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Diagnostics
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Renal Cell Carcinoma: From Diagnosis to Identification of Novel Therapeutic...
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Renal Cell Carcinoma: From Diagnosis to Identification of Novel Therapeutic Targets and Minimally Invasive Treatments

A special issue of Diagnostics (ISSN 2075-4418). This special issue belongs to the section "Pathology and Molecular Diagnostics".

Deadline for manuscript submissions: closed (31 August 2022) | Viewed by 5347

Special Issue Editors

Dr. Matteo Ferro

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Guest Editor
Division of Urology, European Institute of Oncology-IRCCS, 20141 Milan, Italy
Interests: cancer cells; cancer biology; prostate cancer; urology; prostate; bladder cancer; urologic oncology; cancer metastasis; oncology; doppler ultrasonography
Special Issues, Collections and Topics in MDPI journals
Prof. Dr. Andrea Minervini

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Guest Editor
Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy
Unit of Oncologic Minimally- Invasive Urology and Andrology, Careggi Hospital, Florence, Italy
Interests: renal cell carcinoma; prostate cancer; bladder cancer; robotic surgery; biomarkers
Special Issues, Collections and Topics in MDPI journals
Prof. Dr. Alessandro Antonelli

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Guest Editor
Department of Urology, University of Verona, Verona, Italy
Interests: kidney cancer; minimally invasive surgery; reconstructive urology; surgical innovation
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Dr. Angelo Porreca

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Guest Editor
IOV - Istituto Oncologico Veneto – IRCCS, Via Gattamelata, 64, 35128 Padova, Italy
Interests: renal cell carcinoma; prostate cancer; bladder cancer
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Prof. Dr. Giuseppe Lucarelli

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Guest Editor
Andrology and Kidney Transplantation Unit, Department of Emergency and Organ Transplantation—Urology, University of Bari “Aldo Moro”, 70124 Bari, Italy
Interests: kidney cancer; prostate cancer; kidney transplantation; metabolomics
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Prof. Dr. Michele Battaglia

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Guest Editor
Department of Emergency and Organ Transplantation – Urology, Andrology and Kidney Transplantation Unit - University of Bari « Aldo Moro », 70124 Bari, Italy
Interests: renal cell carcinoma; prostate cancer; bladder cancer
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Prof. Dr. Ditonno Pasquale

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Guest Editor
Department of Emergency and Organ Transplantation – Urology, Andrology and Kidney Transplantation Unit - University of Bari « Aldo Moro », 70124 Bari, Italy
Interests: renal cell carcinoma; prostate cancer; bladder cancer
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Prof. Dr. Riccardo Schiavina

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Guest Editor
Department of Urology, University of Bologna, S-Orsola-Malpighi Hospital, Bologna, Italy
Interests: renal cell carcinoma; prostate cancer; bladder cancer; robotic surgery
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Prof. Dr. Ottavio De Cobelli

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Guest Editor
1. Division of Urology, European Institute of Oncology-IRCCS, Milan, Italy
2. Department of Oncology and Haematology-Oncology, Università degli studi di Milano, Milan, Italy
Interests: renal cell carcinoma; prostate cancer; bladder cancer; robotic surgery
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Prof. Dr. Gennaro Musi

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Guest Editor
1. Division of Urology, European Institute of Oncology-IRCCS, Milan, Italy
2. Department of Oncology and Haematology-Oncology, Università degli studi di Milano, Milan, Italy
Interests: renal cell carcinoma; prostate cancer; bladder cancer; robotic surgery
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Renal cell carcinoma (RCC) is the most frequent malignancy affecting the adult kidney and the twelfth most common cancer. The pathophysiology of RCC is complex and arises from a combination of gene mutations (i.e., VHL, PBMR1, SETD2, BAP1, etc.) in addition to other factors such as diabetes, obesity, smoking, and hypertension. In the early stages, the disease is frequently asymptomatic and incidentally diagnosed by imaging, having a good prognosis; conversely, RCC has a high mortality rate in advanced phases, due to poor responses to radiotherapy and chemotherapy. The progressive introduction of high-throughput technologies and recent studies of molecular and genomic profiling have shed new light on the pathophysiology of RCC. Moreover, in recent years, there has been a growing interest in identifying tumor markers not only for diagnostic purposes but also to improve the predictive power of clinical and pathological parameters. This Special Issue of Diagnostics aims to collect studies on minimally invasive treatment and translational research for the management and diagnosis of renal cell carcinoma (RCC).

You may choose our Joint Special Issue in Biomedicines.

Dr. Matteo Ferro
Prof. Dr. Andrea Minervini
Prof. Dr. Alessandro Antonelli
Dr. Angelo Porreca
Prof. Dr. Giuseppe Lucarelli
Dr. Michele Battaglia
Prof. Dr. Ditonno Pasquale
Prof. Dr. Riccardo Schiavina
Prof. Dr. Ottavio De Cobelli
Dr. Gennaro Musi
Guest Editors

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. Diagnostics 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 2600 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

  • renal cell carcinoma
  • biomarker
  • molecular biology
  • diagnosis
  • prognosis
  • pathology

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

Published Papers (2 papers)

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Research

11 pages, 1829 KiB  
Article
Small Renal Masses without Gross Fat: What Is the Role of Contrast-Enhanced MDCT?
by Gerta Repeckaite, Kristina Zviniene, Justina Jankauskiene, Algidas Basevicius and Daimantas Milonas
Diagnostics 2022, 12(2), 553; https://doi.org/10.3390/diagnostics12020553 - 21 Feb 2022
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Abstract
Increased detection of small renal masses (SRMs) has encouraged research for non-invasive diagnostic tools capable of adequately differentiating malignant vs. benign SRMs and the type of the tumour. Multi-detector computed tomography (MDCT) has been suggested as an alternative to intervention, therefore, it is [...] Read more.
Increased detection of small renal masses (SRMs) has encouraged research for non-invasive diagnostic tools capable of adequately differentiating malignant vs. benign SRMs and the type of the tumour. Multi-detector computed tomography (MDCT) has been suggested as an alternative to intervention, therefore, it is important to determine both the capabilities and limitations of MDCT for SRM evaluation. In our study, two abdominal radiologists retrospectively blindly assessed MDCT scan images of 98 patients with incidentally detected lipid-poor SRMs that did not present as definitely aggressive lesions on CT. Radiological conclusions were compared to histopathological findings of materials obtained during surgery that were assumed as the gold standard. The probability (odds ratio (OR)) in regression analyses, sensitivity (SE), and specificity (SP) of predetermined SRM characteristics were calculated. Correct differentiation between malignant vs. benign SRMs was detected in 70.4% of cases, with more accurate identification of malignant (73%) in comparison to benign (65.7%) lesions. The radiological conclusions of SRM type matched histopathological findings in 56.1%. Central scarring (OR 10.6, p = 0.001), diameter of lesion (OR 2.4, p = 0.003), and homogeneous accumulation of contrast medium (OR 3.4, p = 0.03) significantly influenced the accuracy of malignant diagnosis. SE and SP of these parameters varied from 20.6% to 91.3% and 22.9% to 74.3%, respectively. In conclusion, MDCT is able to correctly differentiate malignant versus uncharacteristic benign SRMs in more than 2/3 of cases. However, frequency of the correct histopathological SRM type MDCT identification remains low. Full article
(This article belongs to the Special Issue Renal Cell Carcinoma: From Diagnosis to Identification of Novel Therapeutic Targets and Minimally Invasive Treatments)
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8 pages, 2493 KiB  
Article
PSMA-PET/CT in Patients with Recurrent Clear Cell Renal Cell Carcinoma: Histopathological Correlations of Imaging Findings
by Falk Gühne, Philipp Seifert, Bernhard Theis, Matthias Steinert, Martin Freesmeyer and Robert Drescher
Diagnostics 2021, 11(7), 1142; https://doi.org/10.3390/diagnostics11071142 - 23 Jun 2021
Cited by 20 | Viewed by 2462
Abstract
PET/CT with prostate-specific membrane antigen (PSMA)-targeted tracers has been used in the diagnosis and staging of patients with clear cell renal cell carcinoma (ccRCC). For ccRCC primary tumors, PET parameters were shown to predict histologic grade and features. The aim of this study [...] Read more.
PET/CT with prostate-specific membrane antigen (PSMA)-targeted tracers has been used in the diagnosis and staging of patients with clear cell renal cell carcinoma (ccRCC). For ccRCC primary tumors, PET parameters were shown to predict histologic grade and features. The aim of this study was to correlate PSMA PET/CT with histopathological findings in patients with metastatic recurrence of ccRCC. Patients with ccRCC who underwent PSMA-targeted PET/CT and subsequent histopathological evaluation of suspicious lesions were included. Specimens underwent immunohistochemical marking. Lesion diameter, volume and tracer uptake were correlated with the extent and intensity of molecular PSMA expression and with clinical findings. Twelve PET-positive lesions of nine patients were evaluated. Eleven ccRCC metastases and one prostate carcinoma were detected histopathologically. Molecular PSMA expression was detected in all lesions, which intensity and distribution did not correlate with PET parameters. PSMA-targeted PET/CT is a feasible tool for the evaluation of patients with ccRCC but cannot reliably predict histologic features of metastases. PSMA may also be expressed in malignant lesions other than ccRCC, leading to incidental detection of these tumors. Full article
(This article belongs to the Special Issue Renal Cell Carcinoma: From Diagnosis to Identification of Novel Therapeutic Targets and Minimally Invasive Treatments)
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