Screening and identification of Lynch syndrome: a systematic review of the frequency of Lynch syndrome-associated clinicopathologic and molecular characteristics in Lynch syndrome gynecologic cancers.

BACKGROUND: This study aimed to investigate the frequency of Lynch syndrome-associated clinicopathologic and molecular characteristics in Lynch syndrome gynecologic cancers.
METHODS: A systematic literature search was conducted in the literature databases (Medline, CINAHL, EMBASE, Google Scholar, Cochrane Library, and Clinicaltrials.gov) to identify the studies describing clinicopathologic characteristics, MMR protein immunohistochemistry and/or MSI, MLH1 methylation, and genetic testing in Lynch syndrome gynecologic cancer patients.
RESULTS: A total of 24 of the evaluated studies that met the inclusion criteria were identified. A clinicopathological examination confirmed 242 endometrial cancer, 17 clear cells endometrial cancer, 35 serous endometrial cancer, 30 mixed and 21 other endometrial cancer. Thus, a total of 345 endometrial cancer was confirmed from the screening of 1,317 gynaecological cancer. However, the morphological analysis demonstrated 236 patients with endometrial cancer associated with Lynch syndrome. The frequency of confirmed LS with endometrial cancer was 68.40%. At diagnosis, the median age was 49.94±4.34 years, and the average BMI was 26.07±3.77 kg/m2. Endometrioid histology and stage I disease were the most frequent at 70.97% and 71.19% histological type and FIGO stage, respectively. Similarly, morphological and histological analysis demonstrated a higher degree of grade I cancer (47.28) and lymphovascular invasion (56.52%), respectively. DISCUSSION: Lynch syndrome-associated clinicopathologic and molecular characteristics occur significantly in Lynch syndrome gynecologic cancers and may improve risk stratification and triaging of gynecologic cancers for genetic testing. 2021 Translational Cancer Research. All rights reserved.

Introduction

Lynch syndrome (LS) is an autosomal dominant hereditary syndrome that increases the risk of the early development of multiple cancers, including colorectal (CRC), gynecologic, urothelial, and biliary tract cancers (1). The syndrome is implicated in 5% of endometrial cancers (EC), with a lifetime risk of 40–60% (2,3).

LS has also been linked to cancers of the endocervix (4). The syndrome results from inactivating germline mutations in genes that encode mismatch repair (MMR) proteins. Pathogenic MMR gene mutations associated with LS typically involve four primary genes, including MLH1, PMS2, MSH2, and MSH6 (1,3). MSH2 expression can also be lost due to epigenetic silencing resulting from the germline deletion of the EPCAM gene (5,6).

Immunohistochemistry (IHC) of proteins encoded by the DNA MMR genes and microsatellite instability (MSI) are becoming the mainstay of LS molecular screening, supplementing the family history-based clinical criteria such as Amsterdam II and Bethesda (7-9). IHC tests the expression of MMR proteins in tumour tissue. MLH1 and PMS2 are heterodimers. MLH1 mutation, therefore, results in the loss of expression of both MLH1 and PMS2. Similarly, MSH2 and MSH6 are heterodimers, with MSH2 transformation resulting in the loss of expression of MSH6 (3,7,10). However, isolated mutations of PMS2 and MSH6 can result in the isolated loss of expression of these genes. MLH1 failure can result from epigenetic silencing through promoter hypermethylation (10). Detection of MLH1 methylation with intact MSH2/MSH6 expression suggests a sporadic origin of a tumour (10,11).

MSI testing is a polymerase chain reaction-based (PCR) test that assesses DNA for the presence of somatic changes. The presence of MSI in at least two loci is pathogenic (MSI-High) (10). However, MSI has low sensitivity in MSH2 and MSH6 mutations, with a sensitivity of 55% and 77% in MSH2 and MSH6, versus 90% in MLH1/PMS2 (12). MMR IHC deficiency and MSI-H are present in 28% and 31% of endometrial malignancies, respectively (13). However, LS gynaecological cancers have MMR expression patterns and MSI similarities with sporadic gynaecological malignancies, making molecular criteria insufficient in triaging potential LS cancers (14). Additionally, more than 50% of gynecologic cancers with suspected LS based on these molecular criteria lack pathogenic LS-related germline mutations on genetic testing, indicating a high rate of false-positive LS-related MMR deficiency (15).

Clinical and pathologic studies have identified clinical and pathologic characteristics that may be potentially LS-defining. Some of these characteristics include the presence of synchronous or metachronous malignancies, lower BMI, and tumour characteristics such as lower uterine segment (LUS) involvement, endometrioid differentiation, and tumour-infiltrating lymphocytes (9,16,17). Although the inclusion of these clinicopathologic characteristics in the screening workflow may potentially enhance the sensitivity of LS triaging, the proportion of LS gynaecological cancers that demonstrate these clinicopathologic and molecular features have not been ascertained. Their effectiveness in identifying underlying LS in gynecologic cancer is therefore unclear. Thus, this systematic review describes the clinicopathologic features and frequency of LS associated gynecologic cancer. We present the following article in accordance with the PRISMA reporting checklist (available at https://dx.doi.org/10.21037/tcr-21-677).

Methods

Literature search strategies

A systematic electronic literature search was performed in the Medline, CINAHL, EMBASE, Google Scholar, and Cochrane Library. The search was based on the PICO strategy of PRISMA: Population (gynaecological cancer), Intervention (Clinical characteristics, histopathology, immunohistochemistry (MLH1, MSH2, MSH6, PMS2) with MLH1 methylation testing, Micro-satellite instability (MSI) analysis, Outcome (screening method positivity) and Comparison (germline mutational analysis). The search criteria included the terms ‘gynaecological cancer’, ‘endometrial cancer’, ‘cervical cancer’, ‘lynch syndrome’, ‘screening’, and ‘diagnoses. The date of publication was not limited (). The protocol of this systematic review was not registered in PROSPERO as it is not mandatory (18).

Figure 1

PRISMA flow diagram.

Inclusion criteria

Studies were included based on whether they reported the clinico-histopathologic characteristics of confirmed LS gynecologic cancers including tumour morphology and histological features, findings of LS screening, and diagnosis including MMR IHC and/or MSI, MLH1 methylation and genetic testing, and whether they were primary research studies. Studies that reported only clinicopathologic characteristics or molecular characteristics were included if germline mutation testing findings were reported. Studies were excluded if MLH1 methylation and germline mutation testing were not described.

Data extraction

Data were extracted from the included studies on the following variables: author, publication year, study design, number of patients with gynecologic (endometrial) cancers screened for LS, the average age at cancer diagnosis, number of patients with methylated and non-methylated MMR IHC deficient tumours, MSI-MMR IHC concordance rate, number of patients with positive germline mutation testing, BMI, family history of a LS cancer in a first-degree relative (FDR), number of patients with synchronous/metachronous LS cancers, tumour location, FIGO stage, grade, and histological types and features.

Statistical analysis

The extracted data were analyzed using descriptive statistics, including frequencies, percentages, means, median and standard deviations.

Results

Total 24 studies, including 14 prospective cohort and 7 retrospective cohort studies, 1 case report, one case-control and one prospective-retrospective study, were reviewed. Nineteen studies described both clinicopathologic and molecular characteristics of LS gynaecological cancers. Four and only one studies focused alone on clinicopathologic features and molecular characteristics, respectively.

Clinicopathologic characteristics

A total of 22 studies described the clinicopathologic characteristics of LS gynecologic cancers. The average age at diagnosis was 49.94±4.34 years with a range of 20–79 years. Six studies reported Lynch-syndrome gynecologic cancer in women aged 30 years and below. The body mass index (BMI) was reported in seven studies. The average BMI was 26.07±3.77 kg/m2 with a range of 20.3–32.2 kg/m2. A family history of LS in endometrial cancer was reported in 12 studies. Synchronous or metachronous LS cancers were reported in 12 studies ().

Table 1

Clinical characteristics

Variable (n=population)	Frequency n (%)/S.D
Lynch syndrome gynecologic cancers	517 (100.00)
Median age	49.94±4.34 years (range: 20–79 years)
Median BMI (n=7)	26.07±3.77 kg/m2 (range: 20.3–32.2 kg/m2)
History of Lynch syndrome cancer in an FDR (n=111)	84 (75.68)
Synchronous cancer (n=335)	68 (20.30)

BMI, body mass index; FDR, first degree relative. Percentages are based on sample sizes pooled from studies in which the specific clinical characteristic and its frequency was described. BMI was described in 7 studies.

Tumour location in endometrial cancers was described in eight studies. Out of 161 cases, the tumour was in the LUS in 28 (17.39%) cases in these studies. A variable number of studies reported tumour histology. Out of 341 cases, maximum studies (70.79%) were of endometrioid type. Mixed histology tumours consisted mainly of endometrioid, serous, or clear cell features. They consisted of other histological types, including carcinosarcoma, mucinous, adenosquamous, neuroendocrine, yolk sac, and Mullerian tumour in order of frequency. Among 612 cases, the majority (71.19%) had stage I disease, and among 481 cases, the majority (47.28%) had grade 1 tumours. Out of 78 patients, 20 (25.64%) had tumours with tumour-infiltrating lymphocytes. Twenty-seven (44%) of 61 patients had tumours with peritumoral lymphocytes. The lymphovascular invasion was reported in 13 (56.52%) of 23 cases ().

Table 2

Morphologic and histopathologic characteristics

Tumor characteristic (population)	Frequency, n (%)
Lower uterine segment location (n=161)	28 (17.39) cases
Average age	53.1±7.4 years
Histology
Endometrioid (n=341)	242 (70.97)
Serous (n=204)	17 (8.33)
Clear cell (n=256)	35 (13.67)
Mixed (n=284)	30 (10.56)
Other (n=232)	21 (9.05)
Total endometrial cancer	345
FIGO stage
Stage I (n=243)	173 (71.19)
Stage II (n=179)	27 (15.08)
Stage III/IV (n=190)	37 (19.47)
Grade
I (n=184)	87 (47.28)
II (n=166)	43 (25.90)
III (n=131)	38 (29.01)
Histological characteristics
Tumor infiltrating lymphocytes (n=78)	20 (25.64)
Peritumoral lymphocytes (n=61)	27 (44.26)
Lympho-vascular invasion (n=23)	13 (56.52)

Percentages are based on sample sizes pooled from studies in which the frequency of the specific morphologic and histopathologic characteristic was described.

Molecular characteristics

Twenty studies had complete data on MMR IHC and germline mutation testing findings. A total of 4,247 cases of gynecologic cancer were screened through IHC, MSI, and MLH1 promoter methylation testing. Six hundred twenty-eight cases of IHC deficiency without MLH1 methylation. MLH1 methylation findings were reported in 628 patients among 15 studies.

Out of 724 cases with MLH1 deficiency, 628 (86.74%) cases had MLH1 promoter methylation while 96 (13.26%) were non-methylated. Among the 649 cases with MMR IHC deficiency, unmethylated MLH1 deficiency was present in 96 (14.79%) cases. PMS2 expression was tested in 17 studies demonstrating 114 cases. MMR-MSI concordance rate findings were available in 15 studies. The average concordance rate was 30.37% ().

Table 3

MMR IHC

Population (n)	Number (%)
Screened Lynch syndrome cancers	4,247
Endometrial cancers	4210 (99.12)
Synchronous cancers	22 (0.88)
MLH1 deficient (n=4,247)	724 (17.04)
MLH 1 deficient methylated	628 (86.74)
MLH1 deficient non-methylated	96 (13.26)
Non-methylated MMR IHC Deficient (n=4,247)	649 (15.28)
Non-methylated MMR IHC Deficient
MLH1 deficient	96 (14.79)
PMS2 deficient	114 (17.56)
MSH2 deficient	173 (26.65)
MSH6 deficient	266 (40.98)
MMR IHC vs. MSI Concordance rate	30.37%
Endometrial cancer with Lynch Syndrome (n=345)	236 (68.40)

MMR IHC, mismatch repair protein immunohistochemistry; MSI, Microsatellite instability. Percentages are based on sample sizes pooled from studies in which the specific molecular screening finding was described. PMS2 was tested in 114 of the 649 MMR IHC deficient tumors.

Among the 649 MMR IHC deficient cases, 336 (51.77%) cases underwent genetic testing, 162 (48.2%) of the tested cases were confirmed to have pathogenic LS germline mutations. The germline mutations in cases with confirmed LS were reported in 20 studies (160 cases). Of 160 cases with confirmed germline mutations, MLH1 was mutated in 31 (19.5%) cases, while PMS2 was mutated in 14 (8.8%) cases. MSH2 and MSH6 were mutated in 64 (40.2%) and 51 (32.1%) cases, respectively ().

Table 4

Germline mutation characteristics

Population (n)	Frequency n (%)/S.D
MMR IHC Deficient cases that underwent genetic testing (n=649)	336 (51.77)
Tested MMR IHC Deficient cases with confirmed Lynch syndrome (n=336)	162 (48.2)
Germline mutation status (n=159)
MLH1 Mutation	31 (19.5)
PMS2 Mutation	14 (8.8)
MSH2	64 (40.2)
MSH6	51 (32.1)

MMR ICH, mismatch repair protein immunohistochemistry. Only 336 out of 469 MMR IHC deficient tumors underwent germline mutation testing. Specific germline mutations were described in 159 of 162 cancers with confirmed Lynch syndrome. One tumor had MSH2 and MSH6 germline mutations.

Discussion

A total of 24 studies reporting the clinicopathologic and molecular features of 236 genetically confirmed LS gynecologic cancers. Because of the high proportion of endometrial cancers in the reviewed studies, i.e., 4,210 (99.12%) (), ‘endometrial cancer’ is used synonymously with ‘gynecologic cancer’ in some sections of this review.

The average age at diagnosis of LS gynecologic cancer was 49.94±4.34 years (). Young age at diagnosis of gynecologic cancer is an established characteristic of LS based on the findings of previous studies. Mas-Moya et al. found that patients who underwent genetic testing were younger (51 years) compared to the patients who did not undergo genetic testing (59 years) following molecular screening (19). In this review, the average age at diagnosing gynaecological cancers in patients who underwent molecular screening was 53.1±7.4 years. This review indicates the need for further risk stratification based on diagnosis among at-risk women in the 5th and 6th decades of life.

The average BMI of the patients with confirmed LS was 26.07±3.77 kg/m2 (). Previous studies have found an equivocal association between BMI and LS gynecologic cancers (20). However, the lower BMI obtained in this review compared to previous studies suggests that a lower BMI may also contribute to stratifying the risk of LS in gynecologic cancer patients. Gordhandas et al. found a statistically significant difference in BMI among patients with mutation-confirmed LS (27.6 kg/m2) compared to patients with MMR deficiency (32.6 kg/m2) (21). Similarly, Cohn et al. found that MMR deficient patients who have MSI tumours have a lower BMI (30.5 kg/m2) than MMR deficient patients with MSS tumours (33.8 kg/m2) (22), suggesting the possibility of a BMI related risk continuum. Since obesity is an established risk factor for endometrial cancer (23), BMI can be used to assign the risk for LS in gynecologic cancers, particularly endometrial carcinoma.

In an FDR, a family history of LS cancer was found in 84 (75.68%) (). However, this proportion may be lower since three of the studies that reported the highest percentage of cases with a history of LS cancer in an FDR included participants from high-risk families. A smaller proportion was obtained in a recent meta-analysis which found that family history-based triaging identifies only 56% of endometrial cancers with LS (13). Kahn et al. found that family history-dependent screening of endometrial cancers can miss approximately 43% of LS endometrial cancers (13). This is because most LS gynecologic cancer patients with unknown germline mutation status are likely to be probands.

Sixty-eight of 335 patients had synchronous or metachronous LS malignancies during LS gynecologic cancer diagnosis (). This proportion may be lower since some of the studies did not distinguish between synchronous and metachronous cancers. Other studies have also demonstrated a similar association. In the study conducted by Lu et al., out of nine patients with synchronous ovarian cancer who underwent genetic testing, only 1 (11.1%) had a germline mutation (24). However, the molecular characteristics of these tumours were not reported. Notably, the finding of MMR IHC deficiency in synchronous tumours predicts the existence of underlying LS. All three patients with synchronous tumours and MMR IHC deficiency who underwent germline testing had a pathogenic LS germline mutation (25). Synchronous cancer presentation may therefore complement molecular criteria in defining the risk profile of gynecologic cancer patients for genetic testing.

An LUS location of the LS endometrial cancer was found in 28 (17.39%) of 161 patients (). In the Westin et al. study, 5 out of 6 MMR IHC deficient women with LUS endometrial cancers who underwent genetic testing were confirmed to have LS (17). As such, the finding of LS-associated molecular characteristics in an LUS endometrial tumour may enhance the identification of LS.

In the reviewed studies, endometrioid differentiation was the most frequent (70.97%) histological type (). Gordhandas et al. found that LS gynecologic cancers typically demonstrate heterogenous histologies (21). However, their study did not cater for the variations in the sample sizes of the studies reporting these characteristics. Since 70–80% of all endometrial cancers are endometrioid (23), this review supports the need for universal screening for LS in endometrial cancers.

This review finds significant heterogeneity in the histological grades of LS gynecologic malignancies at diagnosis. Regarding tumour stage, the frequency of stage I disease in LS gynecologic cancers at the time of diagnosis was 71.19% (). This indicates that most gynecologic cancers caused by underlying LS are not advanced at the time of presentation. The high frequency of stage I cases may be related to the non-indolent clinical pattern of endometrial cancers since most women develop symptoms early during disease presentation (26). Tumour grade is therefore potentially non-efficacious in identifying underlying LS.

Twenty (25.64%) out of 78 patients had tumours with tumour-infiltrating lymphocytes feature. Peritumoral lymphocytes and lymphovascular invasion occurred in 44.26% and 56.52% of the cases. However, these characteristics were reported in small sample sizes (20, 27 and 13 cases, respectively). As such, although gynecologic cancer patients can be selected for genetic testing based on these histologic features, the absence of these features does not exclude underlying LS.

In patients with gynaecological cancers who underwent molecular screening, 649 (15.28%) cases had MMR IHC deficiency without MLH1 methylation (). As such, based on the current molecular criteria for triaging LS gynecologic cancers (10), only 15.28% of all gynecologic cancers are likely to be selected for germline mutation testing. Among 4,247 patients, 724 (17.04%) had a loss of MLH1. The frequency of methylation in tumours with loss of expression of MLH1 was 86.74% (628 patients). Kahn et al. obtained similar findings with a frequency of MLH1 loss of 20% and an MLH1 methylation rate of 86% (13). MLH1 methylation appears to have a significant correlation with an MSI-H status. Ten out of 11 MLH1 methylated cases in the Lu et al. study were MSI-H and germline mutation-negative (24). In two studies, an MLH1 methylation rate of 100%was found (27,28). Since one of the major hindrances of universal molecular screening is the prohibitive cost of MSI analysis (10), MLH1 methylation testing in tumours with isolated loss of expression of MLH1 may improve the feasibility of screening, precluding the need for MSI analysis.

According to this review, although the loss of expression of MLH1 in gynecologic cancers mainly results from promoter hypermethylation, the gene is still involved in a proportion of unmethylated MMR IHC deficient tumours comparable to both PMS2 and MSH2. Among unmethylated MMR IHC secondary tumours, loss of expression of MSH6 was the most frequent (40.98%) abnormality. However, this review confirms the findings of previous studies that have shown a predominant implication of the MSH2 and MSH6 genes in abnormal IHC MMR (29).

Approximately 48.2% of the MMR IHC deficient tumours that underwent germline testing confirmed LS. Mills et al. obtained a similar concordance rate (46.7%) between the two diagnostic workups. Several germline mutation variants of undetermined significance have been identified in MMR deficient tumours, which supports the possibility of an unelucidated Lynch-like syndrome (3,28).

MSH2 was the most frequently mutated gene (40%), followed by MSH6 (32%). This indicates that the majority of LS cases arise from mutations within the MSH2/6 heterodimer. MLH1 and PMS2 were mutated in 19.5% and 8.8% of the cases. The frequency of each germline mutation obtained in this study mirrors the findings of other meta-analytic studies (13).

Our finding of endometrial cancer with LS rate was 60.64%, according to the observation of 40–60% in Meyer et al. study (30). This is the first study to examine the frequency of LS-associated clinicopathologic and molecular characteristics in gynecologic cancers with mutation-confirmed LS. Previous studies have predominantly described these characteristics in MMR deficient and sporadic cancers (13,21). This study also used the individual sample sizes of the included studies to derive the proportions of LS gynecologic cancers exhibiting the clinicopathologic features of interest, which increased the accuracy of the findings. Additionally, this review included studies in which methylation findings were reported, hence the methylation status of all patients, and consequently, their valid eligibility for genetic testing was known.

Limitations

One limitation of this review is the small sample of non-endometrial gynecologic cancers. This resulted from the shortage of studies with complete data on the clinicopathologic and molecular characteristics of endometrial gynecologic cancers. Similarly, the suboptimal rate of genetic testing among eligible patients yielded a small number of patients with a positive germline mutation. Reasons for low uptake of gene testing included a loss of follow-up, patient anxiety, rejection of testing, and failure of physicians to refer patients (27,31). However, since this review used a large sample size (4,247 patients), and the overall uptake rate of genetic testing was 73.67%, the small number of confirmed LS cases indicates the low prevalence of LS in gynecologic cancers.

Similarly, in two studies, some of the participants were referred for genetic counselling based on clinical criteria, which may affect the accuracy of the concordance rate between tumour testing and genetic testing (14,17). However, in one of the two studies, all the referred patients were later found to have LS-associated molecular features (17). In contrast, in the other study, most of the referrals met the molecular criteria (14).

Conclusions

This systematic review found that young age at diagnosis, normal or high normal BMI, family history of Lynch cancer syndrome, stage I disease, endometrioid differentiation, low-grade lesion, peritumoral lymphocytes, and lymphovascular invasion are frequent clinicopathologic characteristics of LS gynaecological cancers. The frequency of synchronous malignancies, LUS tumour location, and tumour-infiltrating lymphocytes are low to intermediate. Similarly, the high rate of involvement of the MSH2/MSH6 heterodimer in both MMR IHC deficiency and LS germline mutations, alongside the high frequency of non-LS-related MLH1 loss, indicates that MSH2/MSH6 abnormality is a high-risk molecular characteristic.