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Case report: Pathological complete response to neoadjuvant brigatinib in stage III non-small cell lung cancer with ALK rearrangement.
Seong, Hayoung; Kim, Soo Han; Kim, Mi Hyun; Cho, Jeong Su; Kim, Ahrong; Eom, Jung Seop.
Afiliação
  • Seong H; Department of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
  • Kim SH; Department of Internal Medicine, Pusan National University Hospital, Busan, Republic of Korea.
  • Kim MH; Department of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
  • Cho JS; Department of Internal Medicine, Pusan National University Hospital, Busan, Republic of Korea.
  • Kim A; Department of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
  • Eom JS; Department of Internal Medicine, Pusan National University Hospital, Busan, Republic of Korea.
Front Oncol ; 14: 1343238, 2024.
Article em En | MEDLINE | ID: mdl-39055554
ABSTRACT

Purpose:

The use of neoadjuvant anaplastic lymphoma kinase (ALK)-tyrosine kinase inhibitors (TKIs) has not been extensively explored. The current case report highlights the notable pathological complete response (pCR) achieved following neoadjuvant brigatinib therapy in a patient with stage IIIA ALK-positive non-small cell lung cancer (NSCLC). Case presentation A 32-year-old male presented with incidental lung lesions, ultimately diagnosed as clinical stage T3N1M0, IIIA NSCLC with an ALK gene rearrangement. Following a multidisciplinary discussion, the patient opted for neoadjuvant brigatinib therapy, which significantly reduced the tumor size. Subsequently, surgery with curative intent was performed, revealing pCR with no residual tumor cells. The patient remained disease-free during a 13-month follow-up period.

Conclusion:

This case report provides compelling evidence of pCR following brigatinib therapy in ALK-positive NSCLC, suggesting that surgery after neoadjuvant therapy with brigatinib may offer a safe and effective approach for patients with ALK-positive NSCLC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article