The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.
Phase II trial of docetaxel: a new, highly effective antineoplastic agent in the management of patients with anthracycline-resistant metastatic breast cancer.
Abstract
PURPOSE: To determine the efficacy (objective response rate and duration of response and survival) and toxicity of docetaxel in patients with strictly defined anthracycline-resistant metastatic breast cancer (MBC). PATIENTS AND METHODS: Thirty-five patients with bidimensionally measurable MBC who had progressive disease while receiving anthracycline-containing chemotherapy were registered onto the phase II trial. Docetaxel was administered at a dose of 100 mg/m2 over 1 hour every 21 days. RESULTS: Thirty-four patients were assessable for disease response; 18 (53%; 95% confidence interval [CI], 35% to 70%) achieved a partial response. The median times to disease progression and survival duration were 7.5 and 13.5 months, respectively, for responding patients. The median overall survival duration was 9 months. Two hundred eight cycles (median, five) of docetaxel were administered. Neutropenia with less than 500 cells/microL developed in 31 of 35 patients; it was complicated by fever in 30 (14%) of 208 cycles and in 18 (51%) of 35 patients, including one treatment-related death. Fluid retention was seen in 15 (43%) of 35 patients, including pleural effusions in 11 patients (31%). Moderate skin toxicity, asthenia, and myalgia were observed in 16%, 58%, and 37% of cycles, respectively. CONCLUSION: Docetaxel has the highest reported antitumor activity in anthracycline-resistant MBC. High objective response rates were seen in patients with visceral-dominant involvement, multiple metastatic sites, or extensive previous therapy. Docetaxel is associated with severe but reversible neutropenia, asthenia, and cumulative dose-related fluid retention. Dexamethasone decreased the frequency and severity of skin toxicity and appeared to ameliorate fluid retention.
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Cites
Zubrod, C. G., Schneiderman, M., Frei, E., Brindley, C., Lennard Gold, G., Shnider, B., Oviedo, R., Gorman, J., Jones, R., Jonsson, U., et al. (1960) · Journal of Chronic Diseases · doi:10.1016/0021-9681(60)90137-5 · Cited by 1,034
One-Sample Multiple Testing Procedure for Phase II Clinical Trials
Fleming, T. R. (1982) · Biometrics · doi:10.2307/2530297 · Cited by 1,003
Assessment of response to therapy in advanced breast cancer
Hayward, J. L., Carbone, P. P., Heusen, J. C., Kumaoka, S., Segaloff, A., & Rubens, R. D. (1977) · British Journal of Cancer · doi:10.1038/bjc.1977.42 · Cited by 705
Experimental antitumor activity of taxotere (RP 56976, NSC 628503), a taxol analogue.
Bissery, M.-C., Guénard, D., Guéritte, F., & Lavelle, F. (1991) · PubMed · Cited by 481
Paclitaxel (TaxolTM) and docetaxel (TaxotereTM): Not simply two of a kind
Verweij, J., Clavel, M., & Chevalier, B. (1994) · Annals of Oncology · doi:10.1093/oxfordjournals.annonc.a058903 · Cited by 361
The taxoids: paclitaxel (Taxol®) and docetaxel (Taxotere®)
Pazdur, R., Kudelka, A. P., Kavanagh, J. J., Cohen, P. R., & Raber, M. N. (1993) · Cancer Treatment Reviews · doi:10.1016/0305-7372(93)90010-o · Cited by 278
Chevallier, B., Fumoleau, P., Kerbrat, P., Dieras, V. C., Roche, H. H., Krakowski, I., Azli, N., Bayssas, M., Lentz, M. A., & Glabbeke, M. M. V. (1995) · Journal of Clinical Oncology · doi:10.1200/jco.1995.13.2.314 · Cited by 221
Wilson, W. H., Berg, S. L., Bryant, G., Wittes, R. E., Bates, S., Fojo, A., Steinberg, S. M., Goldspiel, B. R., Herdt, J., & O'Shaughnessy, J. (1994) · Journal of Clinical Oncology · doi:10.1200/jco.1994.12.8.1621 · Cited by 216
A’Hern, R., Smith, I., & Ebbs, S. R. (1993) · British Journal of Cancer · doi:10.1038/bjc.1993.146 · Cited by 197
Vinorelbine (Navelbine) as a salvage treatment for advanced breast cancer
Degardin, M., Bonneterre, J. M., Hecquet, B., Pion, J. M., Adeins, A., Horner, D., & Demaille, A. (1994) · Annals of Oncology · doi:10.1093/oxfordjournals.annonc.a058873 · Cited by 142
Cited by
Nagata, Y., Lan, K.-H., Zhou, X., Tan, M., Esteva, F. J., Sahin, A. A., Klos, K. S., Li, P., Monia, B. P., Nguyen, N. T., et al. (2004) · Cancer Cell · doi:10.1016/j.ccr.2004.06.022 · Cited by 1,858
“controls (Holmes et al., 1991; Valero et al., 1995).”
MethodBruno, R., Hille, D., Riva, A., Vivier, N., ten Bokkel Huinnink, W. W., van Oosterom, A. T., Kaye, S. B., Verweij, J., Fossella, F. V., Valero, V, et al. (1998) · Journal of Clinical Oncology · doi:10.1200/jco.1998.16.1.187 · Cited by 423
Self-citationLucien, F., Pelletier, P.-P., Lavoie, R. R., Lacroix, J.-M., Roy, S., Parent, J.-L., Arsenault, D., Harper, K., & Dubois, C. M. (2017) · Nature Communications · doi:10.1038/ncomms15884 · Cited by 66
Metadata
- Authors
- Valero, V, Holmes, F. A., Walters, R. S., Theriault, R. L., Esparza, L., Fraschini, G., Fonseca, G. A., Bellet, R. E., Buzdar, A. U., & Hortobagyi, G. N.
- Venue
- Journal of Clinical Oncology
- Published
- 1995-12
- Volume
- 13
- Issue
- 12
- Pages
- 2886-2894
- ISSN
- 0732-183X (ISSN-L)
- 1527-7755
- OpenAlex
- W1955744924
- Cited by
- 386
- References
- 10
- FWCI
- 8.25
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Phase II trial of docetaxel: a new, highly effective antineoplastic agent in the management of patients with anthracycline-resistant metastatic breast cancer. https://app.cochat.ai/papers/10.1200/jco.1995.13.12.2886
- The paper
- Valero, V, Holmes, F. A., Walters, R. S., Theriault, R. L., Esparza, L., Fraschini, G., Fonseca, G. A., Bellet, R. E., Buzdar, A. U., & Hortobagyi, G. N. (1995). Phase II trial of docetaxel: a new, highly effective antineoplastic agent in the management of patients with anthracycline-resistant metastatic breast cancer. Journal of Clinical Oncology. https://doi.org/10.1200/jco.1995.13.12.2886
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.