Abstract
We compared the results of randomised trials comparing taxane-containing chemotherapy regimens with regimens not containing a taxane in women with metastatic breast cancer. The specialised register of the Cochrane Breast Cancer Group was searched in March 2004. Eligibility was assessed and data extracted from eligible studies by two reviewers. Hazard ratios (HR) were derived for time-to-event outcomes, and a fixed-effect model was used for meta-analysis. Tumour response rates were analysed as dichotomous variables. Of 21 eligible trials, 16 had published some results and 12 data on overall survival. An estimated 2621 deaths among 3643 women suggest a significant difference in overall survival in favour of taxane-containing regimens (HR 0.93, 95% confidence interval (CI) 0.86–1.00, P=0.05). The treatment effect on survival was similar if only trials of first-line chemotherapy were included, although not statistically significant. There appeared to be an advantage for taxanes in time to progression (HR 0.92, 95% CI 0.85–0.99, P=0.02) and overall response (odds ratio (OR) 1.34, 95% CI 1.18–1.52, P<0.001). There was significant heterogeneity across the trials (P<0.001), partly because of the varying efficacy of the comparator regimens. Taxane-containing regimens improved overall survival in women with metastatic breast cancer. Taxane-containing regimens are more effective than some, but not all, nontaxane-containing regimens.
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Main
Taxanes are among the most active chemotherapy agents used in the management of metastatic breast cancer. Paclitaxel was identified in 1971 as part of a National Cancer Institute (NCI) programme that screened medicinal plants for potential anticancer activity, and was first used in clinical trials in 1983 (Breast cancer: taxane clinical perspectives, 1996). Docetaxel was synthesised in 1986 and is similar to paclitaxel in its mechanism of action.
Initially, the use of taxanes was limited by hypersensitivity reactions, but once these were better managed (largely by premedication with steroids), taxane use became more frequent. Taxanes have become part of standard management in most western countries and are used as single agents or in combination with other chemotherapeutic drugs or the monoclonal antibody trastuzumab (Bernard-Marty et al, 2003).
The effect of taxanes on survival compared with other drugs or drug combinations is unclear. We therefore conducted a systematic review and meta-analysis to identify and synthesise the results of randomised clinical trials comparing taxane-containing chemotherapy regimens with regimens that did not contain a taxane. Prospectively, we asked the following questions:
The planned outcome measures were survival (date randomised to date of death), time to progression (date randomised to date of progression or death), time to treatment failure, overall response, toxicity (specifically leukopenia, neurotoxicity, nausea or vomiting and treatment-related death) and quality of life.
Materials and methods
Properly randomised controlled trials (i.e. where sequence generation and allocation concealment were adequate) comparing any regimen containing a taxane with any regimen not containing a taxane as first-line treatment for metastatic breast cancer were eligible. Trials that included both women with metastatic disease and women with isolated locoregional recurrent disease were eligible for inclusion if it was possible to distinguish between the two groups (data were reported separately) or if women with isolated locoregional recurrence were <20% of the total group. There were no age restrictions. Trials in which the primary intention was to investigate sequencing of treatment regimens were excluded.
The primary outcomes were survival and time to progression for which the hazard ratio (HR) is the most appropriate statistic. When possible, the HR and associated variances were extracted directly from the trial publication/s. If not reported, it was obtained indirectly using the methods described by Parmar et al (1998) using either other available summary statistics or from data extracted from published Kaplan–Meier curves. To allow for immature follow-up, the numbers at risk were adjusted based on estimated minimum and maximum follow-up times
A pooled HR was obtained from the derived observed (O)–expected (E) number of events and the variance for each trial using the fixed effect model (Yusuf et al, 1985). The pooled HR represents the overall risk of an event on taxane-containing chemotherapy vs nontaxane-containing chemotherapy. χ2 tests for heterogeneity were used to test for heterogeneity over all trials (see Alderson et al, 2003). Post hoc subgroup analyses were conducted for the type of taxane and prior exposure to anthracyclines. χ2 tests for interaction were applied to these subgroup analyses.
Results
On 12 March 2004, the search strategy in Table 1 was applied to the specialised register of trials maintained by the Cochrane Breast Cancer Group (see Search Strategy), resulting in the identification of 195 references to potentially eligible trials from the 7164 references on the register. We identified 21 eligible studies, of which three are ongoing (Table 2) (Dieras et al, 1995; Bishop et al, 1999; Chan et al, 1999; Nabholtz et al, 1999, 2003; Sjostrom et al, 1999; Luck et al, 2000; Paridaens et al, 2000; Bonneterre et al, 2001, 2002, 2003; Jassem et al, 2001; Zielinski et al, 2001; Biganzoli et al, 2002; Icli et al, 2002; Talbot et al, 2002; Bontenbal et al, 2003; Sledge et al, 2003; Goldhirsch, 2005; Heidemann, 2005). An additional two studies were identified but excluded: the status of one as a randomised trial was unclear (Gebbia et al, 2003), and the second randomised women to cease vs continue paclitaxel (Gennari et al, 2001). Not all trials reported on all outcomes. Some were less mature studies than others and had been reported in abstract form only.
Although the intention was to include only trials of first-line chemotherapy (i.e. no chemotherapy had been given except as adjuvant therapy), over half of the completed and published trials are of more-than-first-line therapy. All trials meeting the remaining eligibility criteria were therefore included in the review, and separate analyses were conducted for line of therapy. All trials eligible for Question 1 (adding a taxane to a chemotherapy regimen) and Question 2 (comparing any regimen containing a taxane with any regimen not containing a taxane) are of first-line chemotherapy.
It was not possible to assess accurately the quality of randomisation used in most studies owing to lack of information in the published articles. If the imbalance between treatment arms was deemed to be sufficient to lead to a suspicion of bias in the randomisation process, then this is reflected in the quality grade assigned to the randomisation process, details of which have been reported elsewhere (Ghersi et al, 2005).
Over 6300 women had been randomised to the 21 eligible trials, and time-to-event data for overall survival data were available for 57% of them. The data available for Question 3 (comparing a single-agent taxane with any regimen not containing a taxane) were more complete; nine of the 10 eligible trials (representing 2442 or 84% of the 2780 women randomised to this question) had reported overall survival data.
One study was a three-armed trial eligible for both Questions 1 and 3 (Sledge et al, 2003). This was taken into account when the overall effect of taxanes was calculated (by halving the control group).
Overall survival
The trials of first-line chemotherapy suggest that there may be a benefit in terms of overall survival in favour of taxanes, with an HR of 0.92 (95% confidence interval (CI) 0.84–1.02, P=0.11). When all trials are included, there is a statistically significant difference of similar magnitude in favour of taxane-containing regimens, with an HR of 0.93 (95% CI 0.86–1.00, P=0.05). There was no statistically significant heterogeneity across the trials.
The results for those individual trials that reported on survival are shown in Figure 1. Only three of the nine studies eligible for Question 2 (comparing any regimen containing a taxane with any regimen not containing a taxane) provided information on survival, representing 35% of the estimated number of patients. The three trials suggested that there might be a benefit in terms of overall survival in favour of taxanes (HR 0.88, 95% CI 0.76–1.02, P=0.10), but this was not statistically significant.
Nine of the 10 studies eligible for Question 3 (comparing a single-agent taxane with any regimen not containing a taxane) reported on overall survival, which suggests a benefit in favour of the taxane arm (HR 0.94, 95% CI 0.86–1.03, P=0.19) with no statistically significant heterogeneity. A similar but nonsignificant effect was seen if trials with potentially suboptimal comparators (those comparing taxane with mitomycin±vinblastine, and fluorouracil with vinorelbine) (Dieras et al, 1995; Nabholtz et al, 1999; Bonneterre et al, 2002) were excluded (HR 0.97, 95% CI 0.88–1.08, P=0.62), or if the analysis of this subgroup was limited to trials of first-line chemotherapy (HR 0.95, 95% CI 0.83–1.10, P=0.50).
Time to progression
Trials were not consistent in the way they defined this outcome. Trials that started the clock at the time of randomisation were included. Details of the definition used for this outcome for each trial has been reported elsewhere (Ghersi et al, 2005).
The six trials of first-line chemotherapy suggest that there is no detectable difference between taxane and nontaxane-containing regimens (HR 0.99, 95% CI 0.90–1.09, P=0.88). If data from all 11 of the 21 eligible trials reporting this outcome are included, there is a statistically significant benefit in favour or taxanes (HR 0.92, 95% CI 0.85–0.99, P=0.02) (Figure 2). There was, however, significant heterogeneity across trials for all time-to-progression analyses (P<0.00001, I2=89.7%).
Only three of the 21 eligible trials reported data on time to treatment failure. It was therefore not considered appropriate to pool data across trials.
Overall response rates
Sufficient data from 15 of the 21 eligible trials were available to enable an odds ratio (OR) for response rates to be calculated. There were some differences in the definition of response across (but not within) trials. The analysis of the 2787 assessable patients in first-line trials indicate a statistically significant difference in favour of taxane-containing regimens (OR 1.28, 95% CI 1.10–1.50, P=0.002). This difference remained when all trials reporting this outcome were included (OR 1.34, 95% CI 1.18–1.52, P<0.0001). There was significant heterogeneity across trials for this outcome (P<0.0001) (Figure 3).
Toxicity
Four of the nine studies eligible for Question 2 (comparing any regimen containing a taxane with any regimen not containing a taxane) reported on toxicity (Table 3). Taxanes were associated with significantly more leukopenia and neurotoxicity, but less nausea and vomiting in assessable patients. Of those eligible for Question 3 (comparing a single-agent taxane with any regimen not containing a taxane), seven studies reported on leukopenia, nine on nausea or vomiting and neurotoxicity and four on hair loss (Table 4). Taxanes were associated with significantly worse neurotoxicity and hair loss, but less leukopenia and nausea or vomiting.
Quality of life
In all, 10 trials had collected quality-of-life data, eight of which had reported results (Bishop et al, 1999; Chan et al, 1999; Nabholtz et al, 1999, 2003; Hakamies-Blomqvist et al, 2000; Kramer et al, 2000; Carmichael, 2001; Jassem et al, 2001; Biganzoli et al, 2002; Sledge et al, 2003). The type of instrument used and the way in which quality of life was reported varied across trials, as did the completion rate by patients of quality-of-life instruments. Some studies reported problems with patients in poorer health not completing questionnaires (e.g. Nabholtz et al, 1999). For these reasons, it was decided not to statistically pool quality-of-life data. None of the individual trials reported a statistically significant difference in overall quality of life, or in any of the subscales, between taxane- and nontaxane-containing chemotherapy regimens.
Treatment-related death
The trials reported 54 treatment-related deaths: 24 on taxane-containing regimens and 30 on the nontaxane-containing regimens. There was no statistically significant difference between the two groups (OR 0.80, 95% CI 0.48–1.32, P=0.41).
Subgroup analyses
Single-agent taxane compared with single-agent anthracycline
The three trials comparing single-agent taxane with single-agent anthracycline (an estimated 916 events in 1110 women) showed no detectable difference in time to progression (HR 1.10, 95% CI 0.97–1.26, P=0.12) with some evidence of heterogeneity (P=0.001). An estimated 812 deaths in 1110 women showed no detectable difference in overall survival (HR 1.00, 95% CI 0.88–1.15, P=0.94) and no statistically significant heterogeneity.
Single-agent taxane compared with nonanthracycline-containing combinations
The six trials comparing single-agent taxane with a nonanthracycline-containing combination (estimated 966 deaths in 1332 women) favoured taxane-containing regimens for overall survival (HR 0.91, 95% CI 0.80–1.03, P=0.13) with no statistically significant heterogeneity. For time to progression, the five studies with usable data (1020 events in 1156 women) favoured taxane-containing regimens (HR 0.85, 95% CI 0.75–0.96, P<0.0008), with statistically significant heterogeneity (P<0.0001, I2 91.3%).
Type of taxane
Post hoc subgroup analyses were conducted to investigate the treatment effect within the types of taxane. Data from the 2038 women randomised to seven trials using paclitaxel show no detectable difference in overall survival (HR 0.97, 95% CI 0.87–1.07, P=0.54) or in time to progression. Data from the 1605 women randomised to five trials using docetaxel showed a statistically significant difference in overall survival and time to progression in favour of the taxane-containing regimen (HR for overall survival 0.88, 95% CI 0.78–0.98, P=0.02) with no statistically significant heterogeneity.
There was a statistically significant difference in time to progression between women who had received docetaxel compared to those who had received paclitaxel (test for interaction P<0.001) (Figure 4). The interpretation of this result is complicated by the significant heterogeneity in both the docetaxel and paclitaxel trials and may relate to the choice of comparator in these trials.
Previous exposure to anthracyclines
Post hoc subgroup analyses were also used to investigate the treatment effect in patients who had or had not received previous anthracyclines. Data from the 1123 women randomised to the five trials in women who had received anthracyclines favoured taxane-containing regimens in terms of overall survival (HR 0.94, 95% CI 0.82–1.08, P=0.39) and time to progression. There was no detectable difference for either outcome in anthracycline-naive women, although there was a significant difference in favour of taxanes for overall response (OR 1.21, 95% CI 1.03–1.43, P=0.02). There was statistically significant difference in time to progression (P=0.006) between women who had received prior anthracyclines and those who had not (P<0.001) (Figure 5).
Discussion
Despite the relative immaturity of many of the studies included in this review, there is sufficient evidence to conclude that on average, taxane-containing regimens are associated with a statistically significant improvement in overall survival compared with nontaxane-containing regimens. This is consistent with emerging data from trials employing taxanes in the adjuvant setting (Nowak et al, 2004).
Conclusions about the effects of taxanes on other end points (such as response rate and time to progression), the effects of taxanes in various subgroups and the differential effects of paclitaxel and docetaxel are of clinical interest, but are statistically less secure. Taxane-containing regimens were associated with more leukopenia and neurotoxicity, but less nausea and vomiting, than the control group, and the effect on quality of life did not appear to differ in any of the trials.
At the time of this review, overall survival data were available for only 12 of the 20 eligible trials. This may relate to the relative immaturity of some of the trials, or reporting bias (specifically the tendency to report positive results early) may exist. There may also be unpublished trials that were not identified in our search. The treatment effects reported may therefore be overestimated.
The initial eligibility criteria for this review limited trials to those comparing taxane- with nontaxane-containing regimens as first-line chemotherapy. A decision was made to include comparisons of more-than-first-line chemotherapy owing to the limited number of completed trials (most of the first-line trials had not reported survival data). Results for overall survival and time to progression limited to the available first-line treatment trials suggest a benefit in favour of taxane-containing regimens, but this is not statistically significant. Nevertheless, the observed results are consistent with those based on all trials and may be due to lack of statistical power.
Some heterogeneity across the trials is to be expected given the different drugs, dosages and schedules being used and the different patient groups and treatment settings. There is, however, strong statistical evidence of heterogeneity among the trials in the effect of treatment on time to progression and response (P<0.00001), and one explanation for this is the varying efficacy of the comparator regimens. For example, the regimens of mitomycin±vinblastine, and fluorouracil+vinorelbine could be regarded as suboptimal chemotherapy for breast cancer. If these regimens are excluded, the advantages for a single-agent taxane, when compared with a nontaxane-containing regimen, are no longer statistically significant. While opinions will vary regarding those regimens that could be considered to be suboptimal, it is reasonable to conclude that taxanes are more effective than some, but not all, regimens with which they have been compared, and are at least as effective as the other regimens.
The analyses of most relevance to clinical practice are comparisons of the different taxanes, and the contexts in which they are used (i.e. in anthracycline-naïve patients or not). The available data suggest that docetaxel may be more active than paclitaxel, at least when given in 3-weekly schedules. This is based on an indirect comparison of these two drugs in trials with statistical heterogeneity, but is consistent with the preliminary results of a trial directly comparing the taxanes (Jones et al, 2003).
Furthermore, weekly schedules of taxanes are now commonly used and may have a different efficacy-to-toxicity ratio. Ongoing trials, in all stages of breast cancer, are investigating the relative efficacy of different taxanes and different schedules of those taxanes. The benefit of taxanes also appears to be less apparent in patients who have not had previous anthracyclines. While subset analyses may be useful for informing clinical practice, interpreting such analyses requires caution, given the smaller number of patients in each subgroup, and the potential effect of confounding.
This review includes data from 12 studies (3643 randomised women) reporting time-to-event outcomes, and 16 studies (4287 randomised women) reporting response as an outcome. When complete, the data from all 21 eligible studies will contribute information on over 6000 randomised women to future updates of this review.
This paper is based on a Cochrane review published in the Cochrane Library 2004, Issue 3 (see www.CochraneLibrary.net for information). Cochrane reviews are regularly updated as new evidence emerges and in response to comments and criticisms, and the Cochrane Library should be consulted for the current version of the review.
Change history
16 November 2011
This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication
References
Alderson P, Green S, Higgins JPT (eds) (2003) Cochrane Reviewers' Handbook 4.2.2. Chichester, UK, Ltd: John Wiley & Sons, Available at http://www.cochrane.org/resources/handbook/hbook.htm (accessed 31 January 2005)
Bernard-Marty C, Cardoso F, Piccart MJ (2003) Use and abuse of taxanes in the management of metastatic breast cancer. Eur J Cancer 39: 1978–1989
Biganzoli L, Cufer T, Bruning P, Coleman R, Duchateau L, Calvert AH, Gamucci T, Twelves C, Fargeot P, Epelbaum R, Lohrisch C, Piccart MJ (2002) Doxorubicin and paclitaxel vs doxorubicin and cyclophosphamide as first-line chemotherapy in metastatic breast cancer: EORTC 10961. J Clin Oncol 20(14): 3114–3121
Bishop JF, Dewar J, Toner GC, Smith J, Tattersall MH, Olver IN, Ackland S, Kennedy I, Goldstein D, Gurney H, Walpole E, Levi J, Stephenson J, Canetta RL (1999) Initial paclitaxel improves outcome compared with CMFP combination chemotherapy as front-line therapy in untreated metastatic breast cancer. J Clin Oncol 17(8): 2355–2364
Bonneterre J, Dieras V, Tubiana-Hulin M, Bougnoux P, Bonneterre M, Delozier T, Culine S, Dohollou N, Suissa J, Samak R (2001) 6 cycles of epirubicin/docetaxel (ET) vs 6 cycles of 5FU epirubicin/cyclophosphamide (FEC) as first line metastatic breast cancer (MBC) treatment. Proceedings of the American Society of Clinical Oncology Abstract 163, Available at http://www.asco.org/ac/1,1003,_12-002636-00_18-0010-00_19-00163,00.asp (accessed 15 September 2004)
Bonneterre J, Roche H, Monnier A, Guastalla JP, Namer M, Fargeot P, Assadourian S (2002) Docetaxel vs 5-fluorouracil plus vinorelbine in metastatic breast cancer after anthracycline therapy failure. Br J Cancer 87(11): 1210–1215
Bontenbal M, Braun JJ, Creemers GJ, de Boer AC, Janssen JTP, Leys MBL, Schothorst KLC, Schmitz PIM, Bokma JJ, Seynaeve C (2003) Phase III study comparing AT (adriamycin, docetaxel) to FAC (fluorouracil, adriamycin, cyclophosphamide) as first-line chemotherapy in patients with metastatic breast cancer. Eur J Cancer Suppl 1(5): S201
Breast cancer: taxane clinical perspectives (1996) Bristol-Myers Squibb Oncology. Princeton NJ, USA: BMS Publication
Carmichael J (2001) UKCCCR trial of epirubicin and cyclophosphamide vs epirubicin and taxol in the first line treatment of women with metastatic breast cancer. UKCCR ABO1. Proceedings of the American Society of Clinical Oncology 37th Annual Meeting 12–15 May 2001, San Francisco, Alexandria, VA: ASCO. 22app
Chan S, Friedrichs K, Noel D, Pinter T, Van Belle S, Vorobiof D, Duarte R, Gil Gil M, Bodrogi I, Murray E, Yelle L, von Minckwitz G, Korec S, Simmonds P, Buzzi F, Gonzalez Mancha R, Richardson G, Walpole E, Ronzoni M, Murawsky M, Alakl M, Riva A, Crown J, 303 Study Group (1999) Prospective randomized trial of docetaxel vs doxorubicin in patients with metastatic breast cancer. John Crown for the 303 Study Group. J Clin Oncol 17(8): 2341–2354
Dieras V, Marty M, Tubiana N, Corette L, Morvan F, Serin D, Mignot L, Chazard M, Garet F, Onetto N, Helman S, Pouillart P (1995) Phase II randomised study of paclitaxel vs mitomycin in advanced breast cancer. Semin Oncol 22(4 Suppl 8): 33–39
Gebbia V, Blasi L, Borsellino N, Caruso M, Leonardi V, Agostara B, Valenza R (2003) Paclitaxel and epidoxorubicin or doxorubicin vs cyclophosphamide and epidoxorubicin as first-line chemotherapy for metastatic breast carcinoma: a randomised phase II study. Anticancer Res 23(1B): 765–771
Gennari A, Manzione L, Del Mastro L, Amadori D, De Lena M, Moretti G, Grifalchi F, Valsecchi R, Luzi Fedeli S, Carrara B, Conte P (2001) Paclitaxel maintenance treatment following first line chemotherapy with anthracyclines plus paclitaxel in metastatic breast cancer: preliminary results from the Italian MANTA 1 study. Breast Cancer Res Treat 64: 82 (Abstract 325)
Ghersi D, Wilcken N, Simes J, Donoghue E (2005) Taxane-containing regimens for metastatic breast cancer. The Cochrane Database of Systematic Reviews. Issue 2. Art. no.: CD003366, doi: 10.1002/14651858.CD003366.pub2
Goldhirsch A (2005) Phase III randomised study of trastuzumab (Herceptin) alone followed by paclitaxel plus trastuzumab vs upfront combination of trastuzumab and paclitaxel in women with HER2 overexpressing metastatic breast cancer. Available at: http://www.clinicaltrials.gov/ct/gui/show/NCT00004935 (accessed 15 September 2004)
Hakamies-Blomqvist L, Luoma M, Sjostrom J, Pluzanska A, Sjodin M, Mouridsen H, Ostenstad B, Mjaaland I, Ottosson-Lonn S, Bergh J, Malmstrom P, Blomqvist C (2000) Quality of life in patients with metastatic breast cancer receiving either docetaxel or sequential methotrexate and 5-fluorouracil. A multicentre randomised phase III trial by the Scandinavian breast group. Eur J Cancer 36(11): 1411–1417
Heidemann EG (2005) Mitoxantrone with or without docetaxel in treating women with metastatic breast cancer. Available at: http://www.clinicaltrials.gov/ct/ (accessed 15 September 2004)
Icli F, Akbulut H, Uner A, Bulent Y, Altinbas M, Baltali E, Komercu S, Erkisi M, Demirkazik A, Senler FC (2002) Paclitaxel vs cisplatin+VP-16 in advanced breast cancer patients pre-treated with anthracyclines: a phase III randomized study, Turkish Oncology Group. Proceedings of the 27th ESMO Congress Available at http://www.medsessions.com/ESMO2002/ (accessed 15 September 2004)
Jassem J, Pienkowski T, Pluzanska A, Jelic S, Gorbunova V, Mrsic-Krmpotic Z, Berzins J, Nagykalnai T, Wigler N, Renard J, Munier S, Weil C, Central & Eastern Europe and Israel Pacitaxel Breast Cancer Study Group (2001) Doxorubicin and paclitaxel vs fluorouracil, doxorubicin, and cyclophosphamide as first-line therapy for women with metastatic breast cancer: final results of a randomized phase III multicenter trial. J Clin Oncol 19(6): 1707–1715
Jones S, Erban J, Overmayer J, Budd B, Hutchins XL, Lower E, Laufman L, Sundaram S, Urba W, Olsen S, Meyers ML, Ravdin PM (2003) Randomized trial comparing docetaxel and paclitaxel in patients with metastatic breast cancer [abstract 10]. 26th Annual San Antonio Breast Cancer Symposium; 2–6 Dec 2003; San Antonio. Breast Cancer Res Treat 82(1 Suppl 1): S9
Kramer JA, Curran D, Piccart M, de Haes JC, Bruning PF, Klijn JG, Bontenbal M, van Pottelsberghe C, Groenvold M, Paridaens R (2000) Randomised trial of paclitaxel vs doxorubicin as first-line chemotherapy for advanced breast cancer: quality of life evaluation using the EORTC QLQ-C30 and the Rotterdam symptom checklist. Eur J Cancer 36(12): 1488–1497
Luck HJ, Thomssen C, Untch M, Kuhn W, Eidtmann H, du Bois A, Olbricht S, Moebus V, Steinfeld D, Bauknecht T, Schroeder W, Jackisch C (2000) Multicentric phase III study in firstline treatment of advanced metastatic breast cancer. Epirubicin/paclitaxel vs epirubicin/cyclophosphamide. A study of the AGO Breast Cancer Group. Proceedings of the American Society of Clinical Oncology Abstract 280 Available at http://www.asco.org/ac/1,1003,_12-002636-00_18-002-00_19-00100082,00.asp (accessed 15 September 04)
Nabholtz J-M, Paterson A, Dirix L, Dewar J, Chap L, Martin M, Chan S, Tang SC, Dugan W, Gil M, Zaluski J, Russel C, Vogel C, Borg-Olivier O, Riva A, Murawsky M, Azli N, Efremidis A (2001) A phase III randomized trial comparing docetaxel, doxorubicin and cyclophosphamide to FAC as first line chemotherapy for patients with metastatic breast cancer. Proceedings of the American Society of Clinical Oncology Abstract 83 Available at http://www.asco.org/ac/1,1003,_12-002636-00_18-0010-00_19-0083,00.asp (accessed 15 September 04)
Nabholtz J-M, Falkson C, Campos D, Szanto J, Martin M, Chan S, Pienkowski T, Zaluski J, Pinter T, Krzakowski M, Vorobiof D, Leonard R, Kennedy I, Azli N, Murawsky M, Riva A, Pouillart P (2003) Docetaxel and doxorubicin compared with doxorubicin and cyclophosphamide as first-line chemotherapy for metastatic breast cancer: results of a randomized, multicenter, phase III trial. J Clin Oncol 21(6): 968–975
Nabholtz J-M, Senn HJ, Bezwoda WR, Melnychuk D, Deschenes L, Douma J, Vandenberg TA, Rapoport B, Rosso R, Trillet-Lenoir V, Drbal J, Molino A, Nortier JW, Richel DJ, Nagykalnai T, Siedlecki P, Wilking N, Genot JY, Hupperets PS, Pannuti F, Skarlos D, Tomiak EM, Murawsky M, Alakl M, Riva A, Aapro M, for the 304 Study Group (1999) Prospective randomized trial of docetaxel vs mitomycin plus vinblastine in patients with metastatic breast cancer progressing despite previous anthracycline-containing chemotherapy. J Clin Oncol 17(5): 1413–1424
Nowak AK, Wilcken NR, Stockler MR, Hamilton A, Ghersi D (2004) Systematic review of taxane-containing vs non-taxane-containing regimens for adjuvant and neoadjuvant treatment of early breast cancer. Lancet Oncol 5(6): 372–380
Paridaens R, Biganzoli L, Bruning P, Klijn JG, Gamucci T, Houston S, Coleman R, Schachter J, Van Vreckem A, Sylvester R, Awada A, Wildiers J, Piccart M (2000) Paclitaxel vs doxorubicin as first-line single-agent chemotherapy for metastatic breast cancer: a European Organization for Research and Treatment of Cancer Randomized Study with Cross-Over. J Clin Oncol 18(4): 724–733
Parmar MKB, Torri V, Stewart L (1998) Extracting summary statistics to perform meta-analyses of the published literature for survival endpoints. Stat Med 17: 2815–2834
Simes RJ, Wilcken N, Brunswick C, Clarke M, Ganz P, Ghersi D, Henderson IC, Liberati A, Lockwood S, Rodger A, Breast Cancer Group. (2005) About The Cochrane Collaboration (Collaborative Review Groups (CRGs), Issue 2, Art no.: BREASTCA
Sjostrom J, Blomqvist C, Mouridsen H, Pluzanska A, Ottosson-Lonn S, Bengtsson NO, Ostenstad B, Mjaaland I, Palm-Sjovall M, Wist E, Valvere V, Anderson H, Bergh J (1999) Docetaxel compared with sequential methotrexate and 5-fluorouracil in patients with advanced breast cancer after anthracycline failure: a randomised phase III study with crossover on progression by the Scandinavian Breast Group. Eur J Cancer 35(8): 1194–1201
Sledge GW, Neuberg D, Bernardo P, Ingle JN, Martino S, Rowinsky EK, Wood WC (2003) Phase III trial of doxorubicin, paclitaxel and the combination of doxorubicin and paclitaxel as front-line chemotherapy for metastatic breast cancer: an intergroup trial (E1193). J Clin Oncol 21(4): 588–592
Talbot DC, Moiseyenko V, Van Belle S, O'Reilly SM, Albo Conejo E, Ackland S, Eisenberg P, Melnychuk D, Pienkowski T, Burger HU, Laws S, Osterwalder B (2002) Randomised, phase II trial comparing oral capecitabine (Xeloda) with paclitaxel in patients with metastatic/advanced breast cancer pretreated with anthracyclines. Br J Cancer 86: 1367–1372
Yusuf S, Peto R, Lewis J, Collins R, Sleight P (1985) Beta blockade during and after myocardial infarction: an overview of the randomized trials. Progr Cardiovasc Dis 27(5): 335–371
Zielinski C, Beslija S, Cervek J, Mrsic-Krmpotic Z, Tchernozemsky I, Wiltschke C, Ghilezan N, Grgic M, Jassem J, Tzekova V, Kahan Z, Pawlega J, Onat H, Inbar M, Brodowicz T (2001) Gemcitabine/epirubicin/paclitaxel vs 5-fluorouracil/epirubicin/cyclophosphamide as first-line treatment in metastatic breast cancer: interim toxicity analysis of a randomised, multicenter phase III trial of the Central European Cooperative Oncology Group (CECOG) [abstract 1958]. Proceedings of the American Society of Clinical Oncology 37th Annual Meeting 12–15 May 2001, San Francisco, Alexandria, VA: ASCO
Acknowledgements
We thank Nicole Davis for her work in the identification of studies through the Cochrane Breast Cancer Group's specialised register of trials, and Emma Donoghue for eligibility assessment and data extraction. We also acknowledge the contribution made to the original concept for this review by I Craig Henderson, Kathleen Pritchard, Martin Tattersall, Martin Stockler, Christine Brunswick and Alessandro Liberati. This review was completed with a grant from the US Army Medical Research and Materiel Command; Grant identification number: DAMD17-99-1-9392. The funding agency had no involvement in the design and conduct of this review. Davina Ghersi participated in the design the review, developed the protocol, identified, selected and critically appraised the studies to be included in the review, applied eligibility criteria, extracted and entered data, analysed the data and wrote the first draft and approved the final manuscript. Nicholas Wilcken and John Simes both participated in the design of the review and the development of the protocol, and reviewed and approved the manuscript.
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The authors do not have a conflict of interest to declare in relation to this review. All authors, including the contact author, had full access to all of the data in this review and have final responsibility for the decision to submit for publication.
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Ghersi, D., Wilcken, N. & Simes, R. A systematic review of taxane-containing regimens for metastatic breast cancer. Br J Cancer 93, 293–301 (2005). https://doi.org/10.1038/sj.bjc.6602680
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DOI: https://doi.org/10.1038/sj.bjc.6602680
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