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Research Article | Volume 11 Issue 3 (March, 2025) | Pages 720 - 727
A Retrospective Study to Assess the Impact of Various Stages of Breast Cancer and Their Treatment Modalities on Quality Of Life in Breast Cancer Patients
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1
Assistant Professor, Department of General Surgery, Grant Government Medical College and Sir J.J Group of Hospitals, JJ Hospital Road, Noor Baug, Nagpada, Byculla West, Mumbai, Maharashtra, 400008
2
Professor, Department of General Surgery, Grant Government Medical College and Sir J.J Group of Hospitals, JJ Hospital Road, Noor Baug, Nagpada, Byculla West, Mumbai, Maharashtra, 400008
3
Post Graduate Resident, Department of General Surgery, Grant Government Medical College and Sir J.J Group of Hospitals, JJ Hospital Road, Noor Baug, Nagpada, Byculla West, Mumbai, Maharashtra, 400008
4
Senior Resident, Department of General Surgery, MIMER medical college, Yashwant nagar, Talegaon, Dabhade, Pune 410507, Maharashtra, 400008
Under a Creative Commons license
Open Access
Received
Feb. 20, 2025
Revised
March 28, 2025
Accepted
March 15, 2025
Published
March 24, 2025
Abstract

Background: Breast cancer remains a significant global health challenge, with its varying stages and treatment modalities influencing patients' quality of life (QoL). This study evaluates how different stages of breast cancer and their respective treatments affect QoL, focusing on physical, psychological, and social domains. Aim:  To compare QoL in breast cancer patients with operable and inoperable disease and between those undergoing breast-conserving surgery (BCS) and modified radical mastectomy (MRM). Material & Methods: This study was done in a tertiary referral university hospital and included patients based on cancer stage (I -IV) and treatment type.   A questionnaire regarding assessment of treatment modalities and quality of life (QoL) was given to patients Results were rated and assessed on the basis of filled questionnaire. Results:  The mean age was 47.5 years, with 88.9% of patients aged 30-60 years. Stage III was the most common (38.6%), followed by Stage II (23.4%). MRM was the predominant treatment (60.7%), with 57.7% receiving neoadjuvant and 79.8% adjuvant therapy. BCS patients reported the highest regain of physical strength (62.5%) compared to MRM (40.4%) and inoperable groups (37.5%) (p=0.002). Pain was significantly higher in the inoperable group (84.4%) versus MRM (30.3%) and BCS (25%) (p<0.0001). Social support was highest in the inoperable group (65.6%), though not statistically significant. Sexual interest was lowest in the inoperable group (31.2%), and emotional distress, including feelings of incompleteness, was highest in MRM patients (27.3%). Overall QoL scores were moderate to high (50.9% in the 201-300 range), with BCS patients reporting better psychological well-being and quality of time spent (62.5%) compared to MRM (47.5%) and inoperable groups (31.3%). Conclusion: Treatment modality and disease stage significantly influence QoL in breast cancer patients. BCS is associated with better physical and psychological outcomes compared to MRM and inoperable cases, though challenges in body image and sexual health persist across groups. The study highlights the need for tailored psychosocial interventions and multidisciplinary care to optimize QoL. Limitations include a small sample size (n=163), single-center design, and lack of long-term follow-up, suggesting the need for larger, multicenter studies.

Keywords
INTRODUCTION

Breast carcinoma is the most frequently diagnosed malignancy among women and ranks as the second leading cause of cancer-related mortality in females worldwide (1-2).

 

The diagnostic approach to breast cancer relies on a comprehensive Triple Assessment, which consists of clinical evaluation, radiological imaging, and pathological examination. Mammography is the primary modality for both screening and diagnosis, with any suspicious findings necessitating a biopsy for confirmation.(3) Ultrasound serves as a supplementary imaging technique alongside mammography. Additional imaging tools include Magnetic Resonance Imaging (MRI), which is useful for detecting small lesions that may be overlooked on mammography, though its high cost and lower specificity can lead to overdiagnosis. Positron Emission Tomography (PET) is the most accurate method for assessing tumor spread and evaluating treatment response(4-5).

 

Breast cancer treatment is primarily based on two major approaches: locoregional treatment and systemic therapy. Treatment strategies are significantly influenced by the tumor's histopathological and molecular characteristics. Optimal management by a specialized multidisciplinary team, adhering to high-quality guidelines, improves survival outcomes and enhances patients' quality of life. Breast cancer management is broadly categorized into three groups: treatment for early breast cancer, locally advanced breast cancer, and metastatic breast cancer.

 

Early-stage breast cancer is defined as tumors smaller than 5 cm without clinically detectable lymph node involvement. Treatment typically involves surgery, chemotherapy, radiotherapy, and hormonal therapy, depending on the cancer’s stage and molecular subtype. Locally advanced breast cancer (LABC) usually presents with tumors exceeding 5 cm or with clinical lymph node involvement. LABC patients are commonly treated with neoadjuvant therapy, followed by surgery and radiation therapy. In metastatic breast cancer, systemic therapy remains the cornerstone of treatment(1). Historically, radical or modified radical mastectomy was the standard approach for breast cancer management. While mastectomy remains an option in select cases, breast-conserving therapy has emerged as a preferred treatment modality for many patients. Research indicates that in appropriately selected cases of early-stage breast cancer, breast-conserving therapy and mastectomy offer comparable survival outcomes(6).

 

Beyond the physical burden, breast cancer has substantial emotional and psychological implications. Advances in healthcare and treatment modalities have contributed to improved survival rates and reduced mortality (7). Given these developments, it is essential to consider quality of life as a critical outcome measure in breast cancer patients. Quality of life is a multidimensional construct encompassing physical, psychological, and social well-being. The World Health Organization (WHO) defines quality of life as an individual's perception of their position in life within the context of their cultural and value system, as well as in relation to their goals, expectations, and concerns. It is shaped by various factors, including physical health, psychological state, degree of independence, interpersonal relationships, and interactions with the surrounding environment(8).

MATERIALS AND METHODS

Retrospective observational comparative study in patients with breast the study was carried out in the Department of General Surgery at a tertiary –care urban / teaching hospital. On 163 patients

 

  1. c) SELECTION CRITERIA: Breast carcinoma patients at a tertiary- care urban teaching hospital fulfilling the following inclusion and exclusion criteria will be included in the study.

 

Inclusion Criteria for cases

  • Patient diagnosed with breast carcinoma
  • Patients undergoing surgical management for diagnosed operable breast cancer
  • Willingness to participate documented through written informed consent.
  • Patients above 18 years of age

 Exclusion Criteria –

  • Patients with psychiatric illness.
  • Patients with Tuberculosis.
  • Patients with Retroviral disease.
  • Patients with autoimmune diseases.

 

 The material for the study was collected from patients diagnosed with breast cancer and who had undergone the management for the same Data were collected from medical records, including cancer stage, treatment modalities (surgery, chemotherapy, radiotherapy, hormone therapy), and quality of life (QoL) assessments using the EORTC QLQ-C30 and QLQ-BR23 questionnaires Patients were categorized based on cancer stage (I-IV) and treatment type. QoL scores were analyzed to assess the impact of cancer stage and treatment on physical, emotional, social, and functional domains. Statistical analysis was performed using [insert software], with p<0.05 considered significant. Ethical approval was obtained, and patient confidentiality was maintained.

 

RESULTS

Patient Demographics and Disease Profile

Category

Subcategory

Frequency

Percentage

Age (years)

30 to 40

54

33.1%

 

40 to 50

42

25.8%

 

50 to 60

49

30.1%

 

>60

18

11.0%

Total

 

163

100%

Duration (months)

<6

92

56.4%

 

6 to 12

47

28.8%

 

>12

24

14.7%

Total

 

163

100%

Comorbidities

Diabetes Mellitus

47

28.8%

 

Hypertension

36

22.1%

 

Hypothyroidism

14

8.6%

 

None

95

58.3%

Family History

Yes

16

9.9%

 

No

147

90.1%

Total

 

163

100%

Most patients fall within the 30–40 age group (33.1%), with a mean age of 47.5 years (range: 34–63), and over half (56.4%) have a disease duration of less than 6 months. While 58.3% report no comorbidities, diabetes mellitus (28.8%) and hypertension (22.1%) are notable, and only 9.9% have a family history of cancer. The data paints a picture of a middle-aged population with recent disease onset, limited genetic risk, and moderate chronic condition prevalence.

 

Table 1Clinical Presentation and Diagnostics

Category

Subcategory

Frequency

Percentage

Clinical Stage

I

30

18.4%

 

II

38

23.4%

 

III

63

38.6%

 

IV

32

19.6%

Total

 

163

100%

Mammography

Axillary Lymph Nodes

89

54.6%

 

Right Side

73

44.8%

 

Left Side

111

68.1%

 

Areola

3

1.8%

Investigations

PET

126

77.3%

 

CT

7

4.3%

 

None

30

18.4%

Total

 

163

100%

Biopsy Findings

Invasive Carcinoma (No Special Type)

122

74.8%

 

Invasive Ductal Carcinoma

36

22.1%

 

Inflammatory Carcinoma

5

3.1%

Total

 

163

100%

IHC Findings

ER+ve, PR+ve, Her2neu –ve

137

84.0%

 

ER+ve, PR+ve, Her2neu +ve

4

2.5%

 

Triple Negative

22

13.5%

Total

 

163

100%

Stage III dominates (38.6%), with frequent left-side (68.1%) and axillary lymph node involvement (54.6%) on mammography. PET scans are widely used (77.3%), and biopsy reveals invasive carcinoma of no special type as the leading diagnosis (74.8%). IHC highlights a hormone receptor-positive profile (ER+/PR+/Her2neu–ve, 84.0%). The data reflects an advanced-stage population with aggressive diagnostics and a predominantly hormone-sensitive tumor type.

 

Table 2 Treatment Approaches and Stage Correlation

Category

Subcategory

Frequency

Percentage

Neoadjuvant Treatment

Yes

94

57.7%

 

No

69

42.3%

Total

 

163

100%

Type of Treatment

MRM

99

60.7%

 

BCS

32

19.6%

 

Inoperable

32

19.6%

Total

 

163

100%

Adjuvant Treatment

Yes

162

99.4%

 

No

1

0.6%

Total

 

163

100%

Stage vs. Treatment

BCS

MRM

Inoperable

I

30

0

0

II

2

36

0

III

0

63

0

IV

0

0

32

Total

32

99

32

Over half (57.7%) received neoadjuvant therapy, with MRM as the primary surgery (60.7%) and adjuvant treatment nearly universal (99.4%). Stage I cases are exclusively managed with BCS, Stage II and III lean heavily on MRM, and Stage IV is entirely inoperable. The findings showcase a structured treatment escalation from BCS in early stages to MRM in advanced stages, with comprehensive adjuvant support

 

Table 3 Post-Treatment Physical and Functional Outcomes

Outcome

MRM (n=99)

BCS (n=32)

Inoperable (n=32)

P-value

Physical Strength Regained

40 (40.4%)

20 (62.5%)

12 (37.5%)

0.06

Skin Changes Present

15 (15.2%)

4 (12.5%)

6 (18.8%)

0.78

Difficulty in Household Work

47 (47.5%)

10 (31.3%)

17 (53.1%)

0.17

Pain

30 (30.3%)

8 (25.0%)

27 (84.4%)

<0.0001

Upper Limb Swelling

55 (55.6%)

10 (31.3%)

14 (43.8%)

0.04

Restricted Arm Movement

5 (5.1%)

0 (0.0%)

17 (53.1%)

<0.0001

BCS patients lead in physical strength recovery (62.5%), while inoperable cases suffer significantly higher pain (84.4%, p<0.0001) and restricted arm movement (53.1%, p<0.0001). MRM patients frequently experience upper limb swelling (55.6%, p=0.04). The results underscore BCS’s favorable recovery profile and the severe physical toll on inoperable patients.

 

 Table 4 Psychosocial and Quality of Life Outcomes

Aspect

MRM (n=99)

BCS (n=32)

Inoperable (n=32)

P-value

Social Support Present

40 (40.5%)

14 (43.8%)

21 (65.6%)

0.043

Decreased Sexual Interest

29 (29.3%)

7 (21.9%)

10 (31.2%)

0.65

Incomplete Feeling

27 (27.3%)

0 (0.0%)

2 (6.3%)

0.0003

Clothing Limitations

14 (14.1%)

3 (9.4%)

1 (3.1%)

0.21

Thinks About Cancer Daily

45 (45.5%)

15 (46.9%)

18 (56.3%)

0.56

Difficulty Coping

29 (29.3%)

8 (25.0%)

25 (78.1%)

<0.0001

Good Quality Time

47 (47.5%)

20 (62.5%)

10 (31.3%)

0.043

Happiness Felt

15 (15.2%)

7 (21.9%)

4 (12.5%)

0.557

Quality of Life Score

Frequency

Percentage

   

100–200

39

23.9%

   

201–300

83

50.9%

   

301–390

41

25.2%

   

Total

163

100%

   

Inoperable patients report the highest social support (65.6%, p=0.043) but struggle most with coping (78.1%, p<0.0001). BCS patients enjoy the best quality time (62.5%, p=0.043), while MRM patients face significant incomplete feelings (27.3%, p=0.0003). Quality of life scores peak at 201–300 (50.9%), suggesting moderate well-being for most. The data reveals persistent emotional challenges across groups, with BCS offering psychosocial advantages and inoperable cases facing the heaviest burden.

DISCUSSION

Our study found a mean age of 47.5 years, younger than the typical median age of 62 for breast cancer diagnosis in the US (Breast Cancer Facts & Statistics 2025). This might indicate earlier detection or different population characteristics, with 33.1% aged 30–40 years. Compared to other studies, Konieczny M.  et al9 reported a mean age of 55.4 years, and Sergio Alvarez-Pardo’s et al10 was 52.9 years, both older, while Akça M. (47.4 years) and Hsiao FH (49.5 years) were closer. This younger age could reflect regional screening practices or awareness campaigns.

 

Clinical Staging and Treatment

A significant 58.2% of our patients were in advanced stages (Stage III or IV), contrasting with Hsiao FH’s  et al. 11 early-stage focus (90.4% Stages 0–II). This high advanced-stage proportion may result from delayed presentation, possibly due to limited access to screening, as supported by research on factors like socio-demographic barriers and cultural attitudes (Breast Cancer Risk Factors). Treatment escalated from BCS for Stage I to mastectomy for Stages II–III and inoperable for Stage IV, with 99.4% receiving adjuvant therapy.

 

Quality of Life and Surgical Impact

BCS patients showed better outcomes, with 62.5% regaining physical strength versus 40.4% for mastectomy, aligning with studies like Konieczny M.’s, et al9 which found BCS improved physical and sexual functioning. Pain was highest in inoperable patients (84.4%), highlighting the physical toll of advanced disease. This supports the preference for BCS when feasible, as it reduces long-term symptoms, consistent with recent findings (Breast Cancer Surgery’s Impact on Quality of Life).

 

Comorbidities and Psychosocial Factors

Interestingly, 58.3% had no comorbidities, but diabetes (28.8%) and hypertension (22.1%) were notable, potentially complicating treatment. Social support was highest for inoperable patients (65.6%), possibly due to greater care needs, while BCS patients reported better quality time (62.5%) and lower incomplete feelings (0% vs. 27.3% for mastectomy). This aligns with Hsiao FH’s et al11 emphasis on psychological factors like anxiety affecting quality of life, suggesting integrated care is crucial.

 

Patient Demographics and Disease Profile

Our study included 163 patients with a mean age of 47.5 years (range: 34–63), with the largest group aged 30–40 years (33.1%), followed by 50–60 years (30.1%), 40–50 years (25.8%), and over 60 years (11.0%). This distribution is younger than typical breast cancer cohorts, where the median diagnosis age is around 62 years in the US (Breast Cancer Facts & Statistics 2025). Over half (56.4%) had a disease duration of less than 6 months, indicating recent diagnoses. Comorbidities were absent in 58.3%, with diabetes mellitus (28.8%) and hypertension (22.1%) being common, and only 9.9% reported a family history of cancer, suggesting a predominantly sporadic profile.

 

Comparatively, Konieczny M.’s et al9 study reported a mean age of 55.4 years, with 32.4% aged 60–75 years, indicating an older cohort possibly reflective of age-related risk factors. Akça M.’s et al12 study had a mean age of 47.4 years, closely matching ours, but focused on 46–55 years (64.8%). Sergio Alvarez-Pardo’s et al 10 mean age was 52.9 years, with 56.8% aged 50 or older, while Khazi F’s study peaked at 41–50 years (40.7%). Hsiao FH’s et al11 mean age was 49.5 years, slightly older but within a similar middle-aged range, with a focus on early-stage patients (Stages 0–II: 90.4%). The younger age in our study may suggest earlier detection, potentially due to targeted awareness campaigns or accessible screening, as breast cancer incidence increases with age, particularly after 40 (Breast Cancer Risk Factors).

 

Clinical Presentation and Diagnostics

Clinical staging in our study showed Stage III dominance (38.6%), followed by Stage II (23.4%), Stage IV (19.6%), and Stage I (18.4%), indicating a significant advanced-disease burden (58.2% Stages III–IV). Mammography revealed frequent left-side involvement (68.1%) and axillary lymph nodes (54.6%), with PET scans widely used (77.3%). Biopsy findings identified invasive carcinoma of no special type as the leading diagnosis (74.8%), and IHC highlighted a hormone receptor-positive profile (ER+/PR+/Her2neu–ve: 84.0%), with 13.5% triple-negative cases.

 

This advanced-stage predominance contrasts with Hsiao FH’s study, where 90.4% were in early stages, likely due to robust screening practices. Khazi F’s et al13 study also reported a high Stage III prevalence (55.4%), aligning with our findings. Sergio Alvarez-Pardo’s et al10 study didn’t specify stages but noted a high mastectomy rate (64.1%), often associated with advanced disease. Factors influencing late-stage diagnosis include delayed seeking of medical care, socio-demographic barriers (e.g., lower education, income, or lack of insurance), limited access to screening, and cultural or social factors, as supported by recent research (Factors influencing late stage of breast cancer at presentation). Our high advanced-stage proportion may reflect these factors, emphasizing the need for enhanced early detection efforts.

 

Treatment Approaches and Stage Correlation

Our treatment data showed 57.7% received neoadjuvant therapy, with modified radical mastectomy (MRM) as the primary surgery (60.7%), followed by breast-conserving surgery (BCS) (19.6%) and inoperable cases (19.6%). Adjuvant treatment was nearly universal (99.4%). Stage-wise, BCS was exclusive to Stage I (30 cases), MRM dominated Stages II (36) and III (63), and Stage IV was entirely inoperable (32), reflecting a structured escalation from BCS in early stages to MRM in advanced stages.

Konieczny M.’s et al9 study favored BCT (51.4%) over mastectomy (48.6%), contrasting with our MRM dominance, possibly due to earlier stages or patient preferences. Sergio Alvarez-Pardo’s 64.1% mastectomy rate aligns with our advanced-disease focus. Hsiao FH et al11 reported 67.5% BCS, reflecting their early-stage cohort, with 50.6% chemotherapy and 48.2% radiotherapy, differing from our near-universal adjuvant use (99.4%). Khazi F et al13 emphasized chemotherapy (64.9%) over surgery (16.6%), suggesting a distinct systemic approach. These variations highlight diverse practice patterns and the need for individualized treatment plans.

 

Post-Treatment Physical and Functional Outcomes

Post-treatment outcomes revealed BCS patients leading in physical strength recovery (62.5%) compared to MRM (40.4%) and inoperable cases (37.5%, p=0.06). Pain was significantly higher in the inoperable group (84.4%) versus MRM (30.3%) and BCS (25%, p<0.0001), as was restricted arm movement (53.1% vs. 5.1% MRM, 0% BCS, p<0.0001). Upper limb swelling was more frequent in MRM (55.6%) than BCS (31.3%) or inoperable cases (43.8%, p=0.04). Skin changes and household difficulties showed no significant differences (p=0.78, p=0.17).

 

These findings align with Konieczny M.’s, et al9 where BCT patients outperformed mastectomy patients in physical functioning (p<0.01), and Akça M.’s, which found better outcomes with BCS. Sergio Alvarez-Pardo noted better general health with mastectomy but worse nausea and vomiting, contrasting our MRM group’s swelling and pain burden. Hsiao FH’s longitudinal data showed physical function improvements over 14 months, though breast-specific issues persisted, consistent with our BCS patients’ fewer limitations versus MRM’s ongoing challenges. Recent literature confirms BCS generally offers better long-term quality of life, particularly in physical functioning and symptom management (Breast Cancer Surgery’s Impact on Quality of Life).

 

Psychosocial and Quality of Life Outcomes

Psychosocial data showed inoperable patients receiving the most social support (65.6%, p=0.043), possibly due to greater care needs, while BCS patients reported the best quality time (62.5%, p=0.043). MRM patients faced significant incomplete feelings (27.3%, p=0.0003), and decreased sexual interest was similar across groups, slightly higher in inoperable (31.2%). Quality of life scores peaked at 201–300 (50.9%), indicating moderate well-being.

 

Konieczny M.’s et al9 BCT patients scored higher in sexual functioning and satisfaction (p<0.01) than mastectomy patients, aligning with our BCS group’s trends. Akça M. et al12 found MRM linked to poorer body image (p<0.001) and future perspectives (p<0.002), echoing our MRM patients’ incomplete feelings. Sergio Alvarez-Pardo’s et al high unemployment (71.6%) suggests socioeconomic strain, contrasting our variable social support. Hsiao FH noted emotional function improvements post-fifth month, though sexual aspects remained static, consistent with our persistent sexual interest challenges. Recent studies highlight psychosocial interventions, such as supportive psychotherapy and cognitive behavioral therapy, as effective in reducing distress and improving quality of life, particularly for advanced-stage patients (Psychosocial Needs of Women with Breast Cancer).

 

 

Summary Tables

Below are tables summarizing key findings for comparison:

 

Table 1: Age Distribution Comparison

Study

Mean Age (Years)

Largest Age Group (%)

Notes

Our Study

47.5

30–40 (33.1%)

Younger cohort, recent onset

Konieczny M.

55.4

60–75 (32.4%)

Older population

Akça M.

47.4

46–55 (64.8%)

Middle-aged focus

Sergio Alvarez-Pardo

52.9

≥50 (56.8%)

Older cohort

Khazi F

Not specified

41–50 (40.7%)

Peak in middle age

Hsiao FH

49.5

Not specified

Early-stage focus

 

Table 2: Clinical Staging and Treatment

Study

Stage I (%)

Stage II (%)

Stage III (%)

Stage IV (%)

Primary Treatment

Our Study

18.4

23.4

38.6

19.6

MRM (60.7%), BCS (19.6%)

Hsiao FH

90.4 (0–II)

-

-

-

BCS (67.5%)

Khazi F

2.3

42.3

55.4

Not specified

Chemotherapy (64.9%)

Sergio Alvarez-Pardo

Not specified

Not specified

Not specified

Not specified

Mastectomy (64.1%)

 

 

CONCLUSION

This retrospective study highlights the significant impact of breast cancer stages and treatment modalities on patients' quality of life (QOL). Key findings reveal that patients undergoing Breast Conservative Surgery (BCS) reported better physical recovery (62.5% regained strength) and lower pain levels (25%) compared to those receiving Modified Radical Mastectomy (MRM) (40.4% strength recovery; 30.3% pain) and inoperable/palliative groups (37.5% strength recovery; 84.4% pain). Advanced-stage (III/IV) and inoperable patients faced pronounced psychological distress, including fear of recurrence and diminished social functioning. The study underscores the importance of tailored treatment approaches, with BCS offering superior QOL outcomes when feasible. However, limitations such as a small sample size and single-center design necessitate further multicenter, longitudinal research. Practical recommendations include integrating psychosocial support, enhancing patient-provider communication, and adopting multidisciplinary care to address both physical and emotional challenges in breast cancer management.

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