Guest guest Posted September 24, 2010 Report Share Posted September 24, 2010 I am gravely concerned about a member who posted recently that she was breast feeding her baby while on Gleevec. I want her to know that I am not judging her, but merely reiterating what has been passed down to us repeately. In speaking directly to her, I hope you have permission, dear member from your doctor or you could be playing Russian roulette with your baby's health. This is the warning that comes with Gleevec. Women who want to become pregnant should not do so while taking Gleevec or any other TKI. If you need further proof, I urge you to please contact the Novartis Hotline or the instructions that comes in your package. This comes from their webpage: Who should NOT take GLEEVEC Women who are or could be pregnant. Fetal harm can occur when administered to pregnant women; therefore, women should not become pregnant, as well as be advised of the potential risk to the unborn child if GLEEVEC is used during pregnancy. " Women who are breast-feeding because of the potential for serious adverse reactions in nursing infants. " Sexually active females should use adequate birth control while taking GLEEVEC. " Be sure to talk to your doctor and/or healthcare professional about these issues before taking GLEEVEC " http://tinyurl.com/29fl97v --_________________ I further give you warnings from the following information published in the Internet Journal of Oncology. This article was written by Ault MS, RN, FNP-BC, ANP-BC Family Nurse Practitioner, Adult Nurse Practitioner School of Nursing The University of Texas Health Science Center at Houston and I quote from her article (noted in 2010 Volume 7 Number 2). I have known Pat Ault for a long time, also most of the doctors in that department. She would not have been given permission to write this article without the blessings of the doctors at MDACC that she works under and I respect her authority on the subject of CML. You will note that everything I copied is in " quotations " . Some quotes I have excerpted are posted here, but the entire article can be seen at the recited website listed below the quotes, however, it is very lengthy: " Management of CML during pregnancy poses challenges to both hematologists and obstetricians. Currently, consensus is lacking in management of CML in pregnancy; therefore, clinical observations have become important. Most of these observations are derived from small case series or case reports. " Therefore, leukapheresis may be an intermittent short-term alternative option for pregnant patients, and prevents fetal exposure to TERATOGENIC drugs. However, leukapheresis is cumbersome, costly, and a time consuming procedure, with risk of infection, thrombosis and hypotensive events that may affect the fetus and patient. " ........... high concentrations of imatinib are DETECTED IN BREAST MILK. " Investigation of the placentas included standard pathologic analysis, computer assisted morphometry, and fluorescence in situ hybridization (FISH) analysis. This patient was treated with a targeted tyrosine inhibitor during first trimester of a first pregnancy and during the third trimester of a second pregnancy. The umbilical cord blood and breast milk findings were: 1) low imatinib and metabolite concentration levels found in the umbilical blood suggest limited placental transfer in late pregnancy, and 2) HIGH CONCENTRATION LEVELS OF IMATINIB AND METABOLITES WERE FOUND IN THE BREAST MILK. " Rousselot et al (2007) reported imatinib may be discontinued in patients who achieved a complete molecular remission for a period of at least 2 years without evidence of disease progression. " Gambacorti-Passerini et al (2009) reported the IMATINIB CONCENTRATION IN BREAST MILK REACHES A STEADY-STATE LEVEL AT 0.8 ug/ml. The milk intake in infants is known to average 728 to 777 ml/d, (range of 450 to 1165 ml/d); considering this milk intake and the infants are unlikely to receive more than 3 mg/d imatinib daily. This amount is far from therapeutic range, therefore, concluding that mothers with CML could safely breast-feed the infant. However, the effects of low-dose chronic exposure of infants to imatinib are not known, and have not undergone long-term investigation; THEREFORE, BREAST FEEDING SHOULD NOT BE RECOMMENDED AFTER RESUMING THERAPY. ttp://tinyurl.com/2g82tpc FYI, Lottie Duthu Quote Link to comment Share on other sites More sharing options...
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