Impact of breast surgery in de novo stage IV breast cancer
Editorial

Impact of breast surgery in de novo stage IV breast cancer

Tadahiko Shien

Department of Breast and Endocrine Surgery, Okayama University, Okayama, Japan

Correspondence to: Tadahiko Shien, MD, PhD. Department of Breast and Endocrine Surgery, Okayama University, 2-5-1 Shikata-cho, Kita-Ku, Okayama 700-8558, Japan. Email: tshien@md.oayama-u.ac.jp.

Comment on: Fitzal F, Bjelic-Radisic V, Knauer M, et al. Impact of Breast Surgery in Primary Metastasized Breast Cancer: Outcomes of the Prospective Randomized Phase III ABCSG-28 POSYTIVE Trial. Ann Surg 2018. [Epub ahead of print].


Submitted Nov 06, 2018. Accepted for publication Nov 15, 2018.

doi: 10.21037/tcr.2018.11.19


The article, entitled “Impact of Breast Surgery in Primary Metastasized Breast Cancer Outcomes of the Prospective Randomized Phase III ABCSG-28 POSYTIVE Trial”, published in the Annals of Surgery (1), is the third to study to prospectively evaluate the prognostic efficacy of breast surgery in patients with metastases (Table 1). This trial evaluated breast surgery for newly diagnosed de novo stage IV breast cancer patients with no history of systemic therapy. After providing informed consent, patients were allocated to arm A (surgery consisting of either standard breast-conserving surgery or mastectomy including axillary staging and systemic therapy) or to arm B (systemic therapy without surgery). The patients were stratified according to grading, receptor status, HER2 status, metastasis location (visceral vs. bone-only metastases) and planned first-line therapy. As systemic therapy, chemotherapy, anti-HER2 therapy, or anti-hormone therapy was administered according to local standards, with regimens including modern effective drugs. The primary endpoint was overall survival (OS) and the authors reported that they could not demonstrate a prognostic benefit for primary tumor resection. Additionally, they reported worsening of the outcomes of the patients with distant metastasis. The time to distant progression in the surgery arm was shorter (though not significantly) than that in the no-surgery arm (HR 0.598, 95% CI, 0.343–1.043; P=0.0668). These results were very similar to those of the first report on a prospective trial from India (2) but different from the results of many retrospective reports (3). In our view, the limitation of systemic therapies is one of the reasons for this discrepancy. In the Indian trial, the patients did not receive systemic therapies according to breast cancer subtypes. Anti-HER2 targeted therapies were not used for patients with HER2-positive subtype, and very few patients with ER-positive tumors received hormone therapy. In addition, the discontinuation of effective systemic therapy after randomization might result in a poorer outcome, especially distant progression free survival, in the patients with primary tumor resection. However, the patients received modern and continuous systemic therapy in this ABCSG trial and the results were similar to those of prior trials. Given these results, it appears that stage IV breast cancer patients should not undergo primary tumor surgery.

Table 1

The prospective trials which evaluate the prognostic efficacy of primary tumor resection

Trial group Trial number Accrual period (situation) N Initial therapy
India (Tata Memorial Hospital) NTC00193778 2005–2012 (completed) 350 Systemic
JCOG UMIN000005586 (JCOG1017) 2011–2018 (completed) 500/410→570/407 Systemic
ECOG NCT01242800 (ECOG2108) 2011–2015 (completed) 880/660→368/258 Systemic
Turkey NCT00557986 (MF07-01) 2008–2012 (completed) 281 Surgery
ABCSG NCT01015625 (ABCSG 28) 2010–2015 (early stopped) 256→90 Surgery

However, there is an important problem that needs to be addressed. Statistically, the authors planned for a control arm, systemic therapy alone: median survival 24 months, experimental arm, surgery plus systemic therapy: median survival 36 months; HR of 0.666, alpha level 5%, power 80%, drop-out rate 5%, requiring 254 patients (127 in each treatment arm) to be enrolled in order to observe 192 events. However, due to poor recruitment, the study was stopped prematurely after 5 years when only 90 patients had been enrolled, 45 in each arm. The statistical power was thus very low. Moreover, the median survival of the control arm was 54.8 months, which was longer than specified in the protocol plan, such that they would have needed more patients and a longer follow-up period than in their initial plan to detect a 6-month advantage of surgery.

The MF07-01 trial from Turkey evaluated the prognostic effects of breast surgery as the primary treatment and found that breast surgery might prolong OS (4). However, it was not possible to confirm that surgery achieves an 18% improvement of the 3-year survival rate according to their preplanned analysis. On the other hand, a longer follow-up study showed statistically significant improvement in median survival (HR 0.66; 95% CI, 0.49–0.88; P=0.005) (The authors did not plan this analysis as part of their initial protocol).

We know that the most significant treatment to improve the prognosis of metastatic breast cancer patients is the effective systemic therapy. Systemically administered drugs clearly prolong survival. Local therapy, including surgery and/or radiation, is one of the choices of additional treatment. Our aim should be to indicate the most effective treatment strategies for individual cancer patients, employing drugs, surgery and radiation, alone or in various combinations. The goals for them are to prolong their survival and to control symptoms. We want to answer the questions “Who would benefit from breast surgery?” and “When should patients receive surgery?”.

The Japan Clinical Oncology Group (JCOG 1017, UMIN000005586) (5) and Eastern Clinical Oncology Group (ECOG 2108, NCT01242800) are completing the recruitment of recruiting and following patients for a prospective trial. These trials have enough patients to allow statistically meaningful analysis of their hypothesis, and patients received the modern standard systemic therapy, including molecular target therapies, available both before and after randomization. These trials will resolve current controversies and provide many eagerly awaited answers.


Acknowledgments

Funding: This report was supported in part by funding for Practical Research for Innovative Cancer Control (18ck0106307h0002) provided by the Japan Agency for Medical Research and Development, AMED.


Footnote

Provenance and Peer Review: This article was commissioned and reviewed by the Section Editor San-Gang Wu (Department of Radiation Oncology, Xiamen Cancer Center, the First Affiliated Hospital of Xiamen University, Xiamen, China).

Conflicts of Interest: The author has completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tcr.2018.11.19). The author has no conflicts of interest to declare.

Ethical Statement: The author is 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. Fitzal F, Bjelic-Radisic V, Knauer M, et al. Impact of Breast Surgery in Primary Metastasized Breast Cancer: Outcomes of the Prospective Randomized Phase III ABCSG-28 POSYTIVE Trial. Ann Surg 2018; [Epub ahead of print]. [Crossref] [PubMed]
  2. Badwe R, Hawaldar R, Nair N, et al. Locoregional treatment versus no treatment of the primary tumour in metastatic breast cancer: an open label randomised controlled trial. Lancet Oncol 2015;16:1380-8. [Crossref] [PubMed]
  3. Petrelli F, Barni S. Surgery of primary tumors in stage IV breast cancer: an updated meta-analysis of published studies with meta-regression. Med Oncol 2012;29:3282-90. [Crossref] [PubMed]
  4. Soran A, Ozmen V, Ozbas S, et al. Randomized Trial Comparing Resection of Primary Tumor with No Surgery in Stage IV Breast Cancer at Presentation: Protocol MF07-01. Ann Surg Oncol 2018;25:3141-9. [Crossref] [PubMed]
  5. Shien T, Nakamura K, Shibata T, et al. A randomized controlled trial comparing primary tumour resection plus systemic therapy with systemic therapy alone in metastatic breast cancer (PRIM-BC): Japan Clinical Oncology Group Study JCOG1017. Jpn J Clin Oncol 2012;42:970-3. [Crossref] [PubMed]
Cite this article as: Shien T. Impact of breast surgery in de novo stage IV breast cancer. Transl Cancer Res 2019;8(Suppl 2):S118-S119. doi: 10.21037/tcr.2018.11.19

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