Chemoendocrine compared with endocrine adjuvant therapies for node-negative breast cancer: predictive value of centrally reviewed expression of estrogen and progesterone receptors--International Breast Cancer Study Group.


Autoria(s): Viale G.; Regan M.M.; Maiorano E.; Mastropasqua M.G.; Golouh R.; Perin T.; Brown R.W.; Kovács A.; Pillay K.; Ohlschlegel C.; Braye S.; Grigolato P.; Rusca T.; Gelber R.D.; Castiglione-Gertsch M.; Price K.N.; Goldhirsch A.; Gusterson B.A.; Coates A.S.
Data(s)

2008

Resumo

PURPOSE: To centrally assess estrogen receptor (ER) and progesterone receptor (PgR) levels by immunohistochemistry and investigate their predictive value for benefit of chemo-endocrine compared with endocrine adjuvant therapy alone in two randomized clinical trials for node-negative breast cancer. PATIENTS AND METHODS: International Breast Cancer Study Group Trial VIII compared cyclophosphamide, methotrexate, and fluorouracil (CMF) chemotherapy for 6 cycles followed by endocrine therapy with goserelin with either modality alone in pre- and perimenopausal patients. Trial IX compared three cycles of CMF followed by tamoxifen for 5 years versus tamoxifen alone in postmenopausal patients. Central Pathology Office reviewed 883 (83%) of 1,063 patients on Trial VIII and 1,365 (82%) of 1,669 on Trial IX and determined ER and PgR by immunohistochemistry. Disease-free survival (DFS) was compared across the spectrum of expression of each receptor using the Subpopulation Treatment Effect Pattern Plot methodology. RESULTS: Both receptors displayed a bimodal distribution, with substantial proportions showing no staining (receptor absent) and most of the remainder showing a high percentage of stained cells. Chemo-endocrine therapy yielded DFS superior to endocrine therapy alone for patients with receptor-absent tumors, and in some cases also for those with low levels of receptor expression. Among patients with ER-expressing tumors, additional prediction of benefit was suggested in absent or low PgR in Trial VIII but not in Trial IX. CONCLUSION: Low levels of ER and PgR are predictive of the benefit of adding chemotherapy to endocrine therapy. Low PgR may add further prediction among pre- and perimenopausal but not postmenopausal patients whose tumors express ER.

Identificador

http://serval.unil.ch/?id=serval:BIB_A1BF80ADF5C9

isbn:1527-7755[electronic]

pmid:18349391

doi:10.1200/JCO.2007.10.6393

isiid:000254178600005

Idioma(s)

en

Fonte

Journal of Clinical Oncology, vol. 26, no. 9, pp. 1404-1410

Palavras-Chave #Adult; Aged; Antineoplastic Agents, Hormonal/therapeutic use; Antineoplastic Combined Chemotherapy Protocols/administration & dosage; Antineoplastic Combined Chemotherapy Protocols/therapeutic use; Breast Neoplasms/chemistry; Breast Neoplasms/drug therapy; Chemotherapy, Adjuvant; Cyclophosphamide/administration & dosage; Disease-Free Survival; Female; Fluorouracil/administration & dosage; Goserelin/administration & dosage; Humans; Immunohistochemistry; Menopause; Methotrexate/administration & dosage; Middle Aged; Neoplasms, Hormone-Dependent/chemistry; Neoplasms, Hormone-Dependent/drug therapy; Predictive Value of Tests; Receptors, Estrogen/analysis; Receptors, Progesterone/analysis; Tamoxifen/administration & dosage; Treatment Outcome; Tumor Markers, Biological/analysis
Tipo

info:eu-repo/semantics/article

article