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1.
Cancers (Basel) ; 16(2)2024 Jan 15.
Artículo en Inglés | MEDLINE | ID: mdl-38254851

RESUMEN

Radiotherapy (RT) has a fundamental role in the treatment of gynecologic malignancies, including cervical and uterine cancers. Hypofractionated RT has gained popularity in many cancer sites, boosted by technological advances in treatment delivery and image verification. Hypofractionated RT uptake was intensified during the COVID-19 pandemic and has the potential to improve universal access to radiotherapy worldwide, especially in low-resource settings. This review summarizes the rationale, the current challenges and investigation efforts, together with the recent developments associated with hypofractionated RT in gynecologic malignancies. A comprehensive search was undertaken using multiple databases and ongoing trial registries. In the definitive radiotherapy setting for cervical cancers, there are several ongoing clinical trials from Canada, Mexico, Iran, the Philippines and Thailand investigating the role of a moderate hypofractionated external beam RT regimen in the low-risk locally advanced population. Likewise, there are ongoing ultra and moderate hypofractionated RT trials in the uterine cancer setting. One Canadian prospective trial of stereotactic hypofractionated adjuvant RT for uterine cancer patients suggested a good tolerance to this treatment strategy in the acute setting, with a follow-up trial currently randomizing patients between conventional fractionation and the hypofractionated dose regimen delivered in the former trial. Although not yet ready for prime-time use, hypofractionated RT could be a potential solution to several challenges that limit access to and the utilization of radiotherapy for gynecologic cancer patients worldwide.

2.
AME Case Rep ; 6: 25, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35928584

RESUMEN

Background: The Calypso 4-dimensional Localization System allows the delivery of high-dose of radiation to a target guided by the implanted transponders. Calypso beacons are used for prostate and liver tumors treated with stereotactic body radiation therapy (SBRT). Several risks associated with this procedure have been previously observed. Here, we report on two cases where Calypso soft tissue transponders migrated to the lung shortly after implantation in liver. Case Description: Two male patients with hepatocellular carcinoma (HCC) underwent insertion of Calypso beacons in liver under image-guidance in preparation for SBRT. Post-procedure images confirmed the presence of the transponders within the liver. However, few days after implant, further imaging revealed a missing marker, in each patient, that had migrated to the right lung. Patients were asymptomatic and SBRT was delivered uneventfully. Conclusions: This is the first report of migration of Calypso beacons from liver to lung. In order to reduce the risk of migration, a Doppler ultrasound (US) prior to insertion could be performed to ensure that the transponders are at a safe distance from blood vessels. Anchored Calypso beacons, currently approved for insertion in the lung, could be tested as a suitable alternative to soft tissue beacons with a lower risk of migration.

3.
Cureus ; 14(1): e21365, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-35198279

RESUMEN

Transitional cell carcinoma of the endometrium is a rare cancer. We present a 58-year-old Caucasian female was diagnosed with high-grade polyploid transitional cell carcinoma of the endometrium. The pathological findings included a dense serosal adhesion over the fundus and the posterior wall, necrotic and polyploid papillary mass in the endometrial cavity, serosal adhesions and unremarkable parenchyma in the fallopian tubes. Others were the presence of cancer antigen 125 and cytokeratin 7 and absence of cytokeratin 20, actin, estrogen receptor, soluble protein 100, vimentin, and cytokeratin high molecular weight. The case is relevant to practice as it identifies the histological patterns for primary transitional cell carcinoma of the endometrium, including expressing cytokeratin 7 instead of cytokeratin 20. The tumor showed a papillary and solid architecture and composed of undifferentiated to poorly differentiated cells with no defined glandular nor squamous differentiation.

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