TY - JOUR
T1 - Tumor cell dynamics and metastasis in advanced neuroblastoma
AU - Kuroda, Tatsuo
AU - Honna, Toshiro
AU - Morikawa, Nobuyuki
AU - Kitano, Yoshihiro
AU - Fuchimoto, Yasushi
AU - Terawaki, Kan
AU - Kumagai, Masaaki
AU - Tsunematsu, Yukiko
AU - Masaki, Hidekazu
AU - Matsuoka, Kentaro
AU - Saeki, Morihiro
PY - 2005/11/1
Y1 - 2005/11/1
N2 - This study deals with the advancement process of neuroblastoma through clinical observations and circulating tumor cell exploration. Clinical feature, tumor biology, and circulating tumor cell detected by the previously described polymerase chain reaction(PCR) method were analyzed in 31 patients with advanced neuroblastoma treated in our department since 1991 through 2004. Treatment was completed in 28 patients, of whom 17 are alive without the disease and 11 died. The primary lesion was not confirmed in 2 patients with disseminated metastasis, both of whom showed positive circulating tumor cell. Circulating tumor cell was positive in 6 of 9 examined at their first appearance at the hospital, all had stage 4 disease, and 4 of the 6 (66.7%) died of systemic spread of the disease. N-myc was amplified in 15 patients, of whom only 2 (13.3%) died of systemic metastasis. N-myc amplification did not correlate with positive circulating tumor cell. A certain population of neuroblastoma may provide circulating tumor cells from the early period of the disease to form metastatic lesions independently of the primary lesion, which must be regulated by factors other than N-myc. Circulating tumor cells may suggest higher risk for systemic dissemination and poor prognosis.
AB - This study deals with the advancement process of neuroblastoma through clinical observations and circulating tumor cell exploration. Clinical feature, tumor biology, and circulating tumor cell detected by the previously described polymerase chain reaction(PCR) method were analyzed in 31 patients with advanced neuroblastoma treated in our department since 1991 through 2004. Treatment was completed in 28 patients, of whom 17 are alive without the disease and 11 died. The primary lesion was not confirmed in 2 patients with disseminated metastasis, both of whom showed positive circulating tumor cell. Circulating tumor cell was positive in 6 of 9 examined at their first appearance at the hospital, all had stage 4 disease, and 4 of the 6 (66.7%) died of systemic spread of the disease. N-myc was amplified in 15 patients, of whom only 2 (13.3%) died of systemic metastasis. N-myc amplification did not correlate with positive circulating tumor cell. A certain population of neuroblastoma may provide circulating tumor cells from the early period of the disease to form metastatic lesions independently of the primary lesion, which must be regulated by factors other than N-myc. Circulating tumor cells may suggest higher risk for systemic dissemination and poor prognosis.
KW - Circulating tumor cell
KW - Metastasis
KW - Neuroblastoma
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U2 - 10.1007/s00383-005-1503-9
DO - 10.1007/s00383-005-1503-9
M3 - Article
C2 - 16151820
AN - SCOPUS:27944436987
SN - 0179-0358
VL - 21
SP - 859
EP - 863
JO - Pediatric Surgery International
JF - Pediatric Surgery International
IS - 11
ER -