1.Epithelial borderline ovarian tumor: Diagnosis and treatment strategy.
Kimio USHIJIMA ; Kouichiro KAWANO ; Naotake TSUDA ; Shin NISHIO ; Atsumu TERADA ; Hiroyuki KATO ; Kazuto TASAKI ; Ken MATSUKUMA
Obstetrics & Gynecology Science 2015;58(3):183-187
Epithelial borderline ovarian tumors (BOT) are distinctive from benign tumors and carcinoma. They occur in younger women more often than carcinoma, and there is some difficulty making correct diagnosis of BOT. Two subtypes of BOT, serous and mucinous borderline tumor have different characteristics and very different clinical behavior. Serous borderline tumor (SBT) with micropapillary pattern shows more incidence of extra ovarian disease and often coexists with invasive implant. SBT with micropapillary pattern in advanced stage has showed a worse prognosis than typical SBT. Huge mucinous borderline tumors have histologic heterogeneity, and the accuracy of frozen section diagnosis is relatively low. Extensive sampling is required to reach a correct pathological diagnosis. Mucinous adenoma (intestinal type) also runs the risk of recurrence after cystectomy, or intraoperative rupture of cyst. Laparoscopic procedure for BOT has not increased the risk of recurrence. Fertility preserving procedures are generally accepted, except in advanced stage SBT with invasive implants. Only cystectomy shows a significant risk of recurrence. Re-staging surgery and full staging surgery is not necessary for all BOT. We should not attempt to treat them uniformly, by the single diagnosis of "borderline tumor". It depends on histologic type. Close communication with the pathologist is necessary to gain more detail and ask more pathological samples in order to make the optimal treatment strategy for each individual patients.
Adenoma
;
Cystectomy
;
Diagnosis*
;
Female
;
Fertility
;
Frozen Sections
;
Humans
;
Incidence
;
Laparoscopy
;
Mucins
;
Ovarian Diseases
;
Population Characteristics
;
Prognosis
;
Recurrence
;
Rupture
2.Epithelial borderline ovarian tumor: Diagnosis and treatment strategy.
Kimio USHIJIMA ; Kouichiro KAWANO ; Naotake TSUDA ; Shin NISHIO ; Atsumu TERADA ; Hiroyuki KATO ; Kazuto TASAKI ; Ken MATSUKUMA
Obstetrics & Gynecology Science 2015;58(3):183-187
Epithelial borderline ovarian tumors (BOT) are distinctive from benign tumors and carcinoma. They occur in younger women more often than carcinoma, and there is some difficulty making correct diagnosis of BOT. Two subtypes of BOT, serous and mucinous borderline tumor have different characteristics and very different clinical behavior. Serous borderline tumor (SBT) with micropapillary pattern shows more incidence of extra ovarian disease and often coexists with invasive implant. SBT with micropapillary pattern in advanced stage has showed a worse prognosis than typical SBT. Huge mucinous borderline tumors have histologic heterogeneity, and the accuracy of frozen section diagnosis is relatively low. Extensive sampling is required to reach a correct pathological diagnosis. Mucinous adenoma (intestinal type) also runs the risk of recurrence after cystectomy, or intraoperative rupture of cyst. Laparoscopic procedure for BOT has not increased the risk of recurrence. Fertility preserving procedures are generally accepted, except in advanced stage SBT with invasive implants. Only cystectomy shows a significant risk of recurrence. Re-staging surgery and full staging surgery is not necessary for all BOT. We should not attempt to treat them uniformly, by the single diagnosis of "borderline tumor". It depends on histologic type. Close communication with the pathologist is necessary to gain more detail and ask more pathological samples in order to make the optimal treatment strategy for each individual patients.
Adenoma
;
Cystectomy
;
Diagnosis*
;
Female
;
Fertility
;
Frozen Sections
;
Humans
;
Incidence
;
Laparoscopy
;
Mucins
;
Ovarian Diseases
;
Population Characteristics
;
Prognosis
;
Recurrence
;
Rupture
3.Identification of appropriate cone length to avoid positive cone margin in high grade cervical intraepithelial neoplasia.
Kouichiro KAWANO ; Naotake TSUDA ; Shin NISHIO ; Koji YONEMOTO ; Kazuto TASAKI ; Rurika TASAKI ; Kimio USHIJIMA
Journal of Gynecologic Oncology 2016;27(5):e54-
OBJECTIVE: To identify key factors for predicting positive cone margin and appropriate cone length. METHODS: We retrospectively reviewed the margin status of patients who received conization with high grade cervical intraepithelial neoplasia, along with other factors such as patient age, parity, preoperative cytology, size of disease, type of transformation zone, and cone length from patient records. Cut-off value of cone length was analyzed in women younger than 40 years old because we design conization with minimum length especially for women who wish for future pregnancy. Cut-off value of cone length was defined as length corresponds to estimated probability of positive cone margin equal to 0.1 by logistic regression analysis with variables selected by stepwise methods. RESULTS: Among 300 patients, 75 patients had positive cone margin. Multivariable analysis revealed that squamous cell carcinoma at preoperative cytology (p=0.001), 2 or more quadrant disease (p=0.011), and shorter cone length (p<0.001) were risk factors for positive cone margin. Stepwise methods identified cone length and size of lesion as important variables. With this condition, cut-off value of cone length was estimated as 15 mm in single quadrant disease and 20 mm in 2 or more quadrant disease, respectively. CONCLUSION: We identified the independent risk factors of positive cone margin and identified the cut-off value of cone length to avoid positive cone margin in women younger than 40 years old. Conization should be performed not only according to colposcopic findings including type of transformation zone but size of disease and cone length.
Adult
;
Cervical Intraepithelial Neoplasia/*pathology
;
Cervix Uteri/*pathology
;
*Conization
;
Female
;
Humans
;
Middle Aged
;
Retrospective Studies
;
Uterine Cervical Neoplasms/*pathology
4.Antitumor Activity of Oxaliplatin, 5-FU and Paclitaxel Given Alone or in Combination with ZD1839 in Human Gastric Carcinoma Cells in vitro.
Ji Hyun JANG ; Sang Hak LEE ; Jin Hyoung KANG ; Hee Sik SUN ; Kazuto NISHIO ; Nagahiro SAIJO ; Hyo Jeong KUH
Cancer Research and Treatment 2002;34(5):372-381
PURPOSE: Oxaliplatin (LOHP), 5-FU, and paclitaxel (PTX) are considered highly active against advanced gastric carcinomas, and the epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, ZD1839 is considered as a good candidate for the treatment of gastric cancers when given alone or in combination with cytotoxic agents. The present study evaluated the antitumor effects of these agents in SNU-1 human gastric cancer cells either alone or when given as a doublet (i.e., as a cytotoxic-cytostatic combination). MATERIALS AND METHODS: We selected SNU-1 cells that showed DNA mismatch repair (MMR) deficiency and EGFR overexpression. Growth inhibition was measured by MTT and by direct cell counting and cell cycle distribution by flow cytometry. The combination index (CI) was used to describe synergistic interaction. RESULTS: The four drugs showed IC50s ranging from 1.81 nM to 13.2microM. MTT assay appeared to underestimate the cytotoxicity of PTX, which was attributed to a significant resistant fraction (32%). LOHP and PTX induced G2/M arrest, 5-FU increased in S phase, and ZD1839 in-creased in G1 in a concentration dependent manner. PTX ZD1839 showed the greatest synergism and LOHP ZD1839 showed a similar result. The cell cycle effect of PTX was potentiated by the coadministration of ZD1839. A previously developed cytostatic TPi model was used to assess the contribution of cell cycle arrest to overall growth inhibition, and 64% and 80% of the overall growth inhibition was attributed to cell cycle arrest for LOHP and PTX, when exposed to 7.55microM and 10 nM for 72 hr, respectively. CONCLUSION: This study demonstrates the antitumor activity and significant cell cycle arrest effect of ZD1839 against human gastric carcinoma cells and its synergistic interaction with LOHP and PTX. These results provide a preclinical rationale for the clinical development of ZD1839 and its use in combination with LOHP or PTX against human gastric cancers that express EGFR.
Cell Count
;
Cell Cycle
;
Cell Cycle Checkpoints
;
Cytotoxins
;
DNA Mismatch Repair
;
Flow Cytometry
;
Fluorouracil*
;
Humans*
;
Inhibitory Concentration 50
;
Paclitaxel*
;
Protein-Tyrosine Kinases
;
Receptor, Epidermal Growth Factor
;
Robenidine
;
S Phase
;
Stomach Neoplasms