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Generation of Multivirus-specific T Cells to Prevent/treat Viral Infections after Allogeneic Hematopoietic Stem Cell Transplant
Published on: May 27, 2011
Valganciclovir for CMV Prophylaxis After PTCy-Based Allogeneic Hematopoietic Cell Transplantation
Nermen Tawfik1, Ashleigh P Scott2, Catelyn Cashion3
1Clinical Haematology, Alfred Health, Melbourne, Victoria, Australia.
Valganciclovir prophylaxis effectively prevented clinically significant Cytomegalovirus infection (csCMVi) in patients undergoing allogeneic hematopoietic cell transplantation (alloHCT) with post-transplant cyclophosphamide (PTCy) based GVHD prophylaxis. Delayed count recovery was the main barrier to initiating prophylaxis, particularly in haploidentical transplants.
Area of Science:
- Hematopoietic Stem Cell Transplantation
- Infectious Disease Management
- Immunocompromised Patient Care
Background:
- Cytomegalovirus (CMV) reactivation poses a significant risk post-allogeneic hematopoietic cell transplantation (alloHCT), especially with post-transplant cyclophosphamide (PTCy) based prophylaxis.
- Letermovir is effective but costly, necessitating affordable alternatives for CMV infection (csCMVi) prevention.
- Limited data exists on valganciclovir's utility for CMV prophylaxis in PTCy-based alloHCT.
Purpose of the Study:
- To assess the feasibility and effectiveness of using valganciclovir for CMV prophylaxis in adults undergoing alloHCT with PTCy-based GVHD prophylaxis.
- To compare valganciclovir prophylaxis outcomes against a pre-emptive CMV strategy.
Main Methods:
- Retrospective analysis of 244 adults undergoing alloHCT, focusing on CMV-seropositive recipients receiving PTCy-based GVHD prophylaxis and intended valganciclovir prophylaxis.
- Valganciclovir (900 mg daily) initiated post-engraftment until day +100; weekly CMV PCR monitoring was performed.
- Outcomes compared with a contemporaneous cohort using pre-emptive CMV therapy.
Main Results:
- 124 patients met inclusion criteria; 86 (69%) initiated valganciclovir prophylaxis, with delayed count recovery being the primary reason for non-initiation (31%).
- Initiation was less frequent in haploidentical versus matched donor alloHCT (56% vs 80%).
- Valganciclovir prophylaxis significantly reduced csCMVi incidence (13% vs 63% in non-prophylaxis group; aHR 0.09). Haploidentical transplants increased csCMVi risk (aHR 4.5).
Conclusions:
- Valganciclovir is a cost-effective option for preventing csCMVi in CMV-seropositive PTCy-based alloHCT recipients.
- Delayed hematopoietic recovery is a key challenge for prophylaxis initiation, particularly in haploidentical transplantation.
- Valganciclovir prophylaxis demonstrates significant efficacy compared to pre-emptive strategies.
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