Streamlining universal screening for lynch syndrome (LS): Towards improved yield of genetic counseling (GC).

Authors

null

Stefania Sciallero

Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy

Stefania Sciallero , Azzurra Damiani , Simonetta Zupo , Linda Battistuzzi , Alberto Puccini , Carla Bruzzone , Edoardo Gonella , Viviana Gismondi , Mariella Dono , Luca Mastracci , Alberto F. Sobrero , Liliana Varesco , Federica Grillo

Organizations

Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genova, Italy, Azienda Ospedaliera Universitaria San Martino, Genova, Italy, Molecular Diagnostic Unit, Pathology Department, IRCCS Ospedale Policlinico San Martino, Genoa, Italy, Department of Informatics, Bioengineering, Robotics and Systems Engineering , Department of Internal Medicine and Medical Specialties, University of Genoa, Genova, Italy, Medical Oncology Unit 1, IRCCS Ospedale Policlinico San Martino, Genoa, Italy, Unit of Hereditary Cancer, IRCCS Ospedale Policlinico San Martino, Genoa, Italy, Department of Surgical and Diagnostic Sciences (DISC), University of Genova and IRCCS San Martino-IST University Hospital, Genoa, Italy, IRCCS Ospedale San Martino IST, Genova, Italy, Ospedale Policlinico San Martino IRCCS per l'oncologia , Genova, Italy

Research Funding

Other

Background: LS is largely underdiagnosed although Universal Screening (US) in colorectal cancer (CRC) patients through MisMatch Repair deficiency (MMR-d) testing is widely endorsed. Low adherence to guidelines among oncologists may be partly due to a lack of consensus on whether all MMR-d patients should be referred to GC/Genetic Testing (GT). As BRAF mutation rules out LS, we estimated the increased yield of LS diagnosis from GC /GT which could be obtained by selecting candidates for GC through BRAF testing. Methods: From 2011 to 2016, 1447 consecutive stage I-IV CRC surgical patients at a single institution, underwent immunohistochemistry (IHC) for LS using anti MLH1, MSH2, MSH6 and PMS2 antibodies. Oncologists were invited to refer all MMR-d patients to GC/GT. BRAFV600E testing was carried out only in case of MLH1 protein loss at IHC. Results: MMR-d was found in 194 patients (13%), with 171 showing loss of MLH1 expression (88%). Oncologists referred 27 (16%) to GC. Among the 21 who underwent GC, BRAF testing and GT, 9 were BRAF wild type (wt) (43%) and none had LS. Among the 23 MMR-d patients with loss of expression of MSH2, MSH6 or PMS2 (≠MLH1), oncologists referred 9 to GC (39%): 7 underwent GC / GT and 3 carried LS (43%) at GT. Median age was 76 years (range 30-97) in the MMR-d group, 78 (range 41-97) in the MLH1 group and 63 (range 30-86) in the ≠MLH1 group. Overall, LS was diagnosed in 3 of the 28 MMR-d patients (11%) who underwent GC /GT, possibly an underestimate due to the advanced median age of our MLH1 loss patients. Had we only offered GC to the 9 BRAF wt patients among the 21 with MLH1 loss, we could have avoided 12 (57%) of the GC sessions conducted, increasing the yield of LS diagnosis from 3/28 (11%) to 3/16 (19%) (75% increase). Conclusions: When US for LS is adopted, a GC referral rate reduction of 57% among MLH1 loss patients, and an overall increase in the yield of GC of about 75% can be obtained by testing for BRAF mutation before oncologist referral to GC rather than after. As multistep selection of patients by oncologists may be unfeasible, CRC pathology reports with combined MMR-d and BRAF testing (for MLH1 loss at IHC) and an ‘LS suspicion alert’ could improve oncologists’ awareness of LS and compliance with guidelines.

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Abstract Details

Meeting

2019 Gastrointestinal Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Cancers of the Colon, Rectum, and Anus

Track

Cancers of the Colon, Rectum, and Anus

Sub Track

Prevention, Diagnosis, and Screening

Citation

J Clin Oncol 37, 2019 (suppl 4; abstr 503)

DOI

10.1200/JCO.2019.37.4_suppl.503

Abstract #

503

Poster Bd #

D6

Abstract Disclosures

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