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Medvik - BMČ
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Efficacy and safety of weekly carfilzomib (70 mg/m2), dexamethasone, and daratumumab (KdD70) is comparable to twice-weekly KdD56 while being a more convenient dosing option: a cross-study comparison of the CANDOR and EQUULEUS studies

X. Leleu, M. Beksac, T. Chou, M. Dimopoulos, SS. Yoon, HM. Prince, L. Pour, T. Shelekhova, A. Chari, M. Khurana, J. Zhang, M. Obreja, M. Qi, A. Oriol, D. Siegel

. 2021 ; 62 (2) : 358-367. [pub] 20201028

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc21019353

The regimen of carfilzomib, daratumumab, and dexamethasone (KdD) shows activity in patients with relapsed/refractory multiple myeloma. KdD at the twice-weekly 56 mg/m2 carfilzomib dose (KdD56) was used in the randomized phase 3 CANDOR study (NCT03158688), whereas KdD at the once-weekly 70 mg/m2 carfilzomib dose (KdD70) was used in the phase 1 b EQUULEUS study (NCT01998971). We analyzed efficacy data from comparable CANDOR and EQUULEUS patients using inverse probability of treatment weighting (IPTW)-adjusted models. These weights were calculated from propensity scores derived to balance prespecified baseline covariates. The side-by-side and adjusted comparisons showed similar efficacy for overall response rates and progression-free survival in the two groups, with a series of sensitivity analyses showing consistent findings. Safety data were generally consistent with the known safety profiles of each individual drug. Once-weekly KdD70 is comparable to twice-weekly KdD56 in terms of efficacy and safety while being a more convenient dosing option.

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$a The regimen of carfilzomib, daratumumab, and dexamethasone (KdD) shows activity in patients with relapsed/refractory multiple myeloma. KdD at the twice-weekly 56 mg/m2 carfilzomib dose (KdD56) was used in the randomized phase 3 CANDOR study (NCT03158688), whereas KdD at the once-weekly 70 mg/m2 carfilzomib dose (KdD70) was used in the phase 1 b EQUULEUS study (NCT01998971). We analyzed efficacy data from comparable CANDOR and EQUULEUS patients using inverse probability of treatment weighting (IPTW)-adjusted models. These weights were calculated from propensity scores derived to balance prespecified baseline covariates. The side-by-side and adjusted comparisons showed similar efficacy for overall response rates and progression-free survival in the two groups, with a series of sensitivity analyses showing consistent findings. Safety data were generally consistent with the known safety profiles of each individual drug. Once-weekly KdD70 is comparable to twice-weekly KdD56 in terms of efficacy and safety while being a more convenient dosing option.
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$a Beksac, Meral $u Department of Hematology, Ankara University, Ankara, Turkey
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$a Chou, Takaaki $u Department of Internal Medicine, Niigata Cancer Center Hospital, Niigata, Japan
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$a Dimopoulos, Meletios $u Hematology and Medical Oncology, Department of Clinical Therapeutics, National and Kapodistrian University of Athens School of Medicine, Athens, Greece
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$a Yoon, Sung-Soo $u Department of Internal Medicine, Seoul National University, Seoul, South Korea
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$a Prince, H Miles $u Epworth Healthcare and Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Australia
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$a Pour, Ludek $u Department of Internal Medicine, Hematology and Oncology, University Hospital Brno, Brno, Czech Republic
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$a Shelekhova, Tatiana $u Clinic of Professional Pathology, Saratov, Russian Federation
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$a Chari, Ajai $u Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA
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$a Khurana, Monica $u Clinical Development, Oncology, Amgen Inc., Thousand Oaks, CA, USA
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$a Zhang, Jianqi $u Global Biostatistical Science, Amgen Inc., Thousand Oaks, CA, USA
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$a Obreja, Mihaela $u Global Biostatistical Science, Amgen Inc., Thousand Oaks, CA, USA
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$a Oriol, Albert $u Institut Català d'Oncologia and Josep Carreras Research Leukaemia Institute, Hospital Germans Trias i Pujol, Barcelona, Spain
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