Gebelikte Jinekolojik Olmayan Kanserlerlere Genel Yaklaşım
Özet
Gebelikte jinekolojik olmayan kanserlerin insidansı yaklaşık 1/1000 olup en sık meme, tiroid ve serviks kanserleri görülmektedir. Gebelikteki fizyolojik değişiklikler tanı gecikmelerine yol açabileceğinden semptomların dikkatli incelenmesi ve tedavinin multidisipliner bir ekiple bireyselleştirilmesi gerekir. Tanıda ultrasonografi ve MR güvenle kullanılırken, gadolinyum ilk trimesterde önerilmez ve yüksek radyasyonlu BT tercih edilmez. Kemoterapi, fetal organogenez nedeniyle ilk trimesterde yüksek risk taşır; ancak ikinci trimesterden itibaren antrasiklin bazlı rejimler gibi belirli ajanlar uygun dozlarda güvenle uygulanabilir. Terapötik radyoterapi ciddi fetal riskler (mikrosefali, zihinsel gerilik) doğurduğundan gebelikte kontrendikedir ve doğum sonrasına ertelenmelidir. Meme kanseri yönetiminde cerrahi minimal riskle uygulanabilirken, trastuzumab fetal böbrek yetmezliği riski nedeniyle kontrendikedir. Tiroid kanserleri genellikle yavaş ilerler ve cerrahi doğum sonrasına ertelenebilir; ancak agresif tiplerde ikinci trimesterde müdahale edilir ve radyoaktif iyot gebelikte tamamen kontrendikedir. Hodgkin lenfomada stabil hastaların tedavisi ertelenebilirken, agresif olgularda ilk trimesterde tedaviye başlanır. Akut lösemi ise hem anne hem de fetus için yüksek mortalite riski taşıdığından hızla tedavi edilmelidir; ilk trimesterde teratojenik ilaç kısıtlamaları nedeniyle gebeliğin sonlandırılması bir seçenek olabilir. Genel olarak gebeliğin sonlandırılması kanser prognozunu iyileştirmez ve doğum zamanlaması neonatal riskler azaltılarak planlanmalıdır.
The incidence of non-gynecological cancers during pregnancy is approximately 1/1000, with breast, thyroid, and cervical cancers being the most common. Since physiological changes during pregnancy can cause diagnostic delays, careful evaluation of symptoms and a multidisciplinary, individualized treatment approach are essential. Ultrasonography and MRI are safely used for diagnosis, whereas gadolinium is avoided in the first trimester, and CT is generally restricted due to high radiation. Chemotherapy carries significant fetal risks during the first trimester due to organogenesis; however, specific agents like anthracycline-based regimens can be safely administered from the second trimester onward. Therapeutic radiotherapy is contraindicated during pregnancy due to severe fetal risks, such as microcephaly and mental retardation, and must be postponed postpartum. For breast cancer, surgery carries minimal fetal risk, while trastuzumab is contraindicated due to fetal renal failure risks. Thyroid cancers are usually slow-growing, allowing surgery to be delayed postpartum; yet, aggressive types require second-trimester intervention, and radioactive iodine is strictly contraindicated. In Hodgkin lymphoma, treatment for stable patients can be delayed, but aggressive cases require immediate first-trimester therapy. Conversely, acute leukemia demands urgent intervention due to high maternal and fetal mortality, and pregnancy termination may be considered in the first trimester due to the teratogenicity of crucial drugs. Overall, termination does not improve cancer prognosis, and delivery timing should be carefully planned to minimize neonatal morbidity.
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