|
|
Previous Article | Table of Contents | Next Article 
Blood, 1 August 2002, Vol. 100, No. 3, pp. 1104-1105
CORRESPONDENCE
To the editor:
Leukoencephalopathy and papovavirus infection after treatment
with chemotherapy and anti-CD20 monoclonal antibody
Goldberg et al1 recently reported a few unusual
viral infections after high-dose chemotherapy with autologous blood
stem cell rescue associated to peritransplantation rituximab. In their paper, the authors describe 4 cases of either JC papovavirus or cytomegaloviral (CMV) infections after chemotherapy and rituximab administration. Although a direct correlation with anti-CD20 therapy remains to be demonstrated, concerns were expressed about the clustering of these rituximab-treated cases in view of the broad and
increasing use of the anti-CD20 monoclonal antibody in non-Hodgkin lymphoma (NHL) treatment. We report here one additional case of progressive multifocal leukoencephalopathy associated with
peritransplantation rituximab in a heavily pretreated lymphoma patient. A 56-year-old man had a clinical history of Hodgkin
disease, nodular sclerosis, diagnosed in 1974. He had stage II E A
disease and was treated with a mechlorethamine, vincristine,
procarbazine, and prednisone (MOPP) regimen for 6 cycles,
subtotal-nodal irradiation, and splenectomy, achieving a complete
clinical remission. In October 1998 he was diagnosed as having diffuse
large cell NHL, stage IV A. At that time, slides of both diagnoses were
evaluated, confirming the 2 different diseases. Between November 1998 and July 1999 he received cyclophosphamide, hydroxydaunomycin,
vincristine, and prednisone (CHO[P]) for 6 cycles, and then mesna,
ifosfamide, mitoxantrone, and etoposide (MINE) for 6 cycles,
achieving a complete remission. He was admitted in our department 1 year later with progressive disease, presenting with enlarged cervical
nodes and pulmonary, bone, and bone marrow disease localizations.
Serological tests for hepatitis B virus (HBV), hepatitis C
virus (HCV), HIV 1/2, CMV, Epstein-Barr virus (EBV), herpes zoster
virus (HZV), herpes simplex virus (HSV) 1 and 2, and Toxotest were
positive, except for HIV 1/2, indicating past exposure to the
corresponding pathogen. Active infection by HCV-RNA genotype 2a/2c was
also demonstrated (Table 1). The patient
underwent salvage high-dose sequential chemotherapy, including 6 overall doses of rituximab at 375 mg/m2 (R-HDS).2
The treatment lasted from July 2000 to January 2001 and
comprised dexamethasone, cytarabine, and cisplatin ([D]HAP) for 3 cycles cyclophosphamide 5.6 g/m2 plus 2 rituximab 375 mg/m2
infusions before stem cell harvest cytosine arabinoside 1.5 g/m2
every 12 hours for 6 days stem cell rescue and subsequent stem cell
harvest, both preceded by rituximab 375 mg/m2 infusion etoposide
2.4 g/m2 plus cisplatin 100 mg/m2 plus stem cell rescue high-dose BCNU, etoposide, cytosine arabinoside, and melphalan (HD-BEAM) plus stem cell rescue. Two additional weekly doses of rituximab, 375 mg/m2, ended the treatment. Stem cells harvested after
chemotherapy with cytosine arabinoside plus rituximab were negative for
lymphoma cell contamination (as assessed by polymerase chain reaction
[PCR] using a patient's specific primer) and were used to support
the final myeloablative BEAM regimen. The patient achieved a complete
clinical and molecular remission. The treatment was well tolerated, and
the patient was discharged in good clinical conditions. Consolidation
radiotherapy (30 Gy) on sacral region was given on an outpatient
setting. On day +20 from the end of treatment, the patient developed an
asymptomatic CMV infection, documented by a positive pp65 assay (3 and
4 positive nuclei/200 000 cells), and was treated with gancyclovir in
our outpatient department until negativization of the assay in 2 consecutive controls. Seven months later, the patient presented with
progressive pulmonary and bone disease, confirmed by computed
tomography (CT)-scan as well as by histological and immunophenotypic
analysis of the pulmonary localizations. At that time, complete
serological tests were repeated, confirming the presence of HCV-RNA.
The patient was treated with vinorelbine (25 mg/m2) in association with
rituximab, 375 mg/m2, for 7 overall courses, achieving a partial
response. In February 2002, soon after the end of the last dose of
rituximab, the patient experienced mental status changes and ataxia. A
brain CT scan revealed multiple hypodense lesions, while magnetic
resonance imaging (MRI) showed areas of white matter disease consistent with a demyelinating process. A cerebrospinal fluid examination was
positive for BK papovavirus DNA. Despite treatment with cidofovir, the
patient died in April 2002.
The present report adds to the list of unusual viral infections in
patients treated with high-dose chemotherapy and rituximab. Of note,
the BK papovavirus isolated here causes leukoencephalopathy with
10-fold less frequency3 compared with the JC papovavirus responsible for the 2 cases of progressive multifocal
leukoencephalopathy reported by Goldberg et al.1 The
contributory role of rituximab, if any, is only tentative and far from
being proved.4,5 However, this additional case further
strengthens the need for an accurate surveillance and reporting of rare
viral infections that might occur in heavily pretreated lymphoma
patients receiving peritransplantation rituximab.
Paola Matteucci, Michele Magni, Massimo Di Nicola, Carmelo Carlo-Stella, Caterina Uberti, and Alessandro M. Gianni
Correspondence: Paola Matteucci, Istituto Nazionale Tumori,
Medical Oncology C, Milan, Italy
References
1.
Goldberg SL, Pecora AL, Alter RS, et al.
Unusual viral infections (progressive multifocal leukoencephalopathy and cytomegalovirus disease) after high-dose chemotherapy with autologous blood stem cell rescue and peritransplantation rituximab.
Blood.
2002;99:1486-1488[Abstract/Free Full Text].
2.
Magni M, Di Nicola M, Devizzi L, et al.
Successful in vivo purging of CD34containing peripheral blood harvests in mantle cell and indolent lymphoma: evidence for a role of both chemotherapy and rituximab infusion.
Blood.
2000;96:864-869[Abstract/Free Full Text].
3.
Vago L, Cinque P, Sala E, et al.
JCV-DNA and BKV-DNA in the CNS tissue and CSF of AIDS patients and normal subjects: study of 41 cases and review of the literature.
J Acquir Immune Defic Syndr Hum Retrovirol.
1996;12:139-146[Medline]
[Order article via Infotrieve].
4.
Horwitz SM, Breslin S, Negrin RS, et al.
Adjuvant rituximab after autologous peripheral blood stem cell transplant results in delayed immune reconstitution with increase in infectious complications [abstract].
Blood.
2000;96:707a.
5.
Flohr T, Hess GR, Kreiter S, Meyer RG, Huber C, Derigs G.
Immune reconstitution after autologous CD34-positive selected peripheral blood stem cell transplantation combined with rituximab for refractory B-cell non-Hodgkin's lymphoma [abstract].
Blood.
2000;96:709a.

CiteULike Connotea Del.icio.us Digg Reddit Technorati What's this?
Related Articles in Blood Online:
-
Unusual viral infections (progressive multifocal leukoencephalopathy and cytomegalovirus disease) after high-dose chemotherapy with autologous blood stem cell rescue and peritransplantation rituximab
- Stuart L. Goldberg, Andrew L. Pecora, Robert S. Alter, Mark S. Kroll, Scott D. Rowley, Stanley E. Waintraub, Kavita Imrit, and Robert A. Preti
Blood 2002 99: 1486-1488.
[Abstract]
[Full Text]
[PDF]
-
High frequency of point mutations clustered within the adenosine triphosphate-binding region of BCR/ABL in patients with chronic myeloid leukemia or Ph-positive acute lymphoblastic leukemia who develop imatinib (STI571) resistance
- Susan Branford, Zbigniew Rudzki, Sonya Walsh, Andrew Grigg, Chris Arthur, Kerry Taylor, Richard Herrmann, Kevin P. Lynch, and Timothy P. Hughes
Blood 2002 99: 3472-3475.
[Abstract]
[Full Text]
[PDF]
This article has been cited by other articles:

|
 |

|
 |
 
B. Schless, S. Yildirim, D. Beha, F. Keller, and D. Czock
Rituximab in two cases of Goodpasture's syndrome
NDT Plus,
June 1, 2009;
2(3):
225 - 227.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. Focosi, R. E. Kast, F. Maggi, L. Ceccherini-Nelli, and M. Petrini
Lymphotropic Polyomavirus and Progressive Multifocal Leukoencephalopathy
J. Clin. Microbiol.,
January 1, 2009;
47(1):
284 - 284.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A Podolskaya, M Stadermann, C Pilkington, S D Marks, and K Tullus
B cell depletion therapy for 19 patients with refractory systemic lupus erythematosus
Arch. Dis. Child.,
May 1, 2008;
93(5):
401 - 406.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Rey, N. Belmecheri, N. Bouayed, V. Ivanov, D. Coso, J.A. Gastaut, and R. Bouabdallah
JC papovavirus leukoencephalopathy after first line treatment with CHOP and rituximab
Haematologica,
October 1, 2007;
92(10):
e101 - e101.
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J R Berger
Natalizumab and progressive multifocal leucoencephalopathy
Ann Rheum Dis,
November 1, 2006;
65(suppl_3):
iii48 - iii53.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Sandherr, H. Einsele, H. Hebart, C. Kahl, W. Kern, M. Kiehl, G. Massenkeil, O. Penack, X. Schiel, S. Schuettrumpf, et al.
Antiviral prophylaxis in patients with haematological malignancies and solid tumours: Guidelines of the Infectious Diseases Working Party (AGIHO) of the German Society for Hematology and Oncology (DGHO)
Ann. Onc.,
July 1, 2006;
17(7):
1051 - 1059.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|
|