2012
Efficacy and safety of Id-protein-loaded dendritic cell vaccine in patients with multiple myeloma - Phase II study results
ZAHRADOVÁ, Lenka, K. MOLLOVA, Darina OČADLÍKOVÁ, L. KOVAROVA, Zdeněk ADAM et. al.Základní údaje
Originální název
Efficacy and safety of Id-protein-loaded dendritic cell vaccine in patients with multiple myeloma - Phase II study results
Autoři
ZAHRADOVÁ, Lenka (203 Česká republika, garant, domácí), K. MOLLOVA (203 Česká republika), Darina OČADLÍKOVÁ (203 Česká republika, domácí), L. KOVAROVA (203 Česká republika), Zdeněk ADAM (203 Česká republika, domácí), Marta KREJČÍ (203 Česká republika, domácí), Luděk POUR (203 Česká republika, domácí), Andrea KŘIVANOVÁ (203 Česká republika, domácí), Viera SANDECKÁ (703 Slovensko, domácí) a Roman HÁJEK (203 Česká republika, domácí)
Vydání
Neoplasma, Bratislava, 2012, 0028-2685
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Slovensko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 1.574
Kód RIV
RIV/00216224:14110/12:00060980
Organizační jednotka
Lékařská fakulta
UT WoS
000305499900012
Klíčová slova anglicky
dendritic cells; immunotherapy; anticancer vaccines; Id-protein; multiple myeloma
Příznaky
Mezinárodní význam
Změněno: 22. 4. 2013 16:14, Soňa Böhmová
Anotace
V originále
In a phase II clinical study, pretreated multiple myeloma patients with relapsing or stable disease received autologous anticancer vaccine containing dendritic cells loaded with Id-protein. Patients received a total of 6 vaccine doses intradermally in monthly intervals. No clinical responses were observed. During the follow-up with a median of 33.1 months (range: 11-43 months), the disease remained stable in 7/11 (64%) of patients. Immune responses measured by ELISpot were noted in 3/11 (27%) and DTH skin test for Id-protein was positive in 8/11 (73%) of patients; out of those, 1/11 (9%) and 5/11 (46%), respectively, had preexisting immune response to Id-protein before the vaccination began. Outcomes were compared to those of a control group of 13 patients. A trend to lower cumulative incidence of progression in the vaccinated group was observed at 12 months from the first vaccination (p = 0.099). More patients from the control group compared to vaccinated patients required active anticancer therapy [4/11 (36%) vs. 8/13 (62%)]. Vaccines based on dendritic cells loaded with Id-protein are safe and induce specific immune response in multiple myeloma patients. Our results suggest that the vaccination could stabilize the disease in approximately two-thirds of patients.
Návaznosti
LC06027, projekt VaV |
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2B06058, projekt VaV |
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