The role of surgical management in pediatric germ cell tumors (GCTs), NCI case series
Purpose: To review the experience of a tertiary referral center in pediatric germ cell tumors (GCTs) in the last 8 years and to investigate the impact of surgery and site of disease on prognosis. Patients and Methods: We retrospectively analyzed the cases of pediatric germ cell tumors at National Ca...
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Veröffentlicht in: | Journal of Egyptian National Cancer Institute 2008-03, Vol.20 (1), p.70-79 |
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Zusammenfassung: | Purpose: To review the experience of a tertiary referral
center in pediatric germ cell tumors (GCTs) in the last 8
years and to investigate the impact of surgery and site of
disease on prognosis.
Patients and Methods: We retrospectively analyzed
the cases of pediatric germ cell tumors at National Cancer
Institute over an 8 years period. Data concerning diagnosis,
surgery and medical decisions were reviewed and analyzed
for all patients. A total of 34 children with (GCTS) were
found, with a mean age, at presentation, of 6.7 years and
a follow-up period ranging from 3-52 months. One patient
with benign GCT was excluded during analysis of the
results.
Results: Among the 34 patients, there were 14 males
and 20 females with mean age of 6.7 years (range: 9
months-15 years), with male to female ratio 1:1.4. All
patients were symptomatic at presentation, most commonly
with abdominal swelling (18 patients; 52.9%). Anatomic
distribution of GCTs according to sex organ involvement
was either gonadal in 21 patients (61.8%) or extragonadal
in 13 patients (38.2%).
All patients had surgery either in the form of curative
resection or biopsy after formal exploration and evidence
of irresectability. No significant surgical morbidity or
mortality were encountered in our patients. Yolk sac tumor
and malignant teratoma were the commonest histologic
subtypes in our series. Metastatic disease was encountered
in nine out of 33 patients (27.2%). Adjuvant chemotherapy
was administered in 28 out of 33 patients (84.8%), following
surgery, including all patients with extragonadal
disease.
Our patients were followed-up to 52 months. Twentytwo
patients (66.7%) had no recurrence while two patients
(6.1%) died from disease. Pelvic extragonadal site was
the worst site regarding resectability. Complete surgical
resection showed better disease free survival, while those
with irresectable disease had comparable overall survival
while none could be rendered disease free with chemotherapy.
Conclusion: The initial surgical approach to malignant
GCTs at all sites should be complete resection when
possible; the morbidity of extensive surgical resection
should be weighed carefully against the good tumor control
with chemotherapy. Surgical staging does not preclude
preservation of fertility, which should always be considered
in this young age. The site of primary disease plays a role
in the prognosis of pediatric germ cell tumors with the
extragonadal pelvic tumors being the worst regarding
resectabi |
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ISSN: | 1110-0362 1687-9996 |