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Pertuzumab, trastuzumab and taxane-based treatment for visceral organ metastatic, trastuzumab-naïve breast cancer: real-life practice outcomes

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Abstract

Purpose

In this study, we aimed to describe the real-life practice outcomes of pertuzumab–trastuzumab–taxane (PTT) combination in visceral organ metastatic, trastuzumab-naive breast cancer (BC) patients.

Methods

This study was conducted by Turkish Oncology Group and included 317 patients’ data from 36 centers.

Results

Median age was 51 (22–82). Median PFS was 28.5 months, while median OS was 40.3 months. Patients with brain metastases (n: 13, 4.1%) had worse PFS (16.8 m vs. 28.5 m; p = 0.002) and OS (26.7 m vs. 40.3 m; p = 0.009). Patients older than 65 years of age (n: 42, 13.2%) had significantly lower OS results (19.8 m vs. 40.3 m; p = 0.01). Two hundred sixty-eight patients (86.7%) received docetaxel while 37 patients (11.7%) received paclitaxel. PFS and OS were similar between taxane groups. In eight patients (2.5%), 5–40% ejection fraction decrement from baseline was detected without any clinical sign of heart failure.

Conclusions

Our RLP trial included only visceral metastatic, trastuzumab-naïve BC patients including cases with brain involvement who received PTT combination in the first-line treatment. Regardless of negative prognostic characteristics, our results are in parallel with pivotal trial. Further strategies for brain metastasis should be developed to improve outcomes despite encouraging results with PTT treatment. Taxane selection can be personalized and endocrine maintenance may further improve outcomes after taxanes were discontinued. To our knowledge, this is the largest scale real-life clinical practice study of pertuzumab–trastuzumab–taxane therapy to date.

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Availability of data and materials

The data is protected under responsibility of primary author (EE) and senior authors (BO-UD); and available for review process if required.

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Acknowledgements

Turkish Oncology Group (TOG) represented by Esin E., Oksuzoglu B., Bilici A., Kostek O., Cicin I., Kaplan M. A., Aktas B. Y., S. Aksoy, Ozdemir O., Alacacioglu A., Cabuk D., Sumbul A. T., Sakin A., Yetisir E., Paydas S., Er O., Korkmaz T., Yildirim N., Sakalar T., Demir H., Karaagac M., Artac M., Harputluoglu H., Bilen E., Degirmencioglu S., Aliyev A., Olgun P., Cil T., Basaran G., Gumusay O., Demir A., Tanrikulu E., Yumuk P. F., Imamoglu I., Uluc Oyan B., Cetin B., Haksoyler V., Karadurmus N., Erturk I., Yilmaz H., Evrensel T., Beypinar, Kocer, Pilanci K. N., Seker M., Urun Y., Yildirim N., Eren T., Demirci U.

Funding

None declared.

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Authors and Affiliations

Authors

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Contributions

All of the authors contribute to data collection. Concept: EE, BO, UD, GB; Design: EE, BO, UD; Supervision: BO, UD; Analysis and/or Interpretation: EE, UD, IC; Writing: EE; Critical Reviews: BO, UD, FY, AB, IC.

Corresponding author

Correspondence to Ece Esin.

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Conflict of interest

The authors declare no conflict of interest.

Ethics approval and consent to participate

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. The study was approved by the committee of University of Health Sciences, Ankara Oncology Education and Research Hospital (TUEK meeting number: 40-15.5.2018).

Human/animal rights statement

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

Informed consent

Given the retrospective nature of the study, written informed consent was not mandatory according to local regulations.

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Not available.

Additional information

The members of Turkish Oncology Group (TOG) are listed in Acknowledgements.

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Esin, E., Oksuzoglu, B., Bilici, A. et al. Pertuzumab, trastuzumab and taxane-based treatment for visceral organ metastatic, trastuzumab-naïve breast cancer: real-life practice outcomes. Cancer Chemother Pharmacol 83, 131–143 (2019). https://doi.org/10.1007/s00280-018-3712-7

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