期刊文献+

卡铂对视网膜母细胞瘤化疗患儿听力损伤的观察 被引量:3

The ototoxicity of carboplatin in retinoblastoma children
原文传递
导出
摘要 目的观察卡铂在化疗过程中对视网膜母细胞瘤患儿的听力损伤及其严重程度。设计回顾性病例系列。研究对象选择自2009年11月至2011年2月在我院进行卡铂(carboplatin)、依托泊苷(etoposide)、长春新碱(vincristine)方案化疗的视网膜母细胞瘤患者111例,排除相关因素后95例患者(135眼)入选。方法分别在第1、3、6次化疗前进行与年龄相匹配的听力学检查,包括纯音测听(pure-tone audiometry)检查、畸变产物耳声发射(distortion-product otoacoustic emission,DPOAE)检查、听力脑干诱发电位(auditory brainstem response,ABR)检查等。观察化疗过程中双耳听力阈值的变化情况,并判断是否有听力损害。主要指标听力阈值。结果进行化学治疗的平均疗程为5.4次(3~10次)。化疗过程中,95例患者中仅3例出现听力检查结果的异常,其中2例在随后的复查中双耳阈值恢复正常,1例在3次随访听力检查中均提示左耳阈值提高。结论卡铂对视网膜母细胞瘤化疗患者的听力损伤并不常见,程度较轻,但对患儿进行听力监测十分必要。 Objective To analyse the ototoxicity of carboplatin in retinoblastoma children during chemecotherapy with CEV methods.Design Retrospective case series.Participants 95 children(135 eyes) with retinoblastoma in Department of Ophthalmology in Beijing Children's Hospital from November 2009 to February 2011.Methods Pure-tone audiometry,distortion-product otoacoustic emission and auditory brainstem response were used to measure the hearing threshold of bilateral ears at 1st,3rd,and 6th chemecotherapy respectively.Main Outcome Measures The hearing threshold of bilateral ears.Results Three children were found to have elevated hearing threshold during chemotherapy at the 3rd chemecotherapy among all the 95 patients.Two of them were back to normal hearing status in the following measurement.Only one child remained abnormal hearing threshold of his left ear up to 60 dB till the last measurement.Conclusion The ototoxicity of carboplatin during the chemecotherapy of retinoblastoma children is not common,while concurrent audiologic follow-up is required.
出处 《眼科》 CAS 2011年第6期404-407,共4页 Ophthalmology in China
关键词 卡铂 耳毒性 视网膜母细胞瘤 carboplatin ototoxicity retinoblastoma
  • 相关文献

参考文献23

  • 1MacCarthy A,Draper GJ,Steliarova-Foucher E,et al.Retinoblas-toma incidence and survival in European children(1978-1997).Report from the Automated Childhood Cancer Information Systemproject.Eur J Cancer,2006,42:2092-2102.
  • 2Moll AC,Kuik DJ,Bouter LM,et al.Incidence and survival ofretinoblastoma patients in the Netherlands:a register based study1862-1995.Br J Ophthalmol,1997,81:559-562.
  • 3程翼飞,张乐萍.视网膜母细胞瘤化疗进展[J].中国斜视与小儿眼科杂志,2004,12(3):142-144. 被引量:3
  • 4Roarty JD,Mclean IW,Zimmerman LE.Incidence of second neo-plasms in patients with bilateral retinoblastoma.Ophthalmology,1988,95:1583-1587.
  • 5Moll AC,Imhof SM,Bouter LM,et al.Second primary tumors inpatients with retinoblastoma.A review of the literature.Oph-thalmic Genet,1997,18:27-34.
  • 6Shields CL,De Potter P,Himelstein BP,et al.Chemoredection inthe initial management of intraocular retinoblastoma.Arch Oph-thalmol,1996,114:1130-1138.
  • 7丁大连,亓卫东,屈燕,蒋海燕,Richard Salvi.卡铂及其耳毒性[J].中华耳科学杂志,2008,6(2):134-144. 被引量:21
  • 8Bauer FP,Westhofen M,Kehrl W.Carboplatin ototoxicity in headand neck cancer patients.Laryngorhinootologie,1992,71:412-415.
  • 9MacDonald MR,Harrison RV,Wake M,et al.Ototoxicity of carbo-platin:comparing animal and clinical models at the Hospital forSick Children.J Otolaryngol,1994,23:151-159.
  • 10Ettinger LJ,Gayon PS,Krailo MD,et al.A phase II study of car-boplatin in children with recurrent or progressive solid tumors.Cancer,1994,73:1297-1301.

二级参考文献36

  • 1孙建和,杨伟炎,丁大连,孙伟,Sandra McFadden,Richard Salvi.卡铂对灰鼠中枢听觉系统影响研究[J].中国体视学与图像分析,2003,8(2):78-83. 被引量:4
  • 2[1]Ding D,Wang J,Salvi R,et al.Selective loss of inner hair cells and type-I ganglion neurons in carboplatin-treated chinchillas.Mechanisms of damage and protection.Ann N Y Acad Sci,1999,884:152-170.
  • 3[2]Hofstetter P,Ding D,Powers N,et al.Quantitative relationship of carboplatin dose to magnitude of inner and outer hair cell loss and the reduction in distortion product otoacoustic emission amplitude in chinchillas.Hear Res,1997,112(1-2):199-215.
  • 4[3]Wang J,Powers NL,Hofstet1ter P,et al.Effects of selective inner hair cell loss on auditory nerve fiber threshold,tuning and spontaneous and driven discharge rate.Hear Res,1997,107(1-2):67-82.
  • 5[4]Saivi R,Ding D,Wang J,et al.Functional changes in peripheral and central auditory pathways following selective inner hair cell loss.Seminars in Hearing,2003,24(2):135-145.
  • 6[5]Durrant JD,Wang J,Ding D,et al.Are inner or outer hair cells the source of summating potentials recorded from the round window? J Acoust Soc Am,1998,104(1):370-377.
  • 7[6]Salvi RJ,Wang J,Ding D,et al.Auditory deprivation of the central auditory system resulting from selective inner hair cell loss:animal model of auditory neuropathy.Seand Audiol Suppl,1999,51:1-12.
  • 8[9]Zheng XY,Ding D,McFadden SL,et al.Evidence that inner hair cells are the major source of cochlear summating potentials.Hear Res,1997,113(1-2):76-88.
  • 9[12]Ding D,McFadden SL,Salvi RJ.Calpain immunoreactivity and morphological damage in chinchilla inner ears after carboplatin.J Assoc Res Otolaryngol,2002,3(1):68-79.
  • 10[13]Ding D,Wang J,Salvi RJ.Early damage in the chinchilla vestibular sensory epithelium from carboplatin.Audlol Neurootol,1997,2(3):155-167.

共引文献22

同被引文献43

  • 1ABRAMSON D H, SCHEFLER A C. Update on retinoblastoma [J]. Retina, 2004, 24(6) : 828-848.
  • 2KIM J W, ABRAMSON D H, DUNKEL I J. Current manage- ment strategies for intraocular retinoblastoma [ J ]. Drugs, 2007, 67(15) : 2173-2185.
  • 3CHENG Y F, ZHANG L P. The development of retinoblastoma chemical therapy [ J ].中国斜视与小儿眼科杂志,2004,12(3):142-144.
  • 4BESS F H, DODD M J, PARKER R A. Children with minimal sensorineural hearing loss : prevalence, educational performance, and functional status [J]. Ear Hear, 1998, 19(5) : 339-354.
  • 5JEHANNE M, LUMBROSO-LE R L, SAVIGNONI A, et al. A- nalysis of ototoxicity in young children receiving carboplatin in the context of conservative management of unilateral or bilateral reti- noblastoma [ J ]. Pediatr Blood Cancer, 2009, 52 ( 5 ) : 637- 643.
  • 6BRADFORD B R. Chemotherapy induced infertility in patients with testicular cancer [J]. Oncol Nurs Forum, 2012, 39(1):27-30.
  • 7RATAIN M J, KAMINER L S, BITRAN J D, et al. Acute non- lymphocytic leukemia following etoposide and cisplatin combina- tion chemotherapy for advanced non-small-cell carcinoma of the lung [J]. Blood, 1987, 70(5) :1412-1417.
  • 8POTZSCH C, FETSCHER S, MERTELSMANN R, et al. Acute myelomonocytic leukemia secondary to synchronous carcinomas of the breast and lung, and to metachronous renal cell carcinoma [J]. J Cancer Res Clin Oncol, 1997, 123(11-12) : 678-680.
  • 9SHEARER P, KAPOOR G, BECHWITH J B, et al. Secondary acute myelogenous leukemia in patients previously treated for childhood renal tumors: a report from the National Wilms Tumor Study Group [J]. JPediatrHematol Oncol, 2001,23(2) : 109- 111.
  • 10DOMER P H, HEAD D R, RENGANATHAN N, et al. Molecu- lar analysis of 13 cases of MLL/1 lq23 secondary acute leukemia and identification of topoisomerase I1 consensus-binding se- quences near the chromosomal breakpoint of a secondary leukemia with the t(4;11) [J]. Leukemia, 1995, 9(8) : 1305-1312.

引证文献3

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