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Review

Systemic Chemotherapy in Penile Squamous Cell Carcinoma: Mechanisms, Clinical Applications, and Evidence-Based Regimens

by
Michalina Grudzińska
1,*,†,
Mateusz Czajkowski
2,3,†,
Maciej Dolny
2,
Marcin Matuszewski
2,
Piotr Mieczysław Wierzbicki
4,
Agnieszka Rybarczyk
4 and
Oliver Walther Hakenberg
5
1
Student Scientific Circle, Department of Urology, Faculty of Medicine, Medical University of Gdańsk, Marii Skłodowskiej-Curie 3a, 80-210 Gdańsk, Poland
2
Department of Urology, Medical University of Gdańsk, Mariana Smoluchowskiego 17 Street, 80-214 Gdańsk, Poland
3
Penile Disease Center, University Clinical Center of Gdańsk, 80-952 Gdańsk, Poland
4
Department of Histology, Medical University of Gdańsk, Dębinki, 80-211 Gdańsk, Poland
5
Department of Urology, Jena University Hospital, 07747 Jena, Germany
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Cancers 2026, 18(1), 46; https://doi.org/10.3390/cancers18010046 (registering DOI)
Submission received: 9 November 2025 / Revised: 14 December 2025 / Accepted: 22 December 2025 / Published: 23 December 2025

Simple Summary

Penile squamous cell carcinoma (PSCC) is a rare but aggressive malignancy. In its advanced stages, systemic chemotherapy plays a pivotal role; however, the evidence remains limited, and treatment strategies are frequently extrapolated from other cancer types. This review provides a concise and comprehensive overview of the cytotoxic agents used in PSCC, outlining their mechanisms of action, historical development, and current clinical applications. Moreover, major international guidelines are compared to highlight the similarities and differences relevant to daily practice. This review seeks to assist clinicians and researchers in understanding the dynamic landscape of chemotherapeutic options for the treatment of penile cancer.

Abstract

Background/Objectives: Penile squamous cell carcinoma (PSCC) is rare but aggressive. Systemic chemotherapy plays a crucial role in the management of node-positive or metastatic cases; however, the supporting evidence predominantly originates from small, non-randomized studies. This review provides a narrative analysis of the cytotoxic classes and regimens employed in PSCC and compares major clinical guidelines to facilitate informed decision-making in practice. Methods: English-language reports were identified in PubMed/Scopus/Google Scholar without date limits. Selection prioritized objective response, survival and toxicity outcomes, and guidance statements across neoadjuvant, adjuvant, and palliative settings. Results: Bleomycin-containing triplet regimens demonstrated efficacy but were associated with unacceptable pulmonary toxicity, leading to their discontinuation in clinical recommendations. Currently, cisplatin/taxane-based combinations remain fundamental in treatment protocols. The paclitaxel–ifosfamide–cisplatin (TIP) regimen achieves approximately 40–50% objective responses in phase II studies and may enable curative surgery, while taxane–cisplatin–5-fluorouracil (TPF) shows comparable efficacy with higher toxicity. For less fit patients, cisplatin–5-fluorouracil (PF) or carboplatin–taxane doublets are pragmatic alternatives. Single-agent taxanes or vinflunine offer modest second-line benefits. Although EAU–ASCO 2023, ESMO–EURACAN 2024, and NCCN v2.2025 are broadly in consensus, recommendations differ regarding eligibility thresholds and regimen preferences. Overall, the quality of the evidence remains low. Conclusions: TIP remains the reference neoadjuvant option for chemotherapy-fit patients with bulky nodal disease; doublets are reasonable when cisplatin fitness is limited; and bleomycin should be avoided. Harmonized eligibility criteria, biomarker-enriched studies, and coordinated multicenter trials are needed to improve outcomes in this rare malignancy.
Keywords: penile cancer; squamous cell carcinoma; chemotherapy; cisplatin; paclitaxel; neoadjuvant therapy; adjuvant therapy; metastatic disease; guidelines penile cancer; squamous cell carcinoma; chemotherapy; cisplatin; paclitaxel; neoadjuvant therapy; adjuvant therapy; metastatic disease; guidelines

Share and Cite

MDPI and ACS Style

Grudzińska, M.; Czajkowski, M.; Dolny, M.; Matuszewski, M.; Wierzbicki, P.M.; Rybarczyk, A.; Hakenberg, O.W. Systemic Chemotherapy in Penile Squamous Cell Carcinoma: Mechanisms, Clinical Applications, and Evidence-Based Regimens. Cancers 2026, 18, 46. https://doi.org/10.3390/cancers18010046

AMA Style

Grudzińska M, Czajkowski M, Dolny M, Matuszewski M, Wierzbicki PM, Rybarczyk A, Hakenberg OW. Systemic Chemotherapy in Penile Squamous Cell Carcinoma: Mechanisms, Clinical Applications, and Evidence-Based Regimens. Cancers. 2026; 18(1):46. https://doi.org/10.3390/cancers18010046

Chicago/Turabian Style

Grudzińska, Michalina, Mateusz Czajkowski, Maciej Dolny, Marcin Matuszewski, Piotr Mieczysław Wierzbicki, Agnieszka Rybarczyk, and Oliver Walther Hakenberg. 2026. "Systemic Chemotherapy in Penile Squamous Cell Carcinoma: Mechanisms, Clinical Applications, and Evidence-Based Regimens" Cancers 18, no. 1: 46. https://doi.org/10.3390/cancers18010046

APA Style

Grudzińska, M., Czajkowski, M., Dolny, M., Matuszewski, M., Wierzbicki, P. M., Rybarczyk, A., & Hakenberg, O. W. (2026). Systemic Chemotherapy in Penile Squamous Cell Carcinoma: Mechanisms, Clinical Applications, and Evidence-Based Regimens. Cancers, 18(1), 46. https://doi.org/10.3390/cancers18010046

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