Less micrometastatic risk related to circulating tumor cells after endoscopic breast cancer surgery compared to open surgery
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Increase of circulating tumor cells (CTCs) has been found after surgery for various carcinomas but not confirmed for breast cancer, and whether endoscopic surgery confers identical effect to CTCs as open surgery did is not clear. The present study aimed to investigate whether CTCs increase after surgery and whether there is a difference between open surgery and endoscopic surgery.
Pre- and postoperative peripheral blood (5 mL) obtained from 110 female patients with operable breast cancer (53 underwent endoscopic surgery, 57 underwent open radical mastectomy). Quantitative real-time reverse transcription-PCR was done to detect cytokeratin 19 mRNA-positive CTC. CTC detection rate, cell number and the increase after surgery (named micrometastasis) were compared between the two groups.
In the open group, CTC positive rate before and after surgery were 22.81 and 33.33%; median CTC number before and after surgery were 0.21 and 0.43 and 17 patients (29.82%) had increased micrometastatic risk. In the endoscopic group, CTC positive rate before and after surgery were 24.53 and 28.30%; median CTC number before and after surgery were 0.27 and 0.36, and 8 patients (15.09%) had increased micrometastatic risk. There was a suggestive higher postoperative CTC detection rate and CTC number and a significant increased postoperation micrometastatic risk was observed in the open group compared to the endoscopic group (OR = 3.19, 95%CI: 1.05–9.65) after adjustment for clinicopathologic characteristics.
CTC tends to increase in breast cancer patients after surgery, and the micrometastatic risk was higher for open surgery compared to endoscopic surgery.
This study was prospectively registered at Chinese Clinical Trial Register (ChiCTR-OCH-10000859, 24 April 2010).
KeywordsBreast neoplasms Neoplastic cells Circulating tumor cells Micrometastases Endoscopic breast surgery Open surgery
circulating tumor cell
Michigan Cancer Foundation-7 breast cancer cell line
Breast cancer is by far the most common malignancy in women and it is ranked as the leading cause of cancer death . However, relapse and metastasis are still the primary reason for mortality, which mainly result from micrometastasis undetected by conventional approaches in blood, bone marrow or lymph nodes. Recent clinical researches have focused on detection and exploration of micrometastasis in the form of circulating tumor cells (CTC) in peripheral blood, which significantly contributes to distant metastasis . Results from studies have showed a clinical value of detecting and monitoring levels of CTC for evaluation of prognosis and therapeutic regime, as well as providing reference information for clinical decision-making [3, 4, 5]. Evidence from previous clinical investigations showed that tumor surgical manipulations induce tumor cell dissemination during operation of breast, hepatic, colorectal, cervical and prostatic cancers [6, 7, 8, 9, 10, 11, 12], even leading to an increased incidence of distant metastases according to further results of animal studies . In contrast to traditional open surgery, although endoscopic breast cancer surgery is capable of achieving local disease control in the majority of patients, it is considered that special procedures in endoscopic performance, including lipolysis solution, liposuction and endoscopic axillary dissection and so on, might increase the possibility of hematogenous dissemination of tumor cells, and there is a lack of evidence in support of the oncological security of this technique . Accordingly, the aim of this pilot study was to evaluate the effect of the surgical approach on micrometastatic risk correlated to surgery.
Detection of CTC before and after resection of primary breast tumor might be helpful to expand our knowledge about the effect of surgery on dissemination of malignant cells. One of the most frequently used markers for the detection of CTCs in the PB of patients with breast cancer is cytokeratin-19 (CK-19), a cytoskeletal protein expressed on epithelial but not on mesenchymal cells, that is expressed on virtually all breast cancer cells. Previous studies have reported that the detection of CTCs by real-time reverse transcription-polymerase chain reaction (RT-PCR) based on detection of CK-19 mRNA provides a sensitive, accurate approach and allows for reliable quantification of mRNA transcripts in an individual sample [15, 16].
Between 2010 and 2011, a total of 110 female patients with newly diagnosed breast cancer (stageI-III) treated with primary surgery at the Breast Disease Center of Southwest Hospital were prospectively enrolled. A preoperative diagnosis of breast carcinoma by core needle biopsy was required. Before surgery, a complete baseline diagnostic evaluation for the detection of distant metastases was performed, including chest X-rays, liver function tests, ultrasound of the liver and whole-body bone scan when indicated. Patients with distant metastases or open biopsy prior to operation were excluded. The choice of open or endoscopic approach depended on the surgeon to whom the patient was referred, and surgery was performed or supervised by an experienced surgeon. Fifty three of these 110 patients underwent endoscopic subcutaneous mastectomy and axillary dissection, including 20 patients who received immediate breast reconstruction with implant or latissimus dorsi flap and 33 patients who just received endoscopic nipple and/or skin sparing subcutaneous mastectomy first and will received breast reconstruction at a second stage. And 57 patients received open radical mastectomy. There was no difference in the protocol of anesthesia between the two groups. In endoscopic procedures, axillary dissection was performed before subcutaneous mastectomy and an endoscopic work space was maintained by inflation of the subcutaneous tissue using carbon dioxide at a pressure of 8-10 mmHg (1 mmHg = 1.33 kPa). The axillary lymph node dissection was also done for the open surgery cases, although mastectomy is performed followed by axillary dissection in the routine open modified radical mastectomy, while in the endoscopic procedure, axillary dissection is prior to mastectomy. Among the 53 microscopic surgery cases, 20(37.7%) received immediate breast reconstruction.
All the patients also participated in a prospective study for early diagnosis of recurrence, metastasis and prognosis monitoring by circulating breast-tumor cells detecting (ChiCTR-OCH-10000859). Tumor stage was classified according to the sixth edition of the TNM classification of the American Joint Commission on Cancer (6th edition). Written informed consent for the collection of blood samples was obtained from all participating patients and the protocol of this study was approved by the Ethical Committee of the Southwest Hospital (KY201003).
Blood samples, real-time RT-PCR assay for CK-19 mRNA detection
Five mL peripheral blood was drawn from every patient prior to surgery (t0) and 12 h after the operation (t1) and all laboratory analyses were conducted in a blinded fashion. Mononuclear cells, including tumor cells, were harvested by gradient density centrifugation using Ficoll-Hypaque. Total RNA isolation was carried out by using TRNzol reagent (Tiangen Biotech, Beijing, China) according to the manufacturer’s instructions. All RNA preparations and handling steps took place in a laminar flow hood under RNAse-free conditions. The isolated RNA was dissolved in diethylpyrocarbonate-treated water and stored at − 80 °C for future use. The purity and quantity of RNA were determined using a spectrophotometer (260 nm/280 nm). Reverse transcription of RNA was carried out with the PrimeScript™ RT reagent (TOYOBO, Japan). Two μg of total RNA was used as template to synthesize cDNA according to the manufacturer’s instructions. The real-time RT-PCR assay for CK-19 mRNA-positive CTCs has been previously described in detail elsewhere (SYBR Green Realtime PCR Master Mix, TOYOBO, Japan). The number of CTCs in each of the tested samples was expressed as Michigan Cancer Foundation-7 (MCF-7) breast cancer cell line equivalents per 2 μg of total-RNA, as determined by LightCycler system (Roche Diagnostics, Germany) software 3.1, according to the external standard calibration curve. According to the analytic detection limit of our assay, the presence of ≥0.9 MCF-7 cell equivalents/2 μg of total RNA was considered a positive result of CTCs, following the protocol of Stathopoulou et al.  Using this detecting limit as a cut-off, surgery is considered to implement an increased micrometastatic risk if the number of CTCs is increased beyond this cut-off after operation. Moreover, all blood samples were simultaneously tested for the integrity of RNA by demonstrating positive detection of the house keeping β-actin gene.
The Mann-Whitney test was used to compare the non-normally distributed number of CTCs between different surgical groups. The Wilcoxon test was used for paired comparison of the CTC numbers before and after surgery. Unpaired comparison of binomial variables was done using the Chi-square test or Fisher exact test (when the prerequisite of Chi-square test was not fulfilled). The paired comparison of binomial variables was done using the McNemar test. Unpaired comparison of ordinal variables between the two surgical groups was done using the Mann-Whitney test. Mantel-Haenszel stratified analysis was done to exclude the potential confounder bias introduced by tumor size, lymph node status or tumor stage. Propensity score matching was done with control for age, menopausal status, tumor size, lymph node, tumor stage, histology type, estrogen receptors status, progesterone receptors status, HER-2 status and pre-operation CTC status. The matching error was set to 0.1. Then Mc Nemar test was done for comparing the micrometastatic status between the matched two groups. Multi-variate analysis for the association of surgical type and micrometastatic risk was done by binary logistic regression (backward likelihood method), with adjustment for age (transformed into ordinal variable by optimal scaling analysis), menopausal status (premenopausal V.S. postmenopausal), tumor size (T1 to T3), lymph node (pN0 to pN3), tumor stage (I to III), histology type (Invasive ductal V.S. other type), estrogen receptors status (− V.S. +), progesterone receptors status (− V.S. +), HER-2 status (− to +++) and pre-operation CTC status (negative V.S. positive). The entry and removal probability for stepwise was set as default value (0.05 and 0.10, respectively). Furthermore, the interaction of surgical type and pre-operation CTC status was additionally analyzed by binary logistic regression, too. Data analysis was carried out with PASW Statistical software version 18.0 (SPSS Inc. Chicago, IL) and Review Manager 5.0 (The Cochrane Collaboration, Copenhagen).
Characteristics of the recruited patients
Endoscopic group (n = 53)
Open group (n = 57)
Lymph node (pN)
Estrogen receptors status
Progesterone receptors status
Surgery duration, min
Bleeding volume, mL
Detection of CTCs
Comparison for the positive rate of CTCs before and after surgery in the endoscopic and the open group
Endoscopic group (n = 53)
Open group (n = 57)
P value a
P value b
Comparison for number of CTCs before and after surgery in the endoscopic and the open group
Endoscopic group (n = 53)
Open group (n = 57)
P value a
P value b
Micrometastatic risk of CTCs in different breast cancer surgeries
The association between surgery type and micrometastatic risk: multi-variate analysis
Model 0 a
Model 1 b
Model 2 c
OR (95% CI)
OR (95% CI)
OR (95% CI)
2.39 (0.93, 6.13)
2.60 (0.99, 6.80)
3.19 (1.05, 9.65)
0.64 (0.25, 1.65)
2.16 (0.79, 5.87)
0.15 (0.02, 1.12)
1.07 (0.68, 1.67)
0.18 (0.03, 1.21)
2.23 (0.79, 6.28)
Pre-surgery CTC status
0.37 (0.10, 1.35)
6.31 (0.10, 418.40)
1.15 (0.46, 2.87)
1.42 (0.86, 2.33)
1.41 (0.78, 2.55)
1.84 (0.72, 4.73)
1.33 (0.54, 3.28)
0.91 (0.61, 1.38)
0.15 (0.01, 2.56)
Our study shows that a suggestive increased trend for the CTC positive rate (23.64% V.S. 30.91%), either in the open surgery group (22.81% V.S. 33.33%) or in the endoscopic surgery group (24.53% V.S. 28.30%). There is also a suggestive increase in the number of CTCs in each group after surgery (open surgery: 0.21 V.S. 0.43; endoscopic surgery: 0.27 V.S. 0.36). Furthermore, higher micrometastatic risk related to CTC was found in the open surgery group compared to the endoscopical group (OR = 3.19, 95%CI: 1.05–9.65), which indicates that patients who underwent open surgery will take more surgery-related potential metastatic risk.
Review of 16 published studies of CTC before and after surgery therapy
Detection rate preoperatively
Time interval after surgery
Detection rate postoperatively
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Maltoni R et al. 
Pierga JY et al. 
van Dalum G et al. 
Banys M et al. 
Daskalakis M et al. 
Sandri MT et al. 
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Thepjatri N et al. 
Krawczyk N et al. 
Ismail MS et al. 
Hu XC et al. 
Galan M et al. 
Krag DN et al. 
Choy A et al. 
McCulloch P et al. 
The operative treatment of breast cancer has made substantial directional changes. From Halsted’s radical operation to classical modified radical mastectomy, to widely accepted breast conservation, a shift from “maximum tolerable” to “minimum effective” treatment strategy has been evident [29, 30]. Conventional mastectomy is often associated with complications such as an obvious scar, physical defect, upper extremity edema and dysfunction. Mastectomy patients tend to suffer from ongoing anxiety and depression over the disfigurement of their bodies and the loss of a feminine figure. The endoscopic approach emerges as a response to the need for new “minimally invasive” surgical techniques that assure a local tumor control while decreasing surgery-related morbidity [31, 32]. Under endoscopic vision, meticulous dissection and hemostasis can be achieved with the harmonic scalpel, and the average blood loss is less than the conventional method . Endoscopic breast surgery plays an important role in the treatment of patients with early breast cancer. It is suitable for patients with small-to-moderate-sized breasts and reconstruction can be performed immediately or at a second stage, especially for Asian women. Endoscopic nipple and/or skin sparing subcutaneous mastectomy with immediate breast reconstruction restore the patient’s body image and improve cosmesis over open surgery. For instance, in our institution, we performed endoscopic harvesting of latissimus dorsi flap with prosthesis implantation for immediate breast reconstruction after nipple-sparing mastectomy in 2 patients with breast cancer who wished to avoid a long scar on the back. Both patients were satisfied with the esthetic results of the procedure using only 3 small trocar ports instead of a long visible scar on the back .
However, evidence for the safety in support of this technique is lacing. Whether the minimization of invasion by endoscopic surgery leads to a less or more induction of CTCs release is unknown by now. To the best of our knowledge, the present study is the first clinical study evaluating the effect of endoscopic surgery on CTCs in breast cancer patients underwent surgery. When increased micrometastatic risk is defined as the CTC number increased beyond the detection cut-off after operation, less micrometastatic risk was found in the endoscopic operated group, which indicates that patients underwent open surgery will take more surgery-related potential metastatic risk. Although the surgical principles are the same for both surgical approaches, the surgical sequence is different from each other. This difference may partially block cancer cell dissemination enhanced by surgical manipulation. However, a study with long-term follow-up in a larger population is required to confirm the clinical indication of our results. Our study found no significant difference of surgery duration or bleeding volume between the micrometastatic patients and the non-micrometastatic patients. It may indicate that these characteristics are not the main contributor for the higher micrometastatic risk in the open surgery group. The present study has several major limitations. First, the study is of observational design. Bias introduced by potential confounder, such as the subjective decision of therapy strategy affected by the disease status, could not be completed ruled out. Randomized clinical trial would be needed in the future to validate our findings. Second, some specific types of breast cancer such as ductal carcinoma was not recruited with adequate sample size for subgroup analysis. Hence the increase of micrometastatic risk observed in the present study may not be generalized to all cases of breast cancer. Third, although the increase of CTC in peripheral blood was widely accepted to be a promising biomarker of poorer prognosis, the clinical outcome of the patients, such as disease free survival and metastasis rate was not investigated in the present study due to the limited follow-up period and sample size. Whether the long-term risk of endoscopic breast cancer surgery is comparable with open surgery for breast cancer still acquires further study.
The present study found a suggestive increase of CTCs in breast cancer patients after surgery, and the endoscopic surgery was associated with less risk of metastasis related to CTCs compared to open radical mastectomy. The results may indicate that monitoring of CTC status is necessary for the breast cancer patients after surgery, especially for those who underwent open surgery. Future studies are needed to confirm our finding.
JJ, YZ, SL, WY designed the study. SL, WY, XY, LC, LF, HL, KL, YZ, JJ collected the data, designed and developed the database, carried out data analyses and produced the initial draft of the manuscript. SL, WY contributed to drafting the manuscript. All authors participated in the revised manuscript and have read and approved the final submitted manuscript.
This work was supported by Fund of Army Medical University (Third Military Medical University) (grant number 2010XLC03, 2018YFC1707503). The sponsor had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Ethics approval and consent to participate
Written informed consent was obtained from all participating patients and the protocol of this study was approved by the Ethical Committee of the Southwest Hospital (KY201003).
Consent for publication
The authors declare that they have no competing interests.
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