TY - JOUR
T1 - Carfilzomib, cyclophosphamide, and dexamethasone (KCd) for the treatment of triple-class relapsed/refractory multiple myeloma (RRMM)
AU - Pennipede, Dante
AU - Mohyuddin, Ghulam Rehman
AU - Hawkins, Ryan
AU - Ganguly, Siddhartha
AU - Shune, Leyla
AU - Ahmed, Nausheen
AU - Mohan, Meera
AU - Cui, Wei
AU - Mahmoudjafari, Zahra
AU - McGuirk, Joseph
AU - Atrash, Shebli
AU - Abdallah, Al Ola
N1 - Funding Information:
There was no external funding for this study
Publisher Copyright:
© 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
PY - 2021/12
Y1 - 2021/12
N2 - Background: Multiple myeloma (MM) is an incurable hematologic malignancy, and outcomes remain poor for patients with triple-class relapsed/refractory MM (RRMM). Descriptive analyses were performed on available data for patient characteristics, disease course, and outcomes of the KCd on triple-class RRMM patients at our institution. Patients and Methods: Twenty-three patients with triple-class RRMM treated with KCd between June 2017 and October 2020 were included in our analysis. The regimen KCd consisted of 28 days cycles of carfilzomib 20/36 mg/m2 IV on days 1, 2, 8, 9, 15, and 16, cyclophosphamide 300 mg/m2 IV weekly, and dexamethasone (20-40) mg orally weekly. Results: Patients received a median of 6 (3-10) prior regimens. The median number of cycles administered was 4 (1-11) cycles. Overall response rate was 52%, 6 patients (26%) achieved very good partial response (VGPR), 6 patients (26%) achieved partial response (PR), and 5 patients (22%) achieved stable disease (SD). Progression-free survival (PFS) and Overall-survival (OS) were 4 and 11.9 months, respectively. There was no reported treatment-related mortality. The most common grade ≥3 adverse events were neutropenia (26%), thrombocytopenia (56.5%), and anemia (56.5%). Conclusions: KCd showed clinically meaningful efficacy and manageable safety profile in patients with triple-class RRMM in real-world.
AB - Background: Multiple myeloma (MM) is an incurable hematologic malignancy, and outcomes remain poor for patients with triple-class relapsed/refractory MM (RRMM). Descriptive analyses were performed on available data for patient characteristics, disease course, and outcomes of the KCd on triple-class RRMM patients at our institution. Patients and Methods: Twenty-three patients with triple-class RRMM treated with KCd between June 2017 and October 2020 were included in our analysis. The regimen KCd consisted of 28 days cycles of carfilzomib 20/36 mg/m2 IV on days 1, 2, 8, 9, 15, and 16, cyclophosphamide 300 mg/m2 IV weekly, and dexamethasone (20-40) mg orally weekly. Results: Patients received a median of 6 (3-10) prior regimens. The median number of cycles administered was 4 (1-11) cycles. Overall response rate was 52%, 6 patients (26%) achieved very good partial response (VGPR), 6 patients (26%) achieved partial response (PR), and 5 patients (22%) achieved stable disease (SD). Progression-free survival (PFS) and Overall-survival (OS) were 4 and 11.9 months, respectively. There was no reported treatment-related mortality. The most common grade ≥3 adverse events were neutropenia (26%), thrombocytopenia (56.5%), and anemia (56.5%). Conclusions: KCd showed clinically meaningful efficacy and manageable safety profile in patients with triple-class RRMM in real-world.
KW - carfilzomib
KW - cyclophosphamide
KW - multiple myeloma
KW - triple-class refractory myeloma
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U2 - 10.1111/ejh.13697
DO - 10.1111/ejh.13697
M3 - Article
C2 - 34378251
AN - SCOPUS:85113842843
SN - 0902-4441
VL - 107
SP - 602
EP - 608
JO - European Journal of Haematology
JF - European Journal of Haematology
IS - 6
ER -