A prospective study of a long-term follow-up of an observation program for neuroblastoma detected by mass screening

Mio Tanaka1, Hisato Kigasawa, Keisuke Kato

  • 1Division of Pathology, Kanagawa Children's Medical Center, Minami-ku, Yokohama, Japan. mio@zc4.so-net.ne.jp

Pediatric Blood & Cancer
|January 6, 2010
PubMed

Insights

Over 70% of infants with neuroblastoma (NBL) detected via mass screening (MS6M) could be safely observed without surgery. This study evaluated the usefulness of an NBL observation program for selected screened patients.

Area of Science:

  • Pediatric Oncology
  • Cancer Screening
  • Clinical Research

Background:

  • A nationwide mass screening for neuroblastoma (NBL) in 6-month-old infants (MS6M) was conducted in Japan from 1985 to 2003.
  • Most detected NBL tumors exhibited favorable biological features, leading to the establishment of an observation program in 1993 for selected patients.

Purpose of the Study:

  • To evaluate the clinicopathological findings and current status of patients enrolled in the NBL observation program.
  • To assess the usefulness of the observation strategy for managing NBL detected through mass screening.

Main Methods:

  • 53 out of 101 NBL patients detected by MS6M were enrolled in the observation program between 1993 and 2003.
  • Patients were categorized into four groups based on changes in urinary VMA/HVA levels and tumor size.

Main Results:

  • Urinary VMA and HVA levels decreased in 39 of 53 patients; 17 showed undetectable tumors (Group A), and 22 had detectable tumors (Group B).
  • Seven patients (Group C) had variable tumor markers and gradual volume increase; six (Group D) showed short-term increases.
  • Surgical intervention was performed on tumors in Groups C and D, some in Group B, and one multiple tumor case; no unfavorable biologic factors were found in excised tumors.

Conclusions:

  • The observation program, a large series for MS6M, demonstrated that over 70% of eligible patients could be managed non-surgically.
  • This supports the utility of observation for specific neuroblastoma cases identified through infant mass screening.
Abstract