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Case report: Osimertinib administration during pregnancy in a woman with advanced EGFR-mutant non-small cell lung cancer

Lung cancer (LC) is one of the most common causes of death worldwide. The identification of oncogene-addicted driving mutations suitable for targeted therapy has improved clinical outcomes in advanced diseases. Clinical trials, on the other hand, rarely involve vulnerable groups such as pregnant wom...

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Autores principales: Soberanis Pina, Pamela, Lara-Mejía, Luis, Matias-Cruz, Venecia, Barrón, Feliciano, Cardona, Andrés F., Raez, Luis E., Rios-Garcia, Eduardo, Arrieta, Oscar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079944/
https://www.ncbi.nlm.nih.gov/pubmed/37035182
http://dx.doi.org/10.3389/fonc.2023.1108124
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author Soberanis Pina, Pamela
Lara-Mejía, Luis
Matias-Cruz, Venecia
Barrón, Feliciano
Cardona, Andrés F.
Raez, Luis E.
Rios-Garcia, Eduardo
Arrieta, Oscar
author_facet Soberanis Pina, Pamela
Lara-Mejía, Luis
Matias-Cruz, Venecia
Barrón, Feliciano
Cardona, Andrés F.
Raez, Luis E.
Rios-Garcia, Eduardo
Arrieta, Oscar
author_sort Soberanis Pina, Pamela
collection PubMed
description Lung cancer (LC) is one of the most common causes of death worldwide. The identification of oncogene-addicted driving mutations suitable for targeted therapy has improved clinical outcomes in advanced diseases. Clinical trials, on the other hand, rarely involve vulnerable groups such as pregnant women. We report a 37-year-old woman with advanced non-small cell lung cancer (NSCLC) harboring an exon 19 deletion of EGFR treated with afatinib. After the initial treatment, the patient achieved a complete response and had an unplanned pregnancy. Targeted therapy was withheld during the first trimester and resumed with osimertinib in the second trimester in which the patient developed oligohydramnios and intrauterine growth restriction (IUGR) of the baby. Osimertinib was delayed at two different times during the third trimester with complete resolution of the oligohydramnios. The baby was born at 37.3 weeks of gestation (WOG) with no signs of congenital disorders. After delivery, the mother restarted osimertinib and maintained a complete response. This case suggests that osimertinib could be an acceptable option for tumor control during pregnancy in EGFR-mutant NSCLC. This information do not replace current recommendations for avoiding pregnancy and promoting contraceptive usage in patients receiving any cancer therapy.
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spelling pubmed-100799442023-04-08 Case report: Osimertinib administration during pregnancy in a woman with advanced EGFR-mutant non-small cell lung cancer Soberanis Pina, Pamela Lara-Mejía, Luis Matias-Cruz, Venecia Barrón, Feliciano Cardona, Andrés F. Raez, Luis E. Rios-Garcia, Eduardo Arrieta, Oscar Front Oncol Oncology Lung cancer (LC) is one of the most common causes of death worldwide. The identification of oncogene-addicted driving mutations suitable for targeted therapy has improved clinical outcomes in advanced diseases. Clinical trials, on the other hand, rarely involve vulnerable groups such as pregnant women. We report a 37-year-old woman with advanced non-small cell lung cancer (NSCLC) harboring an exon 19 deletion of EGFR treated with afatinib. After the initial treatment, the patient achieved a complete response and had an unplanned pregnancy. Targeted therapy was withheld during the first trimester and resumed with osimertinib in the second trimester in which the patient developed oligohydramnios and intrauterine growth restriction (IUGR) of the baby. Osimertinib was delayed at two different times during the third trimester with complete resolution of the oligohydramnios. The baby was born at 37.3 weeks of gestation (WOG) with no signs of congenital disorders. After delivery, the mother restarted osimertinib and maintained a complete response. This case suggests that osimertinib could be an acceptable option for tumor control during pregnancy in EGFR-mutant NSCLC. This information do not replace current recommendations for avoiding pregnancy and promoting contraceptive usage in patients receiving any cancer therapy. Frontiers Media S.A. 2023-03-24 /pmc/articles/PMC10079944/ /pubmed/37035182 http://dx.doi.org/10.3389/fonc.2023.1108124 Text en Copyright © 2023 Soberanis Pina, Lara-Mejía, Matias-Cruz, Barrón, Cardona, Raez, Rios-Garcia and Arrieta https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Soberanis Pina, Pamela
Lara-Mejía, Luis
Matias-Cruz, Venecia
Barrón, Feliciano
Cardona, Andrés F.
Raez, Luis E.
Rios-Garcia, Eduardo
Arrieta, Oscar
Case report: Osimertinib administration during pregnancy in a woman with advanced EGFR-mutant non-small cell lung cancer
title Case report: Osimertinib administration during pregnancy in a woman with advanced EGFR-mutant non-small cell lung cancer
title_full Case report: Osimertinib administration during pregnancy in a woman with advanced EGFR-mutant non-small cell lung cancer
title_fullStr Case report: Osimertinib administration during pregnancy in a woman with advanced EGFR-mutant non-small cell lung cancer
title_full_unstemmed Case report: Osimertinib administration during pregnancy in a woman with advanced EGFR-mutant non-small cell lung cancer
title_short Case report: Osimertinib administration during pregnancy in a woman with advanced EGFR-mutant non-small cell lung cancer
title_sort case report: osimertinib administration during pregnancy in a woman with advanced egfr-mutant non-small cell lung cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079944/
https://www.ncbi.nlm.nih.gov/pubmed/37035182
http://dx.doi.org/10.3389/fonc.2023.1108124
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