| Literature DB >> 26955792 |
Artur Jurczyszyn1, Norbert Grzasko2,3, Alessandro Gozzetti4, Jacek Czepiel1, Alfonso Cerase4, Vania Hungria5, Edvan Crusoe5, Ana Luiza Miranda Silva Dias5, Ravi Vij6, Mark A Fiala6, Jo Caers7, Leo Rasche8, Ajay K Nooka9, Sagar Lonial9, David H Vesole10, Sandhya Philip10, Shane Gangatharan11, Agnieszka Druzd-Sitek12, Jan Walewski12, Alessandro Corso13, Federica Cocito13, Marie-Christine M Vekemans14, Erden Atilla15, Meral Beksac15, Xavier Leleu16, Julio Davila17, Ashraf Badros18, Ekta Aneja19, Niels Abildgaard20, Efstathios Kastritis21, Dorotea Fantl22, Natalia Schutz22, Tomas Pika23, Aleksandra Butrym24, Magdalena Olszewska-Szopa24, Lidia Usnarska-Zubkiewicz24, Saad Z Usmani25, Hareth Nahi26, Chor S Chim27, Chaim Shustik28, Krzysztof Madry29, Suzanne Lentzsch30, Alina Swiderska31, Grzegorz Helbig32, Renata Guzicka-Kazimierczak33, Nikoletta Lendvai34, Anders Waage35, Kristian T Andersen36, Hirokazu Murakami37, Sonja Zweegman38, Jorge J Castillo39.
Abstract
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.Entities:
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Year: 2016 PMID: 26955792 PMCID: PMC5502095 DOI: 10.1002/ajh.24351
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047