Radyasyonun Kadın Fertilitesi Üzerine Etkileri

Yazarlar

Yeşim Bayoğlu Tekin

Özet

Radyoterapi, günümüzde kanser tedavisinin temel yapı taşlarından biri olmakla birlikte, abdominal veya pelvik bölgeye uygulandığında kadın üreme sistemi üzerinde geri dönüşü olmayan, oldukça yıkıcı etkilere yol açabilmektedir. Kadınlar sınırlı ve yenilenemez bir fertilite kapasitesiyle dünyaya geldiklerinden, iyonlaştırıcı radyasyon overlerdeki germ hücrelerinde DNA hasarı oluşturarak folikül havuzunun hızla tükenmesine, erken menopoza ve kısırlığa neden olur. Over rezervinin takibinde AMH, FSH ve antral folikül sayısı gibi tanısal yöntemler kullanılsa da, radyasyonun dozu ve hastanın yaşı hasarın boyutunu doğrudan belirler. Radyasyon yalnızca overleri değil, uterus yapısını da miyometrial ve endometrial fibrozis, atrofi ve vaskülarizasyon bozuklukları yoluyla zedeleyerek embriyo implantasyonunu olumsuz etkiler. Bu durum, tedavi sonrası sağ kalan hastaların gebeliklerinde erken doğum, düşük doğum ağırlığı, plasenta invazyon anomalileri ve uterus rüptürü riskini ciddi oranda artırmaktadır. Bu toksik etkileri engellemek amacıyla cerrahi olarak over transpozisyonu ve uteropeksi gibi teknikler uygulanırken, farmakolojik alanda sfingosin-1-fosfat ve amifostin gibi koruyucu ajanlar geliştirilmektedir. Ayrıca, kranial ışınlamalar hipotalamus-hipofiz-gonadal aksını bozarak hormonal eksikliklere, erken ergenliğe ve hiperprolaktinemiye sebebiyet verebilir. Bu nedenle, genç kanser hastalarında onkofertilite danışmanlığı ve üreme sağlığını koruyucu stratejilerin multidisipliner bir yaklaşımla planlanması hayati önem taşımaktadır.

Although radiotherapy remains a cornerstone in modern oncology, its application to pelvic or abdominal fields can exert profoundly destructive and irreversible effects on the female reproductive system. Since women are born with a finite, non-renewable ovarian reserve, ionizing radiation triggers accelerated cellular apoptosis and DNA double-strand breaks within germ cells, leading to premature ovarian insufficiency and permanent sterility. While diagnostic markers such as Anti-Müllerian Hormone (AMH), FSH, and antral follicle count are critical for assessing remaining ovarian reserve, the patient's age and cumulative radiation dosage remain the primary determinants of injury severity. Beyond ovarian damage, radiation severely compromises uterine integrity by inducing endometrial atrophy, myometrial fibrosis, and microvascular dysfunction, which directly impair embryo implantation. Consequently, cancer survivors face significantly elevated obstetric complications, including spontaneous abortion, preterm delivery, low birth weight, and uterine rupture. To mitigate these adverse outcomes, fertility preservation techniques are essential, incorporating surgical interventions like ovarian transposition and uteropexy, alongside experimental pharmacological shields such as sphingosine-1-phosphate and amifostine. Additionally, cranial irradiation can disrupt the vital hypothalamic-pituitary-gonadal axis, precipitating gonadotropin deficiency, precocious puberty, and hyperprolactinemia. Therefore, early oncofertility counseling and personalized protective management are crucial to safeguarding the future reproductive health and quality of life for young female survivors.

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Sayfalar

523-535

Gelecek

23 Ağustos 2022

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