Adjuvant chemotherapy followed by goserelin versus either modality alone for premenopausal lymph node-negative breast cancer: a randomized trial. 2003

, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
International Breast Cancer Study Group Coordinating Center and Inselspital, Bern, Switzerland. monica.castiglione@siak.ch

BACKGROUND Although chemotherapy and ovarian function suppression are both effective adjuvant therapies for patients with early-stage breast cancer, little is known of the efficacy of their sequential combination. In an International Breast Cancer Study Group (IBCSG) randomized clinical trial (Trial VIII) for pre- and perimenopausal women with lymph node-negative breast cancer, we compared sequential chemotherapy followed by the gonadotropin-releasing hormone agonist goserelin with each modality alone. METHODS From March 1990 through October 1999, 1063 patients stratified by estrogen receptor (ER) status and radiotherapy plan were randomly assigned to receive goserelin for 24 months (n = 346), six courses of "classical" CMF (cyclophosphamide, methotrexate, 5-fluorouracil) chemotherapy (n = 360), or six courses of classical CMF followed by 18 months of goserelin (CMF --> goserelin; n = 357). A fourth arm (no adjuvant treatment) with 46 patients was discontinued in 1992. Tumors were classified as ER-negative (30%), ER-positive (68%), or ER status unknown (3%). Twenty percent of patients were aged 39 years or younger. The median follow-up was 7 years. The primary outcome was disease-free survival (DFS). RESULTS Patients with ER-negative tumors achieved better disease-free survival if they received CMF (5-year DFS for CMF = 84%, 95% confidence interval [CI] = 77% to 91%; 5-year DFS for CMF --> goserelin = 88%, 95% CI = 82% to 94%) than if they received goserelin alone (5-year DFS = 73%, 95% CI = 64% to 81%). By contrast, for patients with ER-positive disease, chemotherapy alone and goserelin alone provided similar outcomes (5-year DFS for both treatment groups = 81%, 95% CI = 76% to 87%), whereas sequential therapy (5-year DFS = 86%, 95% CI = 82% to 91%) provided a statistically nonsignificant improvement compared with either modality alone, primarily because of the results among younger women. CONCLUSIONS Premenopausal women with ER-negative (i.e., endocrine nonresponsive), lymph node-negative breast cancer should receive adjuvant chemotherapy. For patients with ER-positive (i.e., endocrine responsive) disease, the combination of chemotherapy with ovarian function suppression or other endocrine agents, and the use of endocrine therapy alone should be studied.

UI MeSH Term Description Entries
D008207 Lymphatic Metastasis Transfer of a neoplasm from its primary site to lymph nodes or to distant parts of the body by way of the lymphatic system. Lymph Node Metastasis,Lymph Node Metastases,Lymphatic Metastases,Metastasis, Lymph Node
D008727 Methotrexate An antineoplastic antimetabolite with immunosuppressant properties. It is an inhibitor of TETRAHYDROFOLATE DEHYDROGENASE and prevents the formation of tetrahydrofolate, necessary for synthesis of thymidylate, an essential component of DNA. Amethopterin,Methotrexate Hydrate,Methotrexate Sodium,Methotrexate, (D)-Isomer,Methotrexate, (DL)-Isomer,Methotrexate, Dicesium Salt,Methotrexate, Disodium Salt,Methotrexate, Sodium Salt,Mexate,Dicesium Salt Methotrexate,Hydrate, Methotrexate,Sodium, Methotrexate
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D011960 Receptors, Estrogen Cytoplasmic proteins that bind estrogens and migrate to the nucleus where they regulate DNA transcription. Evaluation of the state of estrogen receptors in breast cancer patients has become clinically important. Estrogen Receptor,Estrogen Receptors,Estrogen Nuclear Receptor,Estrogen Receptor Type I,Estrogen Receptor Type II,Estrogen Receptors Type I,Estrogen Receptors Type II,Receptor, Estrogen Nuclear,Receptors, Estrogen, Type I,Receptors, Estrogen, Type II,Nuclear Receptor, Estrogen,Receptor, Estrogen
D001943 Breast Neoplasms Tumors or cancer of the human BREAST. Breast Cancer,Breast Tumors,Cancer of Breast,Breast Carcinoma,Cancer of the Breast,Human Mammary Carcinoma,Malignant Neoplasm of Breast,Malignant Tumor of Breast,Mammary Cancer,Mammary Carcinoma, Human,Mammary Neoplasm, Human,Mammary Neoplasms, Human,Neoplasms, Breast,Tumors, Breast,Breast Carcinomas,Breast Malignant Neoplasm,Breast Malignant Neoplasms,Breast Malignant Tumor,Breast Malignant Tumors,Breast Neoplasm,Breast Tumor,Cancer, Breast,Cancer, Mammary,Cancers, Mammary,Carcinoma, Breast,Carcinoma, Human Mammary,Carcinomas, Breast,Carcinomas, Human Mammary,Human Mammary Carcinomas,Human Mammary Neoplasm,Human Mammary Neoplasms,Mammary Cancers,Mammary Carcinomas, Human,Neoplasm, Breast,Neoplasm, Human Mammary,Neoplasms, Human Mammary,Tumor, Breast
D003520 Cyclophosphamide Precursor of an alkylating nitrogen mustard antineoplastic and immunosuppressive agent that must be activated in the LIVER to form the active aldophosphamide. It has been used in the treatment of LYMPHOMA and LEUKEMIA. Its side effect, ALOPECIA, has been used for defleecing sheep. Cyclophosphamide may also cause sterility, birth defects, mutations, and cancer. (+,-)-2-(bis(2-Chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorine 2-Oxide Monohydrate,B-518,Cyclophosphamide Anhydrous,Cyclophosphamide Monohydrate,Cyclophosphamide, (R)-Isomer,Cyclophosphamide, (S)-Isomer,Cyclophosphane,Cytophosphan,Cytophosphane,Cytoxan,Endoxan,NSC-26271,Neosar,Procytox,Sendoxan,B 518,B518,NSC 26271,NSC26271
D004334 Drug Administration Schedule Time schedule for administration of a drug in order to achieve optimum effectiveness and convenience. Administration Schedule, Drug,Administration Schedules, Drug,Drug Administration Schedules,Schedule, Drug Administration,Schedules, Drug Administration
D005260 Female Females
D005472 Fluorouracil A pyrimidine analog that is an antineoplastic antimetabolite. It interferes with DNA synthesis by blocking the THYMIDYLATE SYNTHETASE conversion of deoxyuridylic acid to thymidylic acid. 5-FU,5-FU Lederle,5-FU Medac,5-Fluorouracil,5-Fluorouracil-Biosyn,5-HU Hexal,5FU,Adrucil,Carac,Efudex,Efudix,Fluoro-Uracile ICN,Fluoroplex,Fluorouracil Mononitrate,Fluorouracil Monopotassium Salt,Fluorouracil Monosodium Salt,Fluorouracil Potassium Salt,Fluorouracil-GRY,Fluorouracile Dakota,Fluorouracilo Ferrer Far,Fluoruracil,Fluracedyl,Flurodex,Haemato-FU,Neofluor,Onkofluor,Ribofluor,5 FU Lederle,5 FU Medac,5 Fluorouracil,5 Fluorouracil Biosyn,5 HU Hexal,Dakota, Fluorouracile,Fluoro Uracile ICN,Fluorouracil GRY,Haemato FU
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
December 2003, Journal of the National Cancer Institute,
, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
October 2011, Annals of oncology : official journal of the European Society for Medical Oncology,
, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
January 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology,
, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
December 2016, Breast (Edinburgh, Scotland),
, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
August 2006, European journal of cancer (Oxford, England : 1990),
, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
February 2005, British journal of cancer,
, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
January 1992, Cancer investigation,
, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
July 2002, Journal of the National Cancer Institute,
, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
April 2003, Journal of the National Cancer Institute,
, and Monica Castiglione-Gertsch, and Anne O'Neill, and Karen N Price, and Aron Goldhirsch, and Alan S Coates, and Marco Colleoni, and M Laura Nasi, and Marco Bonetti, and Richard D Gelber
March 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology,
Copied contents to your clipboard!