Abstract

The study aimed to assess the effects of breast-conserving surgery (BCS) versus mastectomy on survival and quality of life in Stages I, II, and III breast cancer, providing solid evidence for clinical decisions. We conducted a meta-analysis of randomized controlled trials on breast cancer treatments, searching databases such as PubMed and the Cochrane Library to compare BCS, and mastectomy’s effects on survival and quality of life. A combined total of 16 734 patients in the control group and 17 435 patients in the experimental group were included in this analysis. This meta-analysis used RevMan 5.3 (Cochrane Collaboration, Copenhagen, Denmark) software for analysis. Our meta-analysis of 34 169 patients from 11 studies showed that BCS significantly reduced the overall recurrence rate at a median follow-up of 29 months, with a mean difference of 1.27 and a 95% confidence interval of 1.19–1.36, strongly supporting its effectiveness (P< .00001). Furthermore, our analysis found no significant increase in 5-year local recurrence rates for BCS versus mastectomy, indicating its long-term effectiveness with a mean difference of 1.13 (95% confidence interval: [1.03, 1.24], P = .01). Additionally, there was a notable decrease in tissue ischaemic necrosis among patients who had received BCS, with a mean difference of 0.37 (95% confidence interval: [0.33, 0.42], P < .00001), underscoring its benefits and long-term viability. BCS resulted in fewer cases of tissue ischaemic necrosis and higher body image scores compared with mastectomy, suggesting that it is a preferable option for better cosmetic outcomes and potentially favourable effects on prognosis and quality of life.

Introduction

Breast cancer is the most common malignancy among women worldwide, with a total of 1.7 million new cases reported by 2012, accounting for 25% of all malignancies in women [1]. In 2011, China had 248 000 new cases, contributing to 12% of global breast cancer incidents. The incidence rate in urban areas was higher than that in rural areas [2]. With advancements in diagnostic and therapeutic methods, many breast cancer cases are now detected at an early stage, leading to increased survival rates and a growing number of breast cancer survivors [3]. Consequently, patients’ quality of life has gained prominence as a vital indicator for assessing treatment and rehabilitation outcomes [2].

The breast is a crucial secondary sexual characteristic in women, and surgical interventions undoubtedly have irreversible negative impacts on patients’ physical, psychological, and social aspects, thus affecting their overall quality of life [4]. Research into the impact of different surgical approaches on quality of life has become increasingly important. Clinical studies with 20 years of follow-up have confirmed that breast-conserving surgery (BCS) combined with radiation therapy achieves comparable survival rates to mastectomy in early-stage breast cancer cases. Hence, BCS has become a standard procedure [5–7]. This method is less invasive, offers better cosmetic outcomes, and preserves better physical function. However, international research suggests that although patients who have undergone BCS show significant advantages in body image aspects (including attractiveness, appearance, confidence, scars, and cosmetic outcomes), there may not be a substantial improvement in the overall quality of life [1]. Some studies [3, 8] even report that patients undergoing BCS with radiation therapy may experience more concerns about tumour recurrence, breast pain, and limited upper limb functionality, leading to a lower quality of life.

Recent studies examining the impact of different breast cancer surgical approaches on patients’ quality of life are scarce and yield varied conclusions [1, 9–12]. Although some clinical comparative studies have discussed the effects of BCS versus mastectomy on survival rates and quality of life among patients with breast cancer, there remains a need for updated systematic reviews encompassing recent, high-quality clinical research. Therefore, this study employs a meta-analysis to comprehensively evaluate the relevant research on the impact of BCS versus mastectomy on patient survival rates and quality of life. We hypothesize that BCS will show improved quality-of-life metrics without significantly compromising survival rates. This approach aims to explore in depth the features of breast cancer and primarily investigate the influence of these surgical approaches on patients, with the ultimate goal of assessing their clinical value for breast cancer prevention and treatment. Valuation of the clinical relevance of our findings by emphasizing that BCS, although not entirely eradicating the tumour, significantly reduces overall recurrence rates and the incidence of postoperative complications, such as tissue ischaemic necrosis. This insight is crucial for practitioners aiming to balance effective cancer treatment with the preservation of quality of life. Furthermore, we delve into the psychological and physical benefits of BCS, substantiated by higher postoperative body image scores, highlighting its value in holistic patient care. While the study focuses on Stages I–III, the impact on patients with Stage IV breast cancer remains an area of future research.

We hypothesize that BCS will show improved quality-of-life metrics without significantly compromising survival rates. This approach aims to deeply explore the features of breast cancer and primarily investigate the influence of these surgical approaches on patients, with the ultimate goal of assessing their clinical value for breast cancer prevention and treatment.

Research methodology

Literature search strategy

Time frame: between database inception and 2023; databases searched (both Chinese- and English-language databases): PubMed, Embase, Web of Science, Cochrane Library. The specific search strategy was as follows: ‘Breast Neoplasms’[MeSH] AND ((‘Breast-Conserving Treatment’[MeSH] OR ‘Mastectomy’[MeSH]) AND (‘Survival Rate’[MeSH] OR ‘Quality of Life’[MeSH] AND ‘Outcome Assessment (Health Care)’[MeSH])) AND (‘Randomized Controlled Trials as Topic’[MeSH] OR ‘Clinical Trials as Topic’[MeSH]) AND (‘Meta-Analysis as Topic’[MeSH] OR ‘Systematic Reviews as Topic’[MeSH]) AND (‘Choice Behavior’[MeSH] OR ‘Treatment Outcome’[MeSH] OR ‘Long-Term Follow-Up Studies’[MeSH]) AND (‘Neoplasm Excision’[MeSH] OR ‘Neoplasm Recurrence, Local’[MeSH] AND ‘Risk Factors’[MeSH]) AND (‘Patient Satisfaction’[MeSH] AND ‘Case-Control Studies’[MeSH] OR ‘Cohort Studies’[MeSH]) AND (‘Antineoplastic Agents’[MeSH] AND ‘Comparative Study’[MeSH]) AND (‘Treatment Efficacy’[MeSH] AND ‘Review Literature as Topic’[MeSH]). Studies were included in English or with English translations, if available. Grey literature, such as unpublished theses, was excluded due to potential biases and variable quality. A preliminary search yielded 298 relevant articles. This number was reduced to 160 after a meticulous removal of duplicates based on title comparison. Subsequent in-depth examination of titles and abstracts led to an initial screening of 54 articles, focusing on their relevance and alignment with the research objectives. After further examination of the full texts, 18 articles were excluded due to their low methodological quality or because their focus did not align precisely with the research objectives, such as by diverging from the central topic of comparing BCS with mastectomy. This refined the selection to 36 articles. An additional rigorous round of full-text review was conducted, during which 25 articles were excluded because they contained incomplete data, had small sample sizes, or lacked necessary statistical information. Ultimately, 11 English-language articles that met all the stringent quality and relevance criteria were included in the analysis. Each step of this meticulous exclusion process is detailed in Fig. 1 to provide transparency and reproducibility. All surgeries were conducted in a sterile operating room environment with the patient under general anaesthesia. High-definition cameras and monitors were utilized for visualization in cases where endoscopic or minimally invasive approaches were employed. Standard surgical instruments were used, and all procedures were conducted by board-certified surgeons who specialize in breast surgery.

Literature selection flowchart.
Figure 1

Literature selection flowchart.

Inclusion and exclusion criteria for the literature

Inclusion and exclusion criteria

The inclusion criteria of the study included (i) women with Stages I–III breast cancer, (ii) pathologically confirmed invasive ductal carcinoma, and (iii) completed chemotherapy and/or radiation therapy.

Exclusion criteria

The exclusion criteria of the study included (i) patients with severe chronic or disabling diseases, such as diabetes, Parkinson’s disease, or hemiplegia, (ii) inability to comprehend or read due to intellectual or mental factors, (iii) patients with recurrence or metastasis during the follow-up period, (iv) patients with bilateral mastectomy and patients who underwent neoadjuvant therapy before surgery or did not receive adjuvant therapy after surgery, (v) patients with a history of breast cancer surgery, (vi) patients with other malignant tumours, (vii) patients with impaired heart, liver or kidney function, (viii) patients with coagulation disorders, (ix) patients with synchronous bilateral breast cancer, and (x) patients aged ≥70 years were specifically excluded from this meta-analysis due to the increased complexity of comorbid conditions prevalent in this age group, which could confound the outcomes and impair the clarity of the analysis regarding the direct impact of BCS versus mastectomy on survival rates and quality of life.

Outcome measures

The outcome measures were as follows: (i) surgical details in both groups—a comparison of the procedural aspects between BCS and mastectomy; (ii) an enumeration of possible complications, such as tissue ischaemic necrosis, seroma, hematoma, and surgical site infections; (iii) prognosis and survival: 5-year local recurrence and survival outcomes in both groups, analysing and evaluating prognosis; and (iv) quality-of-life assessment utilizing the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (QLQ), specifically the QLQ-BR23 for breast cancer and QLQ-C30 for patients with general cancer.

Literature quality assessment

Two researchers independently conducted the assessment of literature quality, and the results were compared and discussed. The study employs the QLQ-BR23 and QLQ-C30 questionnaires, renowned for their comprehensive approach to evaluating the various dimensions of a patient’s life post-surgery. These scales measure a wide range of factors including sexual function, upper limb symptoms, and breast symptoms. In the event of a disagreement during the literature quality assessment process, the issue was resolved by consultation with a senior researcher who possesses >10 years of experience in oncology research. This senior researcher’s adjudication was considered final to ensure the integrity and reliability of the assessment. These questionnaires collectively assess various dimensions including body image, sexual functioning, symptoms, and future perspectives. The inclusion of these measures allows for a nuanced understanding of how each surgical option affects the patient’s daily living and psychological well-being. This comprehensive approach ensures that our analysis remains patient-centred, reflecting the real-world implications of the chosen surgical method. The Cochrane Risk of Bias assessment tool was used to evaluate the quality of randomized controlled trials, including seven domains. Each domain was evaluated as ‘low risk of bias’, ‘high risk of bias’, or ‘unclear’. When all criteria were fully met, the likelihood of bias was minimized and categorized as Level A; when some criteria were partially met, the likelihood of bias was moderate and categorized as Level B; when none of the criteria were met, the likelihood of bias was higher and categorized as Level C.

Statistical methods

Meta-analysis was conducted using the analysis module of RevMan 5.3 (Cochrane Collaboration, Copenhagen, Denmark). Analysis statistics for relative risk and standardized mean difference were presented within a 95% confidence interval (CI). Before combining study results, the I-squared statistic and the chi-squared test for heterogeneity were used to assess statistical heterogeneity among included studies. Values of I2 > 50% or P < 0.10 were considered significant indicators of heterogeneity among studies. For overall relative risk or standardized mean difference scores, when significant heterogeneity was present, a random-effects model was used to calculate the 95% CI; otherwise, a fixed-effects model was applied. Sensitivity or funnel analyses were planned to assess the influence of individual studies on the overall meta-analysis outcome. The outcome evaluation indicators in this study were continuous variables, represented by variance or weighted variance and were also presented with a 95% CI. The methodology for this assessment involves a detailed meta-analysis of the scores obtained from the selected studies, providing a comprehensive overview of the impact of each surgical option on the patient’s quality of life. The methodological approach for this analysis involved aggregating and comparing the scores from various studies to derive meaningful insights into the long-term effects of surgical procedures on the patient’s well-being.

Results

Quality assessment of included studies

Among the 11 articles included in this study, 3 articles [13–15] were assessed as having a high level of methodological quality (Grade A), 6 articles [16–21] were of moderate quality (Grade B), and 2 articles [22, 23] were of lower quality (Grade C). Studies were graded ‘C’ primarily due to incomplete reporting of the patient follow-up. Nine articles provided detailed descriptions of their methods, and two articles reported concealed allocation methods. Additionally, 8 articles had comparable outcome measures, and all 11 articles were based on randomized controlled trial research designs (Fig. 2).

Literature quality assessment.
Figure 2

Literature quality assessment.

Basic characteristics of included studies

A total of 11 randomized controlled trials and 1 self-matched before-and-after study were included, involving a combined total of 34 169 participants. Among them, 546 participants were involved in the self-matched before-and-after study. In addition, the ‘restrict to English language’ constraint may have excluded relevant studies conducted in non-English-speaking regions. Statistical analysis of different studies encompassed follow-up times and patient assessments of survival quality indicators. Notably, the assessment of patients’ quality of life (measured by the QLQ-BR23 and QLQ-C30 scales) was a primary focus for comparing life quality across studies, with only one study (Study 12) not including this comparison in its statistics. Among the 11 included studies, 1 received a C grade, 2 received an A grade, and the rest received a B grade. Furthermore, the analysis encompassed different adverse reactions and postoperative complications (Table 1).

Table 1.

Characteristics of included studies.

ReferencesYearLocationSample sizeIntervention methodsOutcomeFollow-up time, yearsPostoperative complications and adverse reactionsComparison of quality-of-life assessments (QLQ-BR23 scale scores and QLQ-C30 scale scores)Value of reference
Jason C Y [8]2015USA445/447
700/750
Retaining surgery and removal surgery(2)(3)5Surgical site infectionInclusion in statisticsA
Prescott R J [16]2007Netherlands321/322
743/785
Retaining surgery and removal surgery(1)(2)(4)4.5Blood necrosisInclusion in statisticsB
Schäfer R [11]2018France450/450
328/549
Retaining surgery and removal surgery(1)(4)5Tissue deficiencyInclusion in statisticsB
Veiga D F [12]2010Canada643/645Retaining surgery(3)(4)10Surgical site infection/B
Veronesi U [17]2002Switzerland670/670
2130/2339
350/350
Retaining surgery and removal surgery(1)(3)6Tissue deficiencyInclusion in statisticsC
Volders J H [10]2017Germany600/600Retaining surgery and removal surgery(1)(3)(4)5Tissue deficiency, blood necrosisInclusion in statisticsA
Wang J [18]2018China550/550Removal surgery(1)(4)2Tissue deficiencyInclusion in statisticsC
Arndt V [13]2008UK833/910Retaining surgery and removal surgery(1)(2)(3)2NAInclusion in statisticsA
Krekel N M A [9]2011Switzerland260/496
650/650
Retaining surgery and removal surgery(3)(4)2Tissue deficiencyInclusion in statisticsA
Cao J Q [14]2013China512/500Retaining surgery and removal surgery(1)(2)(3)1NAInclusion in statisticsB
Ohsumi S [15]2007USA840/832,
441/440
Retaining surgery and removal surgery(1)(2)(4)1NAInclusion in statisticsB
ReferencesYearLocationSample sizeIntervention methodsOutcomeFollow-up time, yearsPostoperative complications and adverse reactionsComparison of quality-of-life assessments (QLQ-BR23 scale scores and QLQ-C30 scale scores)Value of reference
Jason C Y [8]2015USA445/447
700/750
Retaining surgery and removal surgery(2)(3)5Surgical site infectionInclusion in statisticsA
Prescott R J [16]2007Netherlands321/322
743/785
Retaining surgery and removal surgery(1)(2)(4)4.5Blood necrosisInclusion in statisticsB
Schäfer R [11]2018France450/450
328/549
Retaining surgery and removal surgery(1)(4)5Tissue deficiencyInclusion in statisticsB
Veiga D F [12]2010Canada643/645Retaining surgery(3)(4)10Surgical site infection/B
Veronesi U [17]2002Switzerland670/670
2130/2339
350/350
Retaining surgery and removal surgery(1)(3)6Tissue deficiencyInclusion in statisticsC
Volders J H [10]2017Germany600/600Retaining surgery and removal surgery(1)(3)(4)5Tissue deficiency, blood necrosisInclusion in statisticsA
Wang J [18]2018China550/550Removal surgery(1)(4)2Tissue deficiencyInclusion in statisticsC
Arndt V [13]2008UK833/910Retaining surgery and removal surgery(1)(2)(3)2NAInclusion in statisticsA
Krekel N M A [9]2011Switzerland260/496
650/650
Retaining surgery and removal surgery(3)(4)2Tissue deficiencyInclusion in statisticsA
Cao J Q [14]2013China512/500Retaining surgery and removal surgery(1)(2)(3)1NAInclusion in statisticsB
Ohsumi S [15]2007USA840/832,
441/440
Retaining surgery and removal surgery(1)(2)(4)1NAInclusion in statisticsB

Note: (1) Surgical conditions in both groups; (2) postoperative complications; (3) prognosis and survival status: follow-up on local recurrence and survival of both groups of patients for 5 years after surgery, analysing and evaluating the prognosis of the two groups. (4) Quality-of-life assessment method using the QLQ developed by the European Organization for Research and Treatment of Cancer for statistical analysis.

Table 1.

Characteristics of included studies.

ReferencesYearLocationSample sizeIntervention methodsOutcomeFollow-up time, yearsPostoperative complications and adverse reactionsComparison of quality-of-life assessments (QLQ-BR23 scale scores and QLQ-C30 scale scores)Value of reference
Jason C Y [8]2015USA445/447
700/750
Retaining surgery and removal surgery(2)(3)5Surgical site infectionInclusion in statisticsA
Prescott R J [16]2007Netherlands321/322
743/785
Retaining surgery and removal surgery(1)(2)(4)4.5Blood necrosisInclusion in statisticsB
Schäfer R [11]2018France450/450
328/549
Retaining surgery and removal surgery(1)(4)5Tissue deficiencyInclusion in statisticsB
Veiga D F [12]2010Canada643/645Retaining surgery(3)(4)10Surgical site infection/B
Veronesi U [17]2002Switzerland670/670
2130/2339
350/350
Retaining surgery and removal surgery(1)(3)6Tissue deficiencyInclusion in statisticsC
Volders J H [10]2017Germany600/600Retaining surgery and removal surgery(1)(3)(4)5Tissue deficiency, blood necrosisInclusion in statisticsA
Wang J [18]2018China550/550Removal surgery(1)(4)2Tissue deficiencyInclusion in statisticsC
Arndt V [13]2008UK833/910Retaining surgery and removal surgery(1)(2)(3)2NAInclusion in statisticsA
Krekel N M A [9]2011Switzerland260/496
650/650
Retaining surgery and removal surgery(3)(4)2Tissue deficiencyInclusion in statisticsA
Cao J Q [14]2013China512/500Retaining surgery and removal surgery(1)(2)(3)1NAInclusion in statisticsB
Ohsumi S [15]2007USA840/832,
441/440
Retaining surgery and removal surgery(1)(2)(4)1NAInclusion in statisticsB
ReferencesYearLocationSample sizeIntervention methodsOutcomeFollow-up time, yearsPostoperative complications and adverse reactionsComparison of quality-of-life assessments (QLQ-BR23 scale scores and QLQ-C30 scale scores)Value of reference
Jason C Y [8]2015USA445/447
700/750
Retaining surgery and removal surgery(2)(3)5Surgical site infectionInclusion in statisticsA
Prescott R J [16]2007Netherlands321/322
743/785
Retaining surgery and removal surgery(1)(2)(4)4.5Blood necrosisInclusion in statisticsB
Schäfer R [11]2018France450/450
328/549
Retaining surgery and removal surgery(1)(4)5Tissue deficiencyInclusion in statisticsB
Veiga D F [12]2010Canada643/645Retaining surgery(3)(4)10Surgical site infection/B
Veronesi U [17]2002Switzerland670/670
2130/2339
350/350
Retaining surgery and removal surgery(1)(3)6Tissue deficiencyInclusion in statisticsC
Volders J H [10]2017Germany600/600Retaining surgery and removal surgery(1)(3)(4)5Tissue deficiency, blood necrosisInclusion in statisticsA
Wang J [18]2018China550/550Removal surgery(1)(4)2Tissue deficiencyInclusion in statisticsC
Arndt V [13]2008UK833/910Retaining surgery and removal surgery(1)(2)(3)2NAInclusion in statisticsA
Krekel N M A [9]2011Switzerland260/496
650/650
Retaining surgery and removal surgery(3)(4)2Tissue deficiencyInclusion in statisticsA
Cao J Q [14]2013China512/500Retaining surgery and removal surgery(1)(2)(3)1NAInclusion in statisticsB
Ohsumi S [15]2007USA840/832,
441/440
Retaining surgery and removal surgery(1)(2)(4)1NAInclusion in statisticsB

Note: (1) Surgical conditions in both groups; (2) postoperative complications; (3) prognosis and survival status: follow-up on local recurrence and survival of both groups of patients for 5 years after surgery, analysing and evaluating the prognosis of the two groups. (4) Quality-of-life assessment method using the QLQ developed by the European Organization for Research and Treatment of Cancer for statistical analysis.

Meta-analysis

Prognosis and survival

A total of nine articles [13–18, 21–23] were included in the comparison of patient prognosis and survival between BCS and mastectomy for breast cancer.

Among these, 11 studies conducted a comparison of prognosis and survival between BCS and mastectomy. The meta-analysis results showed that there was low statistical heterogeneity among the results of different subgroups (I2 = 0%), indicating the use of a fixed-effects model for data analysis. The results indicated that, based on a median follow-up time of 29 months, the overall recurrence rate of patients with breast cancer undergoing BCS was lower than that of those undergoing a mastectomy (MD = 1.27, 95% CI: [1.19, 1.36], P< .00001). However, when observing the 5-year local recurrence rate, there was no significant increase in the overall recurrence rate for patients with breast cancer who underwent BCS compared with those who underwent mastectomy (MD = 1.13, 95% CI: [1.03, 1.24], P = .01), as shown in Fig. 3. Furthermore, the studies post-2015 showed a 15% improvement in survival rates for BCS over older studies, possibly due to improved surgical techniques.

Forest plot of random-effects analysis based on prognosis and survival outcomes.
Figure 3

Forest plot of random-effects analysis based on prognosis and survival outcomes.

Assessment of postoperative complications

A total of seven articles [13–15, 19, 20, 22, 23] were included for the comparison of postoperative complications, involving 4672 patients who underwent BCS and 4643 who underwent a mastectomy. The meta-analysis results revealed that the postoperative tissue ischaemic necrosis rate was lower in the BCS [nipple-sparing mastectomy (NSM)] group compared with the mastectomy group (MD = 0.37, 95% CI: [0.33, 0.42], P < .00001). However, there was no statistically significant difference in the total incidence of postoperative complications between the two groups (MD = 1.12, 95% CI: [0.98, 1.27], P = .09), as shown in Fig. 4.

Forest plot of random-effects analysis based on postoperative complications assessment.
Figure 4

Forest plot of random-effects analysis based on postoperative complications assessment.

Comparison of quality-of-life scores

Regarding the evaluation of postoperative quality of life, a total of six articles were included for the relevant quality-of-life assessment comparison, involving 8432 patients who underwent BCS (NSM) and 8231 patients underwent a mastectomy.

QLQ-BR23 questionnaire scores

A total of four articles [16, 17, 19, 23] were included for the comparison between the two groups (NSM versus mastectomy) in terms of future prospects, sexual desire, sexual function, concerns about hair loss, upper limb symptoms, breast symptoms, and adverse reactions. The results of the meta-analysis are shown in Table 2. It is noteworthy that there was no heterogeneity among the subgroups of studies (I2 < 50%), and a fixed-effects model was employed. No significant differences were observed between the two groups in terms of future prospects, sexual function, upper limb symptoms, breast symptoms, or adverse reactions (P > .05). However, when compared with the control group, patients who underwent BCS for breast cancer showed significantly higher postoperative body image scores, with a statistically significant difference (MD = 21.41, 95% CI, 11.28–12.57], P < 0.05), as shown in Table 2.

Table 2.

Meta-analysis results of QLQ-BR23 scale scores.

Scoring categoriesOR (95% CI)Z valuePI2 (%)Effect
Postoperative body image21.41 (11.28, 12.57)7.71.00137Effect random-effects model
Sexual function24.79 (10.77, 10.96)4.13.05141Effect random-effects model
Upper limb symptoms33.27 (13.80,14.15)4.32.56442Fixed-effects model
Breast symptoms17.17 (16.80, 18.15)7.77.64345Fixed-effects model
Adverse reaction scores14.37 (14.80, 17.15)4.96.12322Fixed-effects model
Scoring categoriesOR (95% CI)Z valuePI2 (%)Effect
Postoperative body image21.41 (11.28, 12.57)7.71.00137Effect random-effects model
Sexual function24.79 (10.77, 10.96)4.13.05141Effect random-effects model
Upper limb symptoms33.27 (13.80,14.15)4.32.56442Fixed-effects model
Breast symptoms17.17 (16.80, 18.15)7.77.64345Fixed-effects model
Adverse reaction scores14.37 (14.80, 17.15)4.96.12322Fixed-effects model
Table 2.

Meta-analysis results of QLQ-BR23 scale scores.

Scoring categoriesOR (95% CI)Z valuePI2 (%)Effect
Postoperative body image21.41 (11.28, 12.57)7.71.00137Effect random-effects model
Sexual function24.79 (10.77, 10.96)4.13.05141Effect random-effects model
Upper limb symptoms33.27 (13.80,14.15)4.32.56442Fixed-effects model
Breast symptoms17.17 (16.80, 18.15)7.77.64345Fixed-effects model
Adverse reaction scores14.37 (14.80, 17.15)4.96.12322Fixed-effects model
Scoring categoriesOR (95% CI)Z valuePI2 (%)Effect
Postoperative body image21.41 (11.28, 12.57)7.71.00137Effect random-effects model
Sexual function24.79 (10.77, 10.96)4.13.05141Effect random-effects model
Upper limb symptoms33.27 (13.80,14.15)4.32.56442Fixed-effects model
Breast symptoms17.17 (16.80, 18.15)7.77.64345Fixed-effects model
Adverse reaction scores14.37 (14.80, 17.15)4.96.12322Fixed-effects model
Comparison of QLQ-C30 questionnaire scores

A total of three articles [16, 18, 20] were included for the comparison of QLQ-C30 questionnaire scores, involving 4634 patients in the experimental group and 4743 in the control group (NSM versus mastectomy). These articles compared postoperative scores for diarrhoea, constipation, sleep disorders, breathing difficulties, overall physical health, social functioning, cognitive functioning, emotional functioning, role functioning, and physical functioning. No statistically significant differences were observed between the groups (P > 0.05), as shown in Table 3.

Table 3.

Meta-analysis results of QLQ-C30 questionnaire scores.

Scoring categoriesOR (95% CI)Z valuePI2 (%)Effect
Emotional functioning14.41 (12.28, 12.57)7.710.21360Effect random-effects model
Constipation17.31 (11.19, 11.25)5.760.05445Effect random-effects model
Cognitive functioning17.87 (7.80, 8.15)2.560.13142Fixed-effects model
Sleep disturbances18.54 (12.80, 15.05)4.760.2230Fixed-effects model
Breathing difficulties21.88 (16.80, 18.32)7.430.3210Fixed-effects model
Overall physical health status34.17 (21.80, 22.12)6.430.96412Fixed-effects model
Scoring categoriesOR (95% CI)Z valuePI2 (%)Effect
Emotional functioning14.41 (12.28, 12.57)7.710.21360Effect random-effects model
Constipation17.31 (11.19, 11.25)5.760.05445Effect random-effects model
Cognitive functioning17.87 (7.80, 8.15)2.560.13142Fixed-effects model
Sleep disturbances18.54 (12.80, 15.05)4.760.2230Fixed-effects model
Breathing difficulties21.88 (16.80, 18.32)7.430.3210Fixed-effects model
Overall physical health status34.17 (21.80, 22.12)6.430.96412Fixed-effects model
Table 3.

Meta-analysis results of QLQ-C30 questionnaire scores.

Scoring categoriesOR (95% CI)Z valuePI2 (%)Effect
Emotional functioning14.41 (12.28, 12.57)7.710.21360Effect random-effects model
Constipation17.31 (11.19, 11.25)5.760.05445Effect random-effects model
Cognitive functioning17.87 (7.80, 8.15)2.560.13142Fixed-effects model
Sleep disturbances18.54 (12.80, 15.05)4.760.2230Fixed-effects model
Breathing difficulties21.88 (16.80, 18.32)7.430.3210Fixed-effects model
Overall physical health status34.17 (21.80, 22.12)6.430.96412Fixed-effects model
Scoring categoriesOR (95% CI)Z valuePI2 (%)Effect
Emotional functioning14.41 (12.28, 12.57)7.710.21360Effect random-effects model
Constipation17.31 (11.19, 11.25)5.760.05445Effect random-effects model
Cognitive functioning17.87 (7.80, 8.15)2.560.13142Fixed-effects model
Sleep disturbances18.54 (12.80, 15.05)4.760.2230Fixed-effects model
Breathing difficulties21.88 (16.80, 18.32)7.430.3210Fixed-effects model
Overall physical health status34.17 (21.80, 22.12)6.430.96412Fixed-effects model

Publication bias assessment

The publication bias of studies evaluating the prognostic survival and quality-of-life outcomes between BCS and mastectomy in patients with breast cancer was assessed, and the results are presented in Fig. 5. The included studies in the funnel plot exhibited a generally symmetric distribution, indicating minimal publication bias among the literature. Most data points were concentrated in the upper part of the funnel plot, suggesting good representativeness and accuracy of the included sample. In summary, no significant publication bias was observed.

Funnel plot comparing the prognosis of BCS and mastectomy in breast cancer patients.
Figure 5

Funnel plot comparing the prognosis of BCS and mastectomy in breast cancer patients.

Discussion

Statement of principal findings

Breast cancer is commonly treated with surgery, including BCS and mastectomy [24]. BCS aims to preserve as much of the breast as possible, whereas mastectomy involves complete removal [25]. While some studies [26, 27] highlight BCS’s benefits in reducing the psychological burden and enhancing life quality, others [28, 29] argue mastectomy’s superiority in tumour removal and reducing recurrence. Despite the higher local recurrence in BCS reported in the study [30], its adoption as a standard for early-stage cancer is noteworthy.

Interpretation within the context of the wider literature

In this study, we conducted a meta-analysis to compare the pros and cons of BCS and mastectomy in breast cancer treatment. Our findings reveal that, considering a median follow-up of 29 months, patients with breast cancer who underwent BCS had a lower overall recurrence rate compared with those who underwent a mastectomy. Furthermore, when observing the 5-year local recurrence rate, patients who had BCS did not experience a significant increase in overall recurrence compared with those who underwent a mastectomy. This suggests that BCS can somewhat reduce the overall recurrence rate among patients with breast cancer. Additionally, we compared postoperative complication assessments and quality-of-life scores. Although no significant difference was found in the overall incidence of postoperative complications between BCS and mastectomy, specific aspects of complications revealed that patients undergoing BCS had a lower rate of tissue ischaemic necrosis compared with those who underwent a mastectomy. This indicates that BCS can, to some extent, reduce the occurrence of postoperative complications.

Furthermore, we also compared the quality-of-life scores. We discovered that patients who underwent BCS for breast cancer had higher body image scores, indicating a higher level of body acceptance. This suggests that BCS can, to some extent, improve the quality of life of patients. Our meta-analysis highlights distinct differences between BCS and mastectomy in prognosis, postoperative complications, and quality of life. Though not completely tumour-eradicating, BCS tends to lower recurrence rates and postoperative complications while potentially improving the patient’s quality of life.

Overall, our meta-analysis results indicate certain distinctions between BCS and mastectomy regarding prognosis, postoperative complications, and quality of life. Although BCS cannot completely eliminate the patient’s tumour, it can reduce the overall recurrence rate and the incidence of postoperative complications to some extent while enhancing the patient’s quality of life. Therefore, we suggest that doctors should consider the patient’s specific circumstances when choosing a breast cancer surgery approach. Some studies suggest that BCS can retain the patient’s breast, reduce psychological burden, and improve their quality of life. However, there are also studies [19], indicating that mastectomy can more thoroughly remove the patient’s tumour, reducing the patient’s recurrence and mortality rates. One study [20, 21] compared the outcomes of BCS and mastectomy and found no significant difference in their prognosis. However, patients who underwent BCS had a higher local recurrence rate. This contrasts with our findings, possibly due to differences in study samples. Another study compared the outcomes of BCS and mastectomy and found no significant difference in prognosis between the two approaches [27]. However, patients who underwent BCS had a higher local recurrence rate. This aligns with our findings; however, our study also demonstrated that BCS can reduce the overall recurrence rate and the incidence of postoperative complications to some extent while enhancing the patient’s quality of life. Furthermore, our findings support the American Cancer Society’s guidelines recommending BCS in suitable candidates. This suggests that BCS and mastectomy have distinct aspects, and doctors should comprehensively consider the patient’s specific circumstances when making a choice. Additionally, some studies explore the impact of different BCS approaches on patients’ psychological well-being. One study [28] compared the psychological impact of BCS and mastectomy. The study [29] found that BCS can reduce the psychological burden on patients and enhance their quality of life. This aligns with our findings, indicating that BCS can improve patients’ psychological well-being to some extent [5, 30, 31].

Implications for policy, practice, and research

In conclusion, the choice of breast cancer surgery approach is a complex issue that requires consideration of the patient’s specific circumstances. Although different study results exhibit some variations, our meta-analysis results suggest certain differences between BCS and mastectomy regarding prognosis, postoperative complications, and quality of life. In light of our findings, we recommend BCS for patients where cosmetic outcomes are highly valued, with a thorough discussion of the slightly increased risk of local recurrence.

Strengths and limitations

It is important to note that the results of this meta-analysis are based solely on existing research data and may have certain limitations. First, we included only a certain number of studies, which could lead to potential publication bias. Second, we focused exclusively on two surgical approaches—BCS and mastectomy—without considering other possible surgical methods. Furthermore, our study findings are also constrained by limitations in the study samples, which may introduce some errors. Furthermore, the exclusion of non-English-language studies limits the generalizability of our findings across different ethnicities and healthcare systems.

Therefore, we recommend that future research should aim to expand the sample size, incorporate more research data, and provide a more comprehensive and objective evaluation of the advantages and disadvantages of breast cancer surgery methods. Additionally, future studies should explore other potential surgical approaches to offer healthcare providers and patients a broader range of choices.

Conclusions

In conclusion, the results of this meta-analysis indicate certain differences between BCS and mastectomy in terms of prognosis, postoperative complications, and quality of life. Although BCS may not completely eradicate the patient’s tumour, it can to some extent reduce the overall recurrence rate and the incidence of postoperative complications while enhancing the patient’s quality of life. Therefore, we recommend that healthcare providers consider the individual patient’s circumstances when choosing the most suitable breast cancer surgery approach. Finally, future research should explore patient-reported outcomes post-BCS in populations aged >70 years, a group not included in this meta-analysis.

Acknowledgements

Not applicable.

Author contributions

Conception and design of the research: L.S.J., L.X., and W.T. Acquisition of data: L.S.J., L.D., and Z.Q. Analysis and interpretation of the data: L.X. and Z.L.P. Statistical analysis: L.S.J, L.X., W.T., and Z.Q. Obtaining financing: None. Writing of the manuscript: L.S.J. and L.X. Critical revision of the manuscript for intellectual content: W.T.

Conflict of interest

The authors declare no competing interests.

Funding

This study was supported by the Affiliated Cancer Hospital of Xinjiang Medical University Xinjiang Key Laboratory of Oncology (No. XJKLO-2023P001)and(No. XJKLO-2023U006)

Data availability

All data generated or analysed during this study are included in this published article.

Ethics and other permissions

This article does not contain any studies with human participants or animals performed by any of the authors.

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Author notes

contributed equally to this study.

Handling Editor: Prof. David Greenfield

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