Phase II study of bendamustine, bortezomib and dexamethasone as second-line treatment for elderly patients with multiple myeloma: the Intergroupe Francophone du Myelome 2009-01 trial
“…In the BVD regimen, severe adverse events were reported for 65 % of patients mostly due to infections (23.2 %). Few severe hematological side effects were reported (20.5 % neutropenia, 9.5 % thrombocytopenia, 5.5 % anemia) (Rodon et al 2015). In the study conducted by Offidani et al (2013) with the BVD regimen, common severe adverse events were thrombocytopenia (30.5 %), neutropenia (18.5 %), infections (12 %) and neuropathy (8 %).…”
Section: Discussionmentioning
confidence: 95%
“…OS was estimated at 13.3 months. Rodon et al (2015) conducted a phase II study of BVD in elderly patients (>65 years) with one previous line of therapy. ORR was 67 % (CR 10.9 %, VGPR 16.5 %, PR 39.7 %), and median OS was estimated at 23 months.…”
Bendamustine monotherapy is an effective treatment option for heavily pre-treated myeloma patients due to its favorable response rate and mild toxicity.
“…In the BVD regimen, severe adverse events were reported for 65 % of patients mostly due to infections (23.2 %). Few severe hematological side effects were reported (20.5 % neutropenia, 9.5 % thrombocytopenia, 5.5 % anemia) (Rodon et al 2015). In the study conducted by Offidani et al (2013) with the BVD regimen, common severe adverse events were thrombocytopenia (30.5 %), neutropenia (18.5 %), infections (12 %) and neuropathy (8 %).…”
Section: Discussionmentioning
confidence: 95%
“…OS was estimated at 13.3 months. Rodon et al (2015) conducted a phase II study of BVD in elderly patients (>65 years) with one previous line of therapy. ORR was 67 % (CR 10.9 %, VGPR 16.5 %, PR 39.7 %), and median OS was estimated at 23 months.…”
Bendamustine monotherapy is an effective treatment option for heavily pre-treated myeloma patients due to its favorable response rate and mild toxicity.
“…The combination of bendamustine with bortezomib and dexamethasone shows a remarkable antimyeloma activity with manageable toxicity in previously treated MM patients [274,275].…”
MM patient outcome has remarkably improved due to the use of three to four drug combination therapies including PIs and IMiDs, which target the tumor in its bone marrow microenvironment, however MM treatment remains challenging. The use of high-throughput techniques has allowed to discover new insights into MM biology. The identification of candidate therapeutic targets and availability of respective investigative agents will allow for a substantial progress in the development and implementation of personalized medicine in MM.
“…ОЧО соста-вила 67,1 %, из них у 10,9 % пациентов достигнут ПО и у 12,3 % -ОХЧО, у 34,2 % -ЧО. Еще у 13,6 % пациентов достигнута стабилизация заболевания (СЗ), а оставшиеся 10,3 % пациентов были рефрактерными к терапии [12].…”
5,3 (0,8-18,0) мес, а общей выживаемости -25,4 (0,8-47,1) 5.3 (0.8-18.0) months and median overall survival was 25.4 (0.8-47.1) months. Hematologic toxicity was in 53.2 % of patients.
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