Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Sen-ei Hattori is active.

Publication


Featured researches published by Sen-ei Hattori.


Cancer | 1991

Prognostic factors in yolk sac tumors of the ovary. A clinicopathologic analysis of 29 cases

Michiyasu Kawai; Takeo Kano; Yoshihito Furuhashi; Kimio Mizuno; Nobuo Nakashima; Sen-ei Hattori; Sadayuki Kazeto; Seizo Iida; Masahiro Ohta; Yoshitaro Arii; Yutaka Tomoda

Twenty‐nine ovarian cancer patients with yolk sac tumors and germ cell tumors with yolk sac tissue as a component of their disease (16 endodermal sinus tumor, 11 mixed germ cell tumors, one embryonal carcinoma, and one polyembryoma) were treated with cytoreductive surgery and combination chemotherapy. Prognostic factors were investigated in this group. Patients with Stage I disease had a more favorable prognosis (P < 0.003) than those with Stages II and IV disease. The difference in prognosis was significant in cases where residual tumor was absent (P < 0.003) and in cases where ascites was either absent or less than 100 ml in volume (P < 0.05). Endodermal sinus tumor with either an intestinal (P < 0.05) or microcystic pattern (P < 0.01) was more common in survivors than in those who died. The age, preoperative serum alpha‐fetoprotein level, maximum tumor size, and tumor weight had no significant correlation with prognosis. In advanced cases, chemotherapy regimens including cisplatin gave better results than those containing vincristine, dactinomycin, and cyclophosphamide (P < 0.05). The optimal treatment of yolk sac tumors or tumors with yolk sac tissue as a component of the ovary is discussed in light of these results.


European Journal of Cancer | 1993

Randomised study of immunotherapy with OK-432 in uterine cervical carcinoma

Fumitaka Kikkawa; Michiyasu Hawai; Hidenori Oguchi; Masayoshi Kojima; Hisatake Ishikawa; Mitsumasa Iwata; Osamu Maeda; Yutaka Tomoda; Yoshitaro Arii; Kazuo Kuzuya; Masahiro Ohta; Takao Ishizuka; Sen-ei Hattori; Kunio Aoki

OK-432, a streptococcal preparation, was administered to patients with stage Ib and II cervical carcinoma except for adeno- and adenosquamous carcinomas. To evaluate the efficacy of OK-432 precisely, 177 patients were stratified by clinical stage, radiotherapy, and lymph node metastasis after complete radical hysterectomy and pelvic lymphadenectomy. Within each stratum, patients were divided randomly into OK-432 and control groups. 85 patients received OK-432 and 92 patients did not. No significant difference was observed in overall 5-year disease free rates between the OK-432 and the control groups, although the mean diameter of erythema on SU-polysaccharide (SU-PS) skin test was larger in the OK-432 group than in the control group. In stage IIb, a significant difference was observed between the OK-432 and control groups. This difference, however, could be attributed in part to the different incidence of the lymph node metastasis. In stage II without lymph node metastasis, 5-year disease free rate was significantly higher in the OK-432 group.


Gynecologic Oncology | 1990

α-Fetoprotein in malignant germ cell tumors of the ovary

Michiyasu Kawai; Yoshihito Furuhashi; Takeo Kano; Toshiya Misawa; Nobuo Nakashima; Sen-ei Hattori; Yoshie Okamoto; Iwao Kobayashi; Masahiro Ohta; Yoshitaro Arii; Yutaka Tomoda

To investigate the clinical significance of alpha-Fetoprotein (AFP) in malignant germ cell tumors of the ovary, we studied 46 patients who were treated by the Tokai Ovarian Tumor Study Group. The 46 patients had the following tumors: immature teratoma (IT), 17 cases; endodermal sinus tumor (EST), 16 cases; mixed germ cell tumor containing EST, 11 cases; embryonal carcinoma, 1 case; polyembryoma, 1 case. In all 29 non-IT cases, AFP was positive, and in 27 cases (93%) the level was above 1000 ng/ml. In 11 of 17 cases of IT (64.7%), AFP levels were elevated and in 1 case the level was above 1000 ng/ml. Elevation of the AFP level above 1000 ng/ml suggested the presence of EST. AFP levels were monitored in 27 of 29 cases without IT during treatment and follow-up. It was found that AFP levels should be monitored closely for at least 1 year after induction of remission. No recurrence was observed when AFP continued to be negative longer than 1 year. The mean interval to clinical recurrence from the reelevation of AFP was 4 months (1.4-9 months). An increase in the AFP to a positive level, even without clinical signs of recurrence, should be regarded as a recurrence. AFP was found to be a useful tumor marker for the diagnosis and management of malignant germ cell tumors of the ovary.


Journal of Surgical Oncology | 1997

Clinical behavior of borderline ovarian tumors : A Study of 150 cases

Koji Tamakoshi; Fumitaka Kikkawa; Nobuo Nakashima; Akiko Tamakoshi; Michiyasu Kawai; Yoshihito Furuhashi; Sen-ei Hattori; Kazuo Kuzuya; Yoshitaro Arii; Nobuhiko Suganuma; Yutaka Tomoda

We evaluated the clinical features, treatment, and survival status of the patients with borderline ovarian tumors.


Oncology | 1996

Mucinous Carcinoma of the Ovary

Fumitaka Kikkawa; Michiyasu Kawai; Koji Tamakoshi; Nobuhiko Suganuma; Nobuo Nakashima; Yoshihito Furuhashi; Kazuo Kuzuya; Sen-ei Hattori; Yoshitaro Arii; Yutaka Tomoda

Since the incidence of mucinous carcinoma of the ovary is relatively low, with only small numbers of cases at any institution, detailed clinicopathologic studies on the prognosis and the care of patie


Gynecologic and Obstetric Investigation | 1994

Recurrence of epithelial ovarian carcinoma after clinical remission.

Fumitaka Kikkawa; Michiyasu Kawai; Kimio Mizuno; Hisatake Ishikawa; Masayoshi Kojima; Osamu Maeda; Koji Tamakoshi; Nobuhiko Suganuma; Yutaka Tomoda; Sen-ei Hattori; Kazuo Kuzuya

One hundred and eighty-eight patients with epithelial ovarian carcinoma were treated with primary cytoreductive surgery and subsequent combination chemotherapy. The first recurrent findings such as sites and disease-free interval were analyzed in 141 patients who were clinically remitted 6 months after operation or chemotherapy. Fifty-seven cases had a recurrence. Five-year disease-free survival rates were 75, 72, 29, and 0% in stage I, II, III, and IV, respectively. Twenty-one of 22 patients with > 2 cm maximum residual tumor died, although they once achieved clinical remission. Significant differences were observed between histologic types, and the disease-free survival rate was lowest for serous cystadenocarcinoma. Nine of 15 stage IV patients with serous histology experienced remission, but none of the 8 in stage IV with other histologies did so, suggesting that serous adenocarcinoma is sensitive to chemotherapy and conducive to clinical remission. However, all stage IV patients in remission encountered a recurrence. Intra-abdominal cavity and lymph node were frequently the initial recurrent sites (38 and 27%, respectively). On the other hand, the incidence of distant recurrence was as high as 27%, and 8 of 16 cases with distant recurrence were stage I. Survival time after recurrence was not different among initial sites of recurrence and mean survival time was 15 months.


Oncology | 1997

A Randomized Trial of Cisplatin, Vinblastine, and Bleomycin versus Cyclophosphamide, Aclacinomycin, and Cisplatin in Epithelial Ovarian Cancer

Yahito Tokuhashi; Fumitaka Kikkawa; Koji Tamakoshi; Nobuhiko Suganuma; Kazuo Kuzuya; Yoshitaro Arii; Michiyasu Kawai; Sen-ei Hattori; Iwao Kobayashi; Yoshihito Furuhashi; Nobuo Nakashima; Yutaka Tomoda

After primary cytoreductive surgery, a randomized clinical trial was conducted in women with epithelial ovarian cancer to compare the impact on survival between PVB chemotherapy, consisting of cisplatin, vinblastine and bleomycin, and CAP chemotherapy, consisting of cyclophosphamide, aclacinomycin and cisplatin. There were 148 evaluable patients. One hundred and five patients with stage II, III and IV were analyzed in this study, 49 of them received PVB chemotherapy while the remaining 56 patients received CAP chemotherapy. Sixty-four patients fulfilled the criteria for clinical remission set by the Tokai Ovarian Tumor Study Group [Gynecol Oncol 1993;48:342-348]. The remission rate was 73 and 50% in the PVB and CAP groups, respectively, and showed a significant advantage for the PVB group (p = 0.0139). Moreover, the recurrence rate was 44% in the PVB group and 61% in the CAP group after clinical remission, although there was no significant difference between the two groups. The final survival rate was 32% in the PVB group and 24% in the CAP group. There was a significant difference of survival rate between both groups at 24 months (p = 0.0378) and 48 months (p = 0.0450), but finally no significant difference was found at 96 months (p = 0.0660). Compared to the CAP regimen, the PVB combination has a significantly higher efficacy in remission, but there was no significant difference in the long-term survival rate. Furthermore, multivariate analysis demonstrated that the PVB chemotherapy improved the survival, but it was not significant. The authors conclude that PVB chemotherapy may be more effective than CAP chemotherapy for epithelial ovarian cancer.


Gynecologic and Obstetric Investigation | 1997

Distribution of platinum in human gynecologic tissues and pelvic lymph nodes after administration of cisplatin

Yahito Tokuhashi; Fumitaka Kikkawa; Hisatake Ishikawa; Koji Tamakoshi; Sen-ei Hattori; Katsuji Matsuzawa; Takami Inoue; Nobuhiko Suganuma; Yutaka Tomoda

BACKGROUND Defining tissue accumulation of platinum may be of importance, since it may provide a pharmacological explanation for organ-specific cisplatin activity. This study was conducted to evaluate the efficacy of cisplatin at the tissue level in different gynecologic organs. The doses administered were equivalent to those used in neoadjuvant chemotherapy regimens. STUDY DESIGN Cisplatin was administered intravenously to patients with cervical or endometrial cancer 1 h before operation, and platinum accumulations in tissues were assayed by the atomic absorption method. RESULTS Platinum accumulation was highest in the cervix and next highest in the myometrium in both cancers. Platinum accumulation in ovary and lymph node was only 0.58 and 0.57 times that in the myometrium, respectively. In patients with cervical cancer, the platinum accumulations in the myometrium and cervix were significantly higher than in the ovary and lymph node. Platinum accumulation in cervical cancer tissue was lower than in the myometrium and cervix, suggesting that delivery of cisplatin to a cervical cancer is somewhat more difficult than to the normal cervix. In patients with endometrial cancer, there was significantly more accumulation in the cervix than in the ovary and lymph node. CONCLUSIONS These data indicated that cisplatin was easily distributed to the cervix and myometrium, but not to the ovary, lymph node, and cancer tissues.


Acta obstetrica et gynaecologica Japonica | 1988

Establishment and characterization of three new human gestational choriocarcinoma cell lines.

Masahiko Sugiura; Setsuko Goto; Mitsuru Saito; Sentoyo Kato; Sen-ei Hattori; Yutaka Tomoda


Gynecologic Oncology | 1993

Clinical Remission Criteria for Epithelial Carcinoma of the Ovary

Yoshimitsu Morikawa; Michiyasu Kawai; Takeo Kano; Fumitaka Kikkawa; Hidenori Oguchi; Nobuo Nakashima; Takao Ishizuka; Yoshihito Furuhashi; Sen-ei Hattori; Kazuo Kuzuya; Masahiro Ohta; Yoshitaro Arii; Yutaka Tomoda

Collaboration


Dive into the Sen-ei Hattori's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge