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. Author manuscript; available in PMC: 2016 Jan 1.
Published in final edited form as: Int J Cancer. 2014 May 28;136(1):127–137. doi: 10.1002/ijc.28973

Table 1.

Distribution of the 96 patients used in the study according to the type of cohort (original versus validation), adenocarcinoma (colon, pancreas, prostate), and immunotherapy treatment (Tx: GVAX only, GVAX plus ipilimumab, or ipilimumab only). The clinical setting, trial number, and presence or absence of thyroglobulin antibodies at baseline are also shown.

Type of
cohort
Type of
adenocarcinoma
Type of
immunotherapy
Clinical
setting
Clinical trial
number
Total
serum
samples
Total
patients
Patients
without
Tg Abs at
baseline
Patients
who
developed
TgAbs
after Tx
original Colon GVAX only Metastatic NCT00656123 16 8 4 3
original Pancreatic GVAX only Resected NCT00389610 71 12 10 10
validation Pancreatic GVAX only Resected NCT00389610 48 14 11 6
original aPancreatic GVAX + Ipi Metastatic NCT00836407 74 15 12 9
original bProstate GVAX + Ipi Metastatic NCT01510288 126 27 26 21
original aPancreatic Ipi only Metastatic NCT00836407 47 12 10 0
original cProstate Ipi only* Metastatic NCT00323882 52 8 8 0

434 96 81 46

Patients published by

a

Le DT et al. in J Immunotherapy 2013;

b

van den Eertwegh AJ et al. In Lancet Oncology 2012;

c

Slovin SF et al in Ann Oncol 2013.

*

Patients who also received radiotherapy.