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Sensitive MRD Detection from Lymphatic Fluid after Surgery in HPV-Associated Oropharyngeal Cancer.
Earland, Noah; Semenkovich, Nicholas P; Ramirez, Ricardo J; Gerndt, Sophie P; Harris, Peter K; Gu, Zhuosheng; Hearn, Andrew I; Inkman, Matthew; Szymanski, Jeffrey J; Whitfield, Damion; Wahle, Benjamin M; Xu, Zhongping; Chen, Kevin; Alahi, Irfan; Ni, Gabris; Chen, Andrew; Winckler, Wendy; Zhang, Jin; Chaudhuri, Aadel A; Zevallos, Jose P.
  • Earland N; Division of Cancer Biology, Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
  • Semenkovich NP; Division of Biology and Biomedical Sciences, Washington University School of Medicine, St. Louis, Missouri.
  • Ramirez RJ; Division of Biology and Biomedical Sciences, Washington University School of Medicine, St. Louis, Missouri.
  • Gerndt SP; Division of Endocrinology, Metabolism, and Lipid Research, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
  • Harris PK; Department of Otolaryngology-Head and Neck Surgery, Washington University School of Medicine, St. Louis, Missouri.
  • Gu Z; Division of Otolaryngology-Head and Neck Surgery, Allegheny Health Network, Pittsburgh, Pennsylvania.
  • Hearn AI; Division of Cancer Biology, Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
  • Inkman M; Droplet Biosciences, Inc., Cambridge, Massachusetts.
  • Szymanski JJ; Department of Otolaryngology-Head and Neck Surgery, Washington University School of Medicine, St. Louis, Missouri.
  • Whitfield D; Division of Cancer Biology, Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
  • Wahle BM; Division of Cancer Biology, Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
  • Xu Z; Droplet Biosciences, Inc., Cambridge, Massachusetts.
  • Chen K; Department of Otolaryngology-Head and Neck Surgery, Washington University School of Medicine, St. Louis, Missouri.
  • Alahi I; Department of Otolaryngology-Head and Neck Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
  • Ni G; Division of Cancer Biology, Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
  • Chen A; Division of Cancer Biology, Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
  • Winckler W; Department of Computer Science and Engineering, Washington University in St. Louis, St. Louis, Missouri.
  • Zhang J; Division of Cancer Biology, Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
  • Chaudhuri AA; Division of Cancer Biology, Department of Radiation Oncology, Washington University School of Medicine, St. Louis, Missouri.
  • Zevallos JP; Droplet Biosciences, Inc., Cambridge, Massachusetts.
Clin Cancer Res ; 30(7): 1409-1421, 2024 Apr 01.
Article en En | MEDLINE | ID: mdl-37939112
ABSTRACT

PURPOSE:

Our goal was to demonstrate that lymphatic drainage fluid (lymph) has improved sensitivity in quantifying postoperative minimal residual disease (MRD) in locally advanced human papillomavirus (HPV)-associated oropharyngeal squamous cell carcinoma (OPSCC) compared with plasma, and leverage this novel biofluid for patient risk stratification. EXPERIMENTAL

DESIGN:

We prospectively collected lymph samples from neck drains of 106 patients with HPV (+) OPSCC, along with 67 matched plasma samples, 24 hours after surgery. PCR and next-generation sequencing were used to quantify cancer-associated cell-free HPV (cf-HPV) and tumor-informed variants in lymph and plasma. Next, lymph cf-HPV and variants were compared with TNM stage, extranodal extension (ENE), and composite definitions of high-risk pathology. We then created a machine learning model, informed by lymph MRD and clinicopathologic features, to compare with progression-free survival (PFS).

RESULTS:

Postoperative lymph was enriched with cf-HPV compared with plasma (P < 0.0001) and correlated with pN2 stage (P = 0.003), ENE (P < 0.0001), and trial-defined pathologic risk criteria (mean AUC = 0.78). In addition, the lymph mutation number and variant allele frequency were higher in pN2 ENE (+) necks than in pN1 ENE (+) (P = 0.03, P = 0.02) or pN0-N1 ENE (-) (P = 0.04, P = 0.03, respectively). The lymph MRD-informed risk model demonstrated inferior PFS in high-risk patients (AUC = 0.96, P < 0.0001).

CONCLUSIONS:

Variant and cf-HPV quantification, performed in 24-hour postoperative lymph samples, reflects single- and multifeature high-risk pathologic criteria. Incorporating lymphatic MRD and clinicopathologic feature analysis can stratify PFS early after surgery in patients with HPV (+) head and neck cancer. See related commentary by Shannon and Iyer, p. 1223.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Orofaríngeas / Infecciones por Papillomavirus / Neoplasias de Cabeza y Cuello Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Orofaríngeas / Infecciones por Papillomavirus / Neoplasias de Cabeza y Cuello Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article