BJMO - volume 12, issue 6, october 2018
H. Degroote , H. Van Vlierberghe
Advanced hepatocellular carcinoma (HCC) has a poor prognosis and limited therapeutic options. Sorafenib (Nexavar®) was the first drug to demonstrate survival benefit. Recently Regorafenib (Stivarga®) proved to be effective as second-line treatment after progression on Sorafenib. Both are only approved in patients with good performance status and preserved liver function. Alternative treatment options with better efficacy and fewer side effects are still an important medical need. Very recently Lenvatinib (Lenvima®) was granted approval as alternative first-line therapy. Cabozantinib and Ramucirumab showed survival benefit compared to placebo, but are not yet available for clinical use. After promising phase I/II trials, phase III studies with other targeted systemic therapies are being performed. Immunotherapy is another challenging research field that is currently being assessed in clinical trials. Nivolumab (Opdivo®) has received accelerated FDA-approval as second-line therapy. Results are further awaited but will influence the care of patients with advanced hepatocellular carcinoma in the near future.
(BELG J MED ONCOL 2018;12(6):287–292)Read more
BJMO - volume 12, issue 6, october 2018
E. Roussel MD, L. Moris , T. Van den Broeck
Thanks to our improved understanding of the molecular pathogenesis of metastatic renal cell carcinoma, multiple new treatment agents have appeared and extended our therapeutic possibilities. Novel molecular-targeted agents have vastly replaced cytokine therapies but pointed out new challenges in finding the optimal sequence and/or combination in treating metastatic renal cell carcinoma patients. This review focusses on the emerging therapeutic options according to the European Association of Urology guidelines in the rapidly changing renal cell carcinoma landscape.
(BELG J MED ONCOL 2018;12(6):293–300)Read more
BJMO - volume 12, issue 5, september 2018
L. Buisserer , M-D. Tkint de Roodenbeke MD, M. Piccart-Gebhart
Women diagnosed with BRCA1/2 mutation positive breast cancer have an increased lifetime risk of contralateral breast cancer and ovarian cancer. They benefit from risk-reducing surgical strategies such as mastectomy and salpingo-oophorectomy. For patients with BRCA mutations and hormone-receptor positive breast cancer, the option of combined bilateral annexectomy and hormonal therapy with Aromatase Inhibitor can be discussed with high-risk patients. For triple negative breast cancer with BRCA mutation, there is some evidence that adding platinum-agents in the neoadjuvant setting improves the pathologic complete response. Lastly, ongoing clinical trials testing the efficacy of poly (ADP-ribose) polymerase inhibitor therapy in patients with BRCA1/2 mutations will be determinant for the future guideline recommendations in determining best treatment options for these patients.
(BELG J MED ONCOL 2018;12(5):239–246)Read more
BJMO - volume 12, issue 3, may 2018
J.B. Vermorken MD, PhD, O. Zayas
Patients treated for locally advanced cancer of the uterine cervix, FIGO stages IB2 to IVA, may expect a 5-year survival varying from 75% to 16%, respectively. Even though screening programs in Latin America and the Caribbean were established since the 1960´s, advanced stages continue to impact mortality in these countries. Morbidity and quality-of-life are compromised because most of the patients present with symptoms in these later stages. It is crucial to accurately determine tumour size and extension to surrounding organs, not only to establish prognosis, but also for therapy planning. Positron emission tomography combined with computed tomography is the preferred imaging modality but magnetic resonance imaging has high accuracy characterising the primary lesion. Concurrent cisplatin-based chemoradiotherapy is the standard nonsurgical approach, with a relative risk of death of 0.81 compared to the same radiation therapy alone, showing an absolute survival benefit at five years of 6%. Before or after chemoradiation, additional systemic therapy could be used to improve outcomes in patients with locally advanced cancer of the uterine cervix.
(BELG J MED ONCOL 2018:12(3):118–124)Read more
BJMO - volume 12, issue 2, march 2018
A. Janssens MD, PhD, B.I. Hiddinga MD, J. Raskin , J.P. Van Meerbeeck MD, PhD, P. Pauwels MD, PhD
Targeted therapies have transformed the management of non–small-cell lung cancer and placed an increased emphasis on stratifying patients on the basis of the presence of oncogenic drivers. The best characterised molecular driver to date is epidermal growth factor receptor. Selective oral inhibitors of epidermal growth factor receptor that are superior to chemotherapy have become available in clinical practice. Unfortunately progression develops after a median of ten to twelve months. This article provides a framework for understanding clinically relevant resistance mechanisms to epidermal growth factor receptor-tyrosine kinase inhibitors and strategies to delay or overcome resistance, both those clinically available and those in development.
(BELG J MED ONCOL 2018;12(2):68–74)Read more
BJMO - volume 11, issue 8, december 2017
D. Schallier MD, PhD, J. De Grève MD, PhD, K. Vekens , L. Decoster MD, PhD, S. Mignon
Antibodies against programmed cell death-1 (PD-1) and its ligand (PD-L1) have become standard-of-care in the second-line treatment for advanced non-small cell lung cancer after failure of first-line chemotherapy. The observed durable responses as well as the favourable toxicity profile have moved these agents to first-line studies for advanced non-small cell lung cancer. In tumours with high PD-L1 expression, pembrolizumab is registered as the preferred first-line treatment. Further studies are currently focusing on combination strategies. The major future challenge will be selecting the optimal treatment strategy for the patient.
(BELG J MED ONCOL 2017;11(8):380–385)Read more
BJMO - volume 11, issue 6, october 2017
A. Coelho MD, A. Nogueira MD, C. Rolfo MD, PhD, D. Arias Ron , E. Sais MD, F. Passiglia MD, J. Ferri Gandia , R. Porta
After many years of research and many failed attempts, finally the cancer treatments that act on the immune system have paid off. There are several ways to act on the immune system of cancer patients, including vaccination, genetic modification of cells and the inhibition of checkpoint molecules. The latter have had a great development in the last 5 years, not only in the immunogenic tumours but also in other tumours considered non-immunogenic such as lung cancer. In this review we are focusing on the latest findings of immunotherapeutic treatment in non-small cell lung cancer (NSCLC). We review those studies that have led to the approval of some of the drugs targeting immune checkpoints as well as those studies with immune checkpoint inhibitors with the potential to play a role in the treatment of NSCLC.
(BELG J MED ONCOL 2017;11(6):277–283)Read more