Risk factors for, and reversibility of, peripheral neuropathy associated with bortezomib-melphalan-prednisone in newly diagnosed patients with multiple myeloma: Subanalysis of the phase 3 VISTA study

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3130039 31 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Risk factors for, and reversibility of, peripheral neuropathy associated with bortezomib-melphalan-prednisone in newly diagnosed patients with multiple myeloma: Subanalysis of the phase 3 VISTA study
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Objectives: This subanalysis of the phase 3 VISTA trial aimed to assess the frequency, characteristics and reversibility of, and prognostic factors for, bortezomib-associated peripheral neuropathy (PN) in newly diagnosed patients with multiple myeloma ineligible for high-dose therapy who received bortezomib plus melphalan-prednisone.Methods: Patients received nine 6-wk cycles of VMP (bortezomib 1.3 mg/m2, days 1, 4, 8, 11, 22, 25, 29, 32, cycles 1-4, and days 1, 8, 22, 29, cycles 5-9; melphalan 9 mg/m2, days 1-4, cycles 1-9; and prednisone 60 mg/m2, days 1-4, cycles 1-9).Results: Overall, 47% of patients receiving VMP developed PN, including 19% grade 2 and 13% grade ≥3 (<1% grade 4). The PN incidence was dose-related and reached a plateau at a cumulative bortezomib dose of approximately 45 mg/m2. Median time to PN onset was 2.3 months. Bortezomib-associated PN was reversible; 79% of events improved by at least one NCI CTCAE grade within a median of 1.9 months and 60% completely resolved within a median of 5.7 months, with reversibility similar in responding and non-responding patients. By multivariate analysis, baseline neuropathy was the only consistent risk factor for any PN [hazard ratio (HR) 1.785, P = 0.0065], grade ≥2 PN (HR 2.205, P = 0.0032), and grade ≥3 PN (HR 2.438, P = 0.023); age, pre-existing diabetes, International Staging System stage, obesity, and creatinine clearance did not affect the overall rate of PN.Conclusions: Rates of bortezomib-induced PN in the frontline setting were similar to those in relapsed patients and resolved in most cases. (Clinicaltrials.gov identifier: NCT00111319). © 2010 John Wiley & Sons A/S.
Έτος δημοσίευσης:
2011
Συγγραφείς:
Dimopoulos, M.A.
Mateos, M.-V.
Richardson, P.G.
Schlag, R.
Khuageva, N.K.
Shpilberg, O.
Kropff, M.
Spicka, I.
Palumbo, A.
Wu, K.L.
Esseltine, D.-L.
Liu, K.
Deraedt, W.
Cakana, A.
Van De Velde, H.
San Miguel, J.F.
Περιοδικό:
European Journal of Haematology
Τόμος:
86
Αριθμός / τεύχος:
1
Σελίδες:
23-31
Λέξεις-κλειδιά:
bortezomib; melphalan; prednisone, adult; aged; article; cancer patient; clinical trial; creatinine clearance; diabetes mellitus; disease severity; drug megadose; female; human; major clinical study; male; multiple cycle treatment; multiple myeloma; neuropathy; obesity; peripheral neuropathy; priority journal; prognosis; risk factor, Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Boronic Acids; Female; Humans; Male; Melphalan; Middle Aged; Multiple Myeloma; Multivariate Analysis; Peripheral Nervous System Diseases; Prednisone; Pyrazines; Risk Factors
Επίσημο URL (Εκδότης):
DOI:
10.1111/j.1600-0609.2010.01533.x
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