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Eurasian Journal of
            Medicine and Oncology                                     Zercepac  + pyrotinib versus pertuzumab in HER2+ BC
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            ventricular contractions, arrhythmia, sinus tachycardia,   5. Conclusion
            sinus bradycardia, sinus arrhythmia, T-wave changes, and
            changes in cardiac ejection fraction). However, diarrhea   While the HP dual-target regimen remains the neoadjuvant
            showed a statistically significant difference (p<0.001): no   standard for HER2-positive breast cancer, this study
                                                                                                 ®
            cases were reported in the TCbHP group, while all eight   highlights the non-inferiority of Zercepac ’s to originator
            patients in the TCbHPy group experienced varying degrees   trastuzumab, along with its preservative-free formulation
                                                                    cost-efficiency
                                                                                                   HR-negative
                                                               and
                                                                                  advantages.
                                                                                              For
            of diarrhea. Furthermore, all eight patients in the TCbHPy
            group had MP grades above level 4, with a total probability   subgroups,  the  TCbHPy  regimen  demonstrates
            of  75%  (6/8)  achieving  apCR,  bpCR,  or  tpCR.  Two  out   particular promise, achieving high MP regression grades
                                                               (100% grade ≥4) despite modest tpCR rates. The 75%
            of three tpCR patients were HR-negative. As experience
            with Py increased, a triple anti-diarrheal method was   apCR/bpCR composite rate and manageable toxicity
            implemented for first-level prevention: loperamide (two   profile, with appropriate prophylactic measures, suggest
                                                               potential clinical utility, although long-term survival
            tablets per dose, twice daily, not exceeding eight tablets per
            day), smectite powder (one packet per dose, 3 times daily),   outcomes (PFS/OS) require validation in larger cohorts.
            and bifidobacterium (two packets per dose, twice daily).   At present, we are actively collecting and analyzing long-
                                                               term follow-up data, including PFS and OS. We plan
            Before introducing this regimen, the incidence of diarrhea
            in our department included six cases (75%) of Grade  1   to  disclose  these  results  in  subsequent  research  reports.
            and two cases (25%)  of  Grade  2, with no unexpected   Moving forward, studies should prioritize optimized
                                                               dosing strategies and biomarker-driven patient selection
            Grade 3 events. Following the introduction of triple anti-
            diarrheal therapy, as of the manuscript submission date,   to maximize the therapeutic index of Py.
            patient compliance in the Py group in our department   Acknowledgments
            improved significantly. The median duration of diarrhea
            was reduced from 7  days to 3  days (interquartile range:   None.
            2 – 5), and the patient compliance rate increased to 87.5%   Funding
            (7 out of 8), with an initial dose of 400  mg. The tpCR
            rate also improved compared to previous statistics. We   None.
            recognize that the study’s small sample size and single-
            center design may limit the statistical robustness and   Conflict of interest
            generalizability of the findings. Nevertheless, we believe   The authors declare no conflicts of interest.
            the results of this research are of substantial value and can
            serve as a foundational framework for future large-scale,   Author contributions
            multicenter investigations.                        Conceptualization: Hong Gao and Shengying Wang
              In real-world clinical  practice, the  HP  dual-target   Formal analysis: Jiali Lei and Zhaohua Gui
            regimen remains the first choice for neoadjuvant treatment   Methodology: Hong Gao, Jiali Lei, and Zhaohua Gui
            for HER2-positive breast cancer. Zercepac  is not inferior   Writing – original draft: Hong Gao
                                              ®
            to Herceptin in terms of efficacy. With its lack of benzyl   Writing – review & editing: Shengying Wang
            alcohol preservatives and cost advantage, Zercepac  can
                                                      ®
            further reduce expenses for both patients and healthcare   Ethics approval and consent to participate
            systems. Moreover, HR and HER2 status are independent   This retrospective data analysis study, which involved no
            factors influencing tpCR rates across all patients. Based on   disclosure of patient identities and complied with ethical
            the clinical observations in this study, the trastuzumab +   standards, is exempt from obtaining informed consent.
            Py regimen, which combines small and large molecules,   Data are from Anhui Provincial Cancer Hospital, and its
            offers advantages over single-target regimens combined   ethical approval is granted by the Ethics Committee of
            with chemotherapy. It also shows a modest advantage in   Anhui Provincial Cancer Hospital (Approval Number:
            improving the MP grading of primary tumors compared   2024-TJK-06).
            to regimens based solely on large molecules, especially in
            HR-negative, HER2-positive patients. The  combination   Consent for publication
                     ®
            of Zercepac  and Py with chemotherapy warrants further   The authors verbally informed all participants by telephone
            investigation. Whether this regimen can benefit improve   during data collection and follow-up regarding the intent
            PFS or even overall survival (OS) remains to be determined   to publish study results, and all participants provided
            through future clinical follow-up and data collection.  verbal consent.


            Volume 9 Issue 3 (2025)                        119                         doi: 10.36922/EJMO025100044
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