Low-Dose Decitabine-Based Chemoimmunotherapy for Patients with Refractory Advanced Solid Tumors: A Phase I/II Report
Table 4
(a) Result of clinical response. (b) Baseline diagnosis of patients who were assessed in the clinical response.
(a)
Cycles ()
PR (%)
SD (%)
PD (%)
ORR (%)
DAC
8
2
0 (0)
4 (50)
4 (50)
4 (50)
3
4
0 (0)
1 (33.33)
2 (66.67)
1 (33.33)
3*
6
1 (50)
0 (0)
1 (50)
1 (50)
DAC + chemo
18
2
1 (5.6)
12 (66.7)
5 (27.8)
13 (72.3)
11
4
2 (18.2)
4 (36.4)
5 (45.5)
6 (54.5)
11
6
2 (18.2)
5 (45.5)
4 (36.4)
7 (63.6)
DAC + CIK
5
2
0 (0)
4 (80)
1 (20)
4 (80)
5
4
0 (0)
4 (80)
1 (20)
4 (80)
5
6
0 (0)
4 (80)
1 (20)
4 (80)
Note. Data is (%). CIK: cytokine induced killer cells; DAC + chemo: decitabine in combination with chemotherapy; DAC + CIK: decitabine in combination with CIK; PR: partial response; SD: stable disease; PD: progressive disease; ORR: objective response rate. Tumors were assessed every 2 cycles by using RECIST 1.0; RECIST: the Response Evaluation Criteria in Solid Tumors; one patient discontinued treatment attributable to digestive tract hemorrhage.