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. Author manuscript; available in PMC: 2012 Sep 19.
Published in final edited form as: Cancer Chemother Pharmacol. 2010 Oct 28;68(2):379–388. doi: 10.1007/s00280-010-1481-z

Table 4.

Summary of correlative study results and relation to clinical outcomes

Patient Best
response
Time to
progression
(months)
Change in tumor R2 β2
homodimer by in situ
RT–PCR after 3-AP (Fig. 1)
Change in PBMC RRM2
after 3-AP (Fig. 2)
Change in PBMC dCTP
pools after 3-AP (Fig. 3)
4 PD 1.3 Increased Unchanged Not done
6 SD 5.2 Increased Not done Not done
16 PD 2.7 Not done Decreased Not done
27 SD 8.3 Not done Decreased Not done
30 NE NE Not done Not done Significantly decreased
31 SD 13.8 Not done Decreased Significantly increased

All patients except patient 4 had normal liver function; patient 30 was not evaluable for response because of treatment discontinuation after 1 dose due to toxicity

PD progressive disease, SD stable disease, NE not evaluable, PBMC peripheral blood mononuclear cells