Risk factors for hemorrhagic cystitis after allogeneic hematopoietic stem cell transplantation in a letermovir‐exposed CMV‐free population receiving PTCy

Author:

Galli Eugenio1ORCID,Metafuni Elisabetta1ORCID,Gandi Carlo2ORCID,Limongiello Maria Assunta1ORCID,Giammarco Sabrina1ORCID,Mattozzi Andrea3,Santangelo Rosaria45ORCID,Bacigalupo Andrea13,Sorà Federica13ORCID,Chiusolo Patrizia13ORCID,Sica Simona13ORCID

Affiliation:

1. UOC Ematologia e Trapianto di cellule staminali emopoietiche, Dipartimento di Diagnostica per Immagini, Radioterapia Oncologica ed Ematologia, Fondazione Policlinico Universitario A. Gemelli IRCCS Rome Italy

2. UOC Clinica Urologica, Dipartimento di Scienze Mediche e Chirurgiche Addominali ed Endocrino Metaboliche, Fondazione Policlinico Universitario A. Gemelli IRCCS Rome Italy

3. Sezione di Ematologia, Dipartimento di Scienze Radiologiche ed Ematologiche, Università Cattolica del Sacro Cuore Rome Italy

4. UOC Microbiologia, Dipartimento di scienze di laboratorio e infettivologiche Fondazione Policlinico Universitario A. Gemelli IRCCS Rome Italy

5. Sezione di Microbiologia e Virologia, Dipartimento di Scienze biotecnologiche di base, cliniche intensivologiche e perioperatorie, Università Cattolica del Sacro Cuore Rome Italy

Abstract

AbstractHemorrhagic cystitis (HC) is a highly impacting complication in allogeneic hematopoietic stem cell transplantation (HSCT), occurring in 12%–37% of patients. The impact of transplant‐ and patient‐specific variables has been described, with a possible role for JCV and BKV, which may be cooperating with cytomegalovirus (CMV). Here, we analyze 134 letermovir‐exposed, CMV‐free patients, treated with the same cyclophosphamide‐based graft‐versus‐host disease (GVHD) prophylaxis, describing risk factors for HC. The overall incidence of HC was 23%. Patients with HLA mismatched transplant, higher comorbidity score, and receiving three alkylating agents with TBF (thiotepa, busulfan, and fludarabine) conditioning regimen had a higher risk of HC in multivariate analysis (OR: 4.48, 6.32, and 1.32, respectively). A HC‐score including male gender, TBF conditioning, and HLA‐mismatch stratifies the risk of HC in the first 100 days after HSCT. The role of BKV and JCV was not highly impacting in those patients, suggesting a possible synergistic effect between CMV and JCV in causing HC. HC can be interpreted as the combination of patient‐related factors, chemotherapy‐related toxicities—especially due to alkylating agents—and immunological elements.

Publisher

Wiley

Subject

Hematology,General Medicine

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