Department of Obstetrics and Gynecology, University of Chicago Biological Sciences Division, Chicago, Illinois, USA.
Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Int J Gynecol Cancer. 2022 Jul 4;32(7):869-874. doi: 10.1136/ijgc-2021-003340.
The primary objective of this study was to determine whether women whose tumors harbor a somatic mutation have longer recurrence-free survival if they receive traditional adjuvant therapy strategies compared with those who do not.
A retrospective, stage I endometrial cancer cohort from MD Anderson Cancer Center was assessed. Clinical and pathological characteristics and type of adjuvant therapy (cuff brachytherapy, pelvic radiation, chemotherapy) were obtained by review of medical records. exon 3 sequencing was performed. Summary statistics were calculated, and recurrence-free survival was measured using the Kaplan-Meier product-limit estimator.
The analysis included 253 patients, 245 with information regarding adjuvant therapy. Most patients had tumors of endometrioid histology (210/253, 83%) with superficial myometrial invasion (197/250, 79%) and no lymphatic/vascular space invasion (168/247, 68%). Tumor mutations were present in 45 (18%) patients. Patients receiving adjuvant therapy were more likely to have higher-grade tumors, non-endometrioid histology, deep myometrial invasion, and lymphatic/vascular invasion. For patients with low-risk features not receiving adjuvant therapy, the presence of mutation did not significantly impact recurrence-free survival (11.3 years wild-type vs 8.1 years mutant, p=0.65). The cohort was then limited to intermediate-risk tumors, defined as endometrioid histology of any grade with deep myometrial invasion and/or lymphatic/vascular space invasion. When recurrence-free survival was stratified by mutation status and adjuvant therapy, patients with mutations and no adjuvant therapy had the shortest recurrence-free survival at 1.6 years, followed by patients with mutations who received adjuvant therapy (4.0 years), and wild-type with and without adjuvant therapy (8.5 and 7.2 years, respectively) (comparison for all four groups, p=0.01).
In patients with intermediate-risk endometrioid endometrial cancers, the use of adjuvant therapy was associated with an improvement in recurrence-free survival for patients with tumor mutations in .
本研究的主要目的是确定是否存在体细胞突变的肿瘤患者在接受传统辅助治疗策略后与未接受辅助治疗的患者相比,其无复发生存时间是否更长。
对 MD 安德森癌症中心的回顾性 I 期子宫内膜癌队列进行评估。通过病历回顾获取临床和病理特征以及辅助治疗类型(袖口近距离放疗、盆腔放疗、化疗)。进行外显子 3 测序。计算汇总统计数据,并使用 Kaplan-Meier 乘积限估计法测量无复发生存率。
该分析纳入了 253 例患者,其中 245 例有辅助治疗信息。大多数患者的肿瘤组织学为子宫内膜样(210/253,83%),浅肌层浸润(197/250,79%),无淋巴血管间隙浸润(168/247,68%)。45 例(18%)患者存在肿瘤突变。接受辅助治疗的患者更有可能患有高级别肿瘤、非子宫内膜样组织学、深肌层浸润和淋巴血管侵犯。对于未接受辅助治疗的低危特征患者,突变的存在并未显著影响无复发生存率(野生型 11.3 年 vs 突变型 8.1 年,p=0.65)。然后将队列限定为中危肿瘤,定义为任何分级的子宫内膜样组织学伴深肌层浸润和/或淋巴血管间隙浸润。当根据突变状态和辅助治疗分层无复发生存率时,无辅助治疗且存在突变的患者无复发生存率最短,为 1.6 年,其次是接受辅助治疗且存在突变的患者(4.0 年),野生型 突变且有和无辅助治疗的患者分别为 8.5 年和 7.2 年(四组间比较,p=0.01)。
在中危子宫内膜样子宫内膜癌患者中,辅助治疗的应用与肿瘤突变患者无复发生存率的提高相关。