Unmet Clinical Needs in the Management of Idiopathic Multicentric Castleman Disease: A Consensus-based Position Paper From an ad hoc Expert Panel

Author:

Zinzani Pier Luigi12,Paulli Marco3,Arcaini Luca45,Della Torre Emanuel67,Ferrero Simone89,Figuera Amalia10,Frigeri Ferdinando11,Martelli Maurizio12,Sabattini Elena13,Scarpa Riccardo1415,Barosi Giovanni16

Affiliation:

1. IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia “Seràgnoli,” Bologna, Italy

2. Dipartimento di Medicina Specialistica, Diagnostica e Sperimentale, Università di Bologna, Italy

3. Unit of Anatomic Pathology, Department of Molecular Medicine, University of Pavia, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy

4. Department of Molecular Medicine, University of Pavia, Italy

5. Division of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy

6. Università Vita-Salute San Raffaele, IRCCS San Raffaele Scientific Institute, Milan, Italy

7. Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Scientific Institute, Milan, Italy

8. Department of Molecular Biotechnologies and Health Sciences, Hematology Division, University of Torino, Italy

9. Hematology Division, AOU “Città della Salute e della Scienza di Torino,” Torino, Italy

10. Division of Hematology, AOU Policlinico “G. Rodolico-S. Marco,” Catania, Italy

11. UOC Ematologia a Indirizzo Oncologico, AORN “Sant’Anna e San Sebastiano,” Caserta, Italy

12. Hematology Unit, Department of Translational and Precision Medicine, “Sapienza” University, Rome, Italy

13. Hemathopathology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Policinico di S. Orsola, Bologna, Italy

14. Department of Medicine-DIMED, University of Padova, Padua, Italy

15. Internal Medicine I, Ca’ Foncello Hospital, AULSS2 Marca Trevigiana, Treviso, Italy

16. Center for the Study of Myelofibrosis, IRCCS Policlinico S. Matteo Foundation, Pavia, Italy

Abstract

Castleman disease describes a group of heterogeneous clinicopathological disorders now included in the tumor-like lesions with B-cell predominance of the World Health Organization classification. Managing idiopathic multicentric Castleman disease (iMCD) is challenging, because few systematic studies or comparative randomized clinical trials have been conducted. International, consensus evidence-based guidelines for iMCD were published in 2018, but gaps in the therapeutic options for difficult-to-treat patients, who do not respond to siltuximab and other conventional therapies, still exist. This article presents the results of group discussion among an ad hoc constituted Panel of Italian experts to identify and address unmet clinical needs (UCNs) in managing iMCD. Recommendations on the appropriateness of clinical decisions and proposals for new research concerning the identified UCNs were issued through formalized multiple-step procedures after a comprehensive analysis of the scientific literature. The following key UCNs were addressed: strengthening the diagnostic certainty in iMCD patients before planning first-line therapy; management of siltuximab therapy; choice and management of immune-modulating, or chemotherapy agents in patients resistant/intolerant to siltuximab therapy. While most of the conclusions reached by the Panel are consistent with the existing guidelines, some alternative therapeutic options were stressed, and the discussion contributed to bringing forth the issues that need further investigation. Hopefully, this comprehensive overview will improve the practice of iMCD and inform the design and implementation of new studies in the field.

Publisher

Wiley

Subject

Hematology

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