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Advances in Neoadjuvant Chemotherapy and Radiotherapy for Breast Cancer: Surgical Impact and Clinical Outcomes

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Cancer Therapy".

Deadline for manuscript submissions: 30 November 2026 | Viewed by 2424

Special Issue Editor


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Guest Editor
Hospital Universitari de Bellvitge, Barcelona, Spain
Interests: breast cancer

Special Issue Information

Dear Colleagues,

Neoadjuvant chemotherapy (NAC) and radiotherapy (NRT) are essential strategies in the management of locally advanced and high-risk early-stage breast cancer. These therapies facilitate tumor downstaging, enable breast-conserving surgery, and improve patient prognosis. Advances in molecular profiling, targeted therapies, and immunotherapy have further enhanced the efficacy of neoadjuvant regimens, profoundly influencing surgical decisions, postoperative recovery, and personalized care. Despite these advancements, challenges remain in optimizing protocols, minimizing toxicities, and improving quality of life for patients.

We are pleased to invite you to contribute to this Special Issue on "Advances in Neoadjuvant Chemotherapy and Radiotherapy for Breast Cancer: Surgical Impact and Clinical Outcomes." This collection will explore cutting-edge developments in NAC and NRT, focusing on their impact on treatment optimization, surgical strategies (including breast and axillary surgeries), and therapeutic outcomes. Topics will include emerging protocols, the integration of radiotherapy, and the interplay between chemotherapy and radiotherapy in enhancing efficacy.

We welcome original research articles, systematic reviews, and translational studies covering a range of areas, including the following:

  • Innovative clinical protocols and preclinical findings;
  • Personalized approaches to neoadjuvant therapies;
  • Advances in surgical techniques informed by NAC or NRT;
  • Strategies to overcome challenges in treatment optimization.

This Special Issue aims to provide a comprehensive overview of current trends and future directions in neoadjuvant therapies for breast cancer. We are confident that your expertise in [specific area] will bring valuable insights into this collection and help foster impactful discussions in the field.

Thank you for considering this opportunity. We look forward to receiving your contributions and collaborating with you on this exciting endeavor.

Sincerely,

Dr. Amparo García-Tejedor
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as communications are invited. For planned papers, a title and short abstract (about 250 words) can be sent to the Editorial Office for assessment.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Cancers is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2900 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • neoadjuvant chemotherapy
  • radiotherapy
  • breast cancer
  • surgical outcomes
  • tumor downstaging
  • personalized therapy
  • breast-conserving surgery
  • mastectomy
  • clinical outcomes

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Published Papers (1 paper)

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Research

11 pages, 502 KB  
Article
Impact of Chemotherapy Dose Intensity on Pathological Complete Response in Pembrolizumab-Treated Early Triple-Negative Breast Cancer: A Real-World Multicenter Analysis
by Palma Fedele, Stefania Luigia Stucci, Matteo Landriscina, Maria Morritti, Francesco Giuliani, Lucia Moraca, Giuseppe Cairo, Raffaele Ardito, Marianna Giampaglia, Domenico Bilancia, Assunta Melaccio, Antonella Terenzio, Antonio Gnoni, Antonella Licchetta, Federica Fumai, Laura Lanotte, Alessandro Rizzo and Gennaro Gadaleta-Caldarola
Cancers 2025, 17(21), 3554; https://doi.org/10.3390/cancers17213554 - 2 Nov 2025
Cited by 1 | Viewed by 2041
Abstract
Background: Pembrolizumab combined with neoadjuvant chemotherapy significantly improves pCR in early TNBC, but the effect of treatment intensity and baseline clinical factors has been insufficiently explored in real-world settings. Methods: We retrospectively included 169 consecutive patients with stage II–III TNBC treated across 11 [...] Read more.
Background: Pembrolizumab combined with neoadjuvant chemotherapy significantly improves pCR in early TNBC, but the effect of treatment intensity and baseline clinical factors has been insufficiently explored in real-world settings. Methods: We retrospectively included 169 consecutive patients with stage II–III TNBC treated across 11 Italian oncology centers (January 2022–January 2025) with the KEYNOTE-522 regimen. Clinical, pathological, and treatment data were collected, including relative dose intensity (RDI), dose modifications, and toxicities. The primary endpoint was pCR (ypT0/is ypN0). Results: The overall pCR rate was 65.7%, which is consistent with clinical trial data. Dose reductions occurred in 40% of patients and chemotherapy was discontinued in 18%. Patients maintaining RDI ≥85% achieved higher pCR (79.3% vs. 51.2%, p < 0.001). Similarly, patients without dose reductions (72.5% vs. 55.2%, p = 0.031) and those completing all cycles (73.1% vs. 41.0%, p < 0.001) had superior outcomes. Dose modifications occurred mainly during the taxane/carboplatin phase and were predominantly due to hematological toxicities (anemia 44%, neutropenia 30%, and thrombocytopenia 15%), neuropathy (18%), and gastrointestinal events (36%). Higher TILs correlated with increased pCR (70.6% vs. 60.7%, p = 0.049), while BRCA mutations showed a favorable trend. ECOG, BMI, pregnancy history, and comorbidities were not significantly associated with pCR. Conclusions: In this multicenter real-world cohort, maintaining chemotherapy dose intensity (RDI ≥ 85%) and completing all planned cycles were strongly associated with higher pCR rates, reinforcing the clinical importance of minimizing dose reductions and discontinuations during pembrolizumab-based neoadjuvant therapy for TNBC. Full article
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