Chay Wen Yee, McCluggage W Glenn, Lee Cheng-Han, Köbel Martin, Irving Julie, Millar Joanne, Gilks C Blake, Tinker Anna V
*Department of Medical Oncology, British Columbia Cancer Agency, Vancouver, British Columbia, Canada; †National Cancer Centre Singapore, Singapore; ‡Department of Pathology, Belfast Health and Social Care Trust, Belfast, United Kingdom; §Department of Laboratory Medicine and Pathology, Royal Alexandra Hospital, University of Alberta, Edmonton; ∥Department of Pathology and Laboratory Medicine, University of Calgary, Calgary, Alberta; ¶Department of Pathology, Royal Jubilee Hospital and the University of British Columbia, Victoria, British Columbia, Canada; #Department of Oncology, NI Cancer Centre, Belfast Health and Social Care Trust, Belfast, United Kingdom; and **Department of Pathology, Vancouver General Hospital and the University of British Columbia, Vancouver, British Columbia, Canada.
Int J Gynecol Cancer. 2016 Mar;26(3):431-6. doi: 10.1097/IGC.0000000000000639.
The natural history and optimal management of serous tubal intraepithelial carcinoma (STIC), regardless of BRCA status, is unknown. We report the follow-up findings of a series of incidental fallopian tube high-grade serous carcinomas (HGSCs) and STICs identified in women at low risk for hereditary breast and ovarian cancer (HBOC), undergoing surgery for other indications.
Cases of incidental STIC and HGSC were identified from 2008. Patients with known BRCA1 or BRCA2 mutations, or a family history of ovarian or breast cancer before the diagnosis of STIC or HGSC were excluded. A retrospective chart review was conducted to obtain clinical data.
Eighteen cases were identified with a median follow-up of 25 months (range, 4-88 months). Twelve of 18 patients had a diagnosis of STIC with no associated invasive HGSC and 6 had STIC associated with other invasive malignancies. Completion staging surgery was performed on 7 of the 18 patients, including 5 of 12 in which there was STIC only identified on primary surgery; 3 cases were upstaged from STIC only to HGSC based on the staging surgery. Recurrence of HGSC occurred in 2 of the 18 patients. BRCA testing was performed on 3 patients, 1 of whom tested positive for a pathogenic BRCA1 mutation.
Our study suggests that completion staging surgery for incidental STICs in non-BRCA patients may be considered. These patients should be offered hereditary testing. The Pelvic-Ovarian cancer INTerception (POINT) Project is an international registry set up to add to our understanding of STICs.
无论BRCA状态如何,浆液性输卵管上皮内癌(STIC)的自然病史和最佳治疗方案均尚不清楚。我们报告了一系列在因其他指征接受手术的遗传性乳腺癌和卵巢癌(HBOC)低风险女性中偶然发现的输卵管高级别浆液性癌(HGSC)和STIC的随访结果。
从2008年开始确定偶然发现的STIC和HGSC病例。排除在诊断STIC或HGSC之前已知有BRCA1或BRCA2突变,或有卵巢或乳腺癌家族史的患者。进行回顾性病历审查以获取临床数据。
确定了18例病例,中位随访时间为25个月(范围4 - 88个月)。18例患者中有12例诊断为STIC,无相关浸润性HGSC,6例STIC与其他浸润性恶性肿瘤相关。18例患者中有7例进行了全面分期手术,其中12例仅在初次手术中发现STIC的患者中有5例;3例根据分期手术从仅STIC升级为HGSC。18例患者中有2例发生HGSC复发。对3例患者进行了BRCA检测,其中1例致病性BRCA1突变检测呈阳性。
我们的研究表明,对于非BRCA患者偶然发现的STIC,可考虑进行全面分期手术。这些患者应接受遗传检测。盆腔 - 卵巢癌干预(POINT)项目是一个国际登记处,旨在增进我们对STIC的了解。