Retrospective evaluation of premenopausal hormone‐sensitive breast cancer patients treated with adjuvant gonadotropin‐releasing hormone analogue: Anatolian Society of Medical Oncology (ASMO) study
cancer patient
demography
Adult; Breast Neoplasms/*drug therapy/mortality; Disease-Free Survival; Female; Gonadotropin-Releasing Hormone/pharmacology/*therapeutic use; Humans; Medical Oncology; Middle Aged; Retrospective Studies; Young Adult
retrospective study
gonadorelin associated peptide derivative
Medical Oncology
Turkey (republic)
fluorouracil
Gonadotropin-Releasing Hormone
0302 clinical medicine
middle aged
docetaxel
cancer survival
disease free survival
tamoxifen
breast tumor
adult
adjuvant therapy
hormone sensitivity
Middle Aged
medical oncology
3. Good health
trastuzumab
female
priority journal
early cancer
cancer grading
oncology
young adult
Female
pharmacy
Adult
overall survival
premenopause
610
Breast Neoplasms
anthracycline
Article
Disease-Free Survival
multiple cycle treatment
Young Adult
03 medical and health sciences
breast cancer
follow up
Humans
controlled study
human
survival time
Retrospective Studies
treatment duration
major clinical study
mortality
gonadorelin
aromatase inhibitor
cyclophosphamide
DOI:
10.1111/ajco.12685
Publication Date:
2017-04-21T06:22:50Z
AUTHORS (19)
ABSTRACT
AbstractAimThe goal of this study is to evaluate possible factors affecting the survival of patients treated with gonadotropin‐releasing hormone (GnRH) analogues.MethodsDemographic characteristics, treatment modalities, overall survival (OS) and the possible factors affecting the survival a total of 554 premenopausal breast cancer patients in Turkey evaluated retrospectively.ResultsThe median duration of GnRH analogues use was 22 ± 13.6 (range, 1–87) months. Patients were divided into three groups according to the duration of GNRH analogues use; 4–12 months (Group A), 13–24 months (Group B) and ≥25 months (Group C). Overall, 530 patients were analyzed; 23.2%, 45.8%, 30.9% of the patients were in Group A, B and C, respectively. The median follow‐up duration was 34 ± 30.3 (range, 4–188) months. The OS in patients ≤35 years of age was found to be significantly longer than that of patients >35 years of age in Group B (log rank, P = 0.023). The disease‐free survival of the patients in Group A was significantly shorter than that of patients in Group C (log rank, P = 0.003). The OS of Group A patients was significantly shorter in comparison to that of Group B and Group C patients (log rank, P = 0.000) and the OS of Group B patients was significantly shorter than Group C (log rank, P = 0,000).ConclusionThere is currently no definite data on the optimal duration of GnRH analogues use. One of the important results of this study that will provide an insight to the future studies is the improvement gained in OS by the increase in the duration of GnRH analogues use.
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CITATIONS (1)
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