Use of Platinum Derivatives During Pregnancy

被引:92
作者
Mir, Olivier [1 ,2 ]
Berveiller, Paul [3 ]
Ropert, Stanislas [1 ]
Goffinet, Francois [4 ]
Goldwasser, Francois [1 ]
机构
[1] Univ Paris 05, Cochin Teaching Hosp, AP HP, Fac Med,Dept Med Oncol, F-75679 Paris 14, France
[2] Univ Paris 05, Cochin Teaching Hosp, AP HP, Fac Med,Dept Clin Pharmacol, F-75679 Paris, France
[3] Univ Paris 06, St Antoine Teaching Hosp, AP HP, Fac Med,Dept Obstet, Paris, France
[4] Cochin Teaching Hosp, AP HP, Fac Med, Dept Obstet, Paris, France
关键词
carboplatin; cisplatin; pregnancy; cervical cancer; ovarian cancer; nonsmall cell lung cancer;
D O I
10.1002/cncr.23935
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The incidence of cancer during pregnancy is increasing given the trend for women to postpone childbearing. Knowledge of the potential toxicity and terato-genicity of chemotherapy agents is crucial for patient counseling. Platinum derivatives are active against various malignancies that occur more frequently during pregnancy: melanoma, cervical and ovarian cancers, and lung cancer. The authors of this article performed a systematic review of reports documenting the use of platinum derivatives during pregnancy in the English literature from 1977 through January 2008. Forty-three pregnancies were described: 36 patients received cisplatin, 6 patients received carboplatin, and I patient received both drugs. Two fetal malformations occurred after in utero exposure to cisplatin, but the causative link between cisplatin administration and these malformations remains speculative. However, either detectable cisplatin levels or platinum-DNA adducts were observed in neonates who were exposed to platinum derivatives during the third trimester, providing evidence for a late-onset transplacental transfer of these drugs. The administration of platinum derivatives, although feasible during the second and third trimesters of pregnancy, raises concern regarding the transplacental transfer of these drugs in late pregnancy and has unknown short- and long-term effects. Cancer 2008;113:3069-74. (C) 2008 American Cancer Society.
引用
收藏
页码:3069 / 3074
页数:6
相关论文
共 58 条
[31]   Successful treatment of small cell lung cancer during pregnancy [J].
Kluetz, Paul G. ;
Edelman, Martin J. .
LUNG CANCER, 2008, 61 (01) :129-130
[32]  
KOC ON, 1994, EUR J CANCER, V30A, P716
[33]   STAGE OF PREGNANCY-DEPENDENT TRANS-PLACENTAL PASSAGE OF PT-195M AFTER CIS-PLATINUM TREATMENT [J].
KOPFMAIER, P .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1983, 19 (04) :533-536
[34]   MUTAGENIC POTENTIAL OF CIS-DICHLORODIAMMINE PLATINUM-II IN RODENTS [J].
LEVINE, BS ;
PREACHE, MM ;
PERGAMENT, E .
TOXICOLOGY, 1980, 17 (01) :57-65
[35]  
Li RHW, 2007, J REPROD MED, V52, P575
[36]  
MALFETANO JH, 1990, OBSTET GYNECOL, V75, P545
[37]  
Malhotra N, 2000, EUR J GYNAECOL ONCOL, V21, P396
[38]  
MALONE JM, 1986, OBSTET GYNECOL, V68, P86
[39]   Chemotherapy in the treatment of locally advanced cervical cancer and pregnancy [J].
Marana, HRC ;
de Andrade, JM ;
Mathes, ADD ;
Duarte, G ;
da Cunha, SP ;
Bighetti, S .
GYNECOLOGIC ONCOLOGY, 2001, 80 (02) :272-274
[40]   Paclitaxel and carboplatin chemotherapy administered during pregnancy for advanced epithelial ovarian cancer [J].
Méndez, LE ;
Mueller, A ;
Salom, E ;
González-Quintero, VH .
OBSTETRICS AND GYNECOLOGY, 2003, 102 (05) :1200-1202