期刊文献+

术后辅助化疗对绝经前乳腺癌患者性激素和月经周期的影响 被引量:11

Influence of adjuvant chemotherapy on sex hormone levels and menstrual cycles in premenopausal patients with postoperative breast cancer
下载PDF
导出
摘要 目的观察绝经前乳腺癌患者术后辅助化疗对其性激素和月经周期的影响,为临床选择综合治疗方案提供参考。方法应用回顾性分析及统计学方法,将97例绝经前乳腺癌患者按年龄不同分成3组,Ⅰ组:12例,年龄≤30岁;Ⅱ组:34例,年龄在31~40岁之间;Ⅲ组:51例,年龄≥41岁。分析不同组别在化疗过程中外周血血清雌激素(Eestrogen,E2)、孕激素(Progestin,P)、总睾酮(Testosterone,T)水平及其月经周期的变化。结果患者第一次接受化疗前,Ⅰ组患者血清E2、P、T浓度分别为:(283.73±53.12)pg/ml、(13.98±5.67)ng/ml、(48.64±16.73)ng/dl;Ⅱ组分别为:(278.86±59.36)pg/ml、(13.01±6.21)ng/ml、(46.32±17.09)ng/dl;Ⅲ组分别为:(243.11±90.12)pg/ml、(14.01±6.45)ng/ml、(43.89±18.88)ng/dl,各组E2、P或T间差异没有统计学意义(P值均>0.05)。随着患者接受化疗次数的增加,其血清中E2、P浓度在不同周期间差异存在统计学意义(P值均<0.01),即随着化疗周期的增加E2、P浓度逐渐降低;总睾酮(T)浓度在不同化疗周期间差异没有统计学意义(P值均>0.05),即T并没有随着化疗周期的增加而发生改变。化疗周期结束后,患者发生闭经率为41.2%,未闭经组E2、P、T浓度分别为:(53.66±37.91)pg/ml、(5.34±4.22)ng/ml、(43.32±22.04)ng/dl;闭经组分别为:(12.21±5.64)pg/ml、(0.5±0.2)ng/ml、(103.2±29.88)ng/dl,两组E2、P或T间存在差异,差异有统计学意义(P值均<0.01),即化疗诱导闭经后,患者血清E2、P浓度明显降低,血清T浓度显著升高。不同年龄组间闭经发生率及发生时间不同,患者年龄与化疗诱导的闭经发生率呈强正线性相关(r=1,P=0.016),年龄越大的患者接受化疗后,其发生的闭经可能性越大。患者年龄与闭经发生的时间呈强负直线相关(r=-0.99,P=0.031),患者年龄越大,其在化疗期间发生闭经的时间越早。结论绝经前乳腺癌患者术后接受辅助性化疗后,其血清E2、P浓度降低,T浓度反馈性增高,最终可引起患者闭经。 Objective To provide some messages for clinical comprehensive therapy, by investigating the changes of sex hormone levels and menstrual cycles in premenopausal patients with postoperative breast cancer treat- ed with adjuvant chemotherapy. Methods The changes of oestrogen (E2), progestin (P), testosterone (T) in the se- runa of peripheral blood and menstrual cycles were analyzed by retrospective analyses and statistical methods in the process of adjuvant chemotherapy, in 97 premenopausal patients with postoperative breast cancer. The patients were di- vided into three groups according to patient's ages: group I (12 eases, ≤30 years old), group II (34 eases, 31,-40 years old), and group m (51 eases, ≥41 years old). Results Before the first chemotherapy, the levels of E2, P, T in serum of peripheral blood were (283.73+53.12) pg/ml, (13.98±5.67) ng/ml, and (48.64±16.73) ng/dl in group I, (278.86±59.36) pg/ml, (13.01±6.02) ng/ml, and (46.32±17.09) ng/dl in group lI ,,(243.11±90.)/ml, (14.01±6.45) rig/ ml, (43.89±18.88) ng/dl in group III, respectively. There were no significant differences among the three groups (P〉 0.05). However, the levels of E2, P were significantly different with chemotherapy cycles (P〈0.01): the levels of E2, P gradually diminished with chemotherapy cycles. The T concentration did not changed with chemotherapy cycles (P〉 0.05). Total amenorrhoea rate was 41.2% after chemotherapy cycles were over. The levels of E2, P, T were (53.66± 47.91) pg/ml, (5.34±4.22) ng/ml, (43.32±22.04) ng/dl in unamenorrhoea group, (12.21±5.64) pg/ml, (0.5±0.2) ng/ml, (103.2±29.88) ng/dl and in amenorrhoea group, respectively. There were significant differences between unamenor- rhoea group and amenorrhoea group (P〈0.01). The levels of E2, P both significantly reduced, and the T levels were higher in amenorrhoea group. Amenorrhoea rates and time happened amenorrhoea were not the same in different age groups. There was a positive linear correlation between amenorrhoea rates and ages (r=l, P--0.016), amenorrhoea rates were higher in older women than younger women. Time happened amenorrhoea showed negative linear correlation with ages (r=-0.99, P=0.031), which were earlier in older women than younger women. Conclusion In premenopausal patients with postoperative breast cancer, the levels of E2, P in serum of peripheral blood gradually diminish, and the T levels feedback rise during chemotherapy. Amenorrhoea happens when the levels of E2, P diminished to some degree.
出处 《海南医学》 CAS 2013年第13期1919-1921,共3页 Hainan Medical Journal
关键词 乳腺癌 性激素 闭经 辅助化疗 Breast cancer Sex hormone Amenorrhea Adjuvant chemotherapy
  • 相关文献

参考文献14

  • 1杨,韩为东,赵亚力.乳腺癌与雌激素及有关内分泌治疗[J].现代肿瘤医学,2007,15(5):729-730. 被引量:8
  • 2李洪涛,周遵艳,戴丹菁,张文涛,喻世华,陶劲松,杨继元.化疗对乳腺癌患者性激素及月经的影响[J].现代肿瘤医学,2010,18(1):76-77. 被引量:8
  • 3Zeleniuch-Jacquotte A, Afanasyeva Y, Kaaks R, et al, Premenopausal serum androgens and breast cancer risk: A nested case-control study [J]. Breast Cancer Res, 2012, 14(1): R32.
  • 4Kaaks R, Rinaldi S, Key TJ, et al, Postmenopausal serum androgems, oestrogens and breast cancer risk: the European prospective investigation into cancer and nutrition [J]. Endocr Relat Cancer, 2005, 12: 1071-1082.
  • 5Woolcott C, Shvetsov Y, Stanczyk F, et al, Plasma sex hormone concentrations and breast cancer risk in an ethnically diverse population of postmenopausal women: the Multiethnic Cohort Study [J]. Endocr Relat Cancer, 2010, 17: 125-134.
  • 6Absolom K, Eiserl C, Turner L, el ai, Ovarian failure following cancer treatment: current management and quality of life [J]. Oxford journals, 2008, 22(11): 2506-2512.
  • 7Swain SM, Stephanie RL, menopausal women on the lowed-by-docetaxel arm of NSABP B-30 trial [J] Res Treat, 2009, 113: 315-320.
  • 8Vanhuyse M, Fournier C, Bonneterre J. Chemotherapy-induced amenorrhea: influence on disease-free survival and overall survival in receptor-positive premeno -pausal early breast cancer patients [J]. Annals of Oucology, 2005, 16: 1283-1288.
  • 9Minton SM, Munster PN. Chemotherapy-induced amenorrhea and fertility in women undergoing adjuvant treatment for breast cancer [J]. Cancer Control, 2002, 9(6): 466-472.
  • 10Petrek JA, Naughton MJ, Case LD, et al, Incidence, time course, and determinants of menstrual bleeding after breast cancer treatment: a prospective study [J]. Am J Clin Oncol, 2006, 24: 1045-1051.

二级参考文献23

  • 1Goodwin PJ, Ennis M, Pritchard KI, et al. Risk of menopause during the fist year after breast cancer diagnosis [ J ]. J Clin Oncol, 1999, 17:2365 - 2370.
  • 2Del Mastro L, Venturini M, Sertoli MR, et al. Amenotrhea induced by adjuvant chemotherapy in early breast patients:prognostic role and clinical implications [ J]. Breast Cancer Res Treat, 1997,43: 183 - 190.
  • 3Devanesan P,Todorovic R,Zhao J,et al.Catechol estrogen conjugates and DNA adducts in the kidney of male Syrian golden hamtets treated with 4-hydroxyestradiol:potential biomarkers for estrogen-initiated cancer[J].Carcinogenesis,2001,22:489-497.
  • 4Cavalieri EL,Kumar S,Todorovic R,et al.Imbalance of estrogen homeostasis in kidney and liver of hamsters treated with estradiol:implications for estrogen-induced initiation of renal tumors[J].Chem Res Toxicol,2001,14:1041-1050.
  • 5Chakravarti D,Mailander PC,Li KM,et al.Evidence that a burst of DNA depurination in SENCAR mouse skin induces errorprone repair and forms mutations in the H-ras gene[J].Oncogene,2001,20:7945-7953.
  • 6Yao J,Li Y,Chang M,et al.Catechol estrogen 4-hydroxyequilenin is a substrate and an inhibitor of catechol-O-methyltransferase[J].Chem Res Toxicol,2003,16:668-675.
  • 7Jefcoate CR,Liehr JG,Santen R J,et al.Tissue-specific synthesis and oxidative metabolism of estrogens.Estrogens as endogenous carcinogens in the breast and prostate[J].J National Cancer Institute Monograph,2000,27:95-112.
  • 8Klinge CM.Estrogen receptor interaction with co-activators and co-repressors[J].Steroids,2000,65:227-251.
  • 9Zhao YL,Han WD,Li Q,et al.Mechanism of transcriptional regulation of LRP16 gene expression by 17-estradiol in MCF-7 human breast cancer cells[J].J Mol Endoc,2005,34(1):77-89.
  • 10Webb P,Nguyen P,Valentine C,et al.The estrogen receptor enhances AP-1 activity by two distinct mechanisms with different requirements for receptor transactivation functions[J].Mol Endocrinol,1999,13:1672-1685.

共引文献16

同被引文献98

  • 1韩东兴,席吕刚,严琳,陈云霞,刘邦令.化疗对围绝经期乳腺癌患者性激素水平的影响[J].中国癌症杂志,2011,21(6):470-472. 被引量:3
  • 2尹益民,任晓萍,潘文倩,艾红.高频超声及钼靶X线检查在乳腺癌诊断中的应用价值[J].西安交通大学学报(医学版),2012,33(5):572-575. 被引量:79
  • 3张美芬,张俊娥,梁骊敏.乳癌患者配偶的生存质量与压力的相关性研究[J].护理学杂志(外科版),2006,21(8):59-61. 被引量:6
  • 4李惠平,马力文,张淑兰,贾廷珍,邓惠静,张照辉,梁莉,王墨培,肖宇,曹保山,陈森,汪有蕃.绝经前乳腺癌化疗致闭经的观察及临床意义[J].中华肿瘤杂志,2006,28(11):848-851. 被引量:23
  • 5孙燕,石远凯.临床肿瘤内科手册[M].北京:人民卫生出版社,2008:371.
  • 6周岱翰,主编.临床中医肿瘤学[M].北京:人民卫生出版社.2005:185-195.
  • 7Awadalla AW, Ohaeri JU, Gholoum A, et al. Factors associatedwith quality of life of outpatients with breast caneer and gynecologic cancers and their family caregivers: a controlled Study [J]. BMC Cancer, 2011, 12(7): 1021-1022.
  • 8MeQuellon RP, Thaler HT, Cella D, et al. Quality of life outcomes from a randomized trial of eisplatin versus cisplatin plus palitaxel in advance cervical Gynecology Oncology Group study [J]. Gynecol Oncol, 2010, 102(2): 296-297.
  • 9Skolarikos A, Mitsogiannis H, Deliveliofis C. Indications, predic- tion of success, and methods to improve outcome of shock wave lithotripsy of renal and upper ureteral calculi [J]. Arch Ital Urol An- drol, 2010, 82(1): 56-63.
  • 10Wedd A, Curmingham D, Scarffe JH, et al. Randomized trial com- paring epimbicin, cisilatin and fluorouracil versus fluorouracil, doxorubicin and methotrexate in advanced esophageal gastric can- cer [J]. J Clin Oncol, 2011, 15(10): 261-267.

引证文献11

二级引证文献50

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部