Volume 45, Issue 2 pp. 200-204

Breast conservation in BRCA1 or BRCA2 mutation carriers with early stage breast cancer

Kelly Anne Phillips

Kelly Anne Phillips

Departments of Haematology and Medical Oncology and

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Michael J McKay

Michael J McKay

Radiation Oncology, Peter MacCallum Cancer Institute, East Melbourne, Victoria, Australia

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First published: 12 January 2002
Correspondence: Dr Kelly Anne Phillips, Department of Haematology and Medical Oncology, Peter MacCallum Cancer Institute, Locked Bag No. 1, A’Beckett St, Vic. 8006, Australia. Email: [email protected]

KA Phillips FRACP; MJ McKay PhD, FRANZCR.

SUMMARY

The role of breast conservation therapy (limited surgery and irradiation of the breast with/without axilla) in the approximately 5% of breast cancer patients who harbour a germline mutation in BRCA1 or BRCA2, is a largely unexplored area and is seen by some as controversial. The relatively high cumulative risk of second primary cancers in such patients and concern about a possible decreased ability of mutation carriers to repair DNA damage caused by radiation has fuelled this controversy. Published studies of breast conservation therapy in carriers of a mutation in BRCA1 or BRCA2 are reviewed, with particular attention to their methodology. These studies have not demonstrated any increase in radiation sensitivity of normal tissues in mutation carriers, either in terms of increased early or late toxicity or tumourigenesis. Likewise, tumour sensitivity to radiotherapy, which might be expected based on the known functions of the BRCA1 and BRCA2 genes, has not been documented to date in mutation carriers. Further, methodologically rigorous studies of large numbers of breast cancer patients who carry a mutation in BRCA1 or BRCA2 are required to fully elucidate these issues.

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