-
Je něco špatně v tomto záznamu ?
Health-related quality of life maintained over time in patients with relapsed or refractory multiple myeloma treated with daratumumab in combination with bortezomib and dexamethasone: results from the phase III CASTOR trial
V. Hungria, M. Beksac, KC. Weisel, AK. Nooka, T. Masszi, I. Spicka, M. Munder, MV. Mateos, TM. Mark, M. Qi, X. Qin, J. Fastenau, A. Spencer, P. Sonneveld, W. Garvin, T. Renaud, KS. Gries
Jazyk angličtina Země Velká Británie
Typ dokumentu klinické zkoušky, fáze III, časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem
PubMed
33555030
DOI
10.1111/bjh.17321
Knihovny.cz E-zdroje
- MeSH
- biologické modely * MeSH
- bortezomib aplikace a dávkování MeSH
- dexamethason aplikace a dávkování MeSH
- dospělí MeSH
- kvalita života * MeSH
- lidé středního věku MeSH
- lidé MeSH
- míra přežití MeSH
- mnohočetný myelom * farmakoterapie mortalita MeSH
- monoklonální protilátky aplikace a dávkování MeSH
- přežití bez známek nemoci MeSH
- protokoly protinádorové kombinované chemoterapie aplikace a dávkování MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
In the phase III CASTOR trial, daratumumab, bortezomib and dexamethasone (D-Vd) significantly extended progression-free survival compared with bortezomib and dexamethasone (Vd) alone in patients with relapsed/refractory multiple myeloma (RRMM). Here, we present patient-reported outcomes (PROs) from the CASTOR trial. PROs were assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30-item (EORTC QLQ-C30) and the EuroQol 5-dimensional descriptive system questionnaire. Treatment effects through Cycle 8 were measured by a repeated measures mixed-effects model. After Cycle 8, PROs were only collected for patients in the D-Vd group who continued on daratumumab monotherapy. Compliance rates for PRO assessments were high and similar between treatment groups. Mean changes from baseline were generally similar between treatment groups for EORTC QLQ-C30 global health status (GHS), functioning and symptoms, and did not exceed 10 points for either treatment group. Subgroup analyses were consistent with the results observed in the overall population. There was no change in patients' health-related quality of life for the first eight cycles of therapy; thereafter, patients treated with daratumumab over the long-term reported improvements in GHS and pain. These results complement the significant clinical benefits observed with D-Vd in patients with RRMM and support its use in this patient population.
Ankara University Ankara Turkey
Charles University and General Hospital Prague Czech Republic
Erasmus MC Cancer Institute Rotterdam the Netherlands
Janssen Research and Development LLC Raritan NJ USA
Janssen Research and Development LLC Spring House PA USA
Santa Casa Medical School São Paulo Brazil
Semmelweis University Budapest Hungary
University Hospital of Salamanca IBSAL Salamanca Spain
University Medical Center of Hamburg Eppendorf Hamburg Germany
University of Colorado Anschutz Medical Campus Aurora CO USA
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21025769
- 003
- CZ-PrNML
- 005
- 20211026133528.0
- 007
- ta
- 008
- 211013s2021 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1111/bjh.17321 $2 doi
- 035 __
- $a (PubMed)33555030
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Hungria, Vania $u Santa Casa Medical School, São Paulo, Brazil
- 245 10
- $a Health-related quality of life maintained over time in patients with relapsed or refractory multiple myeloma treated with daratumumab in combination with bortezomib and dexamethasone: results from the phase III CASTOR trial / $c V. Hungria, M. Beksac, KC. Weisel, AK. Nooka, T. Masszi, I. Spicka, M. Munder, MV. Mateos, TM. Mark, M. Qi, X. Qin, J. Fastenau, A. Spencer, P. Sonneveld, W. Garvin, T. Renaud, KS. Gries
- 520 9_
- $a In the phase III CASTOR trial, daratumumab, bortezomib and dexamethasone (D-Vd) significantly extended progression-free survival compared with bortezomib and dexamethasone (Vd) alone in patients with relapsed/refractory multiple myeloma (RRMM). Here, we present patient-reported outcomes (PROs) from the CASTOR trial. PROs were assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30-item (EORTC QLQ-C30) and the EuroQol 5-dimensional descriptive system questionnaire. Treatment effects through Cycle 8 were measured by a repeated measures mixed-effects model. After Cycle 8, PROs were only collected for patients in the D-Vd group who continued on daratumumab monotherapy. Compliance rates for PRO assessments were high and similar between treatment groups. Mean changes from baseline were generally similar between treatment groups for EORTC QLQ-C30 global health status (GHS), functioning and symptoms, and did not exceed 10 points for either treatment group. Subgroup analyses were consistent with the results observed in the overall population. There was no change in patients' health-related quality of life for the first eight cycles of therapy; thereafter, patients treated with daratumumab over the long-term reported improvements in GHS and pain. These results complement the significant clinical benefits observed with D-Vd in patients with RRMM and support its use in this patient population.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a senioři nad 80 let $7 D000369
- 650 _2
- $a monoklonální protilátky $x aplikace a dávkování $7 D000911
- 650 _2
- $a protokoly protinádorové kombinované chemoterapie $x aplikace a dávkování $7 D000971
- 650 _2
- $a bortezomib $x aplikace a dávkování $7 D000069286
- 650 _2
- $a dexamethason $x aplikace a dávkování $7 D003907
- 650 _2
- $a přežití bez známek nemoci $7 D018572
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a lidé středního věku $7 D008875
- 650 12
- $a biologické modely $7 D008954
- 650 12
- $a mnohočetný myelom $x farmakoterapie $x mortalita $7 D009101
- 650 12
- $a kvalita života $7 D011788
- 650 _2
- $a míra přežití $7 D015996
- 655 _2
- $a klinické zkoušky, fáze III $7 D017428
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a multicentrická studie $7 D016448
- 655 _2
- $a randomizované kontrolované studie $7 D016449
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Beksac, Meral $u Ankara University, Ankara, Turkey
- 700 1_
- $a Weisel, Katja C $u University Medical Center of Hamburg-Eppendorf, Hamburg, Germany
- 700 1_
- $a Nooka, Ajay K $u Winship Cancer Institute, Emory University, Atlanta, GA, USA
- 700 1_
- $a Masszi, Tamas $u Semmelweis University, Budapest, Hungary
- 700 1_
- $a Spicka, Ivan $u Charles University and General Hospital, Prague, Czech Republic
- 700 1_
- $a Munder, Markus $u Third Department of Medicine, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany
- 700 1_
- $a Mateos, María-Victoria $u University Hospital of Salamanca/IBSAL, Salamanca, Spain
- 700 1_
- $a Mark, Tomer M $u University of Colorado-Anschutz Medical Campus, Aurora, CO, USA
- 700 1_
- $a Qi, Ming $u Janssen Research & Development, LLC, Spring House, PA, USA
- 700 1_
- $a Qin, Xiang $u Janssen Research & Development, LLC, Spring House, PA, USA
- 700 1_
- $a Fastenau, John $u Janssen Research & Development, LLC, Raritan, NJ, USA
- 700 1_
- $a Spencer, Andrew $u Malignant Haematology and Stem Cell Transplantation Service, Alfred Health-Monash University, Melbourne, Australia
- 700 1_
- $a Sonneveld, Pieter $u Erasmus MC Cancer Institute, Rotterdam, the Netherlands
- 700 1_
- $a Garvin, Wendy $u Janssen Research & Development, LLC, Spring House, PA, USA
- 700 1_
- $a Renaud, Thomas $u Janssen Research & Development, LLC, Raritan, NJ, USA
- 700 1_
- $a Gries, Katharine S $u Janssen Research & Development, LLC, Raritan, NJ, USA
- 773 0_
- $w MED00009374 $t British journal of haematology $x 1365-2141 $g Roč. 193, č. 3 (2021), s. 561-569
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33555030 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20211013 $b ABA008
- 991 __
- $a 20211026133534 $b ABA008
- 999 __
- $a ok $b bmc $g 1714692 $s 1146276
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 193 $c 3 $d 561-569 $e 20210208 $i 1365-2141 $m British journal of haematology $n Br J Haematol $x MED00009374
- LZP __
- $a Pubmed-20211013