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Clinical Utility of Tumor-Naïve Presurgical Circulating Tumor DNA Detection in Early-Stage NSCLC.
Hong, Tae Hee; Hwang, Soohyun; Dasgupta, Abhijit; Abbosh, Chris; Hung, Tiffany; Bredno, Jörg; Walker, Jill; Shi, Xiaojin; Milenkova, Tsveta; Horn, Leora; Choi, Joon Young; Lee, Ho Yun; Cho, Jong Ho; Choi, Yong Soo; Shim, Young Mog; Chai, Shoujie; Rhodes, Kate; Roychowdhury-Saha, Manami; Hodgson, Darren; Kim, Hong Kwan; Ahn, Myung-Ju.
Afiliación
  • Hong TH; Department of Thoracic Surgery, Samsung Medical Center, Seoul, Republic of Korea; Department of Thoracic and Cardiovascular Surgery, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
  • Hwang S; Department of Pathology and Translational Genomics, Samsung Medical Center, Seoul, Republic of Korea.
  • Dasgupta A; Early Data Science, Oncology Data Science, Oncology R&D, AstraZeneca, Gaithersburg, Maryland.
  • Abbosh C; Translational Medicine, Oncology R&D, AstraZeneca, Cambridge, United Kingdom; SAGA Diagnostics, Cambridge, United Kingdom.
  • Hung T; GRAIL, LLC, Menlo Park, California.
  • Bredno J; GRAIL, LLC, Menlo Park, California.
  • Walker J; Precision Medicine, Oncology R&D, AstraZeneca, Cambridge, United Kingdom.
  • Shi X; Late Development Oncology, AstraZeneca, Gaithersburg, Maryland.
  • Milenkova T; Global Medicine Development, AstraZeneca, Cambridge, United Kingdom.
  • Horn L; Late Development Oncology, AstraZeneca, Gaithersburg, Maryland.
  • Choi JY; Department of Nuclear Medicine, Samsung Medical Center, Seoul, Republic of Korea.
  • Lee HY; Department of Radiology and Center for Imaging Science, Samsung Medical Center, Seoul, Republic of Korea.
  • Cho JH; Department of Thoracic Surgery, Samsung Medical Center, Seoul, Republic of Korea.
  • Choi YS; Department of Thoracic Surgery, Samsung Medical Center, Seoul, Republic of Korea.
  • Shim YM; Department of Thoracic Surgery, Samsung Medical Center, Seoul, Republic of Korea.
  • Chai S; GRAIL, LLC, Menlo Park, California.
  • Rhodes K; GRAIL, LLC, Menlo Park, California.
  • Roychowdhury-Saha M; GRAIL, LLC, Menlo Park, California.
  • Hodgson D; Translational Medicine, Oncology R&D, AstraZeneca, Cambridge, United Kingdom.
  • Kim HK; Department of Thoracic Surgery, Samsung Medical Center, Seoul, Republic of Korea.
  • Ahn MJ; Department of Hematology-Oncology, Samsung Medical Center, Seoul, Republic of Korea. Electronic address: silkahn@skku.edu.
J Thorac Oncol ; 2024 Jul 09.
Article en En | MEDLINE | ID: mdl-38992468
ABSTRACT

OBJECTIVES:

The use of tumor-informed circulating tumor DNA (ctDNA) testing in patients with early-stage disease before surgery is limited, mainly owing to restricted tissue access and extended turnaround times. This study aimed to evaluate the clinical value of a tumor-naïve, methylation-based cell-free DNA assay in a large cohort of patients with resected NSCLC.

METHOD:

We analyzed presurgical plasma samples from 895 patients with EGFR and anaplastic lymphoma kinase-wild-type, clinical stage I or II NSCLC. The ctDNA status was evaluated for its prognostic significance in relation to tumor volume, metabolic activity, histologic diagnosis, histologic subtypes, and clinical-to-pathologic TNM upstaging.

RESULTS:

Presurgical ctDNA detection was observed in 55 of 414 patients (13%) with clinical stage I lung adenocarcinoma (LUAD) and was associated with poor recurrence-free survival (2-year recurrence-free survival 69% versus 91%; log-rank p < 0.001), approaching that of clinical stage II LUAD. Presurgical ctDNA detection was not prognostic in patients with clinical stage II LUAD or non-LUAD. Within LUAD, tumor volume and positron emission tomography avidity interacted to predict presurgical ctDNA detection. Moreover, presurgical ctDNA detection was predictive of the postsurgical discovery of International Association for the Study of Lung Cancer grade 3 tumors (p < 0.001) and pathologic TNM upstaging (p < 0.001). Notably, presurgical ctDNA detection strongly correlated with higher programmed death-ligand 1 expression in tumors (positive rates 28% versus 55%, p < 0.001), identifying a subgroup likely to benefit from anti-programmed death-ligand 1 therapies.

CONCLUSION:

These findings support the integration of ctDNA testing into routine diagnostic workflows in early-stage NSCLC without the need for tumor tissue profiling. Furthermore, it is clinically useful in identifying patients at high risk who might benefit from innovative treatments, including neoadjuvant immune checkpoint inhibitors.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Thorac Oncol Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Thorac Oncol Año: 2024 Tipo del documento: Article