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In the rapidly evolving world of cancer research and oncology, timely knowledge sharing can make a real difference in patient outcomes and therapeutic development. Whether you're studying tumor biology, clinical oncology, or cutting-edge immunotherapy techniques, our multidisciplinary publishing platform provides an open space for your discoveries — with monetization opportunities built-in.
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Cancer research drives breakthroughs in early detection, treatment protocols, and patient care. Whether your focus is on genomics, targeted therapies, or epidemiological cancer trends, our platform invites contributions from all corners of the oncology community. Your work can inform real-world decisions and fuel future research directions.
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Publishing isn't only about academic recognition; it's also about earning value for your efforts. Our platform gives oncology researchers the option to monetize their content while contributing to the global cancer research conversation. If you're seeking an alternative to conventional medical journals, this is your invitation to submit.
Join a growing network of oncologists, cancer research specialists, and medical writers. Submit your oncology articles today and turn your insights into both impact and income.
Sophie FERLICOT,
Sophie FERLICOT
Université Paris-Saclay Faculté de Médecine: Universite Paris-Saclay Faculte de Medecine
Pierre-Alexandre Just,
Pierre-Alexandre Just
APHP: Assistance Publique - Hopitaux de Paris
Eva Compérat,
Eva Compérat
APHP: Assistance Publique - Hopitaux de Paris
Etienne Rouleau,
Etienne Rouleau
Gustave Roussy Institute: Gustave Roussy
Frédérique Tissier,
Frédérique Tissier
APHP: Assistance Publique - Hopitaux de Paris
Christophe Vaessen,
Christophe Vaessen
APHP: Assistance Publique - Hopitaux de Paris
Stéphane Richard
Stéphane Richard
EPHE: Ecole Pratique des Hautes Etudes
Background: Hereditary papillary renal cell carcinoma (HPRCC) is a rare autosomal dominant disease characterized by the development of multiple and bilateral papillary type I renal cell carcinomas (RCC) and papillary adenomas caused by activating mutations in the MET proto-oncogene. Classically, distinctive histological features of RCC are described according to the familial renal cell carcinoma s...
8 months ago
Ichiro Tsuboi,
Ichiro Tsuboi
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Momoko Araki,
Momoko Araki
Shimane University Faculty of Medicine Department of Clinical Genetics Unit, , Izumo, Japan
Shuhei Yokoyama,
Shuhei Yokoyama
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Gen Tanaka,
Gen Tanaka
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Kazutaka Mitani,
Kazutaka Mitani
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Saori Yosioka,
Saori Yosioka
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Yusuke Kobayashi,
Yusuke Kobayashi
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Hirochika Nakajima,
Hirochika Nakajima
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Taichi Nagami,
Taichi Nagami
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Kohei Ogawa,
Kohei Ogawa
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Chiaki Koike,
Chiaki Koike
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Koichiro Wada
Koichiro Wada
Shimane University Faculty of Medicine Department of Urology, , Izumo, Japan
Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a rare autosomal-dominant disorder caused by a heterozygous germline mutation in the fumarate hydratase (FH) gene. HLRCC is clinically characterized by the development of three tumors: uterine leiomyomata, cutaneous leiomyomata, and renal cell carcinoma (RCC). HLRCC-associated RCC is aggressive and diagnosed at a much earlier age than spor...
8 months ago
Adrenocortical carcinoma (ACC) and pheochromocytoma/paraganglioma (PPGL) are two rare types of adrenal gland malignancies. Regarding hereditary tumors, some patients with ACC are associated with with Li-Fraumeni syndrome (LFS), and those with PPGL with multiple endocrine neoplasia type 2. Recent studies have expanded this spectrum to include other types of hereditary tumors, such as Lynch syndrome...
8 months ago
Current National Comprehensive Cancer Network ® (NCCN ®) guidelines for Colorectal Genetic/Familial High-Risk Assessment provide limited guidance for genetic testing for individuals with already diagnosed hereditary cancer conditions. We are presenting the case of a 36-year-old woman who was diagnosed with Lynch Syndrome at age 23 after genetic testing for a familial variant (c.283del) in the ML...
8 months ago
Hereditary leiomyomatosis and renal cell cancer (HLRCC) is a rare autosomal dominant syndrome caused by a germline mutation in the fumarate hydratase (FH) gene that manifests with cutaneous leiomyomas, uterine fibroids, and renal cell cancer (RCC). Patients with HLRCC-associated RCC (HLRCC-RCC) have aggressive clinical courses, but there is no standardized therapy for advanced HLRCC-RCC. In this s...
8 months ago
Glioblastoma (GB) is the most common brain cancer and has limited survivability with a mean survival time of 15 months and an overall survival of less than 7 % after 5 years. Impediments to delivery of large molecule (e.g. antibodies) and cell therapeutics to a tumor include the blood–brain barrier (BBB) and the blood‐tumor barrier (BTB) which prevent large solutes from crossing from circulati...
8 months ago
Eva Forssell-Aronsson,
Eva Forssell-Aronsson
NULL
PET/CT and PET/MRI are valuable multimodality imaging techniques for visualizing both functional and anatomical information. The most used PET reconstruction algorithm is Ordered Subset Expectation Maximization (OSEM). In OSEM, the image noise increases with increased number of iterations, and the reconstruction needs to be stopped before complete convergence. The Bayesian penalized likelihood (BP...
8 months ago
Ilaria Proietti,
Ilaria Proietti
Dermatology Unit “Daniele Innocenzi”, “A. Fiorini” Hospital, Via Firenze, 1, 04019 Terracina, Italy
Chiara Battilotti,
Chiara Battilotti
Dermatology Unit “Daniele Innocenzi”, “A. Fiorini” Hospital, Via Firenze, 1, 04019 Terracina, Italy
Francesca Svara,
Francesca Svara
Dermatology Unit “Daniele Innocenzi”, “A. Fiorini” Hospital, Via Firenze, 1, 04019 Terracina, Italy
Ersilia Tolino,
Ersilia Tolino
Dermatology Unit “Daniele Innocenzi”, “A. Fiorini” Hospital, Via Firenze, 1, 04019 Terracina, Italy
Nicoletta Bernardini,
Nicoletta Bernardini
Dermatology Unit “Daniele Innocenzi”, “A. Fiorini” Hospital, Via Firenze, 1, 04019 Terracina, Italy
Nevena Skroza,
Nevena Skroza
Dermatology Unit “Daniele Innocenzi”, “A. Fiorini” Hospital, Via Firenze, 1, 04019 Terracina, Italy
Luca Filippi,
Luca Filippi
Nuclear Medicine Unit, Department of Oncohaematology, Fondazione PTV Policlinico Tor Vergata University Hospital, Viale Oxford 81, 00133 Rome, Italy
Concetta Potenza
Concetta Potenza
Dermatology Unit “Daniele Innocenzi”, “A. Fiorini” Hospital, Via Firenze, 1, 04019 Terracina, Italy
The use of hyaluronic acid (HA) fillers in oncology patients undergoing PET-CT scans is a topic of debate due to potential interference with imaging accuracy. A 54-year-old female, postmelanoma metastasectomy in the parotid region with subsequent facial nerve palsy (FNP), received HA filler injections for facial symmetry and functional restoration. Follow-up PET-CT scans showed no interference or ...
8 months ago
Effective management of the COVID-19 pandemic requires widespread and frequent testing of the population for SARS-CoV-2 infection. Saliva has emerged as an attractive alternative to nasopharyngeal samples for surveillance testing as it does not require specialized personnel or materials for its collection and can be easily provided by the patient. We have developed a simple, fast, and sens...
10 months ago