Skip to main content
. 2018 Sep 20;71(2):71–86. doi: 10.1007/s00251-018-1083-1

Table 1.

Overview of reviewed clinical trials

ACT varianta Cancer type N %OR Outcome (CR/PR/SD/AD) Reference
TILs Melanoma 93 56 19 CR, 33 PR (Rosenberg et al. 2011)
TILs Melanoma 101 54 23 CR, 30 PR (Goff et al. 2016)
TILs, single neo-epitope enriched Gastro-intestinal 4 50 1CR, 1 PR (Tran et al. 2015)
TILs reactive to HPV Cervical 9 33 2 CR, 1 PR (Stevanović et al. 2015)
EBV-specific CTLs from cell lines Lymphoma 13 85 11 CR (Heslop et al. 2010)
DC vaccine primed PBLs Ovarian 3 66 1 CR, 1 SD (Kandalaft et al. 2013)
HER2/neu vaccine primed PBLs HER2+ breast and ovarian 7 43 3 PR (Disis et al. 2014)
PBLs w/ engin.
CEA reactive TCR
colon 3 33 1 PR
3 AD severe inflammatory colitis
(Parkhurst et al. 2011)
PBLs w/ engin.
MAGE-A3 reactive TCR
MAGE-A3/12+ tumours 9 55 1 CR, 4 PR
3 AD neurotoxicity (two deaths)
(Morgan et al. 2013)
PBLs w/ engin.
NY-ESO-1 reactive TCR
Melanoma 20 55 4 CR, 7 PR (Robbins et al. 2015)
PBLs w/ engin.
NY-ESO-1 reactive TCR
Synovial cell sarcoma 18 61 1 CR, 10 PR (Robbins et al. 2015)

TAAs: carcinoembryonic antigen (CEA) New York esophageal squamous cell carcinoma-1 (NY-ESO-1), human epidermal growth factor receptor 2 (HER2/neu), and melanoma-associated antigen (MAGE). Epstein-Barr virus (EBV) human papillomavirus (HPV). RECIST criteria were used for describing outcome: complete response (CR), partial response (PR), objective response (OR) both CR and PR. Stable disease (SD), adverse effects (AD). We have chosen not to indicate the patients that eventually progress to disease, as this heavily depends on the follow-up time of the cohorts

aTumour infiltrating lymphocyte (TIL), peripheral blood lymphocyte (PBL), cytotoxic T lymphocyte (CTL), T cell receptor (TCR), tumour-associated antigen (TAA), and dendritic cell (DC). N is the number of patients