Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

A Retrospective Analysis of Dabrafenib and/or Dabrafenib Plus Trametinib Combination in Patients with Metastatic Melanoma to Characterize Patients with Long-Term Benefit in the Individual Patient Program (DESCRIBE III)

VG. Atkinson, P. Quaglino, M. Aglietta, M. Del Vecchio, R. Depenni, F. Consoli, D. Bafaloukos, PF. Ferrucci, S. Tulyte, I. Krajsová, PA. Ascierto, R. Gueli, A. Arance, H. Gogas, H. Banerjee, T. Saliba, E. de Jong, B. Neyns

. 2021 ; 13 (10) : . [pub] 20210518

Jazyk angličtina Země Švýcarsko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc21017732

Grantová podpora
None Novartis

The dabrafenib plus trametinib (dab + tram) combination has demonstrated durable long-term efficacy in patients with BRAF V600-mutant metastatic melanoma. However, real-world data characterizing patients with long-term benefit are limited. DESCRIBE III was a global, observational, retrospective, chart review study in patients with unresectable or metastatic melanoma treated with dab monotherapy and/or dab + tram combination therapy as part of the Named Patient Program or Individual Patient Program. Overall, 509 patients were enrolled. Patients were categorized into three groups based on their observed treatment duration: long-term (on therapy ≥12 months), intermediate (on therapy ≥6 months and <12 months), and short-term (on therapy <6 months) duration of benefit. More patients in the short-term duration of benefit group had baseline characteristics associated with poor prognosis compared with the other two groups. Median lactate dehydrogenase (LDH) levels (368 U/L) at baseline were also higher in the short-term duration of benefit group. No new safety signals were identified. DESCRIBE III identified baseline characteristics associated with long-term benefit of dab + tram. Lower LDH level and <3 metastatic sites at baseline were associated with a longer duration of benefit, confirming that the findings from COMBI-d and COMBI-v are relevant to patients treated in a real-world setting.

Department of Dermatovenerology University Hospital Prague Charles University 12808 Prague Czech Republic

Department of Internal Medicine Laiko General Hospital National and Kapodistrian University of Athens School of Medicine 11527 Athens Greece

Department of Medical Oncology Candiolo Cancer Institute FPO IRCCS 10060 Candiolo Italy

Department of Medical Oncology Hospital Clinic of Barcelona 08036 Barcelona Spain

Department of Medical Sciences Section of Dermatology University of Turin 10124 Turin Italy

Department of Oncology and Hematology University of Modena and Reggio Emilia 41121 Modena Italy

Department of Oncology University of Torino 10124 Turin Italy

Division of Cancer Services Princess Alexandra Hospital University of Queensland Brisbane QLD 4102 Australia

Hematology Oncology and Transfusion Medicine Center Vilnius University 08410 Vilnius Lithuania

Medical Oncology ASST Spedali Civili 25123 Brescia Italy

Medical Oncology Metropolitan Hospital 18547 Athens Greece

Medical Oncology Universitair Ziekenhuis Brussel 1090 Brussels Belgium

Melanoma Unit Cancer Immunotherapy and Innovative Therapies Istituto Nazionale Tumori IRCCS Fondazione G Pascale 80131 Naples Italy

Novartis AG 4057 Basel Switzerland

Novartis Pharmaceuticals Corporation East Hanover NJ 07936 USA

Oncology Unit ASST Sette Laghi 21100 Varese Italy

Tumor Biotherapy Unit Department of Experimental Oncology IEO Istituto Europeo di Oncologia IRCCS 20141 Milan Italy

Unit of Melanoma Medical Oncology Department of Medical Oncology and Hematology Fondazione IRCCS Istituto Nazionale dei Tumori 20133 Milan Italy

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc21017732
003      
CZ-PrNML
005      
20210729104012.0
007      
ta
008      
210726s2021 sz f 000 0|eng||
009      
AR
024    7_
$a 10.3390/cancers13102466 $2 doi
035    __
$a (PubMed)34070224
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a sz
100    1_
$a Atkinson, Victoria G $u Division of Cancer Services, Princess Alexandra Hospital, University of Queensland, Brisbane, QLD 4102, Australia
245    12
$a A Retrospective Analysis of Dabrafenib and/or Dabrafenib Plus Trametinib Combination in Patients with Metastatic Melanoma to Characterize Patients with Long-Term Benefit in the Individual Patient Program (DESCRIBE III) / $c VG. Atkinson, P. Quaglino, M. Aglietta, M. Del Vecchio, R. Depenni, F. Consoli, D. Bafaloukos, PF. Ferrucci, S. Tulyte, I. Krajsová, PA. Ascierto, R. Gueli, A. Arance, H. Gogas, H. Banerjee, T. Saliba, E. de Jong, B. Neyns
520    9_
$a The dabrafenib plus trametinib (dab + tram) combination has demonstrated durable long-term efficacy in patients with BRAF V600-mutant metastatic melanoma. However, real-world data characterizing patients with long-term benefit are limited. DESCRIBE III was a global, observational, retrospective, chart review study in patients with unresectable or metastatic melanoma treated with dab monotherapy and/or dab + tram combination therapy as part of the Named Patient Program or Individual Patient Program. Overall, 509 patients were enrolled. Patients were categorized into three groups based on their observed treatment duration: long-term (on therapy ≥12 months), intermediate (on therapy ≥6 months and <12 months), and short-term (on therapy <6 months) duration of benefit. More patients in the short-term duration of benefit group had baseline characteristics associated with poor prognosis compared with the other two groups. Median lactate dehydrogenase (LDH) levels (368 U/L) at baseline were also higher in the short-term duration of benefit group. No new safety signals were identified. DESCRIBE III identified baseline characteristics associated with long-term benefit of dab + tram. Lower LDH level and <3 metastatic sites at baseline were associated with a longer duration of benefit, confirming that the findings from COMBI-d and COMBI-v are relevant to patients treated in a real-world setting.
655    _2
$a časopisecké články $7 D016428
700    1_
$a Quaglino, Pietro $u Department of Medical Sciences, Section of Dermatology, University of Turin, 10124 Turin, Italy
700    1_
$a Aglietta, Massimo $u Department of Oncology, University of Torino, 10124 Turin, Italy $u Department of Medical Oncology, Candiolo Cancer Institute, FPO-IRCCS, 10060 Candiolo (Torino), Italy
700    1_
$a Del Vecchio, Michele $u Unit of Melanoma Medical Oncology, Department of Medical Oncology and Hematology, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy
700    1_
$a Depenni, Roberta $u Department of Oncology and Hematology, University of Modena and Reggio Emilia, 41121 Modena, Italy
700    1_
$a Consoli, Francesca $u Medical Oncology, ASST Spedali Civili, 25123 Brescia, Italy
700    1_
$a Bafaloukos, Dimitrios $u Medical Oncology, Metropolitan Hospital, 18547 Athens, Greece
700    1_
$a Ferrucci, Pier Francesco $u Tumor Biotherapy Unit, Department of Experimental Oncology, IEO-Istituto Europeo di Oncologia-IRCCS, 20141 Milan, Italy
700    1_
$a Tulyte, Skaiste $u Hematology, Oncology and Transfusion Medicine Center, Vilnius University, 08410 Vilnius, Lithuania
700    1_
$a Krajsová, Ivana $u Department of Dermatovenerology, University Hospital Prague, Charles University, 12808 Prague, Czech Republic
700    1_
$a Ascierto, Paolo A $u Melanoma Unit, Cancer Immunotherapy and Innovative Therapies, Istituto Nazionale Tumori-IRCCS "Fondazione G. Pascale", 80131 Naples, Italy
700    1_
$a Gueli, Rossana $u Oncology Unit, ASST Sette Laghi, 21100 Varese, Italy
700    1_
$a Arance, Ana $u Department of Medical Oncology, Hospital Clinic of Barcelona, 08036 Barcelona, Spain
700    1_
$a Gogas, Helen $u Department of Internal Medicine, Laiko General Hospital, National and Kapodistrian University of Athens School of Medicine, 11527 Athens, Greece
700    1_
$a Banerjee, Hiya $u Novartis Pharmaceuticals Corporation, East Hanover, NJ 07936, USA
700    1_
$a Saliba, Teddy $u Novartis Pharmaceuticals Corporation, East Hanover, NJ 07936, USA
700    1_
$a de Jong, Egbert $u Novartis AG, 4057 Basel, Switzerland
700    1_
$a Neyns, Bart $u Medical Oncology, Universitair Ziekenhuis Brussel, 1090 Brussels, Belgium
773    0_
$w MED00173178 $t Cancers $x 2072-6694 $g Roč. 13, č. 10 (2021)
856    41
$u https://pubmed.ncbi.nlm.nih.gov/34070224 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20210726 $b ABA008
991    __
$a 20210729104010 $b ABA008
999    __
$a ind $b bmc $g 1676404 $s 1138174
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2021 $b 13 $c 10 $e 20210518 $i 2072-6694 $m Cancers $n Cancers $x MED00173178
GRA    __
$a None $p Novartis
LZP    __
$a Pubmed-20210726

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...