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Cancer treatment during pregnancy: from fetal safety to maternal efficacy

Project description

Development of standard of care for cancer treatment during pregnancy

Increasingly frequent cases of cancer during pregnancy present a broad spectrum of difficult and conflicting medical and ethical decisions. The ERC-funded CRADLE project aims to develop a new standard of care for cancer cases during pregnancy, investigating challenges at all levels including the foetus, the mother, and the foetomaternal barrier. Pivotal to this project is the information available from an international registry of pregnant women with cancer, a registry of their children, and biobanks of maternal, placental, cord blood, and tumour samples. The research includes large-scale clinical and laboratory studies, including pharmacological investigations and RNA-sequencing analysis. Successful outcomes will greatly contribute to the well-being of the mother and foetus in a pregnancy complicated by cancer.

Objective

The evolution in drug regulation of the last 50 years has left pregnant women and their fetuses orphaned. This is particularly problematic for cancer during pregnancy, which raises a difficult and conflicting medical ethical decision process and which has recently become increasingly frequent. In 2012 we published the first prospective study indicating that antenatal exposure to cancer treatment can overall be considered safe. Building on this proof of concept, the current proposal wants to take a groundbreaking step towards developing a standard of care for cancer during pregnancy by addressing –in an integrated fashion- the challenges at the level of the fetus, the mother and the fetomaternal barrier. At the core of this proposal lies an international registry of pregnant women with cancer, along with a registry of their children, and biobanks of maternal, placental, cord blood and tumoral tissues. Research track ‘child’ aims to deliver robust evidence of fetal safety. Research track ‘mother’ aims to address the emerging concerns in the oncological management of the mother, and specifically, the possible distinct biology of pregnancy-associated breast cancer, the most frequent cancer type in pregnancy. The research approach includes large-scale clinical follow-up studies along with laboratory studies on patient biomaterials, including pharmacological investigations and RNA-sequencing studies. Complementary to these studies is research track ‘placenta’ in which cutting-edge models of human placental research are used to address the poorly understood physiological basis of the placental barrier function in this specific situation. This ambitious program will rely on a multidisciplinary team of experts. Not only may the scientific deliverables of this proposal constitute a major step forward to the well-being of both mother and fetus in a pregnancy complicated by cancer, the methodological approach may also provide critical impetus to further research in this field.

Host institution

KATHOLIEKE UNIVERSITEIT LEUVEN
Net EU contribution
€ 1 709 375,00
Address
OUDE MARKT 13
3000 Leuven
Belgium

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Region
Vlaams Gewest Prov. Vlaams-Brabant Arr. Leuven
Activity type
Higher or Secondary Education Establishments
Links
Total cost
€ 1 709 375,00

Beneficiaries (2)