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Erschienen in: Annals of Hematology 8/2016

25.05.2016 | Original Article

Cytomegalovirus infection in autologous stem cell transplant recipients in the era of rituximab

verfasst von: Tania Jain, Jisha John, Aditya Kotecha, Abhinav Deol, Tanaz Saliminia, Sanjay Revankar, Pranatharthi Chandrasekar

Erschienen in: Annals of Hematology | Ausgabe 8/2016

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Abstract

The incidence of cytomegalovirus (CMV) reactivation/disease after autologous stem cell transplant (ASCT) is much lower than that after allogeneic stem cell transplantation. With the recent use of rituximab during cancer chemotherapy or conditioning regimens prior to transplantation, there has been an increasing concern of opportunistic infections including CMV. In the present study, we reviewed the patients undergoing ASCT from December 2007 to December 2013 to identify those developing CMV reactivation/disease. Out of the 978 patients who underwent ASCT at the Karmanos Cancer Institute, 239 patients were tested for symptomatic CMV reactivation based on clinical suspicion. Of the tested patients, 7/239 (2.9 %) were documented to have CMV reactivation within 90 days of ASCT. The median time to develop CMV viremia was 32 days from transplantation. Of the 239 patients tested, CMV viremia was detected in 3 out of 72 patients who received rituximab as compared to 4 out of 167 patients who did not. Three of these seven viremic patients were treated with anti-viral drugs; viremia resolved in all patients at a median of 24 days. Three patients were found to develop other bacterial and/or fungal infections following CMV viremia. Two of the seven patients died during 1-year follow-up, due to primary disease progression or Candida sepsis. None of the patients developed proven tissue-invasive CMV disease. The study did not evaluate the incidence of asymptomatic CMV infection/reactivation. Despite prior publications based on limited data, rituximab does not appear to contribute to an increased frequency of symptomatic CMV reactivation following ASCT.
Literatur
1.
Zurück zum Zitat Fassas AB, Bolanos-Meade J, Buddharaju LN et al (2001) Cytomegalovirus infection and non-neutropenic fever after autologous stem cell transplantation: high rates of reactivation in patients with multiple myeloma and lymphoma. Br J Haematol 112:237–241CrossRefPubMed Fassas AB, Bolanos-Meade J, Buddharaju LN et al (2001) Cytomegalovirus infection and non-neutropenic fever after autologous stem cell transplantation: high rates of reactivation in patients with multiple myeloma and lymphoma. Br J Haematol 112:237–241CrossRefPubMed
2.
Zurück zum Zitat Boeckh M, Stevens-Ayers T, Bowden RA (1996) Cytomegalovirus pp 65 antigenemia after autologous marrow and peripheral blood stem cell transplantation. J Infect Dis 174:907–912CrossRefPubMed Boeckh M, Stevens-Ayers T, Bowden RA (1996) Cytomegalovirus pp 65 antigenemia after autologous marrow and peripheral blood stem cell transplantation. J Infect Dis 174:907–912CrossRefPubMed
3.
Zurück zum Zitat Konoplev S, Champlin RE, Giralt S et al (2001) Cytomegalovirus pneumonia in adult autologous blood and marrow transplant recipients. Bone Marrow Transplant 27:877–881CrossRefPubMed Konoplev S, Champlin RE, Giralt S et al (2001) Cytomegalovirus pneumonia in adult autologous blood and marrow transplant recipients. Bone Marrow Transplant 27:877–881CrossRefPubMed
4.
Zurück zum Zitat Bilgrami S, Aslanzadeh J, Feingold JM et al (1999) Cytomegalovirus viremia, viruria and disease after autologous peripheral blood stem cell transplantation: no need for surveillance. Bone Marrow Transplant 24:69–73CrossRefPubMed Bilgrami S, Aslanzadeh J, Feingold JM et al (1999) Cytomegalovirus viremia, viruria and disease after autologous peripheral blood stem cell transplantation: no need for surveillance. Bone Marrow Transplant 24:69–73CrossRefPubMed
5.
Zurück zum Zitat Holmberg LA, Boeckh M, Hooper H et al (1999) Increased incidence of cytomegalovirus disease after autologous CD34-selected peripheral blood stem cell transplantation. Blood 94:4029–4035PubMed Holmberg LA, Boeckh M, Hooper H et al (1999) Increased incidence of cytomegalovirus disease after autologous CD34-selected peripheral blood stem cell transplantation. Blood 94:4029–4035PubMed
6.
Zurück zum Zitat Rossini F, Terruzzi E, Cammarota S et al (2005) Cytomegalovirus infection after autologous stem cell transplantation: incidence and outcome in a group of patients undergoing a surveillance program. Transpl Infect Dis Off J Transplant Soc 7:122–125CrossRef Rossini F, Terruzzi E, Cammarota S et al (2005) Cytomegalovirus infection after autologous stem cell transplantation: incidence and outcome in a group of patients undergoing a surveillance program. Transpl Infect Dis Off J Transplant Soc 7:122–125CrossRef
7.
Zurück zum Zitat Coiffier B, Lepage E, Briere J et al (2002) CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. N Engl J Med 346:235–242CrossRefPubMed Coiffier B, Lepage E, Briere J et al (2002) CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large-B-cell lymphoma. N Engl J Med 346:235–242CrossRefPubMed
8.
Zurück zum Zitat Fenske TS, Hari PN, Carreras J et al (2009) Impact of pre-transplant rituximab on survival after autologous hematopoietic stem cell transplantation for diffuse large B cell lymphoma. Biol Blood Marrow Transplant J Am Soc Blood Marrow Transplant 15:1455–1464CrossRef Fenske TS, Hari PN, Carreras J et al (2009) Impact of pre-transplant rituximab on survival after autologous hematopoietic stem cell transplantation for diffuse large B cell lymphoma. Biol Blood Marrow Transplant J Am Soc Blood Marrow Transplant 15:1455–1464CrossRef
9.
Zurück zum Zitat Goldberg SL, Pecora AL, Alter RS et al (2002) Unusual viral infections (progressive multifocal leukoencephalopathy and cytomegalovirus disease) after high-dose chemotherapy with autologous blood stem cell rescue and peritransplantation rituximab. Blood 99:1486–1488CrossRefPubMed Goldberg SL, Pecora AL, Alter RS et al (2002) Unusual viral infections (progressive multifocal leukoencephalopathy and cytomegalovirus disease) after high-dose chemotherapy with autologous blood stem cell rescue and peritransplantation rituximab. Blood 99:1486–1488CrossRefPubMed
10.
Zurück zum Zitat Suzan F, Ammor M, Ribrag V (2001) Fatal reactivation of cytomegalovirus infection after use of rituximab for a post-transplantation lymphoproliferative disorder. N Engl J Med 345:1000CrossRefPubMed Suzan F, Ammor M, Ribrag V (2001) Fatal reactivation of cytomegalovirus infection after use of rituximab for a post-transplantation lymphoproliferative disorder. N Engl J Med 345:1000CrossRefPubMed
11.
Zurück zum Zitat Lee MY, Chiou TJ, Hsiao LT et al (2008) Rituximab therapy increased post-transplant cytomegalovirus complications in non-Hodgkin’s lymphoma patients receiving autologous hematopoietic stem cell transplantation. Ann Hematol 87:285–289CrossRefPubMed Lee MY, Chiou TJ, Hsiao LT et al (2008) Rituximab therapy increased post-transplant cytomegalovirus complications in non-Hodgkin’s lymphoma patients receiving autologous hematopoietic stem cell transplantation. Ann Hematol 87:285–289CrossRefPubMed
12.
Zurück zum Zitat Kelesidis T, Daikos G, Boumpas D, Tsiodras S (2011) Does rituximab increase the incidence of infectious complications? A narrative review. Int J Infect Dis IJID Off Publ Int Soc Infect Dis 15:e2–e16 Kelesidis T, Daikos G, Boumpas D, Tsiodras S (2011) Does rituximab increase the incidence of infectious complications? A narrative review. Int J Infect Dis IJID Off Publ Int Soc Infect Dis 15:e2–e16
13.
Zurück zum Zitat Al-Rawi O, Abdel-Rahman F, Al-Najjar R et al (2015) Cytomegalovirus reactivation in adult recipients of autologous stem cell transplantation: a single center experience. Mediterr J Hematol Infect Dis 7:e2015049CrossRefPubMedPubMedCentral Al-Rawi O, Abdel-Rahman F, Al-Najjar R et al (2015) Cytomegalovirus reactivation in adult recipients of autologous stem cell transplantation: a single center experience. Mediterr J Hematol Infect Dis 7:e2015049CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Marchesi F, Mengarelli A, Giannotti F et al (2014) High incidence of post-transplant cytomegalovirus reactivations in myeloma patients undergoing autologous stem cell transplantation after treatment with bortezomib-based regimens: a survey from the Rome Transplant Network. Transpl Infect Dis Off J Transplant Soc 16:158–164CrossRef Marchesi F, Mengarelli A, Giannotti F et al (2014) High incidence of post-transplant cytomegalovirus reactivations in myeloma patients undergoing autologous stem cell transplantation after treatment with bortezomib-based regimens: a survey from the Rome Transplant Network. Transpl Infect Dis Off J Transplant Soc 16:158–164CrossRef
15.
Zurück zum Zitat Kim JH, Goulston C, Sanders S et al (2012) Cytomegalovirus reactivation following autologous peripheral blood stem cell transplantation for multiple myeloma in the era of novel chemotherapeutics and tandem transplantation. Biol Blood Marrow Transplant J Am Soc Blood Marrow Transplant 18:1753–1758CrossRef Kim JH, Goulston C, Sanders S et al (2012) Cytomegalovirus reactivation following autologous peripheral blood stem cell transplantation for multiple myeloma in the era of novel chemotherapeutics and tandem transplantation. Biol Blood Marrow Transplant J Am Soc Blood Marrow Transplant 18:1753–1758CrossRef
16.
Zurück zum Zitat Marchesi F, Pimpinelli F, Dessanti ML et al (2014) Evaluation of risk of symptomatic cytomegalovirus reactivation in myeloma patients treated with tandem autologous stem cell transplantation and novel agents: a single-institution study. Transpl Infect Dis Off J Transplant Soc 16:1032–1038CrossRef Marchesi F, Pimpinelli F, Dessanti ML et al (2014) Evaluation of risk of symptomatic cytomegalovirus reactivation in myeloma patients treated with tandem autologous stem cell transplantation and novel agents: a single-institution study. Transpl Infect Dis Off J Transplant Soc 16:1032–1038CrossRef
Metadaten
Titel
Cytomegalovirus infection in autologous stem cell transplant recipients in the era of rituximab
verfasst von
Tania Jain
Jisha John
Aditya Kotecha
Abhinav Deol
Tanaz Saliminia
Sanjay Revankar
Pranatharthi Chandrasekar
Publikationsdatum
25.05.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
Annals of Hematology / Ausgabe 8/2016
Print ISSN: 0939-5555
Elektronische ISSN: 1432-0584
DOI
https://doi.org/10.1007/s00277-016-2700-4

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