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. Author manuscript; available in PMC: 2015 Aug 1.
Published in final edited form as: Cancer Immunol Res. 2014 Mar 28;2(8):725–731. doi: 10.1158/2326-6066.CIR-13-0213

Table 1.

Clinical course and transfusion requirements in response to various regimens.

Month M Spike (mg/dL) RBC transfusion Platelet transfusion Regimen Reason for change in regimen
−6 1.99 0 0 LD
−5 3.15 0 0 LD
−4 2.28 0 0 LDC Disease progression on Ld
−3 3.47 4 4 Melphalan Intolerability to LDC
−2 NM 12 12 None
−1 4.86 6 6 VDD Disease progression
0 5.35 6 6 VDDT/LDT Tadalafil initiated by patient
1 5.07 8 8 LDT Disease progression on VDD
2 4.4 6 6 LDT
3 NM 6 6 LDCT Synergy of Clarithromycin & Lenalidomide
4 3.6 4 4 LDCT
5 1.88 2 0 LDCT
6 1.24 0 0 LDCT
7 0.81 2 0 LDCT
8 0.65 0 0 LDCT
9 0.69 0 0 LDCT
10 0.62 0 0 LDCT
11 0.58 0 0 LDCT
12 0.78 0 0 LDCT
13 0.87 0 0 LDCT
14 0.72 0 0 LDCT
15 0.93 0 0 LDCT
16 1.16 2 0 LDCT

LD: Lenalidomide and dexamethasone; LDC: Lenalidomide, dexamethasone and clarithromycin; VDD: Bortezomib, liposomal doxorubicin and dexamethasone; VDDT: Bortezomib, liposomal doxorubicin, dexamethasone and tadalafil; LDT: Lenalidomide, dexamethasone and tadalafil; LDCT: Lenalidomide, dexamethasone, clarithromycin and tadalafil; NM: not measured. RBC transfusion measured as units of red cells transfused per month. Platelet transfusion measured as units of single donor platelets transfused per month.