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A randomized, non-comparative phase 2 study of neoadjuvant immune-checkpoint blockade in retroperitoneal dedifferentiated liposarcoma and extremity/truncal undifferentiated pleomorphic sarcoma

  • Christina L. Roland,
  • Elise F. Nassif Haddad,
  • Emily Z. Keung,
  • Wei-Lien Wang,
  • Alexander J. Lazar,
  • Heather Lin,
  • Manoj Chelvanambi,
  • Edwin R. Parra,
  • Khalida Wani,
  • B. Ashleigh Guadagnolo,
  • Andrew J. Bishop,
  • Elizabeth M. Burton,
  • Kelly K. Hunt,
  • Keila E. Torres,
  • Barry W. Feig,
  • Christopher P. Scally,
  • Valerae O. Lewis,
  • Justin E. Bird,
  • Ravin Ratan,
  • Dejka Araujo,
  • M. Alexandra Zarzour,
  • Shreyaskumar Patel,
  • Robert Benjamin,
  • Anthony P. Conley,
  • J. Andrew Livingston,
  • Vinod Ravi,
  • Hussein A. Tawbi,
  • Patrick P. Lin,
  • Bryan S. Moon,
  • Robert L. Satcher,
  • Bilal Mujtaba,
  • Russell G. Witt,
  • Raymond S. Traweek,
  • Brandon Cope,
  • Rossana Lazcano,
  • Chia-Chin Wu,
  • Xiao Zhou,
  • Mohammad M. Mohammad,
  • Randy A. Chu,
  • Jianhua Zhang,
  • Ashish Damania,
  • Pranoti Sahasrabhojane,
  • Taylor Tate,
  • Kate Callahan,
  • Sa Nguyen,
  • Davis Ingram,
  • Rohini Morey,
  • Shadarra Crosby,
  • Grace Mathew,
  • Sheila Duncan,
  • Cibelle F. Lima,
  • Jean-Yves Blay,
  • Wolf Herman Fridman,
  • Kenna Shaw,
  • Ignacio Wistuba,
  • Andrew Futreal,
  • Nadim Ajami,
  • Jennifer A. Wargo,
  • Neeta Somaiah

摘要

Based on the demonstrated clinical activity of immune-checkpoint blockade (ICB) in advanced dedifferentiated liposarcoma (DDLPS) and undifferentiated pleomorphic sarcoma (UPS), we conducted a randomized, non-comparative phase 2 trial (NCT03307616) of neoadjuvant nivolumab or nivolumab/ipilimumab in patients with resectable retroperitoneal DDLPS (n = 17) and extremity/truncal UPS (+ concurrent nivolumab/radiation therapy; n = 10). The primary end point of pathologic response (percent hyalinization) was a median of 8.8% in DDLPS and 89% in UPS. Secondary end points were the changes in immune infiltrate, radiographic response, 12- and 24-month relapse-free survival and overall survival. Lower densities of regulatory T cells before treatment were associated with a major pathologic response (hyalinization > 30%). Tumor infiltration by B cells was increased following neoadjuvant treatment and was associated with overall survival in DDLPS. B cell infiltration was associated with higher densities of regulatory T cells before treatment, which was lost upon ICB treatment. Our data demonstrate that neoadjuvant ICB is associated with complex immune changes within the tumor microenvironment in DDLPS and UPS and that neoadjuvant ICB with concurrent radiotherapy has significant efficacy in UPS.