Efficacy of chemotherapy or chemo‐anti‐PD‐1 combination after failed anti‐PD‐1 therapy for relapsed and refractory hodgkin lymphoma: A series from lysa centers

  • Cédric Rossi
    Cancer Research Centre of Toulouse (CRCT), UMR1037 INSERM, Université Toulouse III Paul‐Sabatier, ERL5294 CNRS, Université de Toulouse Toulouse France
  • Julia Gilhodes
    Clinical trials office, Institut universitaire du cancer Toulouse‐ Oncopole Toulouse France
  • Marie Maerevoet
    Institut Jules Bordet Bruxelles, B 1000 Belgium
  • Charles Herbaux
    Department of Hematology Unité GRITA, CHRU Claude Huriez Lille France
  • Franck Morschhauser
    Department of Hematology Unité GRITA, CHRU Claude Huriez Lille France
  • Pauline Brice
    Department of Hematology CHU Paris‐GH St‐Louis Lariboisière F‐Widal ‐ Hôpital Saint‐Louis Paris France
  • Sylvain Garciaz
    Department of Hematology Institut Paoli‐Calmettes Marseille France
  • Cécile Borel
    Department of Hematology Institut universitaire du cancer Toulouse‐ Oncopole Toulouse France
  • Loïc Ysebaert
    Department of Hematology Institut universitaire du cancer Toulouse‐ Oncopole Toulouse France
  • Lucie Obéric
    Department of Hematology Institut universitaire du cancer Toulouse‐ Oncopole Toulouse France
  • Julien Lazarovici
    Department of Hematology Institut Gustave‐Roussy Villejuif France
  • Bénédicte Deau
    Department of Hematology CHU Cochin Paris France
  • Jehan Dupuis
    Department of Hematology CHU Henri Mondor Créteil France
  • Adrien Chauchet
    Department of Hematology CHU Besançon Besançon France
  • Julie Abraham
    Department of Hematology CHU Limoges Limoges France
  • Fontanet Bijou
    Department of Hematology Institut Bergonié Bordeaux France
  • Aspasia Stamatoullas‐Bastard
    Department of Hematology Centre Henri Becquerel Rouen France
  • Jean‐Valère Malfuson
    Department of Hematology hôpital d'instruction des armées Percy Clamart France
  • Camille Golfier
    Department of Hematology Dijon University Hospital Dijon France
  • Camille Laurent
    Anatomy‐pathology Department Institut universitaire du cancer Toulouse‐Oncopole Toulouse France
  • Sarah Pericart
    Anatomy‐pathology Department Institut universitaire du cancer Toulouse‐Oncopole Toulouse France
  • Alexandra Traverse‐Glehen
    Anatomy‐pathology Department Centre Hospitalier Lyon Sud Pierre‐Bénite France
  • Salim Kanoun
    Institut universitaire du cancer Toulouse‐Oncopole, Unit, FranceNuclear Medecine Toulouse
  • Thomas Filleron
    Clinical trials office, Institut universitaire du cancer Toulouse‐ Oncopole Toulouse France
  • René‐Olivier Casasnovas
    Department of Hematology Dijon University Hospital Dijon France
  • Hervé Ghesquières
    Department of Hematology Centre Hospitalier Lyon Sud Pierre‐Bénite France

説明

<jats:title>Abstract</jats:title><jats:p>Anti‐PD‐1 therapy provides high response rates in Hodgkin lymphoma (HL) patients who have relapsed or are refractory (R/R) to autologous stem cell transplantation (ASCT) and brentuximab vedotin (BV), but median progression free survival (PFS) is only one year. The efficacy of treatment following anti‐PD‐1 is not well known. We retrospectively investigated the efficacy of salvage therapies for unsatisfactory response to anti‐PD‐1 therapy, assessed by PET‐CT according to the Lugano criteria, in 30 R/R HL patients. Patients were highly pretreated before anti‐PD‐1 (70% received ASCT and 93% BV). Unsatisfactory responses to anti‐PD1 therapy were progressive disease (PD) (<jats:italic>n</jats:italic> = 24) and partial response (PR) (<jats:italic>n</jats:italic> = 6). For the 24 PD patients, median anti‐PD‐1 related PFS was 7.5 months (95%CI, 5.7‐11.6); 17 received subsequent CT alone (Group 1) and 7 received CT in addition to anti‐PD‐1 (Group 2). 16/24 patients (67%) obtained an objective response. In the 15 patients treated with the same CT, twelve obtained PR or complete response (CR). In Group 1, there were 7 CR (41%), 3 PR (18%), and 7 PD (41%). In Group 2, there were 4 CR (57%), 2 PR (29%), and 1 SD (14%). No unexpected toxicity was observed. Six patients who achieved response proceeded to allogeneic SCT. With a median follow‐up of 12.1 months (7‐14.7), the median PFS following the initiation of CT was 11 months (95% CI 6.3‐not reached) and the median of overall survival was not reached. These observations in highly pretreated HL patients suggest that anti‐PD‐1 therapy might re‐sensitize tumor cells to CT.</jats:p>

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