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http://hdl.handle.net/11452/25100
Başlık: | Evaluation of the outcome benefit conferred by intensive surveillance strategies in women with early-stage endometrial cancer |
Yazarlar: | Kıran, Gürkan Kesterson, Joshua P. Kanis, Margaux Jenna Groman, Adrienne E. Lele, Shashikant B. Uludağ Üniversitesi/Tıp Fakültesi/Kadın Hastalıkları ve Doğum Anabilim Dalı. Özerkan, Kemal AAH-9791-2021 6603345841 |
Anahtar kelimeler: | Oncology Obstetrics & gynecology Endometrial cancer Surveillance |
Yayın Tarihi: | Mar-2011 |
Yayıncı: | Academic Press Inc Elsevier Science |
Atıf: | Kesterson, I. vd. (2011). "Evaluation of the outcome benefit conferred by intensive surveillance strategies in women with early-stage endometrial cancer". Gynecologic Oncology, 121(1), Supplement 1, S11-S12. |
Özet: | Introduction: The optimum follow-up regimen after treatment for early-stage endometrial cancer with curative intent is unknown. The National Comprehensive Cancer Network recommends a physical exam and vaginal cytology every three to six months for two years then at six to 12 month intervals with annual chest X-rays (CXR). However, there is debate as to whether intensive follow-up results in an improvement in outcomes for those with recurrent endometrial cancer. Objective: To determine if intensive surveillance for recurrent cancer in women with early-stage endometrial cancer improves their outcomes. Materials and Methods: The Roswell Park Cancer Institute tumor registry was used to identify patients with Stage I and II endometrial cancer initially diagnosed and treated over an 18-year period, who subsequently recurred. Clinico-pathological variables were abstracted. Patients were divided into two groups, depending on their mode of diagnosis of recurrent cancer: 1) routine screening, or 2) symptomatic. The outcomes between the two groups were compared. Results: Fifty-two patients met inclusion criteria. Twenty-three patients were diagnosed via routine screening methods and 29 were symptomatic at presentation. Groups were equally represented with respect to age, stage, grade, adjuvant therapy, site of recurrence (local, distant), and time to recurrence (p > 0.05). Median survival time was 79 months for those diagnosed during routine screening and 80 months for symptomatic patients (p > 0.05). Conclusion: Pap smear and CXR appear to be of limited utility as the present study has shown that women diagnosed as a result of intensive surveillance did not have a better outcome than those who presented when symptomatic. |
URI: | https://doi.org/10.1016/j.ygyno.2010.12.032 https://www.gynecologiconcology-online.net/article/S0090-8258(10)00915-7/fulltext http://hdl.handle.net/11452/25100 |
ISSN: | 0090-8258 |
Koleksiyonlarda Görünür: | Scopus Web of Science |
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