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Je něco špatně v tomto záznamu ?
External validation of International Prognostic Score for asymptomatic early stage chronic lymphocytic leukaemia and proposal of an alternative score
L. Smolej, P. Turcsányi, Z. Kubová, J. Zuchnická, J. Mihályová, M. Šimkovič, P. Vodárek, M. Krčméryová, H. Móciková, M. Brejcha, M. Špaček, Czech CLL Study Group
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
PROGRES Q40/08
Univerzita Karlova v Praze
FNHK, RVO 0017906
Ministerstvo zdravotnictví České republiky
VFN, RVO 64165
Ministerstvo zdravotnictví České republiky
Ministry of Health
PubMed
33280081
DOI
10.1111/bjh.17074
Knihovny.cz E-zdroje
- MeSH
- čas zasáhnout při rozvinutí nemoci statistika a číselné údaje MeSH
- chromozomální aberace statistika a číselné údaje MeSH
- chronická lymfatická leukemie krev diagnóza mortalita patologie MeSH
- geny pro těžké řetězce imunoglobulinů genetika MeSH
- hybridizace in situ fluorescenční metody MeSH
- kohortové studie MeSH
- lidé MeSH
- lymfadenopatie diagnóza MeSH
- palpace metody MeSH
- počet lymfocytů metody MeSH
- prognóza MeSH
- progrese nemoci MeSH
- rizikové faktory MeSH
- senioři MeSH
- staging nádorů metody MeSH
- výzkumný projekt trendy MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Česká republika MeSH
Most patients with chronic lymphocytic leukaemia (CLL) are nowadays diagnosed without any symptoms and do not require therapy. A prognostic score identifying patients within this large group who are at high risk of disease progression would be highly beneficial. The recently published International Prognostic Score for Early asymptomatic patients (IPS-E) uses combination of absolute lymphocyte count (ALC) >15 × 109 /l, palpable lymphadenopathy, and unmutated immunoglobulin heavy-chain variable-region (IGHV) gene to predict the time to first-line therapy (TTFT). Patients at low, intermediate, and high risk had estimated 5-year TTFT of 8%, 28%, and 61%. We performed an external validation of the IPS-E score using an unselected, consecutive group of 130 Binet A patients. The 5-year TTFT was 11%, 36%, and 78% (C-statistic 0·74). Furthermore, we propose an alternative system (AIPS-E) using cytogenetic aberrations instead of palpable lymphadenopathy. This system yielded 5-year TTFT of 14%, 40%, and 72%. These results were externally validated in 388 Binet A patients from five Czech centres; the 5-year TTFT was 16%, 37%, and 80% (C-statistic 0·74). In conclusion, we have successfully validated the IPS-E score for patients with early stage CLL. In addition, we propose a modified scoring system, the AIPS-E, combining IGHV, fluorescence in situ hybridisation, and ALC.
1st Department of Medicine Haematology University General Hospital Prague Czech Republic
Department of Haematology Oncology Center Nový Jičín Czech Republic Prague Czech Republic
Department of Haematology Oncology University Hospital Olomouc Czech Republic
Citace poskytuje Crossref.org
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