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Clinical Trial
. 2017 Aug;52(8):1194-1198.
doi: 10.1038/bmt.2017.91. Epub 2017 May 15.

Circulating tumor cells as a biomarker for response to therapy in multiple myeloma patients treated within the GMMG-MM5 trial

Affiliations
Clinical Trial

Circulating tumor cells as a biomarker for response to therapy in multiple myeloma patients treated within the GMMG-MM5 trial

S Huhn et al. Bone Marrow Transplant. 2017 Aug.
No abstract available

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Conflict of interest statement

SH, NW, JN, MP, TH, MHu, UB, BH-D, MHä, JD, MG, HK, UG, MHo, PR, AJ, NP and KD declare no conflict of interest. MV and RA are employees of Janssen and hold stock in Johnson & Johnson; HJS—Celgene: honoraria, travel grants and Amgen: honoraria; KW—Honoraria and Advisory Board von Amgen, BMS, Celgene, Janssen, Novartis, Takeda; FL—advisory role: BioNTech, Bristol-Myers-Squibb, Eli Lilly, GANYMED Pharmaceuticals, Merck Sharp & Dohme, Roche Pharma AG. Lecture honoraria: Amgen, Astra Zeneca, Eli Lilly, Merck Sharp & Dohme, Roche Pharma AG, Servier. Research grant: Boehringer Ingelheim, Fresenius Biotech. Travel grants: Amgen, Bayer, Merck Sharp & Dohme, Roche Pharma AG, Taiho Pharmaceutical; IWB—scientific grants Jabssen-Cilag and Celgene. TM is an employee of inVentiv Health; PW—Honoraria and membership on Advisory Boards of Sanofi-Aventis. Membership on Advisory Boards and Travel Grants from Hexal AG; HG—research support (institutions): Celgene, Janssen, Chugai, Novartis, BMS; Advisory Boards (institutions): Janssen, Celgene, Novartis, Amgen Takeda, BMS; Honoraria: Celgene, Janssen, Novartis, Chugai, BMS.

Figures

Figure 1
Figure 1
(a) GMMG-MM5—correlation between tumor load in PB and therapy cycle; N=106. (b) GMMG-MM5—correlation between tumor load in PB and response to therapy. (c) GMMG-MM5 and GMMG-HD4—tumor load in PB at diagnosis and after different Bortezomib-based induction therapy regimes. PAd=bortezomib/doxorubicin/reduced dose dexamethasone (240 mL per cycle); VCD=bortezomib/cyclophosphamide/dexamethasone; PAD=bortezomib/doxorubicin/dexamethasone (480 mg per cycle). (d) GMMG-MM5—tumor load in BM and PB at the time point at which the patients had reached CR (after IT, after ASCT and after Cons.). (e) GMMG-MM5—correlation between tumor load in PB and therapy cycle, stratified for the presence or absence of high-risk cytogenetics (HR=amp(1q) more than three copies, deletion 17p13, t(4:14) and t(14:16); SR=low risk (all others)); HR=1; SR=0. (f) GMMG-MM5—correlation between tumor load in PB and therapy cycle, stratified for ISS Stage. Ordinary boxplots ignoring censoring. (g) GMMG-MM5—correlation between tumor load in BM and PB if PB is positive; N=14 pairs. (h) Tumor load in BM and PB if PB is positive; N=14 pairs.
Figure 1
Figure 1
(a) GMMG-MM5—correlation between tumor load in PB and therapy cycle; N=106. (b) GMMG-MM5—correlation between tumor load in PB and response to therapy. (c) GMMG-MM5 and GMMG-HD4—tumor load in PB at diagnosis and after different Bortezomib-based induction therapy regimes. PAd=bortezomib/doxorubicin/reduced dose dexamethasone (240 mL per cycle); VCD=bortezomib/cyclophosphamide/dexamethasone; PAD=bortezomib/doxorubicin/dexamethasone (480 mg per cycle). (d) GMMG-MM5—tumor load in BM and PB at the time point at which the patients had reached CR (after IT, after ASCT and after Cons.). (e) GMMG-MM5—correlation between tumor load in PB and therapy cycle, stratified for the presence or absence of high-risk cytogenetics (HR=amp(1q) more than three copies, deletion 17p13, t(4:14) and t(14:16); SR=low risk (all others)); HR=1; SR=0. (f) GMMG-MM5—correlation between tumor load in PB and therapy cycle, stratified for ISS Stage. Ordinary boxplots ignoring censoring. (g) GMMG-MM5—correlation between tumor load in BM and PB if PB is positive; N=14 pairs. (h) Tumor load in BM and PB if PB is positive; N=14 pairs.

References

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