
Malignant ovarian germ cell tumors: clinico‐pathological presentation and survival outcomes
Author(s) -
TANGJITGAMOL SIRIWAN,
HANPRASERTPONG JITTI,
MANUSIRIVITHAYA SUMONMAL,
WOOTIPOOM VIRACH,
THAVARAMARA THAOVALAI,
BUHACHAT RAKCHAI
Publication year - 2010
Publication title -
acta obstetricia et gynecologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 102
eISSN - 1600-0412
pISSN - 0001-6349
DOI - 10.3109/00016340903443684
Subject(s) - medicine , germ cell tumors , pathological , germ cell , presentation (obstetrics) , gynecology , ovary , oncology , pathology , obstetrics , chemotherapy , biochemistry , chemistry , gene
Objective . To evaluate clinico‐pathological features, treatment, survival, and prognostic factors of patients with malignant ovarian germ cell tumors. Design . Descriptive study. Setting . Bangkok Metropolitan Administration Medical College and Vajira Hospital and Prince of Songkla University. Population . Malignant ovarian germ cell tumor patients treated between January 1996 and December 2007. Methods . Clinico‐pathological data were collected. Patients with malignant tumors arising from benign cystic teratoma were excluded. Survival and potential prognostic factors were analyzed. Main outcome measures . Clinico‐pathological features, survival. Results . One hundred and thirty patients were identified. The median age was 21 years (range, 4–44 years). The most common complaint was pelvic or abdominal mass (63%). Primary surgery was performed by a gynecologic oncologist in only 39.2% of cases. More than half (64.2%) had early stage disease (stages I–II) and the majority had conservative surgery (73.1%). The most common histopathology was dysgerminoma. Of 124 patients with available follow‐up data, 22 did not receive adjuvant treatment; 1 had whole abdominal radiation; and 101 had chemotherapy. Of 89 patients who were evaluable for responses, 4 patients had progressive disease while 85 had complete response. The five‐year progression‐free survival (PFS) and overall survival (OS) were 82.4% [95% confidence interval (CI), 75.4–89.5%)] and 92.4% (95% CI, 87.6–97.2%), respectively. Only preoperative tumor marker elevation was a significant poor prognostic factor for PFS. Conclusions . Malignant ovarian germ cell tumors have a good prognosis with conservative surgical treatment. Chemotherapy is important. Elevated preoperative serum tumor markers are a poor prognostic factor for PFS.