In this review of hepatic resection
for metastatic breast cancer, the
authors argue that a small group
of women with isolated liver metastases
may be appropriate candidates for
surgical resection. Although some data
have been reported, the few published
studies represent small, retrospective
single-institutional series with no standardized
criteria for resection. Nevertheless,
the potential prospect of
improved patient outcome in the setting
of liver metastases from breast
cancer deserves further consideration.
Tumor Biology
The rationale for resection of metastatic
lesions in breast cancer patients
runs counter to our current understanding
of the biology of metastatic
disease. Since stage IV disease by definition
is a manifestation of cancer progression
outside the primary tumor site,
it represents systemic progression that
is not likely to be curable by regional
treatment only. One possible exception
to this is in the setting of colorectal
metastasis to the liver. Due to the
anatomic drainage pattern of the colon
and rectum, liver metastasis may
represent the sole site of extracolonic
dissemination and may not be associated
with occult disease elsewhere. In
patients who undergo complete resection
of hepatic metastases, the 5-year
survival can exceed 30%.[1,2] However,
even in this patient population,
indicators of increased systemic involvement
based on nodal status, high
preoperative carcinoembryonic antigen
levels, and multiple metastases predict
a poor outcome following hepatic
metastasectomy.
Hepatic involvement is rarely the
first site of metastasis in breast cancer,
seen in no more than 5% of patients
with newly diagnosed stage IV
disease.[3] Visceral metastasis in
breast cancer patients has been associated
with short disease-free survival,
high-grade disease, and poor
prognosis. Thus, patients with liver
involvement are likely to have a short
time to disease progression, and a
narrow window in which surgical
resection may potentially have an impact.
Furthermore, even liver metastases
amenable to resection often
indicate additional occult disease. In
at least two studies, over half of patients
undergoing liver metastasectomy
for breast cancer developed
subsequent metastatic disease in the
liver.[4,5] Given the morbidity of
hepatectomy, preoperative radiographic
confirmation of resectability
remains critical.
Patient Selection
Despite the above concerns, it is
noteworthy that several series have
demonstrated favorable survival following
hepatic resection for metastatic
breast cancer. As with many
invasive interventions in the metastatic
setting, careful patient selection is a
critical determinant of outcome. The
authors suggest that there may exist a
limited population of patients with
metastatic disease who may benefit
from such a procedure. This population
would necessarily exclude those
with extrahepatic disease or extensive
disease in the liver, poor performance
status, or a short disease-free
interval. Although some studies have
shown a worse prognosis after liver
resection in patients with estrogen receptor
(ER)-negative disease, it is not
yet clear whether this factor alone
should exclude a patient from consideration
of hepatic resection if other
criteria are met.
It important to consider, however,
that the improved outcome seen in
patients undergoing liver resection
may stem from tumor biology rather
than the intervention itself. A solitary
liver metastasis and long disease-free
interval may represent indolent disease
rather than serve as an indicator
of who may benefit from hepatic resection
per se. Importantly, the largest
reported series of such patients
showed no association between the
extent of surgical resection (R0, R1,
or R2) and outcome,[5] calling into
question whether the relationship between
hepatic resection and prognosis
is, in fact, a causal one.
Neaodjuvant Chemotherapy
for Liver Metastasis
Although no standardized chemotherapy
protocol exists for preoperative
treatment of stage IV breast
cancer, neoadjuvant treatment is gaining
increased acceptance in the treatment
of colorectal hepatic metastases.
The rationale for this approach includes
the fact that it improves resectability
and allows for a more durable
response by combining local and systemic
therapy. This approach may be
particularly attractive when treating
hepatic metastasis in breast cancer,
since a neoadjuvant trial period may
help identify patients who harbor other
sites of distant disease and thus
would not benefit from surgery.
Outcome Assessment
Using the above criteria, relatively
few patients will present with surgically
resectable disease confined to
the liver alone. In contrast, up to 20%
of patients with colorectal metastases
may be candidates for liver resection.
Furthermore, given the perceived survival
advantage of patients with breast
cancer metastases undergoing liver resection
in retrospective series, it is
unlikely that a prospective randomized
trial could be successfully
conducted.
Therefore, the impact of hepatic
metastasectomy is difficult to interpret
at the present time. Inclusion criteria
differ across studies, technical
conduct of the procedures (eg, use of
ultrasound or radioablative techniques)
is not standardized, and chemotherapy
has been variably used
both before and after surgery. In addition,
the use of hormone therapy in
women with ER-positive disease is
an important factor that could arguably
affect both recurrence and survival
more than local therapy.
Conclusions
Given the existing data, it is reasonable
to consider surgical resection of
hepatic metastases for breast cancer.
However, few patients are good candidates
for this procedure. Because of the
limitations inherent in observational
studies as well as the risks associated
with any hepatic resection, it is important
to identify those patients most likely
to benefit from hepatic metastasectomy.
Future efforts must include the establishment
of standardized criteria for
patient selection, surgical technique,
and adjuvant treatment in order to allow
comparison across studies.
