
CPT-11 and Topotecan are a new semisynthetic derivative of CPT, and have been shown to inhibit DNA topoisomerase I and to have a strong antitumor activity with low toxicity against murine tumor. On the other hard, the new antitumor compounds, NC-190 and IST-622 have been shown to inhibit DNA topoisomerase II, and the clinical study are currently under progress. A phase II study of CPT-11 demonstrated that CPT-11 was a very active agent which a acceptable toxicities against patient with advanced non-small cell lung cancer and small cell lung cancer.
Male, Lung Neoplasms, Antineoplastic Agents, Irinotecan, Drug Administration Schedule, Mice, Carcinoma, Non-Small-Cell Lung, Animals, Humans, Phenazines, Camptothecin, Female, Carcinoma, Small Cell, Topoisomerase I Inhibitors, Topotecan
Male, Lung Neoplasms, Antineoplastic Agents, Irinotecan, Drug Administration Schedule, Mice, Carcinoma, Non-Small-Cell Lung, Animals, Humans, Phenazines, Camptothecin, Female, Carcinoma, Small Cell, Topoisomerase I Inhibitors, Topotecan
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 0 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
