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1.
Arch Gynecol Obstet ; 278(6): 565-8, 2008 Dec.
Article in English | MEDLINE | ID: mdl-17576588

ABSTRACT

INTRODUCTION: Advanced clear cell adenocarcinoma of the ovary is a histologic type with an extremely poor prognosis. No reports have been published concerning useful drugs for salvage chemotherapy for this type of cancer. We performed salvage therapy with gemcitabine in a patient with multiple-drug- resistant, unresectable recurrent clear cell adenocarcinoma of the ovary and succeeded in stabilizing recurrent lesions and controlling carcinomatous peritonitis. CASE REPORT: A 55-year-old woman was in Stage IIIc of clear cell adenocarcinoma of the ovary. She had recurrent tumors after primary cytoreductive surgery, which were unresectable and also resistant to paclitaxel, carboplatin, irinotecan, and oral etoposide. After three courses of fourth-line chemotherapy with gemcitabine for the treatment of carcinomatous peritonitis and hepatic and splenic metastatic lesions, serum CA-125 and the severity of ascites showed marked decreases, and its efficacy for the hepatic and splenic metastatic lesions was classified as 5-month stable disease. The toxicity of this drug was in the acceptable range. CONCLUSION: Gemcitabine is also useful for heavily pretreated clear cell adenocarcinoma of the ovary. It is necessary to consider the use of drugs without cross resistance to platinum and taxanes in the selection of drugs for this cancer.


Subject(s)
Adenocarcinoma, Clear Cell/drug therapy , Antimetabolites, Antineoplastic/therapeutic use , Deoxycytidine/analogs & derivatives , Neoplasm Recurrence, Local/drug therapy , Ovarian Neoplasms/drug therapy , Peritonitis/drug therapy , Salvage Therapy/methods , Adenocarcinoma, Clear Cell/pathology , Deoxycytidine/therapeutic use , Fatal Outcome , Female , Humans , Middle Aged , Neoplasm Recurrence, Local/pathology , Ovarian Neoplasms/pathology , Peritonitis/pathology , Gemcitabine
2.
J Reprod Med ; 52(4): 306-12, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17506371

ABSTRACT

OBJECTIVE: To investigate the factors related to activation of transforming growth factor-beta 1 (TGF-beta1) at sites of endometriosis. STUDY DESIGN: TGF-beta1 is activated by plasmin, which is formed when plasminogen is activated by urokinase-type plasminogen activator (uPA). We studied these factors by immunohistochemistry or immunoassay. RESULTS: TGF-beta1 protein was localized mainly in the cytoplasm of glandular epithelial cells in both endometriotic cysts and normal endometrium, but strongly positive immunostaining was significantly more common in cysts. The levels of TGF-beta1, uPA and plasmin/alpha2-plasmin inhibitor complex were all higher in cyst fluid than in peritoneal fluid. There was little uPA protein expression in the glandular epithelium of normal endometrium, but it was prominent in the cytoplasm of glandular epithelial cells from endometriotic cysts, and strongly positive immunostaining was significantly more common in cysts. CONCLUSION: These results suggest that TGF-beta1 activity is increased at sites of endometriosis due to enhanced production of both uPA and TGF-beta1 by glandular epithelium and because plasmin activates TGF-beta1 after being converted from plasminogen by uPA.


Subject(s)
Endometriosis/metabolism , Fibrinolysin/metabolism , Ovarian Cysts/metabolism , Transforming Growth Factor beta1/metabolism , Urokinase-Type Plasminogen Activator/metabolism , Adult , Chi-Square Distribution , Endometriosis/pathology , Female , Humans , Immunoassay , Immunohistochemistry , Middle Aged , Ovarian Cysts/pathology , Statistics, Nonparametric
3.
Acta Cytol ; 50(3): 323-6, 2006.
Article in English | MEDLINE | ID: mdl-16780029

ABSTRACT

UNLABELLED: BACKGROUND; Papillary serous carcinoma of the peritoneum (PSCP) is a tumor that produces widespread intraperitoneal lesions. Unlike serous ovarian adenocarcinoma, many aspects of its mode of progression and biologic characteristics are unclear. CASE: A 46-year-old woman with PSCP had no detectable ascites and minimal intraperitoneal involvement at the time of the diagnosis, but a paraaortic lymph node metastasis was present. Preoperative endometrial cytology was positive (suspicion of adenocarcinoma). The histologic diagnosis was poorly differentiated serous adenocarcinoma. Cytology of the peritoneal washings demonstrated positive findings, similar to those of endometrial cytology. After cytoreductive surgery, including lymph node dissection and platinum-based chemotherapy, the patient achieved long-term survival. CONCLUSION: PSCP can present with an early paraaortic lymph node metastasis. Endometrial cytology can be valuable in the diagnosis.


Subject(s)
Cystadenocarcinoma, Papillary/pathology , Cystadenocarcinoma, Serous/pathology , Peritoneal Neoplasms/pathology , Adnexa Uteri/pathology , Aorta, Abdominal/diagnostic imaging , Endometrium/pathology , Female , Humans , Lymphatic Metastasis , Middle Aged , Peritoneal Neoplasms/diagnostic imaging , Radiography
4.
Eur J Obstet Gynecol Reprod Biol ; 127(1): 130-6, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16442693

ABSTRACT

OBJECTIVE: To investigate differences in the biological characteristics of ovarian clear cell adenocarcinoma based on the presence/absence of endometriosis and tumor proliferative activity. METHODS: Stage I ovarian clear cell adenocarcinoma patients were divided into groups with and without endometriosis, and immunohistochemical expression of proliferating cell nuclear antigen was determined in surgical specimens. Then xenograft models of human ovarian clear cell adenocarcinoma with or without human ectopic endometrium were created in severe combined immunodeficiency mice, and tumor growth was assessed from the wet weight and the bromodeoxyuridine uptake. Furthermore, a xenograft model of human endometriosis was made with or without ovarian clear cell adenocarcinoma and cytokine production was investigated. RESULTS: The proliferating cell nuclear antigen labeling index was significantly lower in the tumors of patients with endometriosis compared to the tumors of patients without endometriosis. In tumor-bearing mice, the tumor weight and bromodeoxyuridine uptake were both significantly lower when ovarian clear cell adenocarcinoma was associated with endometriosis than in its absence. Release of transforming growth factor-beta1 and interleukin-6 from the ectopic human endometrium was greater in the presence of clear cell adenocarcinoma than without it, and transforming growth factor-beta1 levels showed a significant difference. CONCLUSION: The proliferative activity of early ovarian clear cell adenocarcinoma seems to depend on the association of this cancer with endometriosis. When endometriosis is associated with ovarian clear cell adenocarcinoma, there is a change of its cytokine production that may inhibit tumor growth.


Subject(s)
Adenocarcinoma, Clear Cell/physiopathology , Cell Proliferation , Endometriosis/complications , Endometriosis/physiopathology , Ovarian Neoplasms/physiopathology , Proliferating Cell Nuclear Antigen/analysis , Adenocarcinoma, Clear Cell/chemistry , Adenocarcinoma, Clear Cell/complications , Adenocarcinoma, Clear Cell/pathology , Animals , Bromodeoxyuridine/metabolism , Endometriosis/metabolism , Endometriosis/pathology , Enzyme-Linked Immunosorbent Assay , Female , Humans , Immunohistochemistry , Interleukin-6/analysis , Mice , Mice, SCID , Neoplasm Staging , Ovarian Neoplasms/chemistry , Ovarian Neoplasms/complications , Ovarian Neoplasms/pathology , Transforming Growth Factor beta1/analysis , Transplantation, Heterologous , Tumor Necrosis Factor-alpha/analysis
5.
Gynecol Oncol ; 88(3): 447-50, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12648602

ABSTRACT

BACKGROUND: Pregnancy complicated by endodermal sinus tumor of the ovary has rarely been reported. CASE: A 32-year-old pregnant woman was found to have an ovarian tumor. At 19 weeks of gestation, tumorectomy was performed and a diagnosis of primary endodermal sinus tumor of the ovary (stage Ic) was made. Pregnancy was continued without postoperative chemotherapy. At 36 weeks of gestation, she underwent cesarean section combined with second-look laparotomy. A normal infant was delivered and there were no signs of recurrence. Subsequently, three courses of combination chemotherapy with bleomycin, etoposide, and cisplatin were administered. There was no evidence of recurrence at 27 months after initial treatment. CONCLUSIONS: Successful management of endodermal sinus tumor of the ovary in a pregnant woman is reported.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Endodermal Sinus Tumor/drug therapy , Ovarian Neoplasms/drug therapy , Pregnancy Complications, Neoplastic/drug therapy , Adult , Bleomycin/administration & dosage , Cisplatin/administration & dosage , Etoposide/administration & dosage , Female , Humans , Pregnancy
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