Filling the Gap: The Immune Therapeutic Armamentarium for Relapsed/Refractory Hodgkin Lymphoma.

CAR-T cells Hodgkin Lymphoma immune escape immunotherapy mechanisms of resistance

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
06 Nov 2022
Historique:
received: 20 09 2022
revised: 30 10 2022
accepted: 02 11 2022
entrez: 11 11 2022
pubmed: 12 11 2022
medline: 12 11 2022
Statut: epublish

Résumé

Despite years of clinical progress which made Hodgkin lymphoma (HL) one of the most curable malignancies with conventional chemotherapy, refractoriness and recurrence may still affect up to 20-30% of patients. The revolution brought by the advent of immunotherapy in all kinds of neoplastic disorders is more than evident in this disease because anti-CD30 antibodies and checkpoint inhibitors have been able to rescue patients previously remaining without therapeutic options. Autologous hematopoietic cell transplantation still represents a significant step in the treatment algorithm for chemosensitive HL; however, the possibility to induce complete responses after allogeneic transplant procedures in patients receiving reduced-intensity conditioning regimens informs on its sensitivity to immunological control. Furthermore, the investigational application of adoptive T cell transfer therapies paves the way for future indications in this setting. Here, we seek to provide a fresh and up-to-date overview of the new immunotherapeutic agents dominating the scene of relapsed/refractory HL. In this optic, we will also review all the potential molecular mechanisms of tumor resistance, theoretically responsible for treatment failures, and we will discuss the place of allogeneic stem cell transplantation in the era of novel therapies.

Identifiants

pubmed: 36362802
pii: jcm11216574
doi: 10.3390/jcm11216574
pmc: PMC9656939
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Esther Hazane Leroyer (E)

Service d'Hématologie Clinique, Hôpital Brabois, Centre Hospitalier Regional Universitaire de Nancy, 54500 Vandoeuvre les Nancy, France.

Caroline Ziegler (C)

Service d'Hématologie Clinique, Hôpital Brabois, Centre Hospitalier Regional Universitaire de Nancy, 54500 Vandoeuvre les Nancy, France.

Charline Moulin (C)

Service d'Hématologie Clinique, Hôpital Brabois, Centre Hospitalier Regional Universitaire de Nancy, 54500 Vandoeuvre les Nancy, France.

Arnaud Campidelli (A)

Service d'Hématologie Clinique, Hôpital Brabois, Centre Hospitalier Regional Universitaire de Nancy, 54500 Vandoeuvre les Nancy, France.

Caroline Jacquet (C)

Service d'Hématologie Clinique, Hôpital Brabois, Centre Hospitalier Regional Universitaire de Nancy, 54500 Vandoeuvre les Nancy, France.

Marie Thérèse Rubio (MT)

Service d'Hématologie Clinique, Hôpital Brabois, Centre Hospitalier Regional Universitaire de Nancy, 54500 Vandoeuvre les Nancy, France.
CNRS UMR 7365 IMoPa, Biopole de l'Université de Lorraine, 54505 Vandoeuvre les Nancy, France.

Pierre Feugier (P)

Service d'Hématologie Clinique, Hôpital Brabois, Centre Hospitalier Regional Universitaire de Nancy, 54500 Vandoeuvre les Nancy, France.
INSERM U1256 Nutrition-Génétique et Exposition aux Risques Environnementaux (NGERE), Université de Lorraine, 54506 Vandoeuvre les Nancy, France.

Simona Pagliuca (S)

Service d'Hématologie Clinique, Hôpital Brabois, Centre Hospitalier Regional Universitaire de Nancy, 54500 Vandoeuvre les Nancy, France.
CNRS UMR 7365 IMoPa, Biopole de l'Université de Lorraine, 54505 Vandoeuvre les Nancy, France.

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