TABLE 2

Patient Characteristics, Prior Oncologic Therapy, and Trial Outcome

Patient no.SexAge (y)CohortEastern Cooperative Oncology GroupPrimary sitePrior chemotherapy with or without radiotherapySites of disease at study entryScreening carcinoembryonic antigenEnd-of-study carcinoembryonic antigenOverall response
101Female5411RectumNXRTLiver, lung, LN2.11.4PD
102Male5910ColonFXLN3.13.7PD
103Male5910ColonA5FULN258544SD
104Female6921ColonFX, FI, MLiver, lung, omentum8.8861PD
105Male6020RectumNXRT, FX, FILiver, lung, LN4621,175PD
106Male6620ColonA5FU, FXLiver, pelvis3829SD
107Female6620RectumNXRTLung, omentum, mesentery1.61.6SD
108Male6920ColonFX, hu3S193 (phase I)Liver, LN4.72.3PR
109Male5120ColonFX, FI, M, cetuximabLung, LN27.416.6SD
110Male5230ColonFXLiver11.99.3SD
111Female6130ColonFX, ILung, LN, adrenal35.643.2SD
112Female4130RectumNXRT, FX, FI, C, BLung, liver, psoas, paravertebral mass6451,386.3PD
113Male5840ColonI, FXLung, liver1,0051,538.3PD
114Male6440ColonFXSuprapubic mass, abdominal wall, bowel17.920.5SD
115Male5940ColonFX, ILung, liver, LN15.257.4PD
116Male6650RectumNXRT, ILung, liver, LN243.3408.2SD
117Male6650ColonFXLiver29.116.7SD
118Male4850RectumNXRTLung, lymph nodes42.328.1NA
119Female5550RectumFX, FI + C + BLung, liver, lymph nodesNA183.5SD
  • NXRT = neoadjuvant chemoradiation (5FU); LN = lymph nodes; FX = FOLFOX; A5FU = adjuvant 5FU; SD = stable disease; FI = FOLFIRI; M = mitomycin; I = irinotecan; C = cetuximab; B = bevacizumab; NA = not assessable.