Phase II trial of atezolizumab (Anti-PD-L1) in the treatment of relapsed/refractory IIB/IVB mycosis fungoides/Sézary syndrome patients after previous systemic treatment. EORTC-1652-CLTG "PARCT"

  • Rudolf Stadler*
  • , Gabriele Roccuzzo*
  • , Pablo Ortiz-Romero
  • , Martine Bagot
  • , Pietro Quaglino
  • , Emmanuella Guenova
  • , Constanze Jonak
  • , Evangelia Papadavid
  • , René Stranzenbach
  • , Sandrine Marreaud
  • , Jammbe Musoro
  • , Jose Casas-Martin
  • , Duncan Murray
  • , Samantha Drennan
  • , Jimmy Van Hear
  • , Paul Moss
  • , Delphine Sartori
  • , Maxime Battistella
  • , Rein Willemze
  • , Julia Scarisbrick
  • Robert Knobler
*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

INTRODUCTION: Treatment of advanced mycosis fungoides (MF) and Sézary syndrome (SS) is a challenge. In this international, multicenter, open-label phase II trial, we assessed the efficacy and safety of anti-PD-L1 atezolizumab in stage IIB-IV refractory/relapsed MF and SS.

MATERIALS AND METHODS: Patients received atezolizumab 1200 mg IV Q3w for up to 1 year unless progression or withdrawal. The main study endpoints were overall response rate (ORR), progression-free survival (PFS), time to next systemic treatment (TTNT), and overall survival (OS).

RESULTS: A total of 26 patients were enrolled from seven countries. Seventeen patients met the inclusion criteria. At a median follow-up of 36.6 months, the ORR was 15.4 % in the intention to treat (ITT) and 17.6 % in the per protocol (PP) population, respectively. In the PP group, 58.8 % of patients, and in the ITT group, 53.9 % of patients achieved partial response or stable disease as their best outcome. One complete response was observed after 1 year. Median PFS was 3 months (95 % CI 1.4-4.9) in PP and 3.1 months (95 % CI 2.4-4.0) in ITT. Median OS was not reached for PP and was 22.3 months (20.0-NE) for ITT. Median TTNT was 5.9 months (2.8-NE) in PP and 6.2 months (3.1-14.8) in ITT. The most common grade ≥ 3 adverse events were fatigue (23.1 %) and infections (15.4 %), with two sepsis-related deaths. Atezolizumab was primarily discontinued due to disease progression (50 %).

CONCLUSIONS: Atezolizumab shows moderate activity in pretreated refractory/relapsed MF and SS. Further studies are needed to identify reliable predictors of safety and treatment response.

Original languageEnglish
Article number115484
Number of pages10
JournalEuropean Journal of Cancer
Volume222
DOIs
Publication statusPublished - 03 Jun 2025

Fields of science

  • 301902 Immunology
  • 302 Clinical Medicine
  • 302011 Dermatology

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