Central nervous system involvement by multiple myeloma: A multi-institutional retrospective study of 172 patients in daily clinical practice
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie
Grantová podpora
P30 CA008748
NCI NIH HHS - United States
PubMed
26955792
PubMed Central
PMC5502095
DOI
10.1002/ajh.24351
Knihovny.cz E-zdroje
- MeSH
- analýza přežití MeSH
- chromozomální aberace MeSH
- dospělí MeSH
- kombinovaná terapie MeSH
- lidé středního věku MeSH
- lidé MeSH
- míra přežití MeSH
- mnohočetný myelom komplikace mortalita patologie terapie MeSH
- nádory centrálního nervového systému diagnóza mortalita sekundární terapie MeSH
- prognóza MeSH
- protinádorové látky terapeutické užití MeSH
- radioterapie MeSH
- retrospektivní studie MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- Názvy látek
- protinádorové látky MeSH
The multicenter retrospective study conducted in 38 centers from 20 countries including 172 adult patients with CNS MM aimed to describe the clinical and pathological characteristics and outcomes of patients with multiple myeloma (MM) involving the central nervous system (CNS). Univariate and multivariate analyses were performed to identify prognostic factors for survival. The median time from MM diagnosis to CNS MM diagnosis was 3 years. Thirty-eight patients (22%) were diagnosed with CNS involvement at the time of initial MM diagnosis and 134 (78%) at relapse/progression. Upon diagnosis of CNS MM, 97% patients received initial therapy for CNS disease, of which 76% received systemic therapy, 36% radiotherapy and 32% intrathecal therapy. After a median follow-up of 3.5 years, the median overall survival (OS) from the onset of CNS involvement for the entire group was 7 months. Untreated and treated patients had median OS of 2 and 8 months, respectively (P < 0.001). At least one previous line of therapy for MM before the diagnosis of CNS disease and >1 cytogenetic abnormality detected by FISH were independently associated with worse OS. The median OS for patients with 0, 1 and 2 of these risk factors were 25 months, 5.5 months and 2 months, respectively (P < 0.001). Neurological manifestations, not considered chemotherapy-related, observed at any time after initial diagnosis of MM should raise a suspicion of CNS involvement. Although prognosis is generally poor, the survival of previously untreated patients and patients with favorable cytogenetic profile might be prolonged due to systemic treatment and/or radiotherapy. Am. J. Hematol. 91:575-580, 2016. © 2016 Wiley Periodicals, Inc.
Ankara University Medical School Ankara Turkey
Azienda Ospedaliera Universitaria Senese Siena Italy
Centre Hospitalier Universitaire de Liege Liege Belgium
Cliniques Universitaires Saint Luc Brussels Belgium
Columbia University Medical Center New York New York
Dana Farber Cancer Institute Harvard Medical School Boston Massachusetts
Department of Hematology St John's Cancer Center Lublin Poland
Fondazione IRCCS Policlinico San Matteo University of Pavia Pavia Italy
Fremantle Hospital Fremantle Australia
Gunma University Graduate School of Health Sciences Gunma Japan
Hopital La Miletrie CHU Poitiers France
Hospital Italiano de Buenos Aires Buenos Aires Argentina
Hospital Universitario de Salamanca Salamanca Spain
Jagiellonian University Medical College Cracow Poland
John Theurer Cancer Center at Hackensack UMC New Jersey and Georgetown University Washington DC
Karolinska University Hospital Stockholm Sweden
Levine Cancer Institute Carolinas HealthCare System Charlotte NC
Maria Sklodowska Curie Institute Oncology Center Warsaw Poland
Medical University Warsaw Poland
Memorial Sloan Kettering Cancer Center New York New York
National and Kapodistrian University of Athens Athens Greece
Norwegian University of Science and Technology Trondheim Norway
Odense University Hospital Odense Denmark
Pomeranian Medical University Szczecin Poland
Provincial Hospital Zielona Gora Poland
Queen Mary Hospital University of Hong Kong Hong Kong
Royal Victoria Hospital McGill University Montreal Canada
Santa Casa Medical School Sao Paulo Brazil
Silesian Medical University Katowice Poland
University Hospital Olomouc Olomouc Czech Republic
University Hospital Wuerzburg Wuerzburg Germany
University of Maryland Medical Center Baltimore Maryland
VU University Medical Center Amsterdam the Netherlands
Washington University School of Medicine St Louis Missouri
Weill Cornell Medical College New York New York
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