Long-term quality of life after breast surgery—are breast conserving surgery and mastectomy comparable?
Editorial Commentary

Long-term quality of life after breast surgery—are breast conserving surgery and mastectomy comparable?

Hans-Christian Kolberg1 ORCID logo, Rachel Würstlein2

1Department of Gynecology and Obstetrics, Marienhospital Bottrop, Bottrop, Germany; 2Breast Cancer Center, Department of Gynecology and Obstetrics, Ludwig-Maximilian-University Hospital, Munich, Germany

Correspondence to: Hans-Christian Kolberg, MD, PhD. Department of Gynecology and Obstetrics, Marienhospital Bottrop, Josef-Albers-Str. 70, 46236 Bottrop, Germany. Email: hans-christian.kolberg@mhb-bottrop.de.

Comment on: Diao K, Lei X, He W, et al. Patient-Reported Quality of Life after Breast Conserving Surgery with Radiotherapy versus Mastectomy and Reconstruction. Ann Surg 2023;278:e1096-e1102.


Keywords: Breast cancer; mastectomy; breast conserving surgery; quality of life; patient-reported outcome (PRO)


Submitted Dec 20, 2023. Accepted for publication Feb 27, 2024. Published online Mar 22, 2024.

doi: 10.21037/gs-23-522


In a population-based study of long-term quality of life among breast cancer survivors, Diao et al. demonstrated an association of mastectomy and reconstruction with worse sexual well-being compared to breast conserving surgery and radiotherapy. Patients older than 65 who received breast conserving surgery and radiotherapy and young patients who received mastectomy and autologous reconstruction reported the highest quality of life scores. Of the 1,215 included patients with breast cancer stage 0–II and a median follow up of 9 years, 631 had received breast conserving surgery and radiotherapy and 584 had been treated by mastectomy and reconstruction. All patients answered paper surveys using BREAQST-Q and Patient-Reported Outcome Measurement Information System (PROMIS). Of the items investigated, including psychosocial well-being, physical function and well-being, upper extremity function, satisfaction with breasts and sexual well-being, only sexual well-being showed a statistically significant difference between the two groups as mentioned above. No difference in overall survival could be demonstrated. However, the use of chemotherapy had a negative impact (1).

With a median follow up of 9 years the authors focused on long term quality of life. This is a very important aspect of the analysis, because it is known that quality of life changes over time. Short-term analyses demonstrate a better quality of life in patients after breast conserving surgery compared to mastectomy (2). In a recently published study from Germany, patients after mastectomy had an impairment of quality of life shortly after surgery whereas after 24 months it had improved substantially and was even better than in patients after breast conserving surgery (3). Satisfaction after reconstructive surgery also changes over time. While the satisfaction with the body image improves after breast conserving surgery and simple mastectomy, the opposite has been demonstrated for mastectomy and immediate reconstruction (4). These findings underscore the importance of long-term approaches as chosen in the study conducted by Diao et al. The main goal of breast surgery for early breast cancer—survival—is always a long-term endpoint. But other endpoints like quality of life and body image also have to be investigated with an adequate follow up, because in a situation with curative intent the next 10 to 20 years do matter.

Age plays an important role in the deterioration of quality of life after breast cancer surgery. While this has been demonstrated for all surgical approaches, the effect is more pronounced after mastectomy (5). In another recently published analysis young age was associated with poorer social and sexual function, as well as poorer sexual enjoyment and lower expectations of the future (6). These data demonstrate the importance to include the factor age in all analyses regarding quality of life after breast cancer surgery. The new aspect in the work discussed here is that there is a difference between women younger than 50 and women older than 65 in the long-term quality of life depending on the type of surgery, with younger women being more satisfied with mastectomy and autologous (but not implant) reconstruction and older women with breast conserving surgery and radiation. This result can add a very important aspect in the situation of preoperative counseling.

However, many factors have an impact on the quality of life and this is not always associated with the type of surgery. Thus the interpretation of dichotome results as in the paper of Diao et al. always warrants caution.

Some caveats and limitations of the analysis have to be mentioned. The approach of a long-term follow up resulted in a response rate of only 25% and that may have an impact on the results and furthermore as always in long-term observations included patients with techniques of surgery and radiation as well as systemic regimens that are no longer state of the art. Also adding to the possibility of a selection bias is the fact that the indications for mastectomy are not discussed. Maybe the decision for a mastectomy in a situation where it is not clearly indicated represents an attitude towards life that is also mirrored in long-term quality of life?

The authors only included patients after breast conserving surgery and radiation and after mastectomy and reconstruction. In consequence their analysis allow no conclusions regarding simple mastectomy and mastectomy and post-mastectomy-radiation. This has to be taken into account when using the data for preoperative counseling. Furthermore the statistically significant preference for mastectomy in women younger than 50 occurred only after autologous reconstruction and not after implant based reconstruction.

Despite these limitations the publication of Diao and colleagues from the MD Anderson Cancer Center delivered important information regarding the quality of life after breast cancer surgery. Sexual well-being is better in younger women after mastectomy and autologous reconstruction and in older women after breast conserving surgery and radiation. Although these findings are far from leading to a recommendation they can be of use when discussing surgery with patients who are struggling to find out what their preference is.


Acknowledgments

Funding: None.


Footnote

Provenance and Peer Review: This article was commissioned by the editorial office, Gland Surgery. The article has undergone external peer review.

Peer Review File: Available at https://gs.amegroups.com/article/view/10.21037/gs-23-522/prf

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at https://gs.amegroups.com/article/view/10.21037/gs-23-522/coif). H.C.K. reports payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from Pfizer, Novartis, Roche, Genomic Health/Exact Sciences, Amgen, AstraZeneca, Riemser, Carl Zeiss Meditec, TEVA, Theraclion, Janssen-Cilag, GSK, LIV Pharma, Lilly, Daiichi Sankyo, Gilead, Zuellig; support for attending meetings and/or travel from Carl Zeiss Meditec, LIV Pharma, Novartis, Amgen, Pfizer, Daiichi Sankyo, Tesaro, Gilead, AstraZeneca, Zuellig, Stemline; participation on a Data Safety Monitoring Board or Advisory Board for Pfizer, Novartis, SurgVision, Carl Zeiss Meditec, Amgen, Onkowissen, MSD, Gilead, Daiichi Sankyo, Seagen, Genomic Health/Exact Sciences, Agendia, Lilly and stock from Theraclion SA. The other author has no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


References

  1. Diao K, Lei X, He W, et al. Patient-Reported Quality of Life after Breast Conserving Surgery with Radiotherapy versus Mastectomy and Reconstruction. Ann Surg 2023;278:e1096-e1102. [Crossref] [PubMed]
  2. Vieira RADC, Bailão-Junior A, de Oliveira-Junior I. Does breast oncoplastic surgery improve quality of life? Front Oncol 2023;12:1099125. [Crossref] [PubMed]
  3. Oei SL, Thronicke A, Grieb G, et al. Evaluation of quality of life in breast cancer patients who underwent breast-conserving surgery or mastectomy using real-world data. Breast Cancer 2023;30:1008-17. [Crossref] [PubMed]
  4. Afshar-Bakshloo M, Albers S, Richter C, et al. How breast cancer therapies impact body image - real-world data from a prospective cohort study collecting patient-reported outcomes. BMC Cancer 2023;23:705. [Crossref] [PubMed]
  5. Herbert SL, Flock F, Felberbaum R, et al. Predictors of Decreased Quality of Life in Breast Cancer Survivors Five Years After Diagnosis. J Breast Cancer 2023;26:243-53. [Crossref] [PubMed]
  6. Alvarez-Pardo S, Romero-Pérez EM, Camberos-Castañeda N, et al. Quality of Life in Breast Cancer Survivors in Relation to Age, Type of Surgery and Length of Time since First Treatment. Int J Environ Res Public Health 2022;19:16229. [Crossref] [PubMed]
Cite this article as: Kolberg HC, Würstlein R. Long-term quality of life after breast surgery—are breast conserving surgery and mastectomy comparable? Gland Surg 2024;13(3):452-454. doi: 10.21037/gs-23-522

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