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1 thout the presence of any other cytotoxic or cytostatic agent.
2 II trials may not be appropriate for testing cytostatic agents.
3 dependent manner) may not be appropriate for cytostatic agents.
4 s for modifying trial designs to accommodate cytostatic agents.
5 onse to a broad range of cell cycle specific cytostatic agents.
6 s in the early development stage of targeted cytostatic agents.
7 ns for the early development of target-based cytostatic agents.
8 models for the treatment effect of targeted cytostatic agents.
9 esign to evaluate the activity of a putative cytostatic agent, acknowledging heterogeneity of tumor g
10 etagal-treated vessels (P<0.05), whereas the cytostatic agent Ad-p21 decreased lesion size by 58% (P<
11 ate that in SH-SY5Y cells, suramin acts as a cytostatic agent and can block IGF-II-dependent cell gro
12 ory nerve action potential amplitude for all cytostatic agents and a moderate reduction of nerve cond
13 al trials suggested that sorafenib acts as a cytostatic agent, as many patients experienced prolonged
15 e progression) to evaluate the efficacy of a cytostatic agent in a phase II trial is more relevant th
16 onged by subsequent treatment with the three cytostatic agents in all HCCs may be of clinical importa
18 intenance strategies with both cytotoxic and cytostatic agents in women who achieve a secondary respo
19 As known and described in detail, the three cytostatic agents inhibit different processes necessary
20 ongly suggest that the use of rapamycin as a cytostatic agent may be an efficient tool for the treatm
22 n colon carcinoma (HCC) cells, the effect of cytostatic agents reported to inhibit HCC growth [IFN-al
24 regions of a tumor and release cytotoxic or cytostatic agents; several of these HAPs are currently i
25 erties have been reported previously for the cytostatic agents shown here to up-regulate beta-chemoki
29 Exposure of motor neuron cultures to the cytostatic agent vincristine markedly decreased CAT leve
30 sintercalators (8, 9, 12, and 13) behaved as cytostatic agents, while the monosubstituted acridine an
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