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Article: Combined-modality treatment for isolated recurrences of breast carcinoma: Update on 30 years of experience at the University of Texas M. D. Anderson Cancer Center and assessment of prognostic factors
Title | Combined-modality treatment for isolated recurrences of breast carcinoma: Update on 30 years of experience at the University of Texas M. D. Anderson Cancer Center and assessment of prognostic factors |
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Authors | |
Keywords | Breast carcinoma Chemotherapy Combined modality Isolated recurrence Stage IV-NED |
Issue Date | 2005 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/28741 |
Citation | Cancer, 2005, v. 104 n. 6, p. 1158-1171 How to Cite? |
Abstract | BACKGROUND. In three prospective, single-arm studies, the authors previously showed an improved outcome for anthracycline-naïve patients with isolated sites of recurrent breast carcinoma (BC) who were treated with doxorubicin-based chemotherapy after local therapy (surgery and/or radiotherapy). In the current report, the initial results are presented from a Phase II trial of docetaxel (100 mg/m2 every 21 days for 6 cycles) given after local therapy for recurrent BC (Stage IV BC with no evidence of clinically measurable disease) in patients who received prior adjuvant anthracycline-based chemotherapy, and the authors provide an update of the 3 previous studies. An analysis of prognostic factors for these patients also is presented. METHODS. Eligibility criteria for all studies included histologic proof of recurrent BC that had been resected and/or irradiated with curative intent. Survival was calculated using the Kaplan-Meier method. Univariate survival analyses were performed to test for associations between patient characteristics and outcome (log-rank test). Cox proportional hazards models were used to determine the multivariable correlations between patient characteristics and outcome. RESULTS. The median follow-up for the docetaxel-based trial (n = 26 patients) was 45 months. Early outcomes for this study are promising. The median disease-free survival (DFS) was 44 months, and the 3-year DFS and overall survival (OS) rates were 58% and 87%, respectively. In the 3 doxorubicin-based studies, the median follow-up was 121.5 months for all living patients, and the estimated 20-year DFS and OS rates were both 26%. On multivariable analysis of patients from all 4 studies, the only significant prognostic factor for DFS and OS (P = 0.0006) was the number of involved axillary lymph nodes at initial diagnosis. CONCLUSIONS. A proportion of patients with isolated BC recurrences achieved prolonged DFS with combined-modality treatment. Patients who receive anthracycline-based chemotherapy at primary diagnosis may benefit from local treatment followed by docetaxel-based chemotherapy for isolated recurrences. The only significant independent prognostic factor was the number of involved axillary lymph nodes at initial diagnosis. © 2005 American Cancer Society. |
Persistent Identifier | http://hdl.handle.net/10722/146567 |
ISSN | 2023 Impact Factor: 6.1 2023 SCImago Journal Rankings: 2.887 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Hanrahan, EO | en_HK |
dc.contributor.author | Broglio, KR | en_HK |
dc.contributor.author | Buzdar, AU | en_HK |
dc.contributor.author | Theriault, RL | en_HK |
dc.contributor.author | Valero, V | en_HK |
dc.contributor.author | Crisiofanilli, M | en_HK |
dc.contributor.author | Yin, G | en_HK |
dc.contributor.author | Kau, SWC | en_HK |
dc.contributor.author | Hortobagyi, GN | en_HK |
dc.contributor.author | Rivera, E | en_HK |
dc.date.accessioned | 2012-05-02T08:37:04Z | - |
dc.date.available | 2012-05-02T08:37:04Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | Cancer, 2005, v. 104 n. 6, p. 1158-1171 | en_HK |
dc.identifier.issn | 0008-543X | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/146567 | - |
dc.description.abstract | BACKGROUND. In three prospective, single-arm studies, the authors previously showed an improved outcome for anthracycline-naïve patients with isolated sites of recurrent breast carcinoma (BC) who were treated with doxorubicin-based chemotherapy after local therapy (surgery and/or radiotherapy). In the current report, the initial results are presented from a Phase II trial of docetaxel (100 mg/m2 every 21 days for 6 cycles) given after local therapy for recurrent BC (Stage IV BC with no evidence of clinically measurable disease) in patients who received prior adjuvant anthracycline-based chemotherapy, and the authors provide an update of the 3 previous studies. An analysis of prognostic factors for these patients also is presented. METHODS. Eligibility criteria for all studies included histologic proof of recurrent BC that had been resected and/or irradiated with curative intent. Survival was calculated using the Kaplan-Meier method. Univariate survival analyses were performed to test for associations between patient characteristics and outcome (log-rank test). Cox proportional hazards models were used to determine the multivariable correlations between patient characteristics and outcome. RESULTS. The median follow-up for the docetaxel-based trial (n = 26 patients) was 45 months. Early outcomes for this study are promising. The median disease-free survival (DFS) was 44 months, and the 3-year DFS and overall survival (OS) rates were 58% and 87%, respectively. In the 3 doxorubicin-based studies, the median follow-up was 121.5 months for all living patients, and the estimated 20-year DFS and OS rates were both 26%. On multivariable analysis of patients from all 4 studies, the only significant prognostic factor for DFS and OS (P = 0.0006) was the number of involved axillary lymph nodes at initial diagnosis. CONCLUSIONS. A proportion of patients with isolated BC recurrences achieved prolonged DFS with combined-modality treatment. Patients who receive anthracycline-based chemotherapy at primary diagnosis may benefit from local treatment followed by docetaxel-based chemotherapy for isolated recurrences. The only significant independent prognostic factor was the number of involved axillary lymph nodes at initial diagnosis. © 2005 American Cancer Society. | en_HK |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/28741 | en_HK |
dc.relation.ispartof | Cancer | en_HK |
dc.subject | Breast carcinoma | en_HK |
dc.subject | Chemotherapy | en_HK |
dc.subject | Combined modality | en_HK |
dc.subject | Isolated recurrence | en_HK |
dc.subject | Stage IV-NED | en_HK |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Aged, 80 And Over | en_US |
dc.subject.mesh | Breast Neoplasms - Mortality - Pathology - Therapy | en_US |
dc.subject.mesh | Clinical Trials As Topic | en_US |
dc.subject.mesh | Combined Modality Therapy | en_US |
dc.subject.mesh | Doxorubicin - Administration & Dosage | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Neoplasm Recurrence, Local - Therapy | en_US |
dc.subject.mesh | Neoplasm Staging | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Proportional Hazards Models | en_US |
dc.subject.mesh | Receptors, Estrogen - Analysis | en_US |
dc.subject.mesh | Taxoids - Administration & Dosage | en_US |
dc.title | Combined-modality treatment for isolated recurrences of breast carcinoma: Update on 30 years of experience at the University of Texas M. D. Anderson Cancer Center and assessment of prognostic factors | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Yin, G: gyin@hku.hk | en_HK |
dc.identifier.authority | Yin, G=rp00831 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/cncr.21305 | en_HK |
dc.identifier.pmid | 16047352 | - |
dc.identifier.scopus | eid_2-s2.0-24644470461 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-24644470461&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 104 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 1158 | en_HK |
dc.identifier.epage | 1171 | en_HK |
dc.identifier.isi | WOS:000231743700005 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Hanrahan, EO=8558091200 | en_HK |
dc.identifier.scopusauthorid | Broglio, KR=6602915196 | en_HK |
dc.identifier.scopusauthorid | Buzdar, AU=35379841900 | en_HK |
dc.identifier.scopusauthorid | Theriault, RL=7103232796 | en_HK |
dc.identifier.scopusauthorid | Valero, V=7004692933 | en_HK |
dc.identifier.scopusauthorid | Crisiofanilli, M=8558090600 | en_HK |
dc.identifier.scopusauthorid | Yin, G=8725807500 | en_HK |
dc.identifier.scopusauthorid | Kau, SWC=7005363979 | en_HK |
dc.identifier.scopusauthorid | Hortobagyi, GN=7202399346 | en_HK |
dc.identifier.scopusauthorid | Rivera, E=7101648447 | en_HK |
dc.identifier.issnl | 0008-543X | - |