phosphorus-radioisotopes and Endometrial-Neoplasms

phosphorus-radioisotopes has been researched along with Endometrial-Neoplasms* in 4 studies

Other Studies

4 other study(ies) available for phosphorus-radioisotopes and Endometrial-Neoplasms

ArticleYear
Electrospray ionization-tandem mass spectrometry and 32P-postlabeling analyses of tamoxifen-DNA adducts in humans.
    Journal of the National Cancer Institute, 2004, Jul-21, Volume: 96, Issue:14

    Although the nonsteroidal antiestrogen tamoxifen is used as an adjuvant chemotherapeutic agent to treat hormone-dependent breast cancer and as a chemopreventive agent in women with elevated risk of breast cancer, it has also been reported to increase the risk of endometrial cancer. Reports of low levels of tamoxifen-DNA adducts in human endometrial tissue have suggested that tamoxifen induces endometrial cancer by a genotoxic mechanism. However, these findings have been controversial. We used electrospray ionization-tandem mass spectrometry (ES-MS/MS) and 32P-postlabeling analyses to investigate the presence of tamoxifen-DNA adducts in human endometrial tissue.. Endometrial DNA from eight tamoxifen-treated women and eight untreated women was hydrolyzed to nucleosides and assayed for (E)-alpha-(deoxyguanosin-N2-yl)-tamoxifen (dG-Tam) and (E)-alpha-(deoxyguanosin-N2-yl)-N-desmethyltamoxifen (dG-desMeTam), the two major tamoxifen-DNA adducts that have been reported to be present in humans and/or experimental animals treated with tamoxifen, using on-line sample preparation coupled with high-performance liquid chromatography (HPLC) and ES-MS/MS. The same DNA samples were assayed for the presence of dG-Tam and dG-desMeTam by (32)P-postlabeling methodology, using two different DNA digestion and labeling protocols, followed by both thin-layer chromatography and HPLC.. We did not detect either tamoxifen-DNA adduct by HPLC-ES-MS/MS analyses (limits of detection for dG-Tam and dG-desMeTam were two adducts per 10(9) nucleotides and two adducts per 10(8) nucleotides, respectively) or by 32P-postlabeling analyses (limit of detection for both adducts was one adduct per 10(9) nucleotides) in any of the endometrial DNA samples.. The initiation of endometrial cancer by tamoxifen is probably not due to a genotoxic mechanism involving the formation of dG-Tam or dG-desMeTam.

    Topics: Adult; Aged; Antineoplastic Agents, Hormonal; Chromatography, High Pressure Liquid; DNA Adducts; Endometrial Neoplasms; Estrogen Receptor Modulators; Female; Humans; Middle Aged; Phosphorus Radioisotopes; Radionuclide Imaging; Spectrometry, Mass, Electrospray Ionization; Tamoxifen

2004
Wound seeding associated with endometrial cancer.
    Gynecologic oncology, 1994, Volume: 52, Issue:3

    We report a patient with well-differentiated adenocarcinoma of the endometrium who developed a recurrence in the anterior abdominal wall probably secondary to wound seeding at the time of her original surgery. She underwent total abdominal hysterectomy, bilateral salpingo-oophorectomy. She then received 15 mCi of 32P for positive peritoneal washings. She was free of disease until 2 years later when a large lower incision mass developed. She had no evidence for intra-abdominal disease and a radical resection with a myocutaneous flap was undertaken. Radical resection for isolated metastases may be of benefit for patients with endometrial cancer. Patients with positive cytology should be observed closely for incisional recurrence.

    Topics: Adenocarcinoma; Adult; Endometrial Neoplasms; Female; Humans; Neoplasm Recurrence, Local; Neoplasm Seeding; Phosphorus Radioisotopes

1994
Single-use percutaneous catheters for intraperitoneal P32 therapy.
    Cancer, 1994, May-15, Volume: 73, Issue:10

    Intraperitoneal (IP) radioactive chromic phosphate (P32) remains investigational in the treatment of patients with ovarian and/or endometrial cancer. Single-use percutaneously placed catheters offer the advantage of therapy without additional surgery.. Between August, 1986 and October, 1992, 25 patients underwent bedside percutaneous catheter placement under local anesthesia without ultrasonographic or radiologic guidance, using a specialized central venous catheter.. Catheter insertion was successful in 22 of 25 patients (88%) with good IP distribution. Of these, 18 of 22 patients (82%) underwent successful catheter placement with one attempt and 4 of 22 (18%) after one to three additional attempts. The technical failure rate was 12%. Multiple catheter placement attempts were associated with an increased incidence of complications (r = 0.63). Bowel entry occurred in 4 of 25 patients (16%) during 5 of 43 attempts at catheter placement (12%) but was without clinical sequelae. The likelihood of bowel entry significantly increased with more than two attempts (P = 0.02). A median of 39 days (range, 7-156 days) elapsed between the preceding laparotomy and catheter insertion.. Percutaneous catheter placement is successful and well tolerated in the majority of patients and should be considered for patients receiving IP P32.

    Topics: Adult; Aged; Catheterization; Catheterization, Central Venous; Chromium Compounds; Disposable Equipment; Endometrial Neoplasms; Female; Humans; Middle Aged; Ovarian Neoplasms; Phosphates; Phosphorus Radioisotopes; Retrospective Studies

1994
[Experience in the use of the radioactive isotopes Aul98 and P32 in the therapy of cancer of the endometrium].
    Voprosy onkologii, 1960, Volume: 6(10)

    Topics: Endometrial Neoplasms; Endometrium; Female; Gold Radioisotopes; Humans; Neoplasms; Phosphorus; Phosphorus Radioisotopes; Radioisotopes; Uterine Neoplasms

1960