SMARCA4-Deficient Thoracic Sarcomatoid Tumors Represent Primarily Smoking-Related Undifferentiated Carcinomas Rather Than Primary Thoracic Sarcomas

Natasha Rekhtman, Joseph Montecalvo, Jason C. Chang, Deepu Alex, Ryan N. Ptashkin, Ni Ai, Jennifer L. Sauter, Brie Kezlarian, Achim Jungbluth, Patrice Desmeules, Amanda Beras, Justin A. Bishop, Andrew J. Plodkowski, Mrinal M. Gounder, Adam J. Schoenfeld, Azadeh Namakydoust, Bob T. Li, Charles M. Rudin, Gregory J. Riely, David R. JonesMarc Ladanyi, William D. Travis

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Introduction: Highly aggressive thoracic neoplasms characterized by SMARCA4 (BRG1) deficiency and undifferentiated round cell or rhabdoid morphology have been recently described and proposed to represent thoracic sarcomas. However, it remains unclear whether such tumors may instead represent sarcomatoid carcinomas, and how their clinicopathologic characteristics compare with those of nonsarcomatoid SMARCA4-deficient non–small cell lung carcinomas (SD-NSCC). Methods: We identified 22 SMARCA4-deficient thoracic sarcomatoid tumors (SD-TSTs) with round cell and/or rhabdoid morphology and 45 SD-NSCCs, and comprehensively analyzed their clinicopathologic, immunohistochemical, and genomic characteristics using 341–468 gene next-generation sequencing and other molecular platforms. Results: The relationship of SD-TSTs with NSCC was supported by (1) the presence of NSCC components juxtaposed with sarcomatoid areas in five cases, (2) focal expression of NSCC lineage markers TTF1 or p40 in four additional cases, (3) smoking history in all except one patient (mean = 51 pack-years), accompanied by genomic smoking signature, and (4) high tumor mutation burden (mean = 14.2 mutations per megabase) and mutations characteristic of NSCC in a subset. Compared with SD-NSCCs, SD-TSTs exhibited considerably larger primary tumor size (p < 0.0001), worse survival (p = 0.004), and more frequent presentation at younger age (30–50 years) despite heavier smoking history. Distinctive pathologic features of SD-TSTs included consistent lack of adhesion molecule claudin-4, SMARCA2 (BRM) codeficiency, and frequent expression of stem cell markers. Conclusions: SD-TSTs represent primarily smoking-associated undifferentiated/de-differentiated carcinomas rather than primary thoracic sarcomas. Despite their histogenetic relationship with NSCC, these tumors have unique clinicopathologic characteristics, supporting their recognition as a distinct entity. Further studies are warranted to determine therapeutic approaches to this novel class of exceptionally aggressive thoracic tumors.

Original languageEnglish (US)
Pages (from-to)231-247
Number of pages17
JournalJournal of Thoracic Oncology
Volume15
Issue number2
DOIs
StatePublished - Feb 2020

Keywords

  • BRG1
  • Lung
  • Rhabdoid
  • SMARCA4
  • Sarcomatoid
  • Thoracic

ASJC Scopus subject areas

  • Oncology
  • Pulmonary and Respiratory Medicine

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