EORTC – Contact Details
Country
Europe
Chair
Dr H. Bonnefoi, Hopital Cantonal Universitaire de Genève, Department of Gynecology, Rue Micheli-du-Crest, 24, CH-1211 GENÈVE 14, SWITZERLAND. Tel: +41 22 3824013 Fax: +41 22 3824135/7117 Email: herve.bonnefoi@hcuge.ch
EORTC Data Center
Avenue E. Mounier 83, bte 11, B-1200 BRUSSELS, BELGIUM. Tel: +32 2 774 16 11 Fax: +32 2 772 35 45
Website
EORTC – Study Details
Title
Postoperative adjuvant chemotherapy followed by adjuvant tamoxifen versus nil for node-negative and node-positive patients with operable breast cancer.
EORTC Study No. 10901
Coordinator(s)
P.F. Bruning, Antoni van Leeuwenhoek Ziekenhuis, Plesmanlaan 121, NL-1066 CX AMSTERDAM, THE NETHERLANDS. Tel: +31 20 512 25 69 Fax: +31 20 512 25 72
R. Paridaens, Universitair Ziekenhuis Gasthuisberg, Afdeling Gezwelziekten, Herestraat 49, B-3000 LEUVEN, BELGIUM. Tel: +32 16 34 69 02 Fax: +32 16 34 69 01 Email: robert.paridaens@uz.kuleuven.ac.be
Summary
- Closed in March 1999 (opened in March 1991)
- Target accrual: 1816 patients
Objectives
- To investigate the disease-free interval and overall survival after adjuvant chemotherapy followed by tamoxifen compared to chemotherapy alone in patients curatively treated for primary breast cancer with surgery ± radiotherapy.
- To investigate the influence of the estrogen receptor content of the primary tumor on the results of adjuvant treatment as given in this study.
Scheme
Update
- Study closed in March 1999; 1863 patients randomized.
Related Publications
Please consult our EORTC bibliography website: http://www.eortc.be/Biblio/default.htm
Publication in progress
Topics
- Tamoxifen
- Hormone-receptor-positive breast cancer
Keywords
Primary breast cancer, adjuvant hormonal treatment
***************************************************
Title
Randomized phase III study comparing short, intensive preoperative combination chemotherapy with similar therapy given postoperatively.
EORTC Trial No. 10902
Coordinator(s)
N. Tubiana-Mathieu, CHRU de Limoges, Limoges, FRANCE.
C.J.H. van de Velde, University Hospital, Department of Surgery, P.O. Box 9600, NL-2300 RC LEIDEN, THE NETHERLANDS. Tel: +31 71 526 23 09 Fax: +31 71 526 67 50 Email: velde@surgery.azl.nl
J.P. Julien, Centre H. Becquerel, 1 rue d'Amiens, 76038 ROUEN Cedex, FRANCE. Tel: +33 2 32 08 22 12 Fax: +33 2 32 08 22 82
Summary
- Closed in March 1999 (opened in March 1991)
- Target accrual: 550 patients (100/arm)
Objectives
- To determine whether preoperative chemotherapy, by reducing the size of the primary tumor will permit more breast conserving therapies.
- To determine the disease-free interval and overall survival in patients who have received preoperative chemotherapy versus the same chemotherapy given postoperatively.
- To evaluate the response of the primary tumor to preoperative chemotherapy and correlate this response to disease-free and overall survival.
Scheme
Update
- The final results of the study have been published.
Related Publications
Please consult our EORTC bibliography website: http://www.eortc.be/Biblio/default.htm
Topics
- Perioperative chemotherapy
Keyword
Perioperative chemotherapy
Title
Phase III randomized trial investigating the role of internal mammary and medial supraclavicular (IM-MS) lymph node chain irradiation in stage I–III breast cancer (joint study of the EORTC Radiotherapy Cooperative Group and the EORTC Breast Cancer Cooperative Group).
EORTC Study No. 10925/22922
Coordinator(s)
W.F. van den Bogaert, Radiotherapy Department, U.Z. Gasthuisberg, Herestraat 49, B-3000 LEUVEN, BELGIUM. Tel: +32 16 346 917 Fax: +32 16 346 901
Dr H. Struikmans, Medisch Centrum Haaglanden – Westeinde, P.O. Box 432 - Lijnbaan 32, NL-2501 CK DEN HAAG, THE NETHERLANDS. Tel: +31 30 250 8800 Fax: +31 30 258 1226 Email: h.struikmans@mchaaglanden.nl
A. Fourquet, Institut Curie, Section Médecine et Hospitalière, Rue d' Ulm 26, 75231 PARIS, FRANCE. Tel: +33 144 324 631 Fax: +33 144 324 616
H. Bartelink, Antoni van Leeuwenhoekhuis, Department of Radiotherapy, Plesmanlaan 1121, NL-1066 CX AMSTERDAM, THE NETHERLANDS. Tel: +31 20 512 2122 Fax: +31 20 669 1101
Summary
- Opened in July 1996
- 4000 patients
- Closed to accrual on 15 January 2004
Objectives
To determine the effect of irradiation to the homolateral mammary supraclavicular lymph node chain in operable breast cancer on:
- Overall survival.
- Disease-free survival.
- Metastases-free survival.
- Cause of death (breast cancer, cardiac, others).
Scheme
Update
- Study in follow-up for analysis
Related Publications
Please consult our EORTC bibliography website: http://www.eortc.be/Biblio/default.htm
Topics
- Radiotherapy
Keywords
Irradiation, internal mammary, medial supraclavicular
***************************************************
Title
A survey of the Breast International Group (BIG) to assess the attitude of patients aged <35 years, with early breast cancer, toward the risk of loss of fertility related to adjuvant therapies.
BIG 3-98/EORTC 10002
Coordinator(s)
A. DiLeo, Sandro Pitigliani Medical Oncology Unit, Dept of Oncology, Hospital of Prato, Piazza dell'Ospedale, 59100 PRATO, ITALY. Tel: +39 0574 434 334 Fax: +39 0574 434 246 Email: adileo@usl4.toscana.it
Summary
- Date of activation: 5 May 2003
- Target accrual: 385
Objectives
Primary Endpoint:
- To estimate the attitude of breast cancer patients toward the risk of sterility related to anti-cancer treatments.
Secondary Endpoint:
- To assess a possible relationship between patient attitude and (a) the fact that the patient already has children and (b) the time interval elapsed between the date of breast cancer diagnosis and the date of study participation.
Scheme
Eligibility Criteria:
- Female sex
- Age <35 years at time of breast cancer diagnosis
- Previous or concomitant early breast cancer histologically/cytologically confirmed (stage I or II)
- No evidence of infertility
- No breast cancer relapse
Update
- 275 Patients randomized as of 3 October 2006.
Related Publications
Please consult our EORTC bibliography website: http://www.eortc.be/Biblio/default.htm
Topics
- Young patients
- Fertility and chemotherapy
Keywords
Sterility, young patients, adjuvant therapy
***************************************************
Title
LAMANOMA: Conservative local treatment versus mastectomy after induction chemotherapy in locally advanced breast cancer: a randomized phase III study.
BIG 2-00/EORTC Study No. 10974/22002
Coordinator(s)
Professor J. Jassem, Medical University of Gdansk, Department of Radiotherapy, Ul. Debinki 7, PL-80 211 GDANSK, POLAND. Email: jjassem@amg.gda.pl
Dr E. Van Limbergen, U.Z. Gasthuisberg, Department of Radiotherapy, Herestraat 49, B-3000 LEUVEN, BELGIUM. Email: erik.vanlimbergen@uz.kuleuven.ac.be
Dr G. van Tienhoven, Academisch Medisch Centrum Department of Radiotherapy, Meibergdreef 9, NL-1105 AZ AMSTERDAM, THE NETHERLANDS. Email: g.vantienhoven@amc.uva.nl
Summary
- Opened in October 2001
- Target sample size: 1300
- Closed in 29/12/2003
Objectives
- The main objective is to show that breast conservative treatment (BCT) (exclusive radiotherapy or tumorectomy followed or preceded by radiotherapy) is not inferior to mastectomy plus postoperative radiotherapy in terms of overall survival (primary endpoint) and time to locoregional failure (secondary endpoint) in locally advanced breast cancer patients who first received induction chemotherapy.
- Additionally, quality of life of the two strategies will be compared.
Scheme
Stratification Factors:
- Institution
- Initial stage
- Response to induction chemotherapy
- Menopausal status
Eligible patients will be randomized between BCT arm and mastectomy plus radiotherapy arm.
Update
- Study closed due to poor accrual.
Related Publications
Please consult our EORTC bibliography website: http://www.eortc.be/Biblio/default.htm
Topics
- Breast conservative treatment
- Locally advanced breast cancer
Keywords
Breast conservative treatment, mastectomy, radiotherapy
***************************************************
Title
p53 study: First prospective intergroup translational research trial assessing the potential predictive value of p53 using a functional assay in yeast in patients with locally advanced/inflammatory or large operable breast cancer, prospectively randomized to a taxane versus non-taxane regimen.
BIG 1-00/EORTC 10994
Coordinator(s)
Dr H. Bonnefoi, Hopital Cantonal Universitaire de Genève, Maternite, Rue Micheli-du-Crest, 24, CH-1211 GENÈVE 14, SWITZERLAND. Email: herve.bonnefoi@hcuge.ch
Summary
- Study opened to accrual: March 2001
- Target sample size: 1440 updated to 1850 (see amendment 3 to protocol)
Objectives
- Compare two chemotherapy arms (arm A: without taxanes and arm B: with taxanes) in the two p53 subgroups separately.
- Test for an overall difference between the two chemotherapy arms.
- Test for interaction between the two chemotherapy arms and the p53 status.
Side Studies
- Agreement between p53 assessment by IHC method and functional test in yeast.
- Tumor assessment using cDNA microarray technology.
Scheme
Update
- 1825 patients randomized as of 3 October 2006.
Related Publications
Please consult our EORTC bibliography website: http://www.eortc.be/Biblio/default.htm
Topics
- Taxanes
- Predictive markers
- Locally advanced breast cancer
Keywords
p53, potential predictive factor, taxanes, locally advanced breast cancer, inflammatory breast cancer, large operable breast cancer
***************************************************
Title
After mapping of the axilla: radiotherapy or surgery AMAROS
EORTC 10981/22023
Coordinator(s)
R. Mansel, University of Wales College of Medicine, Heath Park, CARDIFF, CF14 4XN, UNITED KINGDOM. Email: manselre@cf.ac.uk
Dr E. Rutgers, The Netherlands Cancer Institute – Antoni Van Leeuwenhoekziekenhuis, Plesmanlaan 121, NL-1066 CX AMSTERDAM, THE NETHERLANDS. Email: ERutgers@nki.nl
Professor C. Van De Velde, Leiden University Medical Centre, Albinusdreef 2, Postbus 9600, NL-2300 RC LEIDEN, THE NETHERLANDS. Email: C.J.H.van_de_Velde@lumc.nl
Summary
- Study opened in February 2001
- Target sample size: 3485
Objectives
- Prove equivalence in local control between the two treatment modalities of the axilla which reduced the morbidity.
- Prove benefits for all involved parties. Patients will benefit because of the well-controlled use of the sentinel lymph node mapping and the avoidance of unnecessary axillary dissection. This study will yield important information on local control, morbidity, quality of life, and quality of treatment by comparing the different treatment groups.
Scheme
Randomization will take place before the sentinel node procedure. The patient will know before surgery whether she will have a complete axillary dissection or radiotherapy if the sentinel node(s) is (are) tumor positive on frozen section or definitive histology.
Update
- 2726 patients randomized as of 3 October 2006.
Related Publications
Please consult our EORTC bibliography website: http://www.eortc.be/Biblio/default.htm
Topics
- Radiotherapy
- Node-positive breast cancer
- Sentinel node resection
Keywords
Sentinel nodes biopsy, mapping of axilla
***************************************************
Title
A randomized phase II–III trial evaluating the efficacy of capecitabine and vinorelbine in anthracycline and taxane pretreated metastatic breast cancer.
EORTC 10001/160010
Coordinator(s)
M. Piccart, Institut Jules Bordet, Rue Héger-Bordet, 1, BE 1000 BRUSSELS, BELGIUM. Email: martine.piccart@bordet.be
Summary
- Study opened in September 2002
- Study closed in December 2004
- Target sample size: 72
Objectives
- The trial is a two arm, randomized phase II study, with extension to a phase III trial if the appropriate statistical criteria are met at the end of the phase II part.
Phase II
- The principal objective of the phase II trial is to assess the therapeutic activity (as measured by the response rate (RR) using RECIST criteria) of capecitabine and vinorelbine in MBC patients pretreated with taxanes and anthracyclines, or pretreated with taxanes and in whom anthracyclines are medically ontraindicated.
- As a secondary objective, the duration of response will be assessed for patients presenting with an objective response.
Phase III
- The principal objective of the phase III trial is to test for a difference in overall survival in the two treatment arms.
- Secondary objectives are to compare:
– The progression-free survival (PFS).
– The time to treatment failure (TTF).
– Clinical benefit response (CBR) and quality of life (QOL).
– Overall safety, including adverse events and laboratory abnormalities in both arms.
Scheme
Update
- The trial was stopped due to poor accrual.
Related Publications
Please consult our EORTC bibliography website: http://www.eortc.be/Biblio/default.htm
Topics
- Chemotherapy
Keywords
Third line chemotherapy, metastatic breast cancer
***************************************************
Title
Phase I study of lonafarnib (SCH 66336) in combination with Herceptin plus paclitaxel in HER-2 neu overexpressing breast cancer.
EORTC 10051/16023
Coordinator(s)
J.H.M. Schellens, The Netherlands Cancer Institute – Antoni Van Leeuwenhoekziekenhuis, Plesmanlaan 121, NL-1066 CX AMSTERDAM, THE NETHERLANDS. Email: jhm@nki.nl
Summary
- Date of activation: 01/08/2003
- Target sample size: 40
- Main Endpoints: the safety and tolerability profile of the combination through the MTD, the qualitative and quantitative toxicity of the combination, and the recommended dose for phase II.
- Secondary Endpoints: Translational research to document the activity of lonafarnib, pharmacokinetics, pharmacodynamics.
Scheme
Open study with a starting dose of 75 mg twice daily of SCH 66336, 135 mg/m2 of paclitaxel and 4 mg/m2 (maintenance 2 mg/m2) Herceptin. One cycle is 3 weeks. Dose levels are allocated according to a 3 + 3 scheme (3 patients/dose level, up to 6 in case of a DLT). The dose–escalation proceeds in a stepwise manner: for SCH (mg)/PCL (mg/m2): 75/135, 75/175, 100/175, 125/175, 150/175, 175/175.
Update
- 23 patients randomized as of 3 October 2006. Patient accrual temporarily interrupted due to administrative issues.
Related Publications
Please consult our EORTC bibliography website: http://www.eortc.be/Biblio/default.htm
Topics
- HER-2 neu overexpressing breast cancer
Keywords
Lonafarnib, HER-2 neu overexpressing, translational research
***************************************************
Title
MINDACT trial: A prospective, randomized study comparing the Amsterdam 70-gene expression signature (Mammaprint) with common clinical pathological criteria in selecting patients for adjuvant chemotherapy in node-negative breast cancer.
BIG 3-04/EORTC 10041
Coordinator(s)
E.J.T. Rutgers, The Netherlands Cancer Institute – Antoni Van Leeuwenhoekziekenhuis, Plesmanlaan 121, NL-1066 CX AMSTERDAM, THE NETHERLANDS. Email: ERutgers@nki.nl
M. Piccart, Institut Jules Bordet, Rue Héger-Bordet, 1, BE 1000 BRUSSELS, BELGIUM. Email: martine.piccart@bordet.be
F. Cardoso, Institut Jules Bordet, Rue Heger-Bordet, 1, BE 1000 BRUSSELS, BELGIUM. Email: fatima.cardoso@bordet.be
Summary
- Estimated date of activation: October/November 2006
- Target sample size: 6000
- Stratification for:
– R-T: stratifying for institution, risk group (high-risk genetic/low-risk clinical versus low-risk genetic/high-risk clinical), HR status (positive (ER and/or PgR) versus negative (both)), age (<50 versus ≥50), HER-2 (positive versus negative versus unknown), method of axillary evaluation (sentinel only or dissection), type of surgery (mastectomy or quadrantectomy/tumorectomy).
– R-C: stratifying for institution, risk group (high-risk genetic/low-risk clinical versus low-risk genetic/high-risk clinical versus high-risk genetic/high-risk clinical), HR status (positive (ER and/or PgR) versus negative (both)), age (<50 versus ≥50), HER-2 (positive versus negative versus unknown (at the time of R)), method of axillary evaluation (sentinel only or dissection), type of surgery (mastectomy or quadrantectomy/tumorectomy).
– R-E: stratifying for institution, risk group (high-risk genetic/high-risk clinical versus high-risk genetic/low-risk clinical versus low-risk genetic/high-risk clinical versus low-risk genetic/low-risk clinical), chemotherapy (no chemotherapy, chemotherapy without R-chemotherapy, R-chemotherapy arm A, R-chemotherapy arm B), type of endocrine sensitivity (both ER and PgR positive versus either ER or PgR positive), age (<50 versus ≥50), HER-2/neu (positive versus negative versus unknown (at the time of R)), method of axillary evaluation (sentinel only or dissection), type of surgery (mastectomy or quadrantectomy/tumorectomy).
- Main endpoints: R-T: distant metastases-free survival, R-C and R-E: disease-free survival.
- Secondary endpoints: R-T: the proportion of women treated with chemotherapy per treatment decision-making tool, that is clinical prognosis compared to NKI-signature prognosis and overall survival at 5 and 10 years. R-C: overall survival at 5 and 10 years and safety both early and late. R-E: overall survival at 5 and 10 years.
Scheme
Register patients and send tumor biopsy sample for microarray analysis. For those patients who are node negative the genomic prognosis will be performed. Patients with a successful genomic prognostic test are eligible and can be enrolled in MINDACT. After enrollment the two risk assessments (clinical using Adjuvant! Online and genomic using the Amsterdam 70-gene gene signature) are compared and discordant patients are randomized for treatment decision randomization (R-T). Patient who will receive chemotherapy will be offered a further randomization (R-C) between anthracycline-based chemotherapy and docetaxel–capecitabine chemotherapy. Patients with endocrine responsive disease will be offered the endocrine therapy randomization (R-E) between 2 years of tamoxifen followed by 5 years of letrozole or 7 years of letrozole.
Update
- Approved in the Netherlands and France and in regulatory process for other countries. Trial to open in October/November 2006.
Related Publications
Please consult our EORTC bibliography website: http://www.eortc.be/Biblio/default.htm
Topics
- Node-negative breast cancer
Keywords
Lymph node-negative early breast cancer, taxotere, capecitabine, letrozole, microarray, prognosis
