宫腔镜在子宫内膜癌诊治中的应用进展

张颖, 郭银树

中国实用妇科与产科杂志 ›› 2025, Vol. 41 ›› Issue (11) : 1149-1152.

PDF(859 KB)
PDF(859 KB)
中国实用妇科与产科杂志 ›› 2025, Vol. 41 ›› Issue (11) : 1149-1152. DOI: 10.19538/j.fk2025110118
综述与讲座

宫腔镜在子宫内膜癌诊治中的应用进展

作者信息 +
文章历史 +

引用本文

导出引用
张颖, 郭银树. 宫腔镜在子宫内膜癌诊治中的应用进展[J]. 中国实用妇科与产科杂志. 2025, 41(11): 1149-1152 https://doi.org/10.19538/j.fk2025110118
中图分类号: R737.33   

参考文献

[1]
Mazzon I, Corrado G, Morricone D, et al. Reproductive preservation for treatment of stage IA endometrial cancer in a young woman:hysteroscopic resection[J]. Int J Gynecol Cancer, 2005, 15(5):974-978. DOI:10.1111/j.1525-1438.2005.00162.x.
Uterine cancer is the most common type of gynecological neoplasm. Conventionally, the standard treatment for early-stage endometrial cancer is surgical staging with hysterectomy, bilateral salpingo-oophorectomy, and lymph node assessment. However, this leads to definitive sterilization in reproductive-age women. We report a rare case of a young woman with endometrioid endometrial adenocarcinoma successfully treated with reproductive preservation therapy in order to preserve her uterus. Pretreatment evaluation including tumor grade, depth of myometrial invasion, tumor size, and hormone-receptor status indicated a favorable prognosis. The patient was treated with hysteroscopic resection of the endometrial cancer, of the endometrium near lesion, and of the myometrium under lesion plus hormone therapy. Thirty months after operative hysteroscopy, the patient has given birth by cesarean section at 39 weeks of gestation to a male child of 3.2 kg and is now completely free of disease. We therefore conclude that there may be a role for effective treatment of endometrioid carcinomas with preservation of reproductive capacity, even if our preliminary result should be validated by a longer follow-up.
[2]
Ianieri MM, Staniscia T, Pontrelli G, et al. A new hysteroscopic risk scoring system for diagnosing endometrial hyperplasia and adenocarcinoma[J]. J Minim Invasive Gynecol, 2016, 23(5):712-718. DOI:10.1016/j.jmig.2016.02.017.
[3]
李小燕, 蒯丹, 田欢, 等. 子宫内膜增生及子宫内膜癌的宫腔镜评分系统构建与验证[J]. 中国实用妇科与产科杂志, 2024, 40(1):96-100. DOI:10.19538/j.fk2024010119.
[4]
张颖, 段华. 宫腔镜在子宫内膜癌高危因素评估中的应用进展[J]. 首都医科大学学报, 2021, 42(2):214-218.
子宫内膜癌是最常见的妇科恶性肿瘤之一,术前对其高危因素的准确评估是制定个体化治疗方案的基础。宫腔镜在对子宫内膜癌组织分化程度、宫颈受累情况、内膜癌病灶大小以及子宫内膜癌前哨淋巴结的评估中提供了准确、有价值的信息,对制定个体化手术方案、改善患者预后具有十分重要的意义。
[5]
安德烈亚·堤内利(意), 路易斯·阿朗索·帕切科(西), 塞尔吉奥·海莫维奇(西). 等, 宫腔镜学[M]. 北京/西安: 世界图书出版公司, 2024:209-213.
[6]
Akazawa M, Hashimoto K. Artificial intelligence in gynecologic cancers:current status and future challenges - a systematic review[J]. Artif Intell Med, 2021, 120:102164. DOI:10.1016/j.artmed.2021.102164.
[7]
Zhang Y, Wang Z, Zhang J, et al. Deep learning model for classifying endometrial lesions[J]. J Transl Med, 2021, 19(1):10. DOI:10.1186/s12967-020-02660-x.
Hysteroscopy is a commonly used technique for diagnosing endometrial lesions. It is essential to develop an objective model to aid clinicians in lesion diagnosis, as each type of lesion has a distinct treatment, and judgments of hysteroscopists are relatively subjective. This study constructs a convolutional neural network model that can automatically classify endometrial lesions using hysteroscopic images as input.All histopathologically confirmed endometrial lesion images were obtained from the Shengjing Hospital of China Medical University, including endometrial hyperplasia without atypia, atypical hyperplasia, endometrial cancer, endometrial polyps, and submucous myomas. The study included 1851 images from 454 patients. After the images were preprocessed (histogram equalization, addition of noise, rotations, and flips), a training set of 6478 images was input into a tuned VGGNet-16 model; 250 images were used as the test set to evaluate the model's performance. Thereafter, we compared the model's results with the diagnosis of gynecologists.The overall accuracy of the VGGNet-16 model in classifying endometrial lesions is 80.8%. Its sensitivity to endometrial hyperplasia without atypia, atypical hyperplasia, endometrial cancer, endometrial polyp, and submucous myoma is 84.0%, 68.0%, 78.0%, 94.0%, and 80.0%, respectively; for these diagnoses, the model's specificity is 92.5%, 95.5%, 96.5%, 95.0%, and 96.5%, respectively. When classifying lesions as benign or as premalignant/malignant, the VGGNet-16 model's accuracy, sensitivity, and specificity are 90.8%, 83.0%, and 96.0%, respectively. The diagnostic performance of the VGGNet-16 model is slightly better than that of the three gynecologists in both classification tasks. With the aid of the model, the overall accuracy of the diagnosis of endometrial lesions by gynecologists can be improved.The VGGNet-16 model performs well in classifying endometrial lesions from hysteroscopic images and can provide objective diagnostic evidence for hysteroscopists.
[8]
Vitale SG, Buzzaccarini G, Riemma G, et al. Endometrial biopsy:Indications,techniques and recommendations. An evidence-based guideline for clinical practice[J]. J Gynecol Obstet Hum Reprod, 2023, 52(6):102588. DOI:10.1016/j.jogoh.2023.102588.
[9]
Rodolakis A, Scambia G, Planchamp F, et al. ESGO/ESHRE/ESGE Guidelines for the fertility-sparing treatment of patients with endometrial carcinoma[J]. Facts Views Vis Obgyn, 2023, 15(1):3-23. DOI:10.52054/FVVO.15.1.065.
The standard surgical treatment of endometrial carcinoma (EC) consisting of total hysterectomy with bilateral salpingo-oophorectomy drastically affects the quality of life of patients and creates a challenge for clinicians. Recent evidence-based guidelines of the European Society of Gynaecological Oncology (ESGO), the European SocieTy for Radiotherapy & Oncology (ESTRO) and the European Society of Pathology (ESP) provide comprehensive guidelines on all relevant issues of diagnosis and treatment in EC in a multidisciplinary setting. While also addressing work-up for fertility preservation treatments and the management and follow-up for fertility preservation, it was considered relevant to further extend the guidance on fertility sparing treatment.To define recommendations for fertility-sparing treatment of patients with endometrial carcinoma.ESGO/ESHRE/ESGE nominated an international multidisciplinary development group consisting of practicing clinicians and researchers who have demonstrated leadership and expertise in the care and research of EC (11 experts across Europe). To ensure that the guidelines are evidence-based, the literature published since 2016, identified from a systematic search was reviewed and critically appraised. In the absence of any clear scientific evidence, judgment was based on the professional experience and consensus of the development group. The guidelines are thus based on the best available evidence and expert agreement. Prior to publication, the guidelines were reviewed by 95 independent international practitioners in cancer care delivery and patient representatives.The multidisciplinary development group formulated 48 recommendations for fertility-sparing treatment of patients with endometrial carcinoma in four sections: patient selection, tumour clinicopathological characteristics, treatment and special issues.These recommendations provide guidance to professionals caring for women with endometrial carcinoma, including but not limited to professionals in the field of gynaecological oncology, onco-fertility, reproductive surgery, endoscopy, conservative surgery, and histopathology, and will help towards a holistic and multidisciplinary approach for this challenging clinical scenario.A collaboration was set up between the ESGO, ESHRE and ESGE, aiming to develop clinically relevant and evidence-based guidelines focusing on key aspects of fertility-sparing treatment in order to improve the quality of care for women with endometrial carcinoma across Europe and worldwide.
[10]
Bettocchi S, Ceci O, Vicino M, et al. Diagnostic inadequacy of dilatation and curettage[J]. Fertil Steril, 2001, 75(4):803-805. DOI:10.1016/s0015-0282(00)01792-1.
To assess the diagnostic inadequacy of dilatation and curettage (D&C) by comparing histologic findings with this technique with those obtained after hysterectomy.Retrospective clinical study.University-affiliated hospital.Three hundred ninety-seven patients with abnormal uterine bleeding who underwent D&C and, within 2 months, hysterectomy because of histologic findings or persistence of symptoms.Comparison of histologic findings on D&C with those obtained after hysterectomy.In 248 of 397 patients (62.5%), D&C failed to detect intrauterine disorders subsequently found at hysterectomy; the sensitivity was 46%, the specificity was 100.0%, the positive predictive value was 100.0%, and the negative predictive value was 7.1%.Dilatation and curettage is an inadequate diagnostic and therapeutic tool for all uterine disorders; this technique missed 62.5% of major intrauterine disorders, and all endometrial disorders were still present in the removed uterus.
[11]
中华医学会妇产科学分会妇科内镜学组, 中国民族卫生协会女性健康与生殖疾病管理分会, 北京医学会妇科内镜学分会. 宫腔镜子宫内膜癌形态特征在保留生育功能治疗中作用的中国专家共识[J]. 中华妇产科杂志, 2025, 60(2):83-93.DOI:10.3760/cma.j.cn112141-20250106-00012
[12]
Di Spiezio Sardo A, De Angelis MC, Della Corte L, et al. Should endometrial biopsy under direct hysteroscopic visualization using the grasp technique become the new gold standard for the preoperative evaluation of the patient with endometrial cancer?[J]. Gynecol Oncol, 2020, 158(2):347-353. DOI:10.1016/j.ygyno.2020.05.012.
To investigate the diagnostic accuracy of endometrial biopsy performed with hysteroscopic direct visualization using the "grasp technique" for the detection of endometrial carcinoma (EC) histology type and tumor grade.A cross-sectional study including the clinical and pathology records of patients with confirmed EC who underwent definitive surgery at University of Naples was performed. The preoperative diagnosis of endometrial tumor type and grade obtained using the hysteroscopy grasp technique was correlated with the final pathology specimens. Those results were compared to the diagnostic accuracy of the biopsies collected in a cohort of patients who underwent preoperative diagnostic hysteroscopy followed by blind endometrial biopsy using the Novak curette with subsequent surgical definitive treatment at University of Pisa. Statistical analysis was based on frequency data and diagnostic agreement of the pathology results.A total of 129 patients were included in the final analysis. An agreement rate of 104/106 (98.1%) for endometrioid type and 15/23 (65.2%) for non-endometrioid type was obtained between preoperative hysteroscopic grasp endometrial biopsy specimens and the final pathology with a coefficient k for G1, G2 and G3 tumors of 0.928, 0.925 and 0.974, respectively. When compared to 121 patients undergoing preoperative blind Novak endometrial biopsy, the hysteroscopic grasp technique was superior in agreement rates for tumor histotype [diagnostic accuracy (0.922 vs 0.890); K value (0.705 vs 0.642)] and grade when in presence of endometrioid type EC (K Cohen 0.354 for G1, 0.263 for G2 and 0.488 for G3).Preoperative hysteroscopic guided "grasp" endometrial biopsy provides a more accurate diagnosis of EC histology type and tumor grade when in presence of endometrioid type tumor compared to blind endometrial biopsy obtained using the Novak curette.Copyright © 2020 Elsevier Inc. All rights reserved.
[13]
Clarke MA, Long BJ, Sherman ME, et al. Risk assessment of endometrial cancer and endometrial intraepithelial neoplasia in women with abnormal bleeding and implications for clinical management algorithms[J]. Am J Obstet Gynecol, 2020, 223(4):549e1-549e13. DOI:10.1016/j.ajog.2020.03.032.
[14]
Arena A, Palermo R, De Benedetti P, et al. "RAIL BIOPSY" a novel and useful technique for hysteroscopic endometrial target biopsy[J]. J Minim Invasive Gynecol, 2024, 31(11):909-910. DOI:10.1016/j.jmig.2024.06.013.
[15]
Kelly RA, Contos GT, Walker CA, et al. Hysteroscopic morcellation in endometrial cancer diagnosis:increased risk?[J]. J Minim Invasive Gynecol, 2021, 28(9):1625-1632. DOI:10.1016/j.jmig.2021.02.004.
[16]
Lindheim SR, Lincenberg K, Wood MA, et al. The impact of hysteroscopic tissue removal systems on histopathologic analysis for benign and cancerous endometrial pathology:an ex vivo study[J]. J Obstet Gynaecol India, 2019, 69(Suppl 2):182-187. DOI:10.1007/s13224-018-1177-6.
[17]
Zhang Y, Chu R, Zhang Z, et al. Prognostic significance of positive peritoneal cytology in endometrial carcinoma based on ESGO/ESTRO/ESP risk classification:A multicenter retrospective study[J]. Gynecol Oncol, 2023, 176:43-52. DOI:10.1016/j.ygyno.2023.06.578.
This study aimed to determine the prognostic significance of positive peritoneal cytology (PC) on endometrial carcinoma (EC) patients under the ESGO/ESTRO/ESP risk classification.This study retrospectively analyzed EC patients from 27 medical centers in China from 2000 to 2019. Patients were divided into three ESGO risk groups: low-risk, intermediate-risk and high-intermediate risk, and high-risk groups. The covariates were balanced by using the propensity score-based inverse probability of treatment weighting (PS-IPTW). The prognostic significance of PC was assessed by Kaplan-Meier curves and multivariate Cox regression analysis.A total of 6313 EC patients with PC results were included and positive PC was reported in 384 women (6.1%). The multivariate Cox analysis in all patients showed the positive PC was significantly associated with decreased PFS (hazard ratio [HR] 2.20, 95% confidence interval [CI] 1.55-3.13, P < 0.001) and OS (HR 2.25, 95% CI 1.49-3.40, P < 0.001),and the Kaplan-Meier curves also showed a poor survival in the intermediate and high-intermediate risk group (5-year PFS: 75.5% vs. 93.0%, P < 0.001; 5-year OS: 78.3% vs. 96.4%, P < 0.001); While in the low-risk group, there were no significant differences in PFS and OS between different PC status (5-year PFS: 93.1% vs. 97.3%, P = 0.124; 5-year OS: 98.6% vs. 98.2%, P = 0.823); in the high-risk group, significant difference was only found in PFS (5-year PFS: 62.5% vs. 77.9%, P = 0.033).Positive PC was an adverse prognostic factor for EC, especially in the intermediate and high-intermediate risk patients. Gynecologic oncologists should reconsider the effect of positive PC on different ESGO risk groups.Copyright © 2023 Elsevier Inc. All rights reserved.
[18]
Dong H, Wang Y, Zhang M, et al. Whether preoperative hysteroscopy increases the dissemination of endometrial cancer cells:A systematic review and meta-analysis[J]. J Obstet Gynaecol Res, 2021, 47(9):2969-2977.DOI: 10.1111/jog.14897.
To determine whether hysteroscopy (HSC) increases the risk of intraperitoneal dissemination in endometrial cancer patients.
[19]
Du Y, Xu Y, Qin Z, et al. The oncology safety of diagnostic hysteroscopy in early-stage endometrial cancer:a systematic review and meta-analysis[J]. Front Oncol, 2021, 11:742761.DOI:10.3389/fonc.2021.742761.eCollection2021.
[20]
Quintana-Bertó R, Padilla-Iserte P, Gil-Moreno A, et al. Oncological safety of hysteroscopy in endometrial cancer[J]. Int J Gynecol Cancer, 2022, 32(11):1395-1401. DOI:10.1136/ijgc-2022-003586.
It has been suggested that the manipulation of neoplastic tissue during hysteroscopy may lead to dissemination of tumor cells into the peritoneal cavity and worsen prognosis and overall survival. The goal of this study was to assess the oncological safety comparing hysteroscopy to Pipelle blind biopsy in the presurgical diagnosis of patients with endometrial cancer.We performed a retrospective multicentric study among patients who had received primary surgical treatment for endometrial cancer. A multivariate statistical analysis model was used to compare relapse and survival rates in patients who had been evaluated preoperatively either by hysteroscopy or Pipelle biopsy. The relapse rate, disease-free survival, and overall survival were assessed as the main outcomes. The histological type, tumor size, myometrial invasion, International Federation of Gynecology and Obstetrics (FIGO) stage, surgical approach, use of a uterine manipulator, and adjuvant treatment were also included in the analysis.A total of 1731 women from 15 centers were included: 1044 in the hysteroscopy group and 687 in the Pipelle sampling group. 225 patients relapsed during the 10 year follow-up period: 139 (13.3%) in the hysteroscopy group and 86 (12.4%) in the Pipelle sampling group. There is no evidence of an association between the use of hysteroscopy as a diagnostic method and relapse rate (HR 1.24, 95% CI 0.92 to 1.66; p=0.16), lower disease-free survival (HR 1.23, 95% CI 0.92 to 1.66; p=0.15), or overall survival (HR 0.95, 95% CI 0.70 to 1.29; p=0.76).Hysteroscopy is a safe diagnostic method for patients with endometrial cancer with no impact on oncological outcomes when compared with sampling by Pipelle.© IGCS and ESGO 2022. No commercial re-use. See rights and permissions. Published by BMJ.
[21]
Liu S, Zhen L, Zhang S, et al. Comparison of prognosis of patients with endometrial cancer after hysteroscopy versus dilatation and curettage:A multicenter retrospective study[J]. Front Med (Lausanne), 2023, 9:1097133. DOI:10.3389/fmed.2022.1097133.eCollection2022.
[22]
Yang W, Zhao X, Pan J, et al. Safety of diagnostic hysteroscopy for the investigation of type II endometrial cancer:systematic review with meta-analysis[J]. BMJ Open, 2024, 14(10):e087582. DOI:10.1136/bmjopen-2024-087582.
The goal of this study is to evaluate the safety of diagnostic hysteroscopy (HSC) in type II endometrial cancer (EC).
[23]
Namazov A, Helpman L, Eitan R, et al. Assessment of oncological safety and utility of hysteroscopy in high grade endometrial cancers:results from an Israel gynecologic oncology group study[J]. Eur J Obstet Gynecol Reprod Biol, 2024, 293:67-71. DOI:10.1016/j.ejogrb.2023.12.021.
To compare survival measures of women with Stage I high-grade endometrial cancer who underwent either hysteroscopy or a non-hysteroscopic procedure as a diagnostic procedure.298 patients with stage I high grade endometrial cancer who underwent surgery between 2002 and 2014. Patients were divided into two groups: hysteroscopy and non-hysteroscopy (curettage or office endometrial biopsy). Clinical, pathological, and survival measures were compared between the groups. High grade histology included endometroid grade -3, uterine serous papillary carcinoma, clear cell carcinoma, and carcinosarcoma.There were 71 patients in the hysteroscopy group and 227 patients in the non-hysteroscopy group. The median follow-up was 52 months (range 12-120 months). There were no differences between the groups in the 5-year recurrence-free survival (73.9 % vs. 79.7 %; p = 0.65), disease-specific survival (79.3 % vs. 83.6 %; p = 0.87), and overall survival (65.7 % vs. 80.3 %; p = 0.35).Hysteroscopic diagnosis in women with early-stage and high-grade endometrial cancer does not adversely affect the survival outcomes.Copyright © 2023 Elsevier B.V. All rights reserved.
[24]
Zhou H, Lai KF, Xiang Q, et al. Oncological safety of diagnostic hysteroscopy for apparent early-stage type II endometrial cancer:a multicenter retrospective cohort study[J]. Front Oncol, 2022, 12:918693. DOI:10.3389/fonc.2022.918693.eCollection2022.
[25]
翟茁钰, 杨莉, 李赫, 等. 术前诊断性宫腔镜检查对非子宫内膜样癌患者腹水细胞学结果及预后的影响[J]. 中华妇产科杂志, 2023, 58(12):903-910.DOI:10.3760/cma.j.cn112141-20250106-00012.
[26]
中国研究型医院学会妇产科专业委员会. 早期子宫内膜癌保留生育功能治疗专家共识[J]. 中国妇产科临床杂志, 2019, 20(4):369-373.DOI:10.13390/j.issn.1672-1861.2019.04.025.
[27]
郝敏, 侯勇丽. 子宫内膜癌保留生育功能治疗[J]. 中国实用妇科与产科杂志, 2025, 41(3):280-284.DOI:10.19538/j.fk2025030106.
[28]
Garzon S, Uccella S, Zorzato PC, et al. Fertility-sparing management for endometrial cancer:review of the literature[J]. Minerva Med, 2021, 112:55-69. DOI:10.23736/S0026-4806.20.07072-X.
[29]
Lucchini SM, Esteban A, Nigra MA, et al. Updates on conservative management of endometrial cancer in patients younger than 45 years[J]. Gynecol Oncol, 2021, 161(3):802-809.doi: 10.1016/j.ygyno.2021.04.017.
Endometrial cancer is the most common gynecologic malignancy in developed country. Women under the age of 40 represent 5% of all endometrial cancer and the majority are nulliparous at the time of diagnosis. The aim of this review was to compare oncologic and fertility outcomes among different fertility-preserving therapies in patients under 45 years of age with grade 1 or 2 endometrial cancer. A systematic review was conducted, the MEDLINE, EMBASE, and CINAHL databases were searched for articles published during the period from January 2010 through January 2020 in accordance with PRISMA guidelines, using the terms endometrial cancer, fertility sparing treatment and conservative treatment. A total of 661 patients in 38 studies were included. The median age was 32.3 years (range 13--43). Regardless of the primary treatment, it is always accompanied by systemic or local hormonal treatment. The median follow-up time was 47.92 months (range 1-412), 54.9 months (range 3.4-412) for the progesterone group, 38.97 months (range 3-172) for the hysteroscopic resection group and 23.11 months (range 1-115.5) for the Levonorgestrel Intrauterine Device group. The overall complete response rate was 79.4%, [Hysteroscopic Resection: 90%, hormonal treatment: 77.7%, and Levonorgestrel Intrauterine Device: 71.3%] The p = 0.02 when the primary treatment is Hysteroscopic resection, always followed by hormonal therapy either oral progesterone or Levonorgestrel Intrauterine Device. Patients who had tumor resection had lower progression than those who received hormonal treatment or Levonorgestrel Intrauterine Device 3.5% vs. 12.1% vs. 19.5% respectively (p = 0.03). The complete response time was higher in the Hysteroscopic Resection group (p = 0.04) with fewer patients undergoing hysterectomy (p = 0.0001). Patients who underwent Hysteroscopic Resection had higher pregnancy rates compared to medical treatment or Levonorgestrel Intrauterine Device, 34.5%, 27.6% and 18.4%, respectively (p = 0.002). CONCLUSION: Patients who underwent Hysteroscopic Resection followed progestogens agent was associated to a better complete response, high pregnancy rates and minor numbers of hysterectomies.Copyright © 2021 Elsevier Inc. All rights reserved.
[30]
Fan Z, Li H, Hu R, et al. Fertility-preserving treatment in young women with grade 1 presumed stage ⅠA endometrial adenocarcinoma:a meta-analysis[J]. Int J Gynecol Cancer, 2018, 28(2):385-393. DOI:10.1097/IGC.0000000000001164.
[31]
Fan Y, Li X, Wang J, et al. Analysis of pregnancy-associated factors after fertility-sparing therapy in young women with early stage endometrial cancer or atypical endometrial hyperplasia[J]. Reprod Biol Endocrinol, 2021, 19(1):118. DOI:10.1186/s12958-021-00808-y.
Fertility-sparing therapy is an alternative conservative treatment for patients with early stage endometrioid cancer or atypical endometrial hyperplasia. In this study, we investigated pregnancy outcomes and pregnancy-associated factors in young patients receiving hormonal therapy.
[32]
Madár I, Szabó A, Vleskó G, et al. Diagnostic accuracy of transvaginal ultrasound and magnetic resonance imaging for the detection of myometrial infiltration in endometrial cancer:a systematic review and meta-analysis[J]. Cancers (Basel), 2024, 16(5):907. DOI:10.3390/cancers16050907.
In endometrial cancer (EC), deep myometrial invasion (DMI) is a prognostic factor that can be evaluated by various imaging methods; however, the best method of choice is uncertain. We aimed to compare the diagnostic performance of two-dimensional transvaginal ultrasound (TVS) and magnetic resonance imaging (MRI) in the preoperative detection of DMI in patients with EC. Pubmed, Embase and Cochrane Library were systematically searched in May 2023. We included original articles that compared TVS to MRI on the same cohort of patients, with final histopathological confirmation of DMI as reference standard. Several subgroup analyses were performed. Eighteen studies comprising 1548 patients were included. Pooled sensitivity and specificity were 76.6% (95% confidence interval (CI), 70.9–81.4%) and 87.4% (95% CI, 80.6–92%) for TVS. The corresponding values for MRI were 81.1% (95% CI, 74.9–85.9%) and 83.8% (95% CI, 79.2–87.5%). No significant difference was observed (sensitivity: p = 0.116, specificity: p = 0.707). A non-significant difference between TVS and MRI was observed when no-myometrium infiltration vs. myometrium infiltration was considered. However, when only low-grade EC patients were evaluated, the specificity of MRI was significantly better (p = 0.044). Both TVS and MRI demonstrated comparable sensitivity and specificity. Further studies are needed to assess the presence of myometrium infiltration in patients with fertility-sparing wishes.
[33]
Etrusco A, Laganà AS, Chiantera V, et al. Reproductive and oncologic outcomes in young women with stage ⅠA and grade 2 endometrial carcinoma undergoing fertility-sparing treatment:a systematic review[J]. Biomolecules, 2024, 14(3):306. DOI: 10.3390/biom14030306.
Background: Endometrial cancer (EC) is the most common gynecological malignancy in both Europe and the USA. Approximately 3–5% of cases occur in women of reproductive age. Fertility-sparing treatment (FST) options are available, but very limited evidence regarding grade 2 (G2) ECs exists in the current literature. This systematic review aimed to comprehensively evaluate reproductive and oncologic outcomes among young women diagnosed with stage IA or G2EC disease who underwent FST. Methods: A comprehensive search of the literature was carried out on the following databases: MEDLINE, EMBASE, Global Health, The Cochrane Library (Cochrane Database of Systematic Reviews, Cochrane Central Register of Controlled Trials, Cochrane Methodology Register), the Health Technology Assessment Database, and Web of Science. Only original studies that reported the oncologic and reproductive outcomes of patients with stage IA and G2EC tumors who underwent FST were considered eligible for inclusion in this systematic review (CRD42023484892). Studies describing only the FST for endometrial hyperplasia or G1 EC were excluded. Results: Twenty-two papers that met the abovementioned inclusion criteria were included in the present systematic review. Preliminary analysis suggested encouraging oncologic and reproductive outcomes after FST. Conclusions: The FST approach may represent a feasible and safe option for women of childbearing age diagnosed with G2EC. Despite these promising findings, cautious interpretation is warranted due to inherent limitations, including heterogeneity in study designs and potential biases. Further research with standardized methodologies and larger sample sizes is imperative for obtaining more robust conclusions.
[34]
Lee AJ, Yang EJ, Kim NK, et al. Fertility-sparing hormonal treatment in patients with stage I endometrial cancer of grade 2 without myometrial invasion and grade 1-2 with superficial myometrial invasion:Gynecologic Oncology Research Investigators coLLaborAtion study (GORILLA-2001)[J]. Gynecol Oncol, 2023, 174:106-113.DOI:10.1016/j.ygyno.2023.04.027.
[35]
Zhao S, Zhang J, Yan Y, et al. Oncological and reproductive outcomes of endometrial atypical hyperplasia and endometrial cancer patients undergoing conservative therapy with hysteroscopic resection:A systematic review and meta-analysis[J]. Acta Obstet Gynecol Scand, 2024, 103(8):1498-1512. DOI: 10.1111/aogs.14815.
Our objective was to conduct a systematic review and meta‐analysis of studies evaluating the oncological and reproductive outcomes of patients with endometrial atypical hyperplasia (AH) and endometrioid endometrial cancer (EEC) undergoing conservative therapy with hysteroscopic resection (HR).
[36]
Shan W, Wu P, Yang B, et al. Conservative management of grade 2 stage IA endometrial carcinoma and literature review[J]. J Obstet Gynaecol Res, 2021, 47(3):984-991.DOI:10.1111/jog.14646.
To explore the clinical outcomes of megestrol acetate alone or plus metformin in young women with grade 2 stage IA endometrial carcinoma who ask for preserved fertility.

脚注

利益冲突 所有作者均声明不存在利益冲突

基金

国家重点研发计划(2025YFC2708302)

PDF(859 KB)

Accesses

Citation

Detail

段落导航
相关文章

/