INTRODUCTION
In Brazil, it is estimated that breast cancer shall be the most common cancer
among women in 2018 and 2019, accounting for 29.5% of all new cases of cancer in
the country1. The treatment of patients
with breast cancer, and therefore this cancer’s aggressiveness, is set by the
characteristics of the illness at the time of diagnosis. The main interventions
that can be carried out, whether singly or in combination, are surgery
(conservative surgery or mastectomy), radiotherapy, chemotherapy, and hormone
therapy2.
Among the complications that occur after surgery for breast cancer, the most
common one is lymphedema, a chronic condition that is brought about by the
presence of a protein-rich fluid in the interstitial space3-6. The
onset of lymphedema can happen immediately after surgery, in rare cases, or
occur years after treatment6-10.
The etiology and risk factors for lymphedema seem to result from several
different factors, which are not totally known. In general, it is well known
that the main risk factors are: lymphadenectomy and/or axillary radiotherapy;
obesity; and invasive procedures on limbs on the same side as the breast
cancer11,12.
Whenever mastectomy is recommended, breast reconstruction is also considered and
can be performed either immediately or after the initial procedure (late breast
reconstruction)13. However,
considering the fall in morbidity provided by breast reconstruction carried out
immediately after mastectomy, thereby reducing the surgical procedure and
increasing patient satisfaction, it is important to identify the rate at which
lymphedema occurs when this type of surgical procedure is performed.
OBJECTIVE
This study aimed to analyze, through systematic review of literature, the
influence of immediate breast reconstruction on the prevalence of lymphedema
after mastectomy, among patients with breast cancer.
METHODS
To comply with the proposed objective, we used a method based on the Preferred
Reporting Items for Systematic Review and Meta-Analyses (PRISMA)14 guideline for systematic reviews. We
analyzed the most relevant studies that were originally brought out in any
language, up to August 2018, but which were in some way indexed by the
databases: US National Library of Medicine (PubMed), Cochrane Central Register
of Controlled Trials (CENTRAL), Web of Science and Scientific Electronic Library
Online (SciELO), where the searches were carried out.
Seeking to choose high-quality studies of scientific evidence, we sought
meta-analyses and randomized controlled clinical trials (RCCTs) on human
subjects, without any restrictions as to the year of publication.
The following key words have been used, in different combinations: “lymphedema”,
“lymphoedema”, “postmastectomy”, “mastectomy”, “breast cancer surgery”,
“prevalence”, and “incidence”.
Criteria for inclusion and exclusion were applied, as set out in Chart 1.
Chart 1 - Criteria for inclusion and exclusion of publications.
Criteria for Inclusion |
|
|
|
Delineation |
• |
RCCT |
• |
Meta-analysis |
|
• |
Series of cases |
|
Sample |
• |
Humans |
|
|
|
Intervention |
• |
Mastectomy only |
• |
Mastectomy associated with immediate
reconstruction
|
|
• |
Comparison between the approaches as
mentioned
|
|
Period of publication |
• |
Unspecified |
Language |
• |
Undefined |
Criteria for Exclusion |
|
|
|
Delineation |
• |
Poorly explained and/or incomprehensible
methodology
|
• |
Case report |
|
• |
Review of the literature |
|
|
|
|
Intervention |
• |
Mastectomy associated with late breast
reconstruction
|
• |
Non-surgical or unspecified treatment |
|
Method of publication |
• |
Abstract only |
Chart 1 - Criteria for inclusion and exclusion of publications.
The selection of the publications was first made based on an analysis of the
title and of the abstract of the studies obtained resulting from the searches
(Stage 1), then moving on to the elimination of duplicate results obtained in
the different databases as researched (Stage 2). Afterwards, the complete
versions of the publications were read, with the application of the criteria of
inclusion and exclusion (Stage 3), seeking to select the publications to be
included in the sample.
We must point out that the sample for this study has included all the studies
that have enabled the collection of data on the prevalence of lymphedema in
female patients with breast cancer, specifically after mastectomy, or in cases
of mastectomy associated with immediate breast reconstruction, or comparative
studies considering these two surgical approaches. The exclusion criteria were
the same as those used by Menezes at al15, that addressed late breast reconstructions, as also any studies in
which lymphedema occurred only in a cumulative way, not allowing the collection
of data regarding the total number of patients who developed this disease9,16.
In the publications included in the study sample, data were collected regarding
the type and the number of surgical operations, the mean age of the patients,
the method used for diagnosis, the period of monitoring, criteria for the
identification of lymphedema, and the number of patients who exhibited this
disorder. This data were then subjected to a meta-analysis for the establishment
of the results of this study.
The statistical analysis of data, comparing the prevalence of lymphedema between
mastectomized patients who had and had not been subjected to immediate breast
reconstruction, was made using the software SPSS for Windows 15 (IBM SPSS
Software, New York, USA), with use of the exact Fisher test with a significance
level of p < 0.05.
RESULTS
The searches carried out in different databases resulted in a sample of 248
different publications, which was reduced to 71 after the first stage of
analysis (title and abstract), then further reduced to 33 after the second stage
of analysis (removal of duplicates), and finally the group was further reduced,
with only 10 publications remaining after the third and final stage of analysis
(analysis of the full content of the articles); these met the criteria
established for inclusion and exclusion.
Out of the 10 studies included in the sample of this meta-analysis, five
addressed the prevalence of lymphedema in patients subjected to mastectomy
alone10,17-20; two discussed the prevalence of lymphedema in patients
subjected to mastectomy associated with immediate breast reconstruction6,21, while the final three studies compared both approaches22-24.
In all, the publications included in this sample included 2,425 patients who were
submitted only to mastectomy, and 2,772 patients who had been subjected to
mastectomy associated with immediate breast reconstruction; the mean ages of
these two groups were 51.05 and 47.75 years respectively. The patients who were
subjected only to mastectomy had a body mass index (BMI) of 25.97, while those
patients who had mastectomy with immediate breast reconstruction had a mean BMI
of 23.86 (Tables 1 and 2).
Table 1 - General characteristics of the patients subjected to mastectomy
only.
Study |
Surgical operations (n) |
Mean age (years) |
Mean BMI (kg/m2)
|
Follow-up |
Freitas Júnior et al.17 |
109 |
42.0 |
- |
48 months |
Petrek et al.20 |
263 |
52.3 |
- |
20 years |
Nesvold et al.18 |
263 |
55.0 |
26 |
Mean: 48 months |
Park et al.19 |
450 |
50.0 |
- |
24 months |
Avraham et al.22 |
130 |
61 |
26 |
- |
Card et al.23 |
549 |
- |
28.6 |
Mean: 59 months |
Lee et al.24 |
595 |
46.0 |
23.3 |
Mean: 53 months |
Pandey & Shrestha10 |
66 |
- |
- |
12 months |
TOTAL |
2,425 |
- |
- |
- |
MEAN |
- |
51.05 |
25.975 |
- |
Table 1 - General characteristics of the patients subjected to mastectomy
only.
Table 2 - General characteristics of the patients subjected to mastectomy and
immediate breast reconstruction.
Study |
Surgical operations (n) |
Mean age (years) |
Mean BMI (kg/m2)
|
Mean Follow-up |
Avraham et al.22 |
186 |
45 |
24 |
- |
Card et al.23 |
541 |
- |
25.7 |
59 months |
Crosby et al.21 |
1,499 |
50 |
25.7 |
56 months |
Lee et al.24 |
117 |
45.0 |
21.9 |
53 months |
Lee et al.6 |
429 |
43.0 |
22.0 |
45.3 months |
TOTAL |
2,772 |
- |
- |
- |
MEAN |
- |
45.75 |
23.86 |
53.3 months |
Table 2 - General characteristics of the patients subjected to mastectomy and
immediate breast reconstruction.
As we can see in Tables 3 and 4, lymphedema had a prevalence of 20.95%
among patients who had mastectomy only (508/2,425), while in the case of those
patients who had mastectomies associated with immediate breast reconstruction,
the prevalence was 5.23% (145/2,772). The exact Fisher test showed a
statistically significant difference (p < 0.001).
Table 3 - Prevalence of lymphedema after mastectomy alone.
Study |
Surgical operations (n) |
Lymphedema |
Total |
SM |
SM+ALND |
MRM |
SM (n) |
SM+ALND (n) |
MRM (n) |
Total |
n |
% |
Freitas Júnior et al.17 |
109 |
- |
- |
- |
- |
- |
- |
15 |
13.76 |
Petrek et al.20 |
263 |
- |
- |
- |
- |
- |
- |
128 |
48.67 |
Nesvold et al.18 |
263 |
77 |
- |
186 |
6 |
- |
37 |
43 |
16.35 |
Park et al.19 |
450 |
54 |
145 |
251 |
3 |
32 |
77 |
112 |
24.89 |
Avraham et al.22 |
130 |
59 |
71 |
- |
8 |
28 |
- |
36 |
27.69 |
Card et al.23 |
549 |
474 |
100 |
- |
- |
- |
- |
57 |
10.38 |
Lee et al.24 |
595 |
- |
- |
595 |
- |
- |
110 |
110 |
18.49 |
Pandey & Shrestha10 |
66 |
12 |
- |
54 |
2 |
- |
5 |
7 |
10.61 |
TOTAL |
2,425 |
676 |
316 |
1,086 |
19 |
60 |
229 |
508 |
20.95 |
Table 3 - Prevalence of lymphedema after mastectomy alone.
Table 4 - Prevalence of lymphedema after mastectomy associated with immediate
breast reconstruction.
Study |
Surgical operations (n) |
Lymphedema |
|
|
Total |
SM |
SM+ALND |
MRM |
SM (n) |
SM+ALND (n) |
MRM (n) |
Total |
n |
% |
Avraham et al.22 |
186 |
93 |
93 |
- |
6 |
23 |
- |
29 |
15.59 |
Card et al.23 |
541 |
474 |
100 |
- |
- |
- |
- |
21 |
3.88 |
Crosby et al.21 |
1,499 |
1,067 |
432 |
- |
7 |
43 |
- |
50 |
3.34 |
Lee et al.24 |
117 |
- |
- |
117 |
- |
- |
11 |
11 |
9.40 |
Lee et al.6 |
429 |
280 |
149 |
- |
- |
- |
- |
34 |
7.93 |
TOTAL |
2,772 |
1,914 |
774 |
114 |
13 |
66 |
11 |
145 |
5.23 |
Table 4 - Prevalence of lymphedema after mastectomy associated with immediate
breast reconstruction.
DISCUSSION
Interest in the prognosis for patients undergoing treatment for breast cancer has
increased considerably over the last few decades, both as a result of the
increase in the number of new cases as also due to a search for better
therapeutic options2,6,8-10. One of the
factors that has triggered new studies is the occurrence of lymphedema in
patients who have been subjected to mastectomy4-6,11,21,22, a topic
that is still a cause for considerable controversy in the literature, especially
with regard to factors related to etiology.
Here, we must point out that some factors of methodology could justify the
controversy between the results obtained in different studies, such as the
methods and the diagnostic criteria regarding lymphedema, as used by different
authors. Most of the studies included in the sample used in this research used
the method based on measurement of the circumference of the arm as a way to
diagnose lymphedema10,17-19,22.
There was a study that used a perometer together with arm measurement18 or on an exclusive basis24; studies that used subjective evaluation
by a specialist doctor (not using specific instruments, but just mentioning the
appearance of clinical signs and symptoms)6,23; a study that
made use of self-examination20; and
another study that did not even mention the method used21.
As a criterion for diagnosis of lymphedema, most studies used an arm
circumference of over 2 cm as the only criterion10,17,19,22 or together
with an increase of at least 10% in arm volume18. There was also one study that used the presence of hydropsy and
a difference of at least 1.27 cm between arm circumferences20; four studies did not describe the diagnostic criterion
in their methodologies6,21,23,24.
It is well known that lymphedema can appear immediately after mastectomy or even
years after surgery6-10, and two of the studies here that were
analyzed show that most patients showed some signs of lymphedema in the first
year after surgery.17,18.
Age is a controversial causative factor. While two studies included in this study
did not find any statistically significant differences with regard to this
variable19,21, another three studies did indeed show a
rise in the occurrence of lymphedema related to increased age of the patients
who had mastectomies at the time of surgery6,17,24.
Moreover, some authors have associated the development of lymphedema in
post-mastectomy patients with overweight and obesity11,12. In
general, the studies included here confirm this association. Apart from the
studies where overweight and obesity are statistically shown to be causative
factors17,19, in the studies where obesity showed no
statistical association with lymphedema, there was a significant association of
overweight as a causative factor20,22.
Furthermore, some studies have also confirmed that higher BMI levels (BMI >
25) were significantly associated with the occurrence of lymphedema6,21. According to Freitas Júnior et al.17, a possible cause for this positive association between
higher BMI and the onset of lymphedema lies in the greater difficulty for the
lymph to return in patients with a greater amount of fatty tissue.
We also point out that, in this study, the BMI of the patients who had mastectomy
alone was higher (25.97 kg/m2) than that
of patients who had mastectomies associated with immediate breast reconstruction
(23.86 kg/m2). This shows that studies
should standardize selection or division of the patients into groups according
to their BMI to make it more feasible to confirm this factor as an element of
proneness to the occurrence of lymphedema after mastectomy.
Some authors mention that dissection of the axillary lymph node is also a risk
factor for the development of lymphedema after a mastectomy11,12.
This was confirmed by this systematic review, as studies show that
lymphadenectomy significantly increases the occurrence of lymphedema6,19, both when a simple mastectomy is performed along with dissection
of the axillary lymph nodes, as also when the technique of modified radical
mastectomy is used19.
It is well known that immediate breast reconstruction is a technique that confers
many benefits to the patients, especially those whose breast cancers are in the
early stages. These benefits include: prevention of disfiguration of the chest
wall; reduction in costs; increased self-esteem; and general improvement in
quality of life6,23,25. This technique has been prioritized in literature
because it confers these benefits without affecting the biological behavior of
the breast cancer or promoting any relapse or having any interference on
auxiliary chemotherapy23,26.
In this study, we observed that apart from the benefits mentioned in the
literature with regard to immediate breast reconstruction, this technique also
has a potential to reduce the development of lymphedema among patients with
mastectomies. Confirming the findings of some previous studies22-24, the results of this study show that the immediate
breast reconstruction technique brought a significant reduction
(p <0.001) in cases with lymphedema that was present in
5,23% of the patients subjected to mastectomy with immediate reconstruction,
compared to the 20.95% observed among patients who received no breast
reconstruction.
It is important to emphasize that literature states that radiotherapy can be an
important causative factor for the development of lymphedemas among patients who
have had mastectomies for treatment of breast cancer11,12.
However, out of the ten studies included in the sample used in this study, most
of them10,17,18,20-23 did not
address the radiotherapeutic protocols to which the patients were subjected.
This made it infeasible to establish a correlation between this factor and the
development of lymphedema in both the treatment approaches addressed here.
In the three studies that considered this approach6,19,24, there was
an influence of radiotherapy on the development of lymphedema, which increased
according to the use of radiotherapy or the increase of the quantity used. In
this regard, we mention the importance of standardization and division of groups
of patients in further studies addressing this subject.
We also stress the importance of carrying out further studies on the occurrence
of lymphedema in mastectomized patients, with methodologies duly standardized
between them, and with greater monitoring time, especially when comparing
mastectomy alone and the association of mastectomies with immediate or late
breast reconstruction, which is still a gap in the literature. This would favor
the acceptance and acknowledgment of surgical techniques that offer a better
prognosis to patients with breast cancer.
CONCLUSION
Based on our systematic review, we concluded that mastectomy associated with
immediate breast reconstruction positively influenced the prognosis of patients
with breast cancer, resulting in a significantly lower rate of occurrence of
lymphedema, when compared to cases where mastectomy alone was performed.
Provided there are no contraindications, we can use immediate breast
reconstruction after mastectomies on patients undergoing treatment against
breast cancer, in a safe and efficient way, with a view to reducing the risk of
developing lymphedema.
COLLABORATIONS
RVER
|
Analysis and/or data interpretation, conception and design study,
data curation, final manuscript approval, investigation,
methodology, project administration, realization of operations
and/or trials, writing - original draft preparation, writing -
review & editing.
|
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1. Santa Casa de Montes Claros, Montes Claros, MG,
Brazil
2. Aspirante em Treinamento, Sociedade Brasileira
de Cirurgia Plástica, São Paulo, SP, Brazil.
Corresponding author: Rafael Vilela Eiras
Ribeiro Avenida Presidente Itamar Franco, nº 4001 - Dom Bosco, Juiz
de Fora, MG, Brazil Zip Code 36033-318 E-mail:
vilelaeiras@hotmail.com
Article received: August 29, 2018.
Article accepted: November 11, 2018.
Conflicts of interest: none.