2017
DOI: 10.20452/pamw.4032
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Comparative proteomic profiling of sera from patients with refractory multiple myeloma reveals potential biomarkers predicting response to bortezomib-based therapy

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Cited by 15 publications
(15 citation statements)
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“…The development of new biomarkers predicting response to therapy would allow an identification of patients who should receive other first -line therapeutic regimens as the first -line treatment. [18][19][20] As in the previous reports, impaired renal function did not have negative impact on the response rates or PFS. Importantly, patients who responded to therapy showed an improvement in renal function, confirming the efficacy of this protocol in patients with renal failure.…”
supporting
confidence: 79%
“…The development of new biomarkers predicting response to therapy would allow an identification of patients who should receive other first -line therapeutic regimens as the first -line treatment. [18][19][20] As in the previous reports, impaired renal function did not have negative impact on the response rates or PFS. Importantly, patients who responded to therapy showed an improvement in renal function, confirming the efficacy of this protocol in patients with renal failure.…”
supporting
confidence: 79%
“…Furthermore, apoC1 was also reported as a marker for Wilms tumor [197], gastric adenocarcinoma [198], refractory multiple myeloma [199], hepatitis B-related hepatocellular carcinoma [200].…”
Section: Apoc1 In Pathologymentioning
confidence: 99%
“…[6][7][8] Bone marrow plasma cells are obtained by an invasive method of bone marrow biopsy, which is not useful in routine clinical practice. Therefore, Łuczak et al 4 have used proteomic analysis of se rum to overcome this obstacle. They used nano liquid chromatography-tandem mass spectrom etry to analyze digested serum protein samples from 61 proteasome inhibitor naive, transplant eligible patients with MM, who were resistant to the first line chemotherapy protocol CTD (cyclo phosphamide, thalidomide, and dexamethasone) and were scheduled for salvage PAD (bortezo mib, adriamycin [doxorubicin], and dexameth asone) or VTD (bortezomib, thalidomide, and dexamethasone) chemotherapy.…”
mentioning
confidence: 99%