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<p>Chemoradiotherapy (CRT) with consolidative immunotherapy(IO) remains the standard care for unresectable stage III NSCLC, yet survival remains suboptimal in molecular subgroups. Emerging targeted therapies offer the potential for converting unresectable cases to resectable status. We present a 54-year-old female with stage IIIB (T1cN3M0) <i>ERBB2</i> exon 20-mutated lung adenocarcinoma (PD-L1 50%) and supraclavicular metastasis. After three cycles of <i>ERBB2</i>-targeted antibody-drug conjugate combined with programmed death-1 (PD-1) inhibitor, transient Grade 1 interstitial lung disease resolved with steroids. Serial imaging revealed 58% tumor regression, enabling successful R0 resection via VATS lobectomy with lymphadenectomy. Histopathological analysis confirmed complete pathological response in primary and nodal lesions, corroborated by undetectable postoperative minimal residual disease. The patient remained recurrence-free at a 9-month follow-up. This induction targeted-IO strategy enabled surgical conversion in ERBB2-mutant NSCLC with durable remission and acceptable toxicity, warranting investigation in molecular subgroups with limited CRT-IO benefit.</p>

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Case report: a R0 resection successfully induced by T-DXd plus PD-1 inhibitor regimen in a primary unresectable stage IIIB NSCLC with ERBB2-mutation

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年6月10日

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  • Ruijie Zhang,
  • Sida Cheng,
  • Kunkun Sun,
  • Lihong Zhang,
  • Xiang Yan,
  • Fan Yang

摘要

Chemoradiotherapy (CRT) with consolidative immunotherapy(IO) remains the standard care for unresectable stage III NSCLC, yet survival remains suboptimal in molecular subgroups. Emerging targeted therapies offer the potential for converting unresectable cases to resectable status. We present a 54-year-old female with stage IIIB (T1cN3M0) ERBB2 exon 20-mutated lung adenocarcinoma (PD-L1 50%) and supraclavicular metastasis. After three cycles of ERBB2-targeted antibody-drug conjugate combined with programmed death-1 (PD-1) inhibitor, transient Grade 1 interstitial lung disease resolved with steroids. Serial imaging revealed 58% tumor regression, enabling successful R0 resection via VATS lobectomy with lymphadenectomy. Histopathological analysis confirmed complete pathological response in primary and nodal lesions, corroborated by undetectable postoperative minimal residual disease. The patient remained recurrence-free at a 9-month follow-up. This induction targeted-IO strategy enabled surgical conversion in ERBB2-mutant NSCLC with durable remission and acceptable toxicity, warranting investigation in molecular subgroups with limited CRT-IO benefit.