ijms-logo

Journal Browser

Journal Browser

Transforming in Cancer Therapy: Advances in Immunotherapy and Tyrosine Kinase Inhibitors

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Oncology".

Deadline for manuscript submissions: 31 October 2025 | Viewed by 619

Special Issue Editor


E-Mail Website
Guest Editor
The Legacy Heritage Center & Dr. Larry Norton Institute, Soroka Medical Center, Ben Gurion University, Beer Sheva 84105, Israel
Interests: thoracic malignancies; lung cancer; immunotherapy; targeted therapy; biomarkers; resistance mechanisms; EGFR/ALK inhibitors; tumor microenvironment; combination therapy
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

The landscape of solid tumor care is rapidly evolving, with immunotherapy and tyrosine kinase inhibitors (TKIs) leading the charge in transforming treatment strategies. Immunotherapy harnesses the body's immune system to specifically target and destroy tumor cells, offering significant benefits in cancers previously deemed hard to treat. By stimulating immune responses through checkpoint inhibitors, monoclonal antibodies, and CAR-T cells, immunotherapy has shown promise in various malignancies. Targeted TKIs can block specific enzymes or receptors responsible for tumor growth, providing a more precise, less toxic alternative to traditional chemotherapy. These inhibitors have revolutionized the management of cancers.

Immunotherapy and TKIs hold the potential to further improve patient outcomes, reducing recurrence and enhancing survival rates.

For this Special Issue, we invite researchers to contribute original research articles, reviews, and perspectives that examine both the fundamental and practical aspects of tumor–immune cell interactions, with a particular focus on the efficacy of immunotherapy and TKIs. As these therapies are already established in several clinical contexts, we welcome submissions that address emerging challenges and future directions in the field. Topics of interest include, but are not limited to, mechanisms of resistance to TKIs and immune checkpoint blockade, innovative combination therapies (such as TKIs with immunotherapy), biomarker discovery for patient stratification, and next-generation immunotherapies such as bispecific antibodies and neoantigen vaccines. We believe that this Special Issue will serve as a valuable building block in developing more advanced, effective, and personalized cancer therapies.

Dr. Walid Shalata
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 short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

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. International Journal of Molecular Sciences is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. There is an Article Processing Charge (APC) for publication in this open access journal. For details about the APC please see here. 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

  • tyrosine kinase inhibitors
  • immunotherapy
  • monoclonal antibodies
  • CAR-T cells

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • Reprint: MDPI Books provides the opportunity to republish successful Special Issues in book format, both online and in print.

Further information on MDPI's Special Issue policies can be found here.

Published Papers (1 paper)

Order results
Result details
Select all
Export citation of selected articles as:

Research

19 pages, 3201 KiB  
Article
Exploring the Impact of TP53 Mutation and Wild-Type Status on the Efficacy of Immunotherapy in Non-Small Cell Lung Cancer
by Alexander Yakobson, Ronen Brenner, Itamar Gothelf, Natalie Maimon Rabinovich, Ahron Yehonatan Cohen, Ashraf Abu Jama, Nashat Abu Yasin, Fahmi Abu Ghalion, Abed Agbarya and Walid Shalata
Int. J. Mol. Sci. 2025, 26(14), 6939; https://doi.org/10.3390/ijms26146939 - 19 Jul 2025
Viewed by 457
Abstract
TP (tumor protein) 53 mutation status plays a critical role in cancer progression and may influence survival outcomes in non-small cell lung cancer (NSCLC) patients receiving immunotherapy. This study investigates the impact of TP53 mutation status and immunotherapy treatment on survival in NSCLC [...] Read more.
TP (tumor protein) 53 mutation status plays a critical role in cancer progression and may influence survival outcomes in non-small cell lung cancer (NSCLC) patients receiving immunotherapy. This study investigates the impact of TP53 mutation status and immunotherapy treatment on survival in NSCLC patients. This retrospective study analyzed NSCLC patients treated with pembrolizumab or ipilimumab plus nivolumab, stratified by TP53 mutation status and PD-L1 (programmed death-ligand 1) expression (<1%, 1–49%, >50%). Survival outcomes (overall survival (OS) and progression free survival (PFS) were assessed using Kaplan–Meier curves and log-rank tests, with subgroup analysis by histological subtype. In squamous cell cancer (SCC) patients, no significant differences in OS or PFS were found based on TP53 mutation status or treatment type. A trend toward improved survival was observed with pembrolizumab (p = 0.088). In adenocarcinoma patients, significant differences in OS and PFS were observed based on TP53 mutation status. Pembrolizumab showed superior survival outcomes compared to ipilimumab plus nivolumab in TP53 wild-type patients (p < 0.001). PD-L1 ≥ 1% also predicted better outcomes, especially in adenocarcinoma patients. TP53 mutation status and immunotherapy type significantly influence survival outcomes in NSCLC, particularly in adenocarcinoma patients. Pembrolizumab demonstrated superior efficacy in TP53 wild-type patients, with PD-L1 expression further refining survival predictions. These findings underscore the importance of personalized treatment strategies based on TP53 status and PD-L1 expression in NSCLC. Further studies are needed to validate these results and optimize treatment approaches. Full article
Show Figures

Figure 1

Back to TopTop