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Phase II evaluation of nedaplatin and paclitaxel in patients with metastatic esophageal carcinoma

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Abstract

Purpose

To evaluate the efficiency and toxicities of nedaplatin and paclitaxel in patients with metastatic carcinoma of the esophagus.

Methods

Thirty-nine untreated patients with confirmed metastatic tumors were enrolled. Patients were treated with nedaplatin 80 mg/m2 and paclitaxel 175 mg/m2 on day 1. Treatment was repeated every 21 days.

Results

Thirty-six patients were eligible to be evaluated to have had a response. The overall response rate was 43.6% (17/39), with complete response and partial response rates of 2.6 and 41%, respectively. The median progression-free survival and overall survival time was 6.1 and 10.3 months, respectively. Grade 3/4 toxicities were only observed in six patients [neutropenia in three patients (7.7%) and nausea/vomiting in three patients (7.7%)].

Conclusion

Comparing to other regimens, combination of nedaplatin and paclitaxel achieved an encouraging clinical outcome, with relatively minimal toxicities for patients with metastatic esophageal carcinoma.

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Correspondence to Li Ren.

Additional information

Y. Gong and L. Ren contributed equally to this work.

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Gong, Y., Ren, L., Zhou, L. et al. Phase II evaluation of nedaplatin and paclitaxel in patients with metastatic esophageal carcinoma. Cancer Chemother Pharmacol 64, 327–333 (2009). https://doi.org/10.1007/s00280-008-0874-8

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  • DOI: https://doi.org/10.1007/s00280-008-0874-8

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