Pegylated Liposomal Doxorubicin in Vindesine-Based and Bortezomib-Based Regimens for Patients With Newly Diagnosed Multiple Myeloma: A Retrospective Study of Efficacy and Safety.
Pegylated Liposomal Doxorubicin in Vindesine-Based and Bortezomib-Based Regimens for Patients With Newly Diagnosed Multiple Myeloma: A Retrospective Study of Efficacy and Safety.
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聚乙二醇化脂质体多柔比星在基于长春地辛和硼替佐米的治疗方案中用于新诊断的多发性骨髓瘤患者:疗效和安全性的回顾性研究。
DOI:
10.3389/fonc.2021.597453
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发表时间:
2021
影响因子:
4.7
通讯作者:
Wang X
中科院分区:
文献类型:
--
作者:
Zhai Y;Yuan D;Ge X;Hu S;Li P;Fang X;Li Y;Zhou X;Wang X
Although pegylated liposomal doxorubicin (PLD) has been approved in combination with bortezomib for relapsed/refractory multiple myeloma (MM), the antitumor efficacy and tolerability of PLD in different regimens for patients with newly diagnosed MM (NDMM) have not been fully defined. A total of 249 NDMM patients diagnosed between January 2008 and October 2019 were included in this retrospective study. Among them, 112 patients received vindesine-based chemotherapy (35 vDD and 77 vAD) and 137 received bortezomib-based chemotherapy (58 VDD and 79 VD). In bortezomib-containing regimens, the complete response rate (48.3 vs. 30.4%, p = 0.033) and very good partial response or better rate (74.1 vs. 57.0%, p = 0.038) of VDD were significantly higher than those of VD subgroup. While no superior survival was found between VDD and VD subgroup. In vindesine-containing regimens, no statistical significance was identified between vDD and vAD in terms of response rate and survival. The occurrence rates of all cardiac AEs were similar between VDD and VD. The vDD regimen was similar with vAD in the aspect of response rate, survival, and toxicity in NDMM patients. The addition of PLD to VD brought deeper response without increased toxicity, while no superior survival was found.
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影响因子:
28.5
作者:
Liu, Jiangmei;Liu, Weiping;Wang, Lijun
通讯作者:
Wang, Lijun
影响因子:
45.3
作者:
Jakubowiak, Andrzej J.;Kendall, Tara;Kaminski, Mark S.
通讯作者:
Kaminski, Mark S.
影响因子:
3.1
作者:
Nishihori, Taiga;Baz, Rachid;Alsina, Melissa
通讯作者:
Alsina, Melissa
影响因子:
6.2
作者:
Orlowski RZ;Nagler A;Sonneveld P;Bladé J;Hajek R;Spencer A;Robak T;Dmoszynska A;Horvath N;Spicka I;Sutherland HJ;Suvorov AN;Xiu L;Cakana A;Parekh T;San-Miguel JF
通讯作者:
San-Miguel JF
影响因子:
20.3
作者:
Mitsiades, N;Mitsiades, CS;Anderson, KC
通讯作者:
Anderson, KC