Persistent human parvovirus B19 infection in children under maintenance chemotherapy for acute lymphocytic leukemia

J Pediatr Hematol Oncol. 2004 Aug;26(8):497-503. doi: 10.1097/01.mph.0000134463.09543.99.

Abstract

Objective: To report on B19 infection management and chemotherapy schedule consequences in five children treated for acute lymphocytic leukemia (ALL).

Patients and methods: Between May 2001 and February 2002, five patients between 4 and 12 years of age, receiving maintenance chemotherapy for ALL, presented with symptoms suggesting B19 infection (pallor, fatigue, petechiae and pancytopenia in four patients; generalized rash in two patients; acute hepatitis in one patient). Qualitative polymerase chain reaction (PCR) on peripheral blood was used for diagnosis and follow-up of infection; quantitative PCR was used for viral load measurement. Intravenous nonspecific high-dose immunoglobulin therapy was administered until PCR was negative.

Results: Qualitative B19 DNA was found in the peripheral blood of all patients, confirming the infection. Viral load at diagnosis ranged from 10 to 10 particles/mL blood. B19 DNA was detectable in four patients at 45, 21, 40, and 44 weeks, respectively. Chemotherapy was delayed in all patients. No clear benefit of intravenous immunoglobulin was noted.

Conclusions: Infection with B19 is rarely reported in patients with ALL, but it should be suspected when unexplained pancytopenia occurs during chemotherapy. Persistent B19 infection remains a challenge in the management of patients receiving maintenance chemotherapy for ALL, as no specific therapy such as a specific immunoglobulin or vaccine exists. The role of viral load measurement needs to be established in terms of its use in follow-up and evaluation of the therapeutic response.

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Child
  • Child, Preschool
  • DNA, Viral / analysis
  • Erythema Infectiosum / diagnosis
  • Erythema Infectiosum / etiology*
  • Erythema Infectiosum / therapy
  • Female
  • Humans
  • Immunocompromised Host*
  • Immunoglobulins, Intravenous / therapeutic use
  • Male
  • Parvovirus B19, Human / genetics
  • Parvovirus B19, Human / isolation & purification*
  • Polymerase Chain Reaction
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / virology

Substances

  • Antineoplastic Agents
  • DNA, Viral
  • Immunoglobulins, Intravenous