“…Studies have shown that PTD regimen (PD regimen combined with thalidomide) achieved promising results, with CR/nCR of 30 ∼ 50%, adverse reactions tolerable, and grade 3/4 PN of about 15%, thus it is considered to be one of the best triplet regimens for MM from the economic perspective and adverse reaction concerns (Cavo et al, 2010;Ludwig et al, 2013;Huang et al, 2014;Leiba et al, 2014;Gentile et al, 2017;Blommestein et al, 2019). However, based on our practice, PTD is poorly tolerated, with a PN incidence of more than 80%, and nearly 50% of patients developed grade 2/3 PN (He et al, 2014).This may be partly due to the fact that patients in the before-2013 group were all treated with bortezomib by IV, while the incidence and severity of PN are significantly higher in the patients treated with bortezomib by IV compared to that by SC Arnulf et al, 2012;Merz et al, 2015;Xu et al, 2018). The incidence of PN in 18 patients treated with PTD regimen in the after-2013 group was significantly decreased, thereinto, the incidence of grade 2 and higher was 22.2% (4/18), which was similar to a previous study in China (Wang et al, 2016).…”