Skip to main content
Erschienen in: BMC Cancer 1/2020

Open Access 01.12.2020 | Research article

Preoperative clinical characteristics scoring system for differentiating uterine leiomyosarcoma from fibroid

verfasst von: Guorui Zhang, Xin Yu, Lan Zhu, Qingbo Fan, Honghui Shi, Jinghe Lang

Erschienen in: BMC Cancer | Ausgabe 1/2020

Abstract

Background

Morcellation may lead to intraperitoneal spread of tumor cells, thus making prognosis of undiagnosed uterine leiomyosarcoma (ULMS) worse. However, preoperative diagnosis of ULMS remains challenging. This study aimed to design a preoperative clinical characteristics scoring system for differentiating ULMS from uterine fibroid.

Methods

This study enrolled 45 ULMS patients and 180 uterine fibroid patients in Peking Union Medical College Hospital from January 2013 to December 2018.

Results

The incidence of occult ULMS was 0.59% (95% CI, 0.39–0.71%). Age ≥ 40 years old (OR 2.826, 95%CI 1.326–5.461), tumor size ≥7 cm (OR 6.930, 95% CI 2.872–16.724), neutrophil-to-lymphocyte ratio (NLR) ≥ 2.8 (OR 3.032, 95%CI 1.288–7.13), number of platelet ≥298 × 109/L (OR 3.688, 95%CI 1.452–9.266) and lactate dehydrogenase (LDH) ≥ 193 U/L (OR 6.479, 95%CI 2.658–15.792) were independent predictors of ULMS. A preoperative clinical characteristics scoring system was designed based on OR values, with a total score of 7 points. Tumor size ≥7 cm, LDH ≥ 193 U/L were assigned 2 points, while age ≥ 40 years old, NLR ≥ 2.8 and number of platelet ≥298 × 109/L were assigned 1 point. Score ≥ 4 points was a useful predictor in diagnosing ULMS from fibroid (sensitivity 0.800, specificity 0.778).

Conclusions

The incidence of occult ULMS was low. Age ≥ 40 years old, tumor size ≥7 cm, LDH ≥ 193 U/L, NLR ≥ 2.8 and number of platelet ≥298 × 109/L were independent predictors of ULMS. The preoperative clinical characteristics scoring system could be helpful in preoperative diagnosis of occult ULMS.
Hinweise

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
ULMS
Uterine leiomyosarcoma
NLR
Neutrophil to lymphocyte ratio
LDH
Lactate dehydrogenase

Background

Uterine fibroid is the most common benign tumor in gynecology, affecting 40–60% of all reproductive women, and is the main cause of hysterectomy worldwide. Minimally invasive surgeries, including myomectomy and hysterectomy, have advantages of low complication rate, mild pain and quick recovery. Morcellation provides possibility of minimally invasive surgery in giant uterine fibroid. Uterine leiomyosarcoma (ULMS) is a rare uterine malignant tumor originating from smooth muscle cell of uterine myometrium, with high malignancy and poor prognosis. The 5-year overall survival rate for International Federation of Gynecology and Obstetrics (FIGO) stage III-IV ULMS is approximately 25–33% [1]. Morcellation may lead to intraperitoneal spread of tumor cells, thus making prognosis of undiagnosed ULMS patients worse. Compared to open surgery group, incidence of peritoneal dissemination in stage I and II ULMS increases (44% vs. 12.9%) in morcellation group [2]. Besides, intraperitoneal recurrence rate of ULMS is higher in morcellation group than open surgery group (72.2% vs 41.2%) [3], and 3-year overall survival rate is lower (64% vs. 73%) [4]. Therefore, preoperative diagnosis of ULMS, which can reduce the risk of tumor spread caused by morcellation, is of great significance.
However, it remains challenging in differentiating ULMS from uterine fibroid preoperatively. Ultrasonography is a preferred imaging modality, and ULMS characterizes unclear boundary, low resistance and high velocity blood flow. Unfortunately, ultrasonography has no definite diagnostic value due to great heterogeneity of ULMS. MRI performs slightly better, but does not facilitate a diagnosis with certainty. Furthermore, the great cost and limited access reduce its indications for uterine tumor.
Therefore, the objective of this study is to design a preoperative clinical characteristics scoring system for differentiating ULMS from uterine fibroid.

Methods

Patients and study design

This study retrospectively enrolled 45 ULMS patients receiving surgery in Peking Union Medical College Hospital, a complicated and severe cases referral center in China, from January 2013 to December 2018. The inclusion criteria were: a) postoperative pathological conformation of ULMS; b) initial treatment (no surgical intervention was performed previously); c) no evidence of tumor dissemination before surgery. 180 patients with uterine fibroid were enrolled in the control group, who were matched according to time of surgery (± 1 year) and surgeons, at a ratio of 1:4. Patients with inflammatory disease or other malignant tumors were excluded.

Data collection

Patients’ clinical data, ultrasonographic features, laboratory tests and surgical methods in ULMS group and control group were retrospectively retrieved. Ultrasonographic features included the largest diameter of uterus, number of fibroid and the largest diameter of fibroid. Laboratory tests included the number of neutrophil, lymphocyte, platelet, neutrophil to lymphocyte ratio (NLR), and serum lactate dehydrogenase (LDH) level. Ultrasonography and laboratory tests were performed within one month prior to surgery. This study was approved by the Institutional Review Board of Peking Union Medical College Hospital and written informed consents were obtained.

Statistical analysis

SPSS20.0 was used for data analysis. Continuous variables were compared by independent sample student T test, and categorized variables by Chi-square test or Fisher exact test. Multiple logistic regression analysis was performed to define risk factors of ULMS, which formed the scoring system. The scoring system was evaluated by ROC curve with sensitivity and specificity. A p-value of < 0.05 was considered as statistical significance.

Results

Incidence of occult ULMS

From January 2013 to December 2018, 50 pathologically diagnosed ULMS patients received initial treatments in Peking Union Medical College Hospital. Of all, 5 cases were suspected as malignancy prior to operation due to evidence of tumor dissemination, and 45 cases were defined as occult ULMS. During the same period, 8169 uterine fibroid patients underwent myomectomies or hysterectomies (transabdominal, laparoscopic, transvaginal or hysteroscopic). The incidence of occult ULMS was 0.59% (95% CI, 0.39–0.71%).

Patients characteristics

45 patients in ULMS group and 180 patients in control group were enrolled in this study. The preoperative clinical characteristics of the two groups were shown in Table 1. Patients in ULMS group were older (47.0 vs 41.2 years old, P < 0.001), with a higher postmenopausal rate (20.0 vs 5.0%, P = 0.003). There were no significant differences in BMI, clinical manifestations (including abnormal vaginal bleeding and compression symptoms) between the two groups. Ultrasonographic manifestations showed that the maximum diameter of uterus (9.6 vs 8.0 cm, P = 0.009) and the largest diameter of fibroids (7.8 vs 6.2 cm, P < 0.001) in ULMS group were significantly larger than control group. As to laboratory tests, LDH level (212.3 vs 169.1 U/L, P < 0.001), number of neutrophil (5.4 vs 3.5 × 109/L, P < 0.001) and platelet (323.4 vs 272.1 × 109/L, P = 0.005), NLR (3.3 vs 2.3, P = 0.007) in ULMS group were significantly higher than control group,. There were no significant differences in number of lymphocyte, hematocrit, CA125 and CA199 level.
Table 1
The preoperative clinical characteristics of ULSM group and control group
 
ULMS group (N = 45)
Control group (N = 180)
P
Age, yrs
47.0 ± 9.7
41.2 ± 7.7
<0.001
Postmenopausal
9 (20.0)
9 (5.0)
0.003
Gravidity
2.2 ± 1.9
1.9 ± 1.4
0.169
Parity
1.1 ± 0.6
0.8 ± 0.6
0.008
BMI, kg/m2
23.0 ± 2.9
22.8 ± 3.5
0.801
Manifestations
27 (60.0)
106 (58.9)
0.892
 Abnormal uterine bleeding
20 (44.4)
85 (47.2)
0.738
 Compression symptoms
4 (8.9)
23 (12.8)
0.612
Overall uterine size, cm
9.6 ± 2.6
8.0 ± 2.4
0.009
Myoma size, cm
7.8 ± 2.3
6.2 ± 2.5
<0.001
 ≥8 cm
24
32
<0.001
Solitary presumed myoma
19
72
0.786
CA125, IU/L, in 140 cases
30.0 ± 39.6
23.9 ± 17.6
0.218
CA199, IU/L, in 72 cases
9.8 ± 8.9
20.2 ± 31.0
0.136
Neutrophil, × 109/L
5.4 ± 3.2
3.5 ± 1.2
<0.001
Lymphocyte, × 109/L
1.8 ± 0.6
2.5 ± 1.2
0.669
NLR
3.3 ± 2.5
2.3 ± 1.1
0.007
HCT, %
37.0 ± 5.3
37.6 ± 3.8
0.446
Platelet, ×109/L
323.4 ± 112.2
272.1 ± 71.4
0.005
LDH, U/L
212.3 ± 57.2
169.1 ± 27.0
<0.001
Initial surgery
  
<0.001
 Total hysterectomy
33
57
 
 Myomectomy
12
123
 
Data was given as mean ± SD or n (%)
ULSM uterine leiomyosarcoma, BMI body mass index, NLR neutrophil-to-lymphocyte ratio, LDH, lactate dehydrogenase, HCT hematocrit

Risk factors of ULMS

To differentiate ULMS from uterine fibroid, ROC curves of single factor, including age, the largest diameter of fibroid, LDH level, NLR and number of platelet were drawn respectively. The cutoff value of each factor was determined according to ROC curves, with age ≥ 40 years old, tumor size ≥7 cm, LDH ≥ 193 U/L, NLR ≥ 2.8 and number of platelet ≥298 × 109/L.
Multivariate logistic regression analysis was performed to evaluate risk factors of ULMS. And Table 2 showed that age ≥ 40 years old (OR 2.826, 95%CI 1.326–5.461), tumor size ≥7 cm (OR 6.930, 95% CI 2.872–16.724), NLR ≥ 2.8 (OR 3.032, 95%CI 1.288–7.13), number of platelet ≥298 × 109/L (OR 3.688, 95%CI 1.452–9.266) and LDH ≥ 193 U/L (OR 6.479, 95%CI 2.658–15.792), were independent predictors of ULMS.
Table 2
Risk factors of ULMS were evaluated by multivariate logistic regression analysis
Factor
P value
OR
95%CI
Age ≥ 40 yrs
0.044
2.826
1.326–5.461
Postmenopausal
0.122
2.642
0.770–9.068
Tumor size ≥7 cm
<0.001
6.930
2.872–16.724
NLR ≥ 2.8
0.011
3.032
1.288–7.139
Platelet ≥298 × 109/L
0.006
3.688
1.452–9.266
LDH ≥ 193 U/L
<0.001
6.479
2.658–15.792
ULSM uterine leiomyosarcoma, NLR neutrophil-to-lymphocyte ratio, LDH lactate dehydrogenase, OR odd ratio, CI confidential interval

A preoperative clinical characteristics scoring system

A preoperative clinical characteristics scoring system was designed based on OR values of the above factors. As shown in Table 3 and Fig. 1, tumor size ≥7 cm, LDH ≥ 193 U/L were assigned 2 points, while age ≥ 40 years old, NLR ≥ 2.8 and number of platelet ≥298 × 109/L were assigned 1 point. The total score was 7 points, and each patient was scored according to the scoring system.
Table 3
A preoperative clinical characteristics scoring system for differentiating ULMS from fibroid
Score
0
1
2
Age, yrs
<40
≥ 40
Myoma size, cm
<7
≥ 7
NLR
<2.8
≥ 2.8
LDH, U/L
<193
≥ 193
Platelet, ×109/L
<298
≥ 298
ULSM uterine leiomyosarcoma, NLR neutrophil-to-lymphocyte ratio, LDH lactate dehydrogenase
Scores of ULMS group and control group, together with sensitivities and specificities of different scores, were shown in Table 4. ROC curve of the scoring system was shown in Fig. 2. According to ROC curve, the optimal cutoff value was established at 4 points, with sensitivity of 0.800 and specificity of 0.778 in diagnosing ULMS from fibroid.
Table 4
Scores of ULMS group and control group, and sensitivity, specificity and accuracy of different scores
Scoring
≥0
≥1
≥2
≥3
≥4
≥5
≥6
≥7
ULMS group
45
45
45
39
36
25
16
6
Control group
180
156
118
66
40
11
2
0
Total
225
201
163
105
76
36
18
6
Sensitivity
1
1
1
0.867
0.800
0.556
0.356
0.133
Specificity
0
0.133
0.344
0.633
0.778
0.939
0.989
1
Accuracy(%)
20.0
30.7
47.6
68.0
78.2
86.2
86.2
82.6
ULSM uterine leiomyosarcoma

Exploring efficacy of the scoring system among patients under 40 years old

Patients under 40 years old with suspected uterine fibroid were more likely to retain uterus and received myomectomy due to fertility demands. Therefore, it was of greater clinical significance to distinguish ULMS from fibroid among patients under 40. In this study, there were 85 patients under 40, including 7 ULMS patients and 78 fibroid patients. The cutoff value of each risk factor was set according to ROC curves, with tumor size ≥7 cm, LDH ≥ 189 U/ L, NLR ≥ 1.69 and number of platelet ≥251 × 109 / L. Accordingly the scoring system was revised as: tumor size ≥7 cm and LDH ≥ 189 U/L assigned 2 points, while NLR ≥ 1.69 and number of platelet ≥251 × 109 / L assigned 1 point. The total score was 6 points. 5 out of 7 ULMS patients and 9 out of 78 patients were scored ≥3, with sensitivity of 0.714 and specificity of 0.885. Since the number of ULMS patients under 40 was limited in this study, larger sample researches were needed to validate the finding in future.

Discussion

In this study, the incidence of occult ULMS was 0.59%. Multivariate logistic regression analysis showed that age ≥ 40 years old, tumor size ≥7 cm, LDH ≥ 193 U/L, NLR ≥ 2.8 and number of platelet ≥298 × 109/L were independent predictors of ULMS. The preoperative clinical characteristic scoring system was designed according to the OR values of different risk factors, and scores ≥4 points was an useful predictor in diagnosing ULMS from fibroid, with sensitivity of 0.800 and specificity of 0.778.
Uterine sarcoma was a rare interstitial tissue derived malignant tumor, accounting for 3–7% of uterine malignant tumors. ULMS was the most common type, accounting for 63% of uterine sarcoma [5]. Clinical manifestations of ULMS were nonspecific, and most were found accidentally after hysterectomy or myomectomy. The incidence of occult ULMS was 0.0–0.64% (median 0.22%) among presumed leiomyoma [6]. The study with the largest sample size till now reported that, rate of occult sarcoma was 0.36% (1/278) among 34,728 hysterectomies performed for presumed fibroids, and the rate of occult ULMS was 0.23% (1/429) [3]. Incidence of ULMS in this study was 0.59%, consistent with previous reports.
Age was a predictor of ULMS. A multicenter retrospective study reported 221 patients of ULMS and 81 patients of endometrial stromal sarcoma were diagnosed at an average age of 55 years old, and 59% were postmenopausal [7]. Hosh et al. found that the age-adjusted incidence rate for patients aged 50 years or older was higher than younger patients (6.4/10 vs 1.5/10, P < 0.0001), based on Surveillance, Epidemiology, and End Results (SEER) database [8]. In this study, patients in ULMS group were older (47.0 vs 41.2 years old, P < 0.001) than control group, and age ≥ 40 years old (OR 2.826, 95%CI 1.326–5.461) was an independent predictor of ULMS.
Tumor size might be a predictor of ULMS. In 2017, the European Society of Gastrointestinal Endoscopy (ESGE) confirmed that certain signs could cause suspicion of sarcoma, including a lesion exceeding 8 cm [9]. In a study of 15 ULMS patients, tumor size > 7 cm (adjusted-OR 0.973; 95% CI, 0.75–1.26; P = 0.08) might be a predictor of ULMS [10]. Another study involving 31 uterine sarcoma patients showed that large tumor size (> 8.0 cm) was an independent risk factor (P = 0.048) [11]. Results in this study also indicated that tumor size of ULMS was significantly larger than fibroid (7.8 vs 6.2 cm, P < 0.001), and tumor size ≥7 cm was an independent predictor of ULMS (OR 6.930, 95% CI 2.872–16.724). However, some studies had opposite results. Chen’s study with 66 cases of uterine sarcoma showed no difference in size between uterine sarcoma and fibroid (9.6 vs 8.5 cm, P = 0.40) [12].
Recent studies had confirmed that NLR might a markers for diagnosis and prognosis of malignant tumors. It was generally believed that inflammation was involved in the process of tumor proliferation, angiogenesis, metastasis and therapeutic response. The concentration of inflammatory cells in tumor microenvironment was high. Some secondary hematological changes might occur in tumor patients, including lymphocyte decrease, neutrophil and platelet elevation. In recent years, studies had found that NLR and platelet to lymphocyte ratio (PLR) might be markers for diagnosis and prognosis of colorectal cancer, ovarian epithelial cancer, liver cancer, pleural malignant mesothelioma, non-small cell lung cancer and breast cancer [13, 14]. Moreover, a meta-analysis enrolling 2820 patients in 14 studies showed that NLR before treatment was associated with the prognosis of soft tissue sarcoma [15]. A few studies focused on the diagnostic value of NLR in uterine sarcoma. Kim compared NLR with serum CA125 as preoperative diagnostic markers for uterine sarcoma, and NLR (> 2.12) was found to be more accurate (sensitivity, 74.5%; specificity, 70.3%) [16]. A study of 31 cases of ULMS, endometrial stromal sarcoma and undifferentiated sarcoma showed that NLR > 2.1 (P = 0.041) was an independent predictor of uterine sarcoma [11]. In this study enrolling 45 ULMS patients, number of neutrophil (5.4 vs 3.5 × 109/L, P < 0.001), NLR (3.3 vs 2.3, P = 0.007) and number of platelet (323.4 vs 272.1 × 109/L, P = 0.005) increased significantly; and NLR ≥ 2.8 (OR 3.032, 95%CI 1.288–7.139) and number of platelet ≥298 × 109/L (OR 3.688, 95%CI 1.452–9.266) were independent predictors of ULMS.
LDH level was one of the markers in cancer diagnosis and prognosis. Metabolism of cancer cells was characterized by increased glucose uptake and lactic acid production. LDH reversibly catalyzed the conversion of pyruvate to lactate or lactate to pyruvate. Elevated LDH level was a negative prognostic biomarker not only because it was a key enzyme involved in cancer metabolism, but also it allowed neoplastic cells to suppress and evade the immune system by altering tumor microenvironment [17]. An immunohistochemical stain study of 50 uterine sarcoma and 26 fibroids revealed that the positivity rates for LDH-A and LDH-D were significantly higher in patients with uterine sarcoma (P < 0.05) [18]. Nagai summarized 15 cases of uterine sarcoma and showed that LDH > 279 U/L was an independent predictor in the diagnosis of uterine sarcoma [19]. LDH was also used in the diagnosis of other gynecological tumors. A study involving 20 cases found that LDH might be one of the diagnostic markers for ovarian epithelial cancer (AUC = 0.77) [20]. In addition, LDH was considered as a prognostic factor for sarcoma. LDH level before treatment was an effective marker of the prognosis of Ewing’s sarcoma [21]. In this study, LDH level in ULMS group was higher (212.3 vs 169.1 U/L, P < 0.001) than control, and LDH ≥ 193 U/L (OR 6.479, 95%CI 2.658–15.792) was an independent predictor of ULMS.
Due to the limited diagnostic value of single factor in ULMS, a few researchers had explored scoring systems incorporating multiple factors to increase diagnostic value. Nagai enrolled 9 patients with ULMS, 3 patients with adenosarcoma and 3 patients with endometrial stromal sarcoma [22]. A revised pre-operative sarcoma scoring system was designed, including age, serum LDH level and cytological finding, with a maximum score of 10 points and an optimal cut-off value of 4 points. The accuracy, positive predictive value, and negative predictive value were 93.7, 92.3 and 94.0%, respectively. Since adenosarcoma and endometrial stromal sarcoma were more easily detected by cytological examinations than ULMS, the results of this study were perhaps not suitable for ULMS. In Cho’s study, sarcoma index was calculated by summing the number of risk factors. Higher sarcoma index was associated with increased risk of uterine sarcoma (0, 13.6%; 1, 21.7%; 2, 62.5%; 3, 100%) [11]. In this study, according to the OR values of different risk factors, a preoperative clinical characteristics scoring system was designed, including factors of age ≥ 40 years old, tumor size ≥7 cm, LDH ≥ 193 U/L, NLR ≥ 2.8 and number of platelet ≥298 × 109/L, with optimal cutoff value 4 points, sensitivity 0.800 and specificity 0.778.
As far as we knew, this was the largest sample study focusing on preoperative diagnosis of ULMS. The scoring system promoted to preoperative diagnosis of ULMS and reduced risk of dissemination of ULMS caused by morcellation. The main limitation of this study was it was a single center based retrospective study. And multicenter studies with larger sample size were needed to confirm the relevant conclusions.

Conclusion

The incidence of occult ULMS was low and preoperative diagnosis was difficult. Age ≥ 40 years old, tumor size ≥7 cm, LDH ≥ 193 U/L, NLR ≥ 2.8 and number of platelet ≥298 × 109/L were independent predictors of ULMS. The ULMS preoperative clinical characteristics scoring system could be helpful in preoperative diagnosis of occult ULMS.

Acknowledgements

None.
The study was approved by the Institutional Review Board of Peking Union Medical College Hospital. And written informed consents were obtained.
Not applicable.

Competing interests

The authors declare that they have no conflicts of interest.
Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://​creativecommons.​org/​licenses/​by/​4.​0/​. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Literatur
1.
Zurück zum Zitat D'Angelo E, Prat J. Uterine sarcomas: a review. Gynecol Oncol. 2010;116(1):131–9.CrossRef D'Angelo E, Prat J. Uterine sarcomas: a review. Gynecol Oncol. 2010;116(1):131–9.CrossRef
2.
Zurück zum Zitat Park JY, Park SK, Kim DY, Kim JH, Kim YM, Kim YT, et al. The impact of tumor morcellation during surgery on the prognosis of patients with apparently early uterine leiomyosarcoma. Gynecol Oncol. 2011;122(2):255–9.CrossRef Park JY, Park SK, Kim DY, Kim JH, Kim YM, Kim YT, et al. The impact of tumor morcellation during surgery on the prognosis of patients with apparently early uterine leiomyosarcoma. Gynecol Oncol. 2011;122(2):255–9.CrossRef
3.
Zurück zum Zitat Raine-Bennett T, Tucker LY, Zaritsky E, Littell RD, Palen T, Neugebauer R, et al. Occult uterine sarcoma and Leiomyosarcoma: incidence of and survival associated with Morcellation. Obstet Gynecol. 2016;127(1):29–39.CrossRef Raine-Bennett T, Tucker LY, Zaritsky E, Littell RD, Palen T, Neugebauer R, et al. Occult uterine sarcoma and Leiomyosarcoma: incidence of and survival associated with Morcellation. Obstet Gynecol. 2016;127(1):29–39.CrossRef
4.
Zurück zum Zitat George S, Barysauskas C, Serrano C, Oduyebo T, Rauh-Hain JA, Del Carmen MG, et al. Retrospective cohort study evaluating the impact of intraperitoneal morcellation on outcomes of localized uterine leiomyosarcoma. Cancer. 2014;120(20):3154–8.CrossRef George S, Barysauskas C, Serrano C, Oduyebo T, Rauh-Hain JA, Del Carmen MG, et al. Retrospective cohort study evaluating the impact of intraperitoneal morcellation on outcomes of localized uterine leiomyosarcoma. Cancer. 2014;120(20):3154–8.CrossRef
5.
Zurück zum Zitat Trope CG, Abeler VM, Kristensen GB. Diagnosis and treatment of sarcoma of the uterus. Rev Acta Oncol. 2012;51(6):694–705.CrossRef Trope CG, Abeler VM, Kristensen GB. Diagnosis and treatment of sarcoma of the uterus. Rev Acta Oncol. 2012;51(6):694–705.CrossRef
6.
Zurück zum Zitat Wong M, De Wilde RL, Isaacson K. Reducing the spread of occult uterine sarcoma at the time of minimally invasive gynecologic surgery. Arch Gynecol Obstet. 2018;297(2):285–93.CrossRef Wong M, De Wilde RL, Isaacson K. Reducing the spread of occult uterine sarcoma at the time of minimally invasive gynecologic surgery. Arch Gynecol Obstet. 2018;297(2):285–93.CrossRef
7.
Zurück zum Zitat Wais M, Tepperman E, Bernardini MQ, Gien LT, Jimenez W, Murji A. A multicentre retrospective review of clinical characteristics of uterine sarcoma. J Obstet Gynaecol Can. 2017;39(8):652–8.CrossRef Wais M, Tepperman E, Bernardini MQ, Gien LT, Jimenez W, Murji A. A multicentre retrospective review of clinical characteristics of uterine sarcoma. J Obstet Gynaecol Can. 2017;39(8):652–8.CrossRef
8.
Zurück zum Zitat Zhao WC, Bi FF, Li D, Yang Q. Incidence and clinical characteristics of unexpected uterine sarcoma after hysterectomy and myomectomy for uterine fibroids: a retrospective study of 10,248 cases. Onco Targets Ther. 2015;8:2943–8.PubMedPubMedCentral Zhao WC, Bi FF, Li D, Yang Q. Incidence and clinical characteristics of unexpected uterine sarcoma after hysterectomy and myomectomy for uterine fibroids: a retrospective study of 10,248 cases. Onco Targets Ther. 2015;8:2943–8.PubMedPubMedCentral
9.
Zurück zum Zitat Halaska MJ, Haidopoulos D, Guyon F, Morice P, Zapardiel I, Kesic V, et al. European Society of Gynecological Oncology Statement on fibroid and uterine Morcellation. Int J Gynecol Cancer. 2017;27(1):189–92.CrossRef Halaska MJ, Haidopoulos D, Guyon F, Morice P, Zapardiel I, Kesic V, et al. European Society of Gynecological Oncology Statement on fibroid and uterine Morcellation. Int J Gynecol Cancer. 2017;27(1):189–92.CrossRef
10.
Zurück zum Zitat Oduyebo T, Hinchcliff E, Meserve EE, Seidman MA, Quade BJ, Rauh-Hain JA, et al. Risk factors for occult uterine sarcoma among women undergoing minimally invasive gynecologic surgery. J Minim Invasive Gynecol. 2016;23(1):34–9.CrossRef Oduyebo T, Hinchcliff E, Meserve EE, Seidman MA, Quade BJ, Rauh-Hain JA, et al. Risk factors for occult uterine sarcoma among women undergoing minimally invasive gynecologic surgery. J Minim Invasive Gynecol. 2016;23(1):34–9.CrossRef
11.
Zurück zum Zitat Cho HY, Kim K, Kim YB, No JH. Differential diagnosis between uterine sarcoma and leiomyoma using preoperative clinical characteristics. J Obstet Gynaecol Res. 2016;42(3):313–8.CrossRef Cho HY, Kim K, Kim YB, No JH. Differential diagnosis between uterine sarcoma and leiomyoma using preoperative clinical characteristics. J Obstet Gynaecol Res. 2016;42(3):313–8.CrossRef
12.
Zurück zum Zitat Chen I, Firth B, Hopkins L, Bougie O, Xie RH, Singh S. Clinical Characteristics Differentiating Uterine Sarcoma and Fibroids. JSLS. 2018;22(1):e2007.00066. Chen I, Firth B, Hopkins L, Bougie O, Xie RH, Singh S. Clinical Characteristics Differentiating Uterine Sarcoma and Fibroids. JSLS. 2018;22(1):e2007.00066.
13.
Zurück zum Zitat Fest J, Ruiter R, Mulder M, Groot Koerkamp B, Ikram MA, Stricker BH, et al. The systemic immune-inflammation index is associated with an increased risk of incident cancer-A population-based cohort study. Int J Cancer. 2020;146(3):692–8. Fest J, Ruiter R, Mulder M, Groot Koerkamp B, Ikram MA, Stricker BH, et al. The systemic immune-inflammation index is associated with an increased risk of incident cancer-A population-based cohort study. Int J Cancer. 2020;146(3):692–8.
14.
Zurück zum Zitat Huang H, Liu Q, Zhu L, Zhang Y, Lu X, Wu Y, et al. Prognostic value of preoperative systemic immune-inflammation index in patients with cervical Cancer. Sci Rep. 2019;9(1):3284. Huang H, Liu Q, Zhu L, Zhang Y, Lu X, Wu Y, et al. Prognostic value of preoperative systemic immune-inflammation index in patients with cervical Cancer. Sci Rep. 2019;9(1):3284.
15.
Zurück zum Zitat Liu G, Ke LC, Sun SR. Prognostic value of pretreatment neutrophil-to-lymphocyte ratio in patients with soft tissue sarcoma: a meta-analysis. Medicine (Baltimore). 2018;97(36):e12176.CrossRef Liu G, Ke LC, Sun SR. Prognostic value of pretreatment neutrophil-to-lymphocyte ratio in patients with soft tissue sarcoma: a meta-analysis. Medicine (Baltimore). 2018;97(36):e12176.CrossRef
16.
Zurück zum Zitat Kim HS, Han KH, Chung HH, Kim JW, Park NH, Song YS, et al. Neutrophil to lymphocyte ratio for preoperative diagnosis of uterine sarcomas: a case-matched comparison. Eur J Surg Oncol. 2010;36(7):691–8.CrossRef Kim HS, Han KH, Chung HH, Kim JW, Park NH, Song YS, et al. Neutrophil to lymphocyte ratio for preoperative diagnosis of uterine sarcomas: a case-matched comparison. Eur J Surg Oncol. 2010;36(7):691–8.CrossRef
17.
Zurück zum Zitat Ding J, Karp JE, Emadi A. Elevated lactate dehydrogenase (LDH) can be a marker of immune suppression in cancer: interplay between hematologic and solid neoplastic clones and their microenvironments. Cancer Biomark. 2017;19(4):353–63.CrossRef Ding J, Karp JE, Emadi A. Elevated lactate dehydrogenase (LDH) can be a marker of immune suppression in cancer: interplay between hematologic and solid neoplastic clones and their microenvironments. Cancer Biomark. 2017;19(4):353–63.CrossRef
18.
Zurück zum Zitat Song KJ, Yu XN, Lv T, Chen YL, Diao YC, Liu SL, et al. Expression and prognostic value of lactate dehydrogenase-a and -D subunits in human uterine myoma and uterine sarcoma. Medicine (Baltimore). 2018;97(14):e0268.CrossRef Song KJ, Yu XN, Lv T, Chen YL, Diao YC, Liu SL, et al. Expression and prognostic value of lactate dehydrogenase-a and -D subunits in human uterine myoma and uterine sarcoma. Medicine (Baltimore). 2018;97(14):e0268.CrossRef
19.
Zurück zum Zitat Nagai T, Takai Y, Akahori T, Ishida H, Hanaoka T, Uotani T, et al. Novel uterine sarcoma preoperative diagnosis score predicts the need for surgery in patients presenting with a uterine mass. Springerplus. 2014;3:678.CrossRef Nagai T, Takai Y, Akahori T, Ishida H, Hanaoka T, Uotani T, et al. Novel uterine sarcoma preoperative diagnosis score predicts the need for surgery in patients presenting with a uterine mass. Springerplus. 2014;3:678.CrossRef
20.
Zurück zum Zitat Bastani A, Asghary A, Heidari MH, Karimi-Busheri F. Evaluation of the sensitivity and specificity of serum level of prostasin, CA125, LDH, AFP, and hCG+beta in epithelial ovarian cancer patients. Eur J Gynaecol Oncol. 2017;38(3):418–24.PubMed Bastani A, Asghary A, Heidari MH, Karimi-Busheri F. Evaluation of the sensitivity and specificity of serum level of prostasin, CA125, LDH, AFP, and hCG+beta in epithelial ovarian cancer patients. Eur J Gynaecol Oncol. 2017;38(3):418–24.PubMed
21.
Zurück zum Zitat Li S, Yang Q, Wang H, Wang Z, Zuo D, Cai Z, et al. Prognostic significance of serum lactate dehydrogenase levels in Ewing's sarcoma: a meta-analysis. Mol Clin Oncol. 2016;5(6):832–8.CrossRef Li S, Yang Q, Wang H, Wang Z, Zuo D, Cai Z, et al. Prognostic significance of serum lactate dehydrogenase levels in Ewing's sarcoma: a meta-analysis. Mol Clin Oncol. 2016;5(6):832–8.CrossRef
22.
Zurück zum Zitat Nagai T, Takai Y, Akahori T, Ishida H, Hanaoka T, Uotani T, et al. Highly improved accuracy of the revised PREoperative sarcoma score (rPRESS) in the decision of performing surgery for patients presenting with a uterine mass. Springerplus. 2015;4:520.CrossRef Nagai T, Takai Y, Akahori T, Ishida H, Hanaoka T, Uotani T, et al. Highly improved accuracy of the revised PREoperative sarcoma score (rPRESS) in the decision of performing surgery for patients presenting with a uterine mass. Springerplus. 2015;4:520.CrossRef
Metadaten
Titel
Preoperative clinical characteristics scoring system for differentiating uterine leiomyosarcoma from fibroid
verfasst von
Guorui Zhang
Xin Yu
Lan Zhu
Qingbo Fan
Honghui Shi
Jinghe Lang
Publikationsdatum
01.12.2020
Verlag
BioMed Central
Erschienen in
BMC Cancer / Ausgabe 1/2020
Elektronische ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-020-07003-z

Weitere Artikel der Ausgabe 1/2020

BMC Cancer 1/2020 Zur Ausgabe

CAR-M-Zellen: Warten auf das große Fressen

22.05.2024 Onkologische Immuntherapie Nachrichten

Auch myeloide Immunzellen lassen sich mit chimären Antigenrezeptoren gegen Tumoren ausstatten. Solche CAR-Fresszell-Therapien werden jetzt für solide Tumoren entwickelt. Künftig soll dieser Prozess nicht mehr ex vivo, sondern per mRNA im Körper der Betroffenen erfolgen.

Blutdrucksenkung könnte Uterusmyome verhindern

Frauen mit unbehandelter oder neu auftretender Hypertonie haben ein deutlich erhöhtes Risiko für Uterusmyome. Eine Therapie mit Antihypertensiva geht hingegen mit einer verringerten Inzidenz der gutartigen Tumoren einher.

Alphablocker schützt vor Miktionsproblemen nach der Biopsie

16.05.2024 alpha-1-Rezeptorantagonisten Nachrichten

Nach einer Prostatabiopsie treten häufig Probleme beim Wasserlassen auf. Ob sich das durch den periinterventionellen Einsatz von Alphablockern verhindern lässt, haben australische Mediziner im Zuge einer Metaanalyse untersucht.

Antikörper-Wirkstoff-Konjugat hält solide Tumoren in Schach

16.05.2024 Zielgerichtete Therapie Nachrichten

Trastuzumab deruxtecan scheint auch jenseits von Lungenkrebs gut gegen solide Tumoren mit HER2-Mutationen zu wirken. Dafür sprechen die Daten einer offenen Pan-Tumor-Studie.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.