T. Feys MBA, MSc

Rapid PCR testing as adjunct to next-generation sequencing for the detection of alterations in patients with non-small-cell lung cancer

Next-generation sequencing (NGS) is increasingly replacing single gene assays in the screening for therapeutic biomarkers in patients with NSCLC. While NGS has the clear advantage that it can detect all targetable oncogenic driver alterations simultaneously, this technique does come with the risk for a longer turnaround time, in part as a result of the centralized way in which this testing is often organized. However, with a delayed test result, you risk that some patients with a high disease burden miss the opportunity to be treated with a specific targeted therapy, or even die before the NGS result comes in. To mitigate this risk, it may be interesting to adopt a rapid PCR-based testing strategy for selected oncogenic driver mutations in parallel to broad NGS testing.

Antibody-drug conjugates in the treatment of advanced breast cancer

Antibody-drug conjugates (ADCs) combine the high specificity of monoclonal antibodies with the high anti-tumor activity of small molecular cytotoxic payloads. In 2013, the human epidermal growth factor receptor 2 (HER2)-targeted ADC ado-trastuzumab emtansine (T-DM1) entered the treatment arsenal for patients with metastatic breast cancer (BC), making it the first ADC to be approved for the treatment of a solid tumor. The pace of ADC development for solid tumors has since increased dramatically, with currently more than 100 ADCs being investigated in clinical trials. Specifically in breast cancer, there are now 3 EMA-approved ADCs: T-DM1, trastuzumab deruxtecan (T-DXd) and sacituzumab govitecan (SG). This article will briefly touch upon the key components and mode of action of ADCs after which the clinical experience with the EMA-approved ADCs in breast cancer will be discussed.

The KRAS oncogene: a long and winding road to druggability

The Kirsten rat sarcoma viral oncogene homolog (KRAS) is mutated in about a quarter of all human cancers and is at the centre of several pathways involved in tumorigenesis. As such, novel therapeutic strategies that can target this oncoprotein are potentially extremely valuable. However, since its discovery as on oncogene, almost four decades have gone by without any major breakthrough in the therapeutic targeting of mutant KRAS. In recent years, however, we are finally witnessing a paradigm shift with the discovery of druggable pockets on KRAS and the clinical activity of covalent KRAS^G12C inhibitors such as sotorasib and adagrasib.

Highlights in thoracic oncology

SUMMARY

In the field of thoracic oncology, many refinements and longer follow-up results of previously reported trials were presented during the annual ASCO 2022 meeting. Although there were no presentations of new, truly practice-changing trials, several exciting and promising data are worthwhile to mention in this highlights in thoracic oncology overview.

(Belg J Med Oncol 2022;16(5):229–35)

Highlights in breast cancer

SUMMARY

ASCO 2022 featured a couple of breast cancer-related presentations with the potential to shake up the clinical practice. First and foremost, results of the DESTINY-Breast 04 study demonstrated a significant progression-free (PFS) and overall survival (OS) benefit with trastuzumab deruxtecan in the treatment of HER2-low metastatic breast cancer (mBC) patients who received 1–2 prior lines of therapy. By effectively creating a new category of breast cancer, this trial will redefine the classical breast cancer classification and will significantly expand the population of patients who can benefit from HER2-targeted therapy. In TROpICS-02, sacituzumab govitecan, an antibody-drug conjugate directed against TROP-2, was found to delay the disease progression of patients with heavily pre-treated HR+/HER2- advanced breast cancer. Also in HR+/HER2- advanced breast cancer, the MAINTAIN study demonstrated a significant PFS benefit with the continued use of a CDK4/6 inhibitor with a switch in endocrine therapy partner in women who progressed while being treated with a CDK4/6 inhibitor. Finally, ASCO 2022 also showed that the significant PFS benefit obtained from adding the CDK4/6 inhibitor palbociclib to letrozole in the first-line treatment of postmenopausal women with HR+ advanced breast cancer did not translate into a significant OS benefit.

(Belg J Med Oncol 2022;16(5):251–6)

New oncology reimbursements in Belgium

OVERVIEW OF BELGIAN REIMBURSEMENT NEWS

(BELG J MED ONCOL 2022;16(5):257)

New oncology reimbursements in Belgium

OVERVIEW OF BELGIAN REIMBURSEMENT NEWS

(BELG J MED ONCOL 2022;16(4):209)