Abstract
Purpose Endometrial cancer (EC) is often the sentinel cancer in women with Lynch Syndrome (LS). However, efforts to implement universal LS screening in EC patients have been hampered by a lack of evidence detailing the proportion of EC patients that would be expected to screen positive for LS.
Methods Studies were identified by electronic searches of Medline, Embase, Cochrane CENTRAL and Web of Science. Proportions of test positivity were calculated by random and fixed-effects meta-analysis models. I2 score was used to assess heterogeneity across studies.
Results Fifty-three studies, including 12,633 EC patients, met the inclusion criteria. The overall proportion of endometrial tumors with microsatellite instability or mismatch repair (MMR) deficiency by immunohistochemistry (IHC) was 0.27 (95%CI 0.25-0.28, I2:71%) and 0.26 (95%CI 0.25-0.27, I2:88%), respectively. Of those women with abnormal tumor testing, 0.29 (95%CI 0.25-0.33, I2:83%) had LS-associated pathogenic variants on germline testing; therefore around 3% of ECs can be attributed to LS. Pre-selection of EC cases did increase the proportion of germline LS diagnoses.
Conclusion The current study suggests that prevalence of LS in EC patients is 2-3%, similar to that of colorectal cancer patients; therefore our data supports the implementation of universal EC screening for LS.
Methods Studies were identified by electronic searches of Medline, Embase, Cochrane CENTRAL and Web of Science. Proportions of test positivity were calculated by random and fixed-effects meta-analysis models. I2 score was used to assess heterogeneity across studies.
Results Fifty-three studies, including 12,633 EC patients, met the inclusion criteria. The overall proportion of endometrial tumors with microsatellite instability or mismatch repair (MMR) deficiency by immunohistochemistry (IHC) was 0.27 (95%CI 0.25-0.28, I2:71%) and 0.26 (95%CI 0.25-0.27, I2:88%), respectively. Of those women with abnormal tumor testing, 0.29 (95%CI 0.25-0.33, I2:83%) had LS-associated pathogenic variants on germline testing; therefore around 3% of ECs can be attributed to LS. Pre-selection of EC cases did increase the proportion of germline LS diagnoses.
Conclusion The current study suggests that prevalence of LS in EC patients is 2-3%, similar to that of colorectal cancer patients; therefore our data supports the implementation of universal EC screening for LS.
Original language | English |
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Journal | Genetics in Medicine |
Early online date | 14 May 2019 |
DOIs | |
Publication status | E-pub ahead of print - 14 May 2019 |
Keywords
- Systematic review
- Lynch Syndrome
- endometrial cancer
- mismatch repair (MMR) immunohistochemistry
- microsatellite instability (MSI)