1998
DOI: 10.1016/s0889-8545(05)70007-3
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Chemotherapy in Pregnancy

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Cited by 80 publications
(60 citation statements)
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References 14 publications
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“…However, after the second trimester, Pentheroudakis et al reported that there was no major difference in the incidence rate of malformations or IUGR between infants from normal pregnancies and those from pregnancies in which chemotherapy was administered (8). Additionally, many reports indicate that the use of chemotherapy after the second trimester is relatively safe (1,(7)(8)(9)(10)(11)(12), suggesting that while chemotherapy is not recommended, it can be practically administered.…”
Section: Discussionmentioning
confidence: 99%
“…However, after the second trimester, Pentheroudakis et al reported that there was no major difference in the incidence rate of malformations or IUGR between infants from normal pregnancies and those from pregnancies in which chemotherapy was administered (8). Additionally, many reports indicate that the use of chemotherapy after the second trimester is relatively safe (1,(7)(8)(9)(10)(11)(12), suggesting that while chemotherapy is not recommended, it can be practically administered.…”
Section: Discussionmentioning
confidence: 99%
“…increased rate of fetal malformations (8,16,36,37). From the second trimester onwards, growth restriction is the main risk of chemotherapy.…”
Section: Accepted Articlementioning
confidence: 99%
“…disorders affecting future generations (16,37,87,88). Of note, during the time from conception until implantation (6 to 10 days after fertilization), the embryo is undifferentiated, and repair and recovery are possible through multiplication of multipotential cells to replace those that might have been lost.…”
Section: Accepted Articlementioning
confidence: 99%
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“…Pregnancy does not appear to affect the course of CML, there is still a risk of leukostasis as well as risk of placental insufficiency with consequent below normal fetal birth weight, increased prematurity, and increased mortality if CML left untreated for the duration of pregnancy. 2 Imatinib mesylate (ST1571, Gleevec, Norvatis) entered clinical trials in 1998 and has since been shown to induce dramatic hematologic and cytogenetic response in CML. 3 Imatinib has been found to be antiangiogenic in animal models.…”
Section: Introductionmentioning
confidence: 99%