Outcomes of patients with relapsed or refractory primary mediastinal B‐cell lymphoma treated with anti‐CD19 CAR‐T cells: CARTHYM, a study from the French national DESCAR‐T registry
Jean Galtier,
Charles Mesguich,
Pierre Sesques,
Vivien Dupont,
Emmanuel Bachy,
Roberta Di Blasi,
Catherine Thieblemont,
Thomas Gastinne,
Guillaume Cartron,
Gabriel Brisou,
François‐Xavier Gros,
Justine Decroocq,
Franck Morschhauser,
Marie‐Thérèse Rubio,
Laurianne Drieu La Rochelle,
Fabien Le Bras,
Sylvain Carras,
Adrien Chauchet,
Jacques‐Olivier Bay,
Magalie Joris,
Mickael Loschi,
Aline Tanguy‐Schmidt,
Alexandra Marquet,
Vincent Camus,
Steven Le Gouill,
Roch Houot,
Krimo Bouabdallah
Affiliations
Jean Galtier
CHU de Bordeaux, Service d'hématologie Clinique et de thérapie cellulaire Bordeaux France
Charles Mesguich
CHU de Bordeaux, Service de médecine nucléaire Bordeaux France
Pierre Sesques
Hospices civils de Lyon, Service d'hématologie clinique Lyon France
Vivien Dupont
LYSARC, Département de biostatistiques Lyon France
Emmanuel Bachy
Hospices civils de Lyon, Service d'hématologie clinique Lyon France
Roberta Di Blasi
Hôpital Saint‐Louis, Service d'hématologie clinique, Assistance publique ‐ Hôpitaux de Paris Paris France
Catherine Thieblemont
Hôpital Saint‐Louis, Service d'hématologie clinique, Assistance publique ‐ Hôpitaux de Paris Paris France
Thomas Gastinne
CHU de Nantes, Service d'hématologie clinique Nantes France
Guillaume Cartron
CHU de Montpellier, Service d'hématologie clinique Montpellier France
Gabriel Brisou
Institut Paoli Calmettes, Service d'hématologie clinique Marseille France
François‐Xavier Gros
CHU de Bordeaux, Service d'hématologie Clinique et de thérapie cellulaire Bordeaux France
Justine Decroocq
Hôpital Cochin, Service d'hématologie clinique, Asistance publique ‐ Hôpitaux de Paris Paris France
Franck Morschhauser
CHRU de Lille, Service d'hématologie clinique Lille France
Marie‐Thérèse Rubio
CHRU de Nancy, Service d'hématologie clinique Nancy France
Laurianne Drieu La Rochelle
CHU de Tours, Service d'hématologie clinique Tours France
Fabien Le Bras
Hôpital Henri Mondor, Service d'hématologie clinique, Assistance publique ‐ Hôpitaux de Paris Paris France
Sylvain Carras
CHU de Grenoble, Service d'hématologie clinique Grenoble France
Adrien Chauchet
CHU de Besançon, Service d'hématologie clinique Bensaçon France
Jacques‐Olivier Bay
CHU de Clermont‐Ferrand, Service d'hématologie clinique Clermont‐Ferrand France
Magalie Joris
CHU d'Amiens, Service d'hématologie clinique Amiens France
Mickael Loschi
CHU de Nice, Service d'hématologie clinique Nice France
Aline Tanguy‐Schmidt
CHU d'Angers, Service d'hématologie clinique Angers France
Alexandra Marquet
LYSARC Lyon France
Vincent Camus
Département d'Hématologie Centre Henri Becquerel Rouen France
Steven Le Gouill
Institut Curie, Service d'hématologie clinique Paris France
Roch Houot
CHU de Rennes, Service d'hématologie clinique Rennes France
Krimo Bouabdallah
CHU de Bordeaux, Service d'hématologie Clinique et de thérapie cellulaire Bordeaux France
ABSTRACT Primary mediastinal B‐cell lymphoma (PMBL) is often cured with dose‐dense anthracycline‐based regimens but the prognosis at relapse or progression remains poor. While anti‐CD19 CAR‐T cell therapy has dramatically improved outcomes in relapsed or refractory large B‐cell lymphoma, far less is known about their efficacy in PMBL. Using the systematic record of all patients treated with CAR‐T cells prospectively included in the DESCAR‐T registry in France, along with centrally reviewed positon‐emission tomography (PET) imaging, we describe the outcomes and key determinants of treatment success in PMBL patients treated over a 6‐year period. Among 82 patients infused in the registry we observed a best complete response (CR) rate, 2‐year progression‐free survival (PFS), and 2‐year overall survival (OS) of 68.1%, 57.4%, and 73.8%, respectively. Outcomes were even better for the 62 patients infused with axicabtagene ciloleucel, with best CR rate, 2‐year PFS, and 2‐year OS reaching 74.5%, 70.4%, and 86.9%, respectively. Achieving a Deauville score of 1–4 or a ΔSUVmax reduction of more than 24% at the 1‐month evaluation was associated with excellent outcomes, whereas increased total metabolic tumor volume baseline PET increased the risk of treatment failure. Surprisingly, neither the response to bridging therapy nor the type of bridging therapy (chemotherapy versus immune checkpoint inhibitors) were associated with long‐term outcomes. In conclusion, this study confirms that anti‐CD19 CAR‐T cells as a valid standard‐of‐care for relapsed and refractory PMBL and highlights key determinants of treatment success.