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Sökning: WFRF:(Rudenstam Carl Magnus) > Timing of CMF chemo...

Timing of CMF chemotherapy in combination with tamoxifen in postmenopausal women with breast cancer: role of endocrine responsiveness of the tumor.

Colleoni, M (författare)
Li, S (författare)
Gelber, R D (författare)
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Coates, A S (författare)
Castiglione-Gertsch, M (författare)
Price, K N (författare)
Lindtner, J (författare)
Rudenstam, Carl-Magnus, 1930 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna, Avdelningen för kirurgi,Institute of Surgical Sciences, Department of Surgery
Crivellari, D (författare)
Collins, J (författare)
Pagani, O (författare)
Simoncini, E (författare)
Thürlimann, B (författare)
Murray, E (författare)
Forbes, J (författare)
Erzen, D (författare)
Holmberg, Stig B, 1946 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna, Avdelningen för kirurgi,Institute of Surgical Sciences, Department of Surgery
Veronesi, A (författare)
Goldhirsch, A (författare)
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 (creator_code:org_t)
Elsevier BV, 2005
2005
Engelska.
Ingår i: Annals of oncology : official journal of the European Society for Medical Oncology / ESMO. - : Elsevier BV. - 0923-7534. ; 16:5, s. 716-25
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • BACKGROUND: Controversy persists about whether chemotherapy benefits all breast cancer patients. PATIENTS AND METHODS: In the International Breast Cancer Study Group (IBCSG) trial VII, 1212 postmenopausal patients with node-positive disease were randomized to receive tamoxifen for 5 years or tamoxifen plus three concurrent courses of cyclophosphamide, methotrexate and 5-fluorouracil ('classical' CMF) chemotherapy, either early, delayed or both. In IBCSG trial IX, 1669 postmenopausal patients with node-negative disease were randomized to receive either tamoxifen alone or three courses of adjuvant classical CMF prior to tamoxifen. Results were assessed according to estrogen receptor (ER) content of the primary tumor. RESULTS: For patients with node-positive, ER-positive disease, adding CMF either early, delayed or both reduced the risk of relapse by 21% (P=0.06), 26% (P=0.02) and 25% (P=0.02), respectively, compared with tamoxifen alone. There was no difference in disease-free survival when CMF was given prior to tamoxifen in patients with node-negative, ER-positive tumors. CONCLUSIONS: CMF given concurrently (early, delayed or both) with tamoxifen was more effective than tamoxifen alone for patients with node-positive, endocrine-responsive breast cancer, supporting late administration of chemotherapy even after commencement of tamoxifen. In contrast, sequential CMF and tamoxifen for patients with node-negative, endocrine-responsive disease was ineffective.

Nyckelord

Adult
Aged
Aged
80 and over
Antineoplastic Combined Chemotherapy Protocols
therapeutic use
Breast Neoplasms
drug therapy
mortality
surgery
Confidence Intervals
Cyclophosphamide
therapeutic use
Dose-Response Relationship
Drug
Drug Administration Schedule
Drug Therapy
Combination
Female
Fluorouracil
therapeutic use
Humans
Mastectomy
Segmental
Methotrexate
therapeutic use
Middle Aged
Neoplasms
Hormone-Dependent
drug therapy
mortality
surgery
Postmenopause
Probability
Prognosis
Reference Values
Risk Assessment
Survival Rate
Tamoxifen
therapeutic use
Time Factors
Treatment Outcome

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