| Literature DB >> 26715148 |
Haruhito Totani1, Masaki Ri2, Chie Kato1, Takahiro Nakashima1, Nana Suzuki1, Shinya Hagiwara1, Takashi Kanamori1, Satsuki Murakami1, Arisa Masuda1, Shiori Kinoshita1, Takashi Yoshida1, Tomoko Narita1, Asahi Ito1, Shigeru Kusumoto1, Takashi Ishida1, Hirokazu Komatsu1, Shinsuke Iida1.
Abstract
Proteasome inhibitors (PIs) in combination with immunomodulatory drugs (IMiDs) have been shown to be effective against relapsed/refractory multiple myeloma (RRMM). To determine the optimal dosing schedule of once weekly bortezomib (BTZ) combined with lenalidomide (LEN) and dexamethasone (DEX), especially in the outpatient setting, we conducted a phase I dose escalation study. A 21-day cycle of BTZ 1.3 mg/m(2) on days 1 and 8, LEN 10 mg/day (cohort 1) or 15 mg/day (cohort 2) on days 1-14, and DEX 20 mg/day on days 1, 2, 8, and 9 was administered. Three patients were enrolled in each cohort. No dose-limiting toxicity was observed in either cohort. Although hematological toxicities estimated as >grade 3 were common, non-hematological toxicities of grade 3 or higher were rare. Two cases of newly diagnosed peripheral neuropathy (PN) were observed, while no grade 3/4 PN was observed. Two patients achieved partial response and two achieved stable disease. The recommended doses of BTZ and LEN were determined to be 1.3 mg/m(2) and 15 mg, respectively. Combination therapy of once weekly BTZ with LEN and DEX was well tolerated and shows promise as a regimen for patients with RRMM previously treated with both PIs and IMiDs.Entities:
Keywords: BLd; Bortezomib; Lenalidomide; Multiple myeloma; Refractory
Mesh:
Substances:
Year: 2015 PMID: 26715148 DOI: 10.1007/s12185-015-1925-7
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490