ABSTRACT:
BACKGROUND:
Stage shift is widely considered a major determinant of the survival benefit
conferred by breast cancer screening. However, factors and mechanisms
underlying such a prognostic advantage need further clarification. We sought to
compare the molecular characteristics of screen detected vs. symptomatic breast
cancers and assess whether differences in tumour biology might translate into
survival benefit.
METHODS:
In a
clinical series of 448 women with operable breast cancer, the Kaplan-Meier
method and the log-rank test were used to estimate the likelihood of cancer
recurrence and death. The Cox proportional hazard model was used for the
multivariate analyses including mode of detection, age at diagnosis, tumour
size, and lymph node status. These same models were applied to subgroups
defined by molecular subtypes.
RESULTS:
Screen
detected breast cancers tended to show more favourable clinicopathological
features and survival outcomes compared to symptomatic cancers. The luminal A
subtype was more common in women with mammography detected tumours than in
symptomatic patients (68.5 vs. 59.0%, p=0.04). Data analysis across categories
of molecular subtypes revealed significantly longer disease free and overall
survival for screen detected cancers with a luminal A subtype only (p=0.01 and
0.02, respectively). For women with a luminal A subtype, the independent
prognostic role of mode of detection on recurrence was confirmed in Cox
proportional hazard models (p=0.03). An independent role of modality of
detection on survival was also suggested (p=0.05).
CONCLUSIONS:
Molecular
subtypes did not substantially explain the differences in survival outcomes
between screened and symptomatic patients. However, our results suggest that
molecular profiles might play a role in interpreting such differences at least
partially. Further studies are warranted to reinterpret the efficacy of
screening programmes in the light of tumour biology.
Source: Molecular profiles
of screen detected vs. symptomatic breast cancer and their impact on survival:
results from a clinical series. Crispo A (anna.crispo@tin.it),
Barba M, D Aiuto G, De Laurentiis M, Grimaldi M, Rinaldo M, Caolo G, D Aiuto M,
Capasso I, Esposito E, Amore A, Di Bonito M, Botti G, Montella M. BMC Cancer.
2013 Jan 10;13(1):15.
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