TY - JOUR
T1 - Extramedullary intracranial localization of multiple myeloma and treatment with novel agents
T2 - A retrospective survey of 50 patients
AU - Gozzetti, Alessandro
AU - Cerase, Alfonso
AU - Lotti, Flavia
AU - Rossi, Davide
AU - Palumbo, Antonio
AU - Petrucci, Maria Teresa
AU - Patriarca, Francesca
AU - Nozzoli, Chiara
AU - Cavo, Michele
AU - Offidani, Massimo
AU - Floridia, Michele
AU - Berretta, Salvatore
AU - Vallone, Roberto
AU - Musto, Pellegrino
AU - Lauria, Francesco
PY - 2012/3/15
Y1 - 2012/3/15
N2 - BACKGROUND: Intracranial involvement in multiple myeloma is extremely rare. The effect of new drugs (eg, thalidomide, bortezomib, lenalidomide) with respect to old drugs (eg, alkylators, steroids) has not been reported. METHODS: We collected clinical and biological data of patients presenting with an osteo-dural or primary dural multiple myeloma (OD-DMM) or a central nervous system myelomatosis (CNS-MM) by sending a questionnaire to the centers of the Gruppo Italiano Malattie Ematologiche dell'Adulto (GIMEMA). RESULTS: A total of 50 patients were registered. New therapies were used in 35 patients, whereas 15 patients received old treatments. Twenty-five out of 50 patients obtained a complete remission or a very good partial remission (CR+VGPR). Overall survival (OS) for CNS-MM was 6 months, for OD-DMM 25 months. OS was 25 months for patients treated with new agents versus 8 months with old agents. Improved OS and progression-free survival were predicted by response (CR+VGPR) and by patients who underwent stem cell transplantation versus chemotherapy. β2-Microglobulin >5 mmol/L was a poor prognostic factor. Multivariate analysis showed poor survival for patients with β2-microglobulin >5 mmol/L and better survival for patients achieving CR+VGPR. CONCLUSIONS: The overall data highlight the relevance of therapy with new drugs in intracranial myeloma, providing a framework for future clinical trials.
AB - BACKGROUND: Intracranial involvement in multiple myeloma is extremely rare. The effect of new drugs (eg, thalidomide, bortezomib, lenalidomide) with respect to old drugs (eg, alkylators, steroids) has not been reported. METHODS: We collected clinical and biological data of patients presenting with an osteo-dural or primary dural multiple myeloma (OD-DMM) or a central nervous system myelomatosis (CNS-MM) by sending a questionnaire to the centers of the Gruppo Italiano Malattie Ematologiche dell'Adulto (GIMEMA). RESULTS: A total of 50 patients were registered. New therapies were used in 35 patients, whereas 15 patients received old treatments. Twenty-five out of 50 patients obtained a complete remission or a very good partial remission (CR+VGPR). Overall survival (OS) for CNS-MM was 6 months, for OD-DMM 25 months. OS was 25 months for patients treated with new agents versus 8 months with old agents. Improved OS and progression-free survival were predicted by response (CR+VGPR) and by patients who underwent stem cell transplantation versus chemotherapy. β2-Microglobulin >5 mmol/L was a poor prognostic factor. Multivariate analysis showed poor survival for patients with β2-microglobulin >5 mmol/L and better survival for patients achieving CR+VGPR. CONCLUSIONS: The overall data highlight the relevance of therapy with new drugs in intracranial myeloma, providing a framework for future clinical trials.
KW - bortezomib
KW - central nervous system
KW - head
KW - intracranial
KW - lenalidomide
KW - multiple myeloma
KW - thalidomide
UR - http://www.scopus.com/inward/record.url?scp=84857996397&partnerID=8YFLogxK
U2 - 10.1002/cncr.26447
DO - 10.1002/cncr.26447
M3 - Article
SN - 0008-543X
VL - 118
SP - 1574
EP - 1584
JO - Cancer
JF - Cancer
IS - 6
ER -