Details

Autor(en) / Beteiligte

• Amayiri, Nisreen
• Tabori, Uri
• Campbell, Brittany
• Bakry, Doua
• Aronson, Melyssa
• Durno, Carol
• Rakopoulos, Patricia
• Malkin, David
• Qaddoumi, Ibrahim
• Musharbash, Awni
• Swaidan, Maisa
• Bouffet, Eric
• Hawkins, Cynthia
• Al‐Hussaini, Maysa

Titel

High frequency of mismatch repair deficiency among pediatric high grade gliomas in J ordan

Ist Teil von

• International journal of cancer, 2016-01, Vol.138 (2), p.380-385

Erscheinungsjahr

2016

Quelle

Wiley Online Library Journals Frontfile Complete

Beschreibungen/Notizen

• Biallelic mismatch repair deficiency (bMMRD) is a cancer predisposition syndrome affecting primarily individuals from consanguinous families resulting in multiple childhood cancers including high grade gliomas (HGG). This is the first study to assess the prevalence of bMMRD among patients with HGG in countries where consanguinity is high. We collected molecular and clinical information on all children diagnosed with HGG and supratentorial primitive neuroectodermal tumors (sPNET) between 2003 and 2013 at King Hussein Cancer Center, Jordan. Comparison was made to a similar cohort from Toronto. Clinical data regarding presence of café au lait macules(CAL), family history of cancer, consanguinity, pathology and treatment were collected. Tumors were centrally reviewed and tested for MMRD by immunohistochemistry of the corresponding proteins. Forty‐two patients fulfilled the inclusion criteria, including 36 with HGG. MMRD was observed in 39% of HGG of whom79% also lost MMR staining in the corresponding normal cells suggestive of bMMRD. P53 dysfunction was highly enriched in MMR deficient tumors ( p  = 0.0003).The frequency of MMRD was significantly lower in Toronto cohort (23%, p  = 0.03). Both evidence of CAL and consanguinity correlated with bMMRD ( p  = 0.005 and 0.05,respectively) but family history of cancer didn't. HGG with all three bMMRD risk factors had evidence of MMRD and all children affected by multiple bMMRD related cancers had identical gene loss by immunohistochemical staining. In Jordan, the frequency of clinical and immunohistochemical alterations suggestive of bMMRD in pediatric HGG is high. Genetic testing will enable appropriate counseling and cancer screening to improve survival of these patients. What's new? Homozygous germline mutations in mismatch repair (MMR) genes can result in biallelic MMR deficiency (bMMRD), a devastating childhood cancer syndrome frequently associated with consanguinity. This study suggests that in Jordan, where consanguinity is common, the prevalence of MMR dysfunction among pediatric patients with high grade glioma (HGG) may be alarmingly high. In the Jordan cohort, bMMRD occurrence was correlated with consanguinity and presence of café au lait macules. Because bMMRD‐related HGGs do not respond to conventional treatment regimens and additional tumor development is common, accurate diagnosis is essential. The findings presented here emphasize the importance of genetic testing.