LUCINAE Registry: Thoracic Cancers During Pregnancy

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorOncology Institute of Southern Switzerland

About this trial

The LUCINAE Registry is an international, multicenter observational study collecting data on patients with thoracic cancers (including lung cancer) who are expecting a child. This includes women diagnosed during pregnancy, women who become pregnant during or after cancer, and men receiving cancer treatment at the time their partner conceives.

Because thoracic cancers during pregnancy are rare, there is limited information to guide clinical decisions. This registry aims to describe patient characteristics, diagnostic approaches, treatments, and maternal and fetal outcomes. Data are collected retrospectively and prospectively from participating centers.

The results of this registry are expected to improve understanding of thoracic cancers in this setting and support the development of future clinical recommendations.

Eligibility criteria

Qualifiers

Patients receiving a diagnosis of thoracic cancer during pregnancy

Patients who became pregnant while having active thoracic cancer

Patients previously treated for a thoracic cancer and becoming pregnant in the 5 years following end of treatment OR Men with a diagnosis of thoracic cancer (including lung cancer, mesothelioma, thymic epithelial tumors, neuroendocrine tumors or sarcoma of the thorax and other rare thoracic entities), who were undergoing active oncological treatment at the time their partner conceived their child.

2. Available information about pregnancy outcomes

Disqualifiers

1. Patient missing data about thoracic cancer stage and diagnosis

2. For retrospective patients, documented refusal to the use of clinical data for research purposes

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

100 Participants
are grouped into 2 trial groups

Sponsors and collaborators

Oncology Institute of Southern Switzerland

Lead sponsor

Clinical Trial Unit Ente Ospedaliero Cantonale

Collaborator