IV Guideline
1 Introduction
1.1 Epidemiology, classification, staging
|
Consensus-based Statement 1.S1
|
|
Expert consensus
|
Strength of consensus +++
|
|
Uterine sarcomas (homologous) are a heterogeneous group of rather rare malignancies (1.5 – 3/100 000) of the uterine musculature, endometrial stroma or uterine connective tissue.
|
|
Consensus-based Recommendation 1.E1
|
|
Expert consensus
|
Strength of consensus +++
|
|
References: [1], [2]
|
|
The terminology and the morphological diagnosis of uterine sarcomas must be based on the most current edition of the WHO classification.
|
|
Consensus-based Recommendation 1.E2
|
|
Expert consensus
|
Strength of consensus +++
|
|
References: [2]
|
|
The postoperative staging of uterine sarcomas must be based on the most current pTNM classification.
|
The WHO classification lists the following entities as malignant mesenchymal tumors or malignant mixed epithelial-mesenchymal tumors [2], [3]:
-
leiomyosarcoma (LMS),
-
low-grade endometrial stromal sarcoma (LG-ESS),
-
high-grade endometrial stromal sarcoma (HG-ESS),
-
undifferentiated uterine sarcoma (UUS),
-
adenosarcoma (AS),
-
PECome (perivascular epithelioid cell tumor), malignant variant.
The diagnosis of other extremely rare sarcomas of the uterus (e.g. rhabdomyosarcoma as an example of a heterologous sarcoma) must be based on the WHO classification of soft tissue sarcomas [4].
This guideline considers the more common entities (LMS, LG-ESS, HG-ESS and UUS or AS) to the exclusion of extremely rare types (rhabdomyosarcoma in adulthood, angiosarcoma, osteosarcoma, chondrosarcoma, liposarcoma, myxofibrosarcoma, alveolar soft part sarcoma and epithelioid sarcoma). A chapter on “Rhabdomyosarcoma of the uterus in children and adolescents” was added to the guideline.
The mean patient age at onset of disease is between 50 and 70 years, depending on the tumor type. Identified risk factors include tamoxifen therapy. Moreover, the incidence of uterine sarcomas is 2 to 3 times higher for women of African descent compared to Asian women or women of European descent.
Carcinosarcomas, which used to be referred to as uterine sarcomas in earlier classifications (also known as malignant mixed Müllerian tumors), are no longer classified as uterine sarcomas but as uterine carcinomas [5], [6]. For this reason, this tumor entity is now discussed in the German national S3 guideline “032-034OL Diagnosis, Treatment and Follow-up of Patients with Endometrial Cancer” [7] (Staging – [Tables 5] and [6]).
Table 5 FIGO and TNM stages for leiomyosarcomas and endometrial stromal sarcomas* of the uterus.
|
FIGO/TNM stage
|
Definition
|
|
* Tumors simultaneously present in the corpus uteri and the ovary/pelvis accompanied by ovarian/pelvic endometriosis must be classified as independent primary tumors.
|
|
I/T1
|
|
Tumor limited to the uterus
|
|
|
IA/T1a
|
Tumor 5 cm or less in greatest dimension
|
|
IB/T1b
|
Tumor larger than 5 cm in greatest dimension
|
|
II/T2
|
|
Tumor extends beyond the uterus, within the pelvis
|
|
|
IIA/T2a
|
Involvement of the adnexa (unilateral or bilateral)
|
|
IIB/T2b
|
Tumor has spread to extrauterine pelvic tissue excluding the adnexa
|
|
III/T3
|
|
Tumor has infiltrated abdominal tissue
|
|
N1
|
IIIA/T3a
|
One site
|
|
IIIB/T3b
|
More than one site
|
|
IIIC
|
Metastasis of pelvic and/or para-aortic lymph nodes
|
|
IV/T4
|
IVA/T4
|
Tumor has infiltrated bladder and/or rectum
|
|
IVB
|
Distant metastasis
|
Table 6 FIGO and TNM stages for adenosarcomas* of the uterus.
|
FIGO/TNM stage
|
Definition
|
|
* Tumors simultaneously present in the corpus uteri and the ovary/pelvis accompanied by ovarian/pelvic endometriosis must be classified as independent primary tumors.
|
|
I/T1
|
|
Tumor limited to the uterus
|
|
|
IA/T1a
|
Tumor limited to the endometrium/endocervix without myometrial infiltration
|
|
IB/T1b
|
Tumor has infiltrated less than half of the myometrium
|
|
IC/T1c
|
Tumor has infiltrated ≥ 50% of the myometrium
|
|
II/T2
|
|
Tumor has spread to the pelvis
|
|
|
IIA/T2a
|
Involvement of the adnexa (unilateral or bilateral)
|
|
IIB/T2b
|
Tumor has spread to extrauterine pelvic tissue excluding the adnexa
|
|
III/T3
|
|
Intraabdominal tumor spread
|
|
N1
|
IIIA/T3a
|
One site
|
|
IIIB/T3b
|
More than one site
|
|
IIIC
|
Metastasis of pelvic and/or para-aortic lymph nodes
|
|
IV/T4
|
IVA/T4
|
Tumor has infiltrated bladder and/or rectal mucosa
|
|
IVB
|
Distant metastasis
|
1.2 Symptoms, general diagnostic work-up (including imaging), general pathology
1.2.1 Symptoms
|
Consensus-based Statement 1.S2
|
|
Expert consensus
|
Strength of consensus +++
|
|
Uterine sarcomas are not associated with any specific symptoms.
|
Generally suspicious symptoms include a “rapidly growing uterus” despite low estrogen levels in the postmenopausal period.
Although it has been suggested that rapid growth of the uterus (e.g., an increase in size resembling 6 weeks of pregnancy over a period of one year [8]) may be an indication for sarcoma, an analysis by Parker and colleagues of more than 1300 patients (of whom around 350 had “rapid growth”) found no increased risk of sarcoma compared to the respective controls (0.27 vs. 0.23%) [9].
Finally, it should be noted that there is no valid definition of what constitutes “rapid growth” nor has any useful data been published which would permit this parameter to be usefully evaluated in terms of being able to differentiate between myomas and sarcomas.
1.2.2 Imaging
|
Consensus-based Recommendation 1.E3
|
|
Expert consensus
|
Strength of consensus +++
|
|
Because of the high potential for metastasis, histologically verified uterine sarcomas should be investigated further, including imaging (CT/MRI) of the thorax and abdomen.
|
|
Consensus-based Recommendation 1.E4
|
|
Expert consensus
|
Strength of consensus +++
|
|
Imaging procedures or diagnostic interventions may not be able to exclude uterine sarcoma.
|
No imaging procedures (sonography, CT, MRT, PET-CT) have any specific or reliable criteria for detecting sarcomas [10].
In general, transvaginal ultrasound is the most important primary diagnostic procedure used to evaluate the uterus.
Computed tomography may be used for abdominal imaging. This is particularly suitable for staging and to identify distant metastasis.
If a patient is known to have a sarcoma, the patient should also have a thoracic CT scan which can then serve as the basis for current management, with the findings used for follow-up.
1.2.3 General pathology
1.2.3.1 Specimens after hysterectomy or surgery of uterine sarcoma
|
Consensus-based Recommendation 1.E5
|
|
Expert consensus
|
Strength of consensus +++
|
|
References: [2], [11], [12], [13]
|
|
The morphological work-up must find out all of the information listed below.
-
Grading of the histological tumor type based on the WHO classification
-
Grading of ESS
-
Evidence for/no evidence of lymph node or blood vessel infiltration (L and V status)
-
Evidence for/no evidence of perineural infiltration (PNI status)
-
Staging (pTNM)
-
Infiltration depth into the myometrium or (endo-)cervical stroma
-
Three-dimensional tumor size, in cm
-
Metric data for the minimal distance between the sarcoma and the respective relevant resection margin
-
R classification (UICC)
-
Estrogen and progesterone receptor expression
|
|
Consensus-based Recommendation 1.E6
|
|
Expert consensus
|
Strength of consensus +++
|
|
As uterine sarcomas may be characterized by a high degree of intra-tumoral heterogeneity, all tumors with a maximum diameter of < 2 cm must be fully investigated. Tumors with diameters of > 2 cm must be embedded in paraffin, using one paraffin block per centimeter greatest tumor dimension.
|
|
Consensus-based Recommendation 1.E7
|
|
Expert consensus
|
Strength of consensus +++
|
|
If the findings do not provide clear information about the malignancy or subtype, a pathological examination must be carried out to investigate the tumor further.
|
|
Consensus-based Recommendation 1.E8
|
|
Expert consensus
|
Strength of consensus +++
|
|
All patients with a diagnosis of uterine sarcoma must be presented to an interdisciplinary tumor conference.
|
|
Consensus-based Recommendation 1.E9
|
|
Expert consensus
|
Strength of consensus +
|
|
The presentation must be done at a DKG-certified gynecological cancer center or sarcoma center.
|
1.3 Genetic predisposition
|
Consensus-based Recommendation 1.E10
|
|
Expert consensus
|
Strength of consensus +++
|
|
If conditions for a germline analysis of the TP53 gen are present, patients must be offered genetic counseling with subsequent analysis to exclude LFS.
|
The majority of sarcomas occur sporadically. Nevertheless, a diagnosis of uterine sarcoma in childhood or early adulthood may be an indication of Li-Fraumeni syndrome (LFS), an inherited familial predisposition to certain cancers.
2 Uterine leiomyosarcoma
2.1 Introduction, clinical and diagnostic work-up
In Northern Europe, sarcomas occur in about 0.4 cases/100 000 women across all age groups with the highest incidence found in women between the ages of 45 and 59 years [14].
The median age at onset of disease is 50 years [15].
Clinical symptoms reported by the patient can include abnormal bleeding (e.g. mid-cycle bleeding postmenopausal bleeding) and, depending on the size of the lesion, a sensation of pressure in the vagina or abdomen. However, in around 50% of cases (e.g., in women with postmenopausal bleeding), the results of curettage and/or endometrial biopsy can be false-negative and do not allow LMS to be clearly excluded [16].
2.2 Histopathological diagnosis
The WHO classification lists both classic and spindle cell leiomyosarcoma as well as an epithelioid and a myxoid variant in its histological differentiation of sarcomas [2].
The WHO classification does not grade uterine LMS [2].
A diagnosis of smooth muscle tumor of uncertain malignant potential (STUMP) [17] should only be made in exceptional cases if it is not possible to clearly differentiate between (classic) LMS and leiomyoma [18], [19], [20].
[Fig. 1] shows a diagnostic algorithm for smooth muscle tumors [17], [18], [20], [21], [22], [23].
Fig. 1 Diagnostic algorithm of smooth muscle tumors of the uterus. [rerif]
2.3 Prognosis
LMS are very aggressive tumors with an unfavorable prognosis. The rate of recurrence ranges from 53 to 71%, and the average 5-year overall survival rate is between 40 and 50% [24], [25].
Additional prognostic factors are age, tumor-free resection margins, mitotic index and vascular invasion [24], [26]. The most important iatrogenic negative prognostic factors are morcellation or tumor injury, e.g. caused by a “myomectomy” [27].
2.4 Surgical treatment
|
Consensus-based Recommendation 2.E11
|
|
Expert consensus
|
Strength of consensus +++
|
|
Treatment of early-stage tumors must include complete removal of the uterus without morcellation but must include bilateral resection of the adnexa.
In premenopausal patients, the ovaries may be preserved.
|
|
Consensus-based Recommendation 2.E12
|
|
Expert consensus
|
Strength of consensus +++
|
|
Systematic pelvic and para-aortic lymphadenectomy should not be carried out if the lymph nodes are diagnostically unremarkable.
|
Total hysterectomy is the gold standard for the surgical management of LMS which are limited to the uterus. The decision whether the adnexa need to be resected will usually depend on the patientʼs menopausal status. In young women, the ovaries can be preserved without affecting prognosis [26], [28], [29]. Ovarian metastasis is rare, with an incidence of just 3%, and occurs almost exclusively in cases with intraperitoneal spread [29].
The incidence of primary pelvic and para-aortic lymph node metastasis is low in cases with LMS. If lymph node involvement is present (involvement is often already detected intraoperatively), then extrauterine or hematogenous metastasis is usually also present. This means that systematic pelvic and para-aortic lymphadenectomy is not associated with a better prognosis, and it is therefore generally not recommended [28], [30], [31].
2.5 Adjuvant systemic therapy and radiotherapy
|
Consensus-based Recommendation 2.E13
|
|
Expert consensus
|
Strength of consensus +++
|
|
Adjuvant chemotherapy should not be generally administered. Depending on the presence of other risk factors (e.g. higher stage tumor) it may be administered in individual cases after carefully weighing up the potential drawbacks/benefits with the patient.
|
|
Consensus-based Recommendation 2.E14
|
|
Expert consensus
|
Strength of consensus +++
|
|
Radiotherapy should not be carried out after complete resection of a stage I/II LMS.
|
Adjuvant systemic therapy is not generally indicated as no randomized controlled study has been able to provide evidence for any benefit in terms of overall survival [32].
Based on the current results of both prospective phase II trials and a phase III trial, it appears that patients with leiomyosarcoma whose tumor is limited to the uterus (stage I – III A with involvement limited exclusively to the uterine serosa) could benefit from systemic therapy after surgery with no residual tumor.
In this context, it was found in a small phase III trial (n = 81 patients, 19 of whom presented with carcinosarcoma) that a combination of doxorubicin/ifosfamide/cisplatin had a significant positive effect on 3-year progression-free survival (55% had additional radiotherapy vs. 41% in the control group who had only radiotherapy), but it was accompanied by significantly higher toxicity [33].
Another phase II trial (n = 47) which used combination chemotherapy with docetaxel and gemcitabine followed by doxorubicin had similarly good results in terms of PFS but with lower toxicity (3-year PFS: 57%) [34], [35].
Based on these results, it would appear that adjuvant chemotherapy should at least be discussed in certain individual cases, even if there is, as yet, no evidence that it leads to a significant improvement in overall survival.
A randomized study reported that adjuvant pelvic irradiation with 50.4 Gy in cases with stage I or II disease resulted in improved local control in a patient population with different sarcoma entities [36], but in the subgroup of patients with leiomyosarcomas (n = 99) no effect was found on either the local rate of recurrence (20% with radiotherapy, 24% without radiotherapy) or the overall survival rate. This means that radiotherapy is not generally indicated after complete resection of a stage I/II LMS. Radiotherapy can be considered in patients with R1/2 resection and locally advanced disease if the tumor is limited to the pelvis.
2.6 Treatment for metastasis and recurrence
|
Consensus-based Recommendation 2.E15
|
|
Expert consensus
|
Strength of consensus +++
|
|
If the diagnosis is metastasized LMS, the first-line therapy must consist of doxorubicin.
|
There is some evidence to suggest that when treating patients with uterine leiomyosarcoma and recurrence or metastasis, complete surgical resection is associated with a better prognosis compared to chemotherapy and/or radiotherapy [37], [38], [39], [40]. Two studies carried out in a selected patient population reported improved survival rates (median survival: 45 vs. 31 months and 2.0 vs. 1.1 years, respectively) after complete resection of metastases in patients with leiomyosarcoma [37], [41].
Palliative systemic therapy is indicated for patients with diffuse metastasis and patients with recurrence/metastasis which cannot be/can no longer be treated with surgery. Such a therapy should be discussed in detail with the patient and the associated toxicity needs to be considered carefully.
There are only a few effective substances such as ifosfamide, gemcitabine or doxorubicin which can be used for mono-chemotherapy, and they are reported to have moderate rates of response (partial or complete remission) of between 17 and 25% [42], [43].
Paclitaxel, cisplatin, topotecan and etoposide are less effective and have low response rates of less than 10% [44] – [47].
In contrast, although combination chemotherapies have higher response rates compared to monotherapies, the toxicity associated with combination therapies is higher [48], [49], [50].
Only one prospective randomized phase II trial has shown that combination therapy is superior to mono-chemotherapy in terms of survival; therapy consisted of a combination of docetaxel/gemcitabine [51]. However, another study with a comparable design was unable to confirm the findings of the first study, so that it is still ultimately not clear whether this combination offers a benefit for patients [52].
According to more recent data from a phase III trial, a combination of docetaxel and gemcitabine offered no benefits compared to monotherapy with doxorubicin to either the overall patient population with soft tissue sarcomas or the subgroup with uterine LMS (median overall survival: 67 vs. 76 weeks; HR: 1.14, 95% CI: 0.83 – 1.57; p = 0.41 for the total patient population, n = 257) [53].
The use of trabectedin in second-line chemotherapy in a metastatic setting after prior administration of anthracyclines was investigated in phase II trials and should be the antitumoral drug of choice to treat this indication. Although the expected remission rates are very low, disease may be stabilized in up to 50% of cases [54].
Pazopanib, a multiple tyrosine kinase inhibitor, is another second-line therapy option which has been investigated in a double-blind, placebo-controlled phase III trial, although patients with a range of sarcoma types of varying histologies and with metastasis were included in the study. As regards the rate of remission and the percentage of patients who experienced disease stabilization, the same statement applies to pazopanib as for trabectedin. In this study, pazopanib significantly increased the progression-free survival period both in the overall patient population and in the subgroup of patients with leiomyosarcoma [55].
3 Low-grade endometrial stromal sarcomas
3.1 Introduction, clinical and diagnostic work-up
The median age at onset of disease is the 6th decade of life [15].
These tumors typically manifest as pathological bleeding, sometimes together with an enlarged uterus and corresponding symptoms.
The WHO classification of malignant endometrial stromal tumors ([Fig. 2]) differentiates between
-
low-grade endometrial stromal sarcomas,
-
high-grade endometrial stromal sarcomas and
-
undifferentiated uterine sarcomas [17].
Fig. 2 Synopsis of the morphology, immunohistochemistry and molecular pathology of endometrial stromal sarcomas (ESS) and undifferentiated uterine sarcomas (UUS). [rerif]
3.2 Prognosis
Tumor stage is the most important prognostic factor for low-grade ESS [56]. The disease-specific 5-year survival rate for low-grade ESS is 80 – 90% and the 10-year survival rate is approximately 70% [57], [58]. If the tumor is limited to the uterus at the time of diagnosis (stage I), then the rates are even higher: 100 and 90%, respectively. The rate drops to 40% for higher stage disease [31]. Positive hormone receptors are a favorable prognostic factor with regard to overall survival [59].
3.3 Surgical treatment
|
Consensus-based Recommendation 3.E16
|
|
Expert consensus
|
Strength of consensus +++
|
|
Treatment of early-stage disease must consist of complete resection of the uterus without morcellation but with complete bilateral resection of the adnexa.
|
|
Consensus-based Recommendation 3.E17
|
|
Expert consensus
|
Strength of consensus +++
|
|
Reference: [60]
|
|
There are currently no data about the oncological safety of hormone replacement therapy after previous primary treatment of a low-grade ESS. Because the tumor biology of low-grade ESS is highly estrogen-dependent, patients should be dissuaded from starting hormone replacement therapy.
|
|
Consensus-based Recommendation 3.E18
|
|
Expert consensus
|
Strength of consensus +++
|
|
Systematic pelvic and para-aortic lymphadenectomy should not be carried out if the lymph nodes are diagnostically unremarkable.
|
The treatment of choice is total hysterectomy (without morcellation) and resection of both adnexa [61].
There is a lot of evidence regarding the endocrine dependence of LG-ESS. A retrospective analysis of 153 patients with LG-ESS found a significantly increased rate of recurrence when the ovaries of premenopausal patients were not removed. Neither this analysis nor two other evaluations of the SEER database found that this had a negative impact on overall survival. Thus, the benefits of ovarian preservation in younger patients must be carefully weighed against the risk of a higher probability of recurrence and must be critically discussed with affected patients [62], [63], [64].
Lymph node involvement does not appear to have an impact on prognosis. Systemic lymphadenectomy and any adjuvant therapy options based on systemic lymphadenectomy are therefore not expected to extend survival times, meaning that lymphadenectomy cannot be routinely recommended [10], [58], [64], [65].
3.4 Adjuvant systemic therapy and radiotherapy
|
Consensus-based Recommendation 3.E19
|
|
Expert consensus
|
Strength of consensus +++
|
|
Adjuvant endocrine therapy should not be generally carried out, although it may be considered depending on the presence of other risk factors (e.g. higher tumor stage) in individual cases after carefully weighing up the drawbacks/benefits with the patient.
|
|
Consensus-based Recommendation 3.E20
|
|
Expert consensus
|
Strength of consensus +++
|
|
Adjuvant chemotherapy must not be carried out.
|
|
Consensus-based Recommendation 3.E21
|
|
Expert consensus
|
Strength of consensus +++
|
|
Adjuvant radiotherapy must not be carried out.
|
Postoperative adjuvant endocrine therapy may be discussed with patients with FIGO stage III disease and higher or after accidental morcellation, although prospective studies are lacking. The data from comparative retrospective analyses of adjuvant treatment support the use of either medroxyprogesterone acetate 200 mg/d (in Germany only available as 250 mg doses) or megestrol acetate 160 mg/d or as an alternative to aromatase inhibitors (letrozole 2.5 mg/d, anastrozole 1 mg/d or exemestane 25 mg/d). The appropriate duration for adjuvant treatment has not been sufficiently investigated. A period of 5 years is currently being discussed [66], [67], [68].
There are no valid data available on adjuvant chemotherapy.
A large epidemiological study from the USA carried out in 3650 patients with uterine sarcoma showed that adjuvant pelvic irradiation (± brachytherapy) had a significant positive effect on loco-regional recurrence-free survival for both the total patient population [69] and the subgroup of patients with ESS (n = 361: after 5 years: 97 vs. 93%; after 8 years 97 vs. 87%). But another large epidemiological study from the USA in a total of 1010 patients with ESS was unable to confirm that adjuvant radiotherapy had a significant benefit on overall survival [58]. The only relevant randomized study on the use of pelvic radiation in patients with uterine sarcoma [36] included 30 patients with endometrial stromal sarcomas but did not carry out a separate survival analysis for this subgroup of patients. Because of the unclear data and the medium- and long-term side effects of adjuvant radiotherapy when loco-regional control is already good, this treatment is not generally indicated.
3.5 Treatment for metastasis and recurrence
|
Consensus-based Recommendation 3.E22
|
|
Expert consensus
|
Strength of consensus +++
|
|
Tamoxifen is contraindicated for LG-ESS.
|
Endometrial stromal sarcomas usually have a better prognosis compared to leiomyosarcomas. However, recurrence is possible even after decades [70]. In every case with recurrence or metastasis, it is important to check whether surgery with the aim of complete macroscopic resection is possible [71].
The targeted administration of percutaneous radiotherapy is a palliative option for local or loco-regional recurrence which cannot be completed resected [72], [73].
Systemic therapy can be administered in cases with postoperative residual tumor, inoperable recurrence with distant metastasis of low-grade endometrial stromal sarcoma. Because of the high expression of estrogen and progesterone receptors, progestogens or aromatase inhibitors are used to treat low-grade endometrial stromal sarcomas [74], [75], [76], [77].
A retrospective analysis of a small case series found medroxyprogesterone acetate 200 mg/d (in Germany only available in doses of 250 mg) or megestrol acetate 160 mg/d to be effective. Response rates of up to 82% were reported [75]. Alternatively, although there is less data available, aromatase inhibitors (letrozole 2.5 mg/d, anastrozole 1 mg/d or exemestane 25 mg/d) also appear to have a positive effect [76].
Because it is a risk factor for uterine sarcoma, tamoxifen must not be used for endocrine therapy [78].
Any ongoing therapy with tamoxifen should be discontinued. If the use of tamoxifen is indicated because of breast cancer, treatment should be switched to an aromatase inhibitor.
4 High-grade endometrial stromal sarcomas and undifferentiated uterine sarcomas
4.1 Introduction, clinical and diagnostic work-up
Although there are distinct pathological anatomical differences between HG-ESS and UUS, both entities share a number of similarities in terms of their incidence, clinical presentation, prognosis and even therapy, which is why they are discussed together here. The staging corresponds to that for LMS.
The median age at onset of disease is 60 years. These tumors also typically manifest as pathological bleeding, sometimes together with an enlarged uterus and the corresponding symptoms.
As previously mentioned, the term “undifferentiated endometrial sarcoma (UES)” which was still included in the WHO classification of 2003 [79] is no longer included in the most recent WHO classification [2] and should therefore no longer be used.
4.2 Prognosis
As regards prognosis, the prognosis for HG-ESS is between that of the more favorable prognosis associated with LG-ESS and the prognosis for aggressively progressive undifferentiated uterine sarcomas (UUS) [80].
However, because disease is often only detected in its later stages, the prognosis is generally unfavorable with a median overall survival of just 1 – 2 years [81], [82].
4.3 Surgical treatment
|
Consensus-based Recommendation 4.E23
|
|
Expert consensus
|
Strength of consensus +++
|
|
Treatment of early-stage disease must consist of complete resection of the uterus without morcellation but with complete bilateral resection of the adnexa.
|
|
Consensus-based Recommendation 4.E24
|
|
Expert consensus
|
Strength of consensus +++
|
|
Systematic pelvic and para-aortic lymphadenectomy should not be carried out if the lymph nodes are diagnostically unremarkable.
|
The treatment of choice also consists of complete hysterectomy (without morcellation) and bilateral adnexal resection. It is not clear whether the adnexa of premenopausal women can be left in situ.
Although positive pelvic and/or para-aortic lymph nodes are associated with a poorer prognosis, there is currently no indication that surgical removal followed by consequent adjuvant therapy would lead to an improvement of this limited prognosis.
4.4 Adjuvant systemic therapy and radiotherapy
|
Consensus-based Recommendation 4.E25
|
|
Expert consensus
|
Strength of consensus +++
|
|
Adjuvant chemotherapy should not be routinely carried out, but it may be considered in individual cases depending on the presence of additional risk factors (e.g. higher tumor stage).
|
There are currently no valid data which indicate that postoperative endocrine therapy would benefit patients, even though evidence for hormone receptors is rare.
There are currently no valid data on the benefit of adjuvant chemotherapy, which means that it must be discussed on an individual basis.
The data on adjuvant radiotherapy is similarly limited. A multicenter retrospective analysis evaluated 59 patients with endometrial stromal tumors, 29 of whom had undifferentiated uterine sarcoma (58% had stage I or II disease (FIGO 1988) [83]). 86% of patients received pelvic teletherapy (median dose for the total patient population: 48 Gy) and 51% received brachytherapy. Overall survival after 5 years of patients with undifferentiated uterine sarcomas was 65% and 40% had loco-regional control. Multivariate analysis showed that in the total patient population (endometrial stromal sarcoma and undifferentiated uterine sarcoma) pelvic radiotherapy was associated with a significantly improved overall survival. However, because of the limited case numbers and the retrospective analysis it is not possible to draw definitive conclusions.
4.5 Treatment for metastasis and recurrence
There are some indications that certain recurrences are histologically heterogeneous (displaying aspects of both high- and low-grade tumors) and that in tumors with evidence of receptors, endocrine therapy only affects the low-grade part and not the high-grade part, although it is this high-grade component which ultimately determines prognosis [84].
In contrast to LG-ESS, endocrine therapy does not play any role.
As regards the use of chemotherapy, this tumor entity can be treated similarly to other high-grade soft tissue sarcomas, although overall specific data on this point are limited.
5 Uterine adenosarcoma
5.1 Introduction, clinical and diagnostic work-up
This rare entity occurs in patients of all ages [85] but peaks in the 6th and 7th decades of life.
According to the WHO classification, adenosarcomas (AS) are defined as mixed epithelial-mesenchymal tumors of the uterus composed of benign epithelial and malignant mesenchymal components [86], [87].
If the mesenchymal component corresponds to a high-grade sarcoma (high-grade polymorphism, a higher mitotic rate, poss. myometrial or cervical stromal invasion and venous invasion with evidence of heterologous elements) and if this is detected in > 25% of the tumor, the diagnosis is an AS with sarcomatous overgrowth [88].
5.2 Prognosis
The rate of recurrence for adenosarcoma without sarcomatous overgrowth is 15 – 25%, but this increases to 45 – 70% for patients with sarcomatous overgrowth. A higher rate of recurrence has also been reported for cases with deeper myometrial invasion, lymph node invasion, a highly malignant heterologous stromal component and/or extrauterine spread. The mortality rate for a typical adenosarcoma is 10 – 25%, but it can be as high as 75% for adenosarcoma with sarcomatous overgrowth.
5.3 Surgical treatment
As with other sarcomas, the treatment of choice is hysterectomy without morcellation. It is not clear whether the adnexa should also be removed.
The benefit of systematic pelvic and para-aortic lymphadenectomy is also not clear [66]. The probability of lymph node involvement is only 3 – 4% [89]. Because of this low incidence and the fact that in this analysis lymph node status has no impact on patient survival, systematic lymphadenectomy is not routinely recommended.
5.4 Adjuvant systemic therapy and radiotherapy
To date, no benefit has been reported for any adjuvant therapy. Based on 1884 cases in the National Cancer Database, chemotherapy has no effect on survival and postoperative radiotherapy even has a negative impact on survival [89].
As with other uterine sarcomas, neither adjuvant systemic therapy nor radiotherapy are currently indicated after complete surgical resection.
If surgical resection was incomplete or in cases with advanced disease, the treating physician should consider whether sarcomatous overgrowth is present and/or whether hormone receptor expression is present; subsequent treatment should be similar to that for HG-ESS or LG-ESS.
5.5 Treatment for metastasis and recurrence
Because of the lack of data, the approach should be similar to that used for other uterine sarcomas, and surgery with complete resection is recommended.
Radiotherapy may be used as palliation to treat local inoperable recurrence or postoperatively to treat isolated findings.
There is no optimal regimen for systemic therapy. Recurrence of adenosarcoma with sarcomatous overgrowth should be treated the same way as other high-grade sarcomas [90]. Recurrence of adenosarcoma without sarcomatous overgrowth but with hormone receptor expression should be treated the same way as LG-ESS.
6 Follow-up
|
Consensus-based Recommendation 7.E26
|
|
Expert consensus
|
Strength of consensus +++
|
|
In the first 2 – 3 years after primary therapy, patients must be regularly followed up every three months with follow-up consisting of speculum examination, vaginal and rectal examination and, if necessary, ultrasound.
|
|
Consensus-based Recommendation 7.E27
|
|
Expert consensus
|
Strength of consensus +++
|
|
An additional diagnostic work-up for the early detection of metastasis may be beneficial.
|
Follow-up serves to ensure the success to treatment and safeguard the patientʼs quality of life.
It is, however, not clear whether intervention following the early detection of unilocular recurrence leads to an improvement in overall survival.
Nevertheless, the use of imaging as part of the further diagnostic work-up for the early detection of metastasis may be beneficial (cf. the specific chapters on individual entities).
7 Morcellation
|
Consensus-based Recommendation 8.E28
|
|
Expert consensus
|
Strength of consensus +++
|
|
The use of morcellation techniques to remove uterine sarcomas results in a worse prognosis. Patients must be informed of this.
|
|
Consensus-based Recommendation 8.E29
|
|
Expert consensus
|
Strength of consensus +++
|
|
Morcellation must not be carried out in a postmenopausal patient if the patient has been diagnosed with a newly developed “myoma”, a large rapidly growing “myoma” or a “myoma” which has become symptomatic for the first time.
|
|
Consensus-based Recommendation 8.E30
|
|
Expert consensus
|
Strength of consensus +++
|
|
Contained in-bag morcellation cannot not exclude the possibility of tumor cell dissemination.
|
|
Consensus-based Recommendation 8.E31
|
|
Expert consensus
|
Strength of consensus +++
|
|
Patients who had a morcellation procedure to remove a uterine sarcoma must present to a DKG-certified gynecological cancer center very soon after morcellation.
|
|
Consensus-based Recommendation 8.E32
|
|
Expert consensus
|
Strength of consensus +++
|
|
Adjuvant systemic therapy should not be generally carried out; nevertheless, because of the higher risk of recurrence after morcellation, systemic therapy should be considered depending on the histological subtype.
|
Morcellation of what is assumed to be benign tissue can occur during uterus-preserving surgery for the management of fibroid myomas or during total and subtotal hysterectomy, although postoperative examination of the resected specimen may reclassify it as a uterine sarcoma. Morcellation of the uterus or of parts of the uterus such as myomas and body of the uterus can occur during both endoscopic and vaginal procedures.
The prevalence of undetected uterine sarcomas during hysterectomies and myomectomies as reported in the literature varies between 1/204 and 1/7400 (0.49 – 0.014%) [91]. A summary analysis of the rate of accidentally operated uterine sarcomas in 10 international studies with 8753 procedures resulted in an incidence of 0.24% [91]. A meta-analysis of 10 120 patients from 9 studies resulted in a comparable incidence of accidentally operated uterine sarcomas of 0.29% [92]. A German analysis carried out in 2017 of 475 morcellation procedures performed from 2004 to 2014 reported a risk of 0.35% (1/280) for the accidental morcellation of a previously unknown uterine sarcoma during hysterectomy and no case of uterine sarcoma detected during 195 myoma morcellations (0/195) [93]. Another German study of 10 731 LSH operations reported a rate of 0.06% uterine sarcomas and 0.07% endometrial carcinomas [94].
Endoscopic intraabdominal morcellation of undetected sarcomas during hysterectomy, conservative surgical management of uterine myomas and laparoscopic supracervical hysterectomy (LSH) have been particularly associated with worsening of the oncological prognosis in terms of recurrence-free survival and overall survival [91], [95], [96], [97], [98], [99], [100].
In a systematic review of the literature and meta-analysis of 4 studies with 202 patients (75 with and 127 without morcellation) done in 2015, the rate of recurrence was higher after morcellation (62 vs. 39%; odds ratio [OR]: 3.16; 95% confidence interval [CI]: 1.38 – 7.26) as was the intraabdominal rate of recurrence (39 vs. 9%; OR: 4.11; 95% CI: 1.92 – 8.81). The overall survival rate after morcellation was also significantly lower (48 vs. 29%; OR: 2.42; 95% CI: 1.19 – 4.92) [101]. However, there was no difference in the extra-abdominal rate of recurrence. These data have been confirmed by other studies [102], [103], [104], [105], [106] but not by all [107], [108], [109], [110]. All of the studies were retrospective observational studies.
There is very little data on the prognosis of patients who had accidental morcellation of a uterine malignancy during vaginal hysterectomy. Wasson et al. analyzed 2296 vaginal hysterectomies, with morcellation carried out in 611 cases [111]. The incidence of accidentally morcellated malignancies was 0.82% (5/611): 3 cases were endometrial carcinomas and 2 cases were sarcomas. There was no recurrence in 5/5 cases; mean disease-free survival was 48 months. Another analysis of more than 3000 hysterectomies which included a total of 18 sarcomas confirmed the observation that transvaginal morcellation does not increase the rate of recurrence [112].
It is not possible to definitively exclude uterine sarcomas preoperatively based on clinical symptoms, growth patterns, ultrasound, CT, PET-CT or MR [91], [113].
Caution is always warranted if risk factors are present. In addition to age, the most common, known risk factor for uterine sarcoma is ongoing or completed tamoxifen therapy [114]. In addition, hereditary tumor syndromes such as Li-Fraumeni syndrome (which is associated with sarcoma) or Lynch syndrome and PTEN syndrome (which are associated with endometrial carcinoma) are also contra-indications for morcellation [115].
The occurrence of sonographically visible or palpable uterine tumors in the postmenopausal period is unphysiological as is increased growth of a known “myoma”. Although none of these factors have been confirmed to be risk factors for uterine sarcoma, either in isolation or in combination, from a clinical and pathophysiological perspective it may be wise to assume that such cases may have an increased risk of uterine sarcoma.
The use of contained in-bag morcellation to prevent the dissemination of malignant cells has been described in various studies [116], [117], [118], [119]. However, the technique of in-bag morcellation has not been clinically validated yet, and it is therefore not possible to make a reliable statement about the oncological safety of this technique [91], [99], [100].
As regards the appropriate procedure after morcellation of a sarcoma, all further approaches should be guided by the statements made in the position paper of the German Society of Gynecology and Obstetrics [91] and international recommendations and statements [95], [96], [97], [98], [99], [100]. The statements also apply to open or endoscopic tumor resections with or without morcellation [108]. The consensus is that the appropriate oncologic surgery recommended for the individual tumor entity should be carried out as soon as possible. It has not been confirmed whether this approach affects overall survival.
8 Information for Patients
|
Consensus-based Recommendation 9.E33
|
|
Expert consensus
|
Strength of consensus +++
|
|
Patients must be given the opportunity to include their partner or family members in talks and discussions.
|
|
Consensus-based Recommendation 9.E34
|
|
Expert consensus
|
Strength of consensus +++
|
|
Patients should be informed about contacting self-help groups.
|
