATI, K. SHOUMARIYEH, N. VON BUBNOFF, S. MULLER, M. TRIGGIANI, R. PARENTE, J. SCHWAAB, M. KUNDI, A.B. FORTINA, F. CAROPPO, K. BROCKOW, A. ZINK, D. FUCHS, I. ANGELOVA-FISCHER, A,S. YAVUZ, Michael DOUBEK (203 Czech Republic, guarantor, belonging to the institution), M. MATTSSON, H. HAGGLUND, J. PANSE, A. SIMONOWSKI, V. SABATO, T. SCHUG, M. JENTZSCH, C. BREYNAERT, J. VARKONYI, V. KENNEDY, O. HERMINE, J. ROSSIGNOL, M. AROCK, P. VALENT and W.R. SPERR.
Edition Theranostics, Lake Haven, Ivyspring International Publisher, 2021, 1838-7640.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30204 Oncology
Country of publisher Australia
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 11.600
RIV identification code RIV/00216224:14740/21:00121919
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.7150/thno.51872
UT WoS 000582957500019
Keywords in English Mastocytosis; sex difference; cytogenetics; molecular mutations; survival
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Natálie Hílek, učo 414715. Changed: 11/4/2022 15:05.
Abstract
In systemic mastocytosis (SM), the clinical features and survival vary greatly. Patient-related factors determining the outcome in SM are largely unknown. Methods: We examined the impact of sex on the clinical features, progression-free survival (PFS), and overall survival (OS) in 3403 patients with mastocytosis collected in the registry of the European Competence Network on Mastocytosis (ECNM). The impact of cytogenetic and molecular genetic aberrations on sex differences was analyzed in a subset of patients. Results: Of all patients enrolled, 55.3% were females. However, a male predominance was found in a subset of advanced SM (AdvSM) patients, namely SM with an associated hematologic neoplasm (SM-AHN, 70%; p < 0.001). Correspondingly, organomegaly (male: 23% vs. female: 13%, p = 0.007) was more, whereas skin involvement (male: 71% vs. female: 86%, p = 0.001) was less frequent in males. In all patients together, OS (p < 0.0001) was significantly inferior in males, and also within the WHO sub-categories indolent SM, aggressive SM (ASM) and SM-AHN. PFS was significantly (p = 0.0002) worse in males when all patients were grouped together; due to low numbers of events, this significance persisted only in the subcategory smoldering SM. Finally, prognostically relevant cytogenetic abnormalities (10% vs. 5%, p = 0.006) or molecular aberrations (SRSF2/ASXLI/RUNXI profile; 63% vs. 40%, p = 0.003) were more frequently present in males. Conclusions: Male sex has a major impact on clinical features, disease progression, and survival in mastocytosis. Male patients have an inferior survival, which seems related to the fact that they more frequently develop a multi-mutated AdvSM associated with a high-risk molecular background.
PrintDisplayed: 6/5/2024 23:25