Borst
VieCuri eerste ziekenhuis van Limburg met nieuwe techniek voor opsporen tumor in de borst
Na een proefperiode is de nieuwe techniek sinds augustus 2024 de standaard bij VieCuri. VieCuri is het eerste ziekenhuis van Limburg met deze nieuwe techniek. Jaarlijks voert VieCuri meer dan 200 operaties uit in het kader van borstkanker, een groot deel daarvan zijn borstsparende operaties bij niet voelbare tumoren waarvoor een lokalisatie nodig is. De […]

Aanbevolen

De toekomst van kanker: nanorobots als behandeling
Eerder kon u lezen over de verwachte toename van kanker bij mannen in de toekomst indien niet wordt ingegrepen. Nieuw onderzoek kan mogelijk helpen bi...
De toekomst van kanker: verwachte stijging bij mannen
De studie is gepubliceerd in Cancer, een peer-reviewed tijdschrift van de American Cancer Society,  en toont aan dat het aantal kankergevallen bi...

Oncologie nieuws

Borst

Clonal Hematopoiesis in Women With Breast Cancer
ascopubs.org
Journal of Clinical Oncology, Ahead of Print.
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Hoofd-hals

Risk of Malignant Transformation of Oral Lichen Planus and Oral Lichenoid Lesions: A Single Centre, 10?Year Review
onlinelibrary.wiley.com
Oral lichen planus (OLP) and oral lichenoid lesions (OLL) are common chronic inflammatory diseases associated with malignant transformation. Risk fact...
Examining the Impact of Race and Sex on the Incidence of Positive Surgical Margins in Oral Cavity Squamous Cell Carcinoma
onlinelibrary.wiley.com
The aim of this study was to compare the incidence of positive surgical margins (PSMs) between different races and sexes in a national cohort.
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Immuno-oncologie

Combined molecular subclass and immune phenotype correlate to atezolizumab plus radiation therapy response in invasive bladder cancer: BPT-ART Phase II study
redjournal.org
Bladder preservation therapy in combination with atezolizumab and radiation therapy (BPT-ART) trial, which was a multicenter, open-label, single-arm phase II study, showed a promisingly high interim clinical complete response (cCR) rate of 84.4% (38/45). In the present study, we aimed to identify potential tissue biomarkers for achieving cCR via BPT-ART.
Prediction of checkpoint inhibitor immunotherapy efficacy for cancer using routine blood tests and clinical data
nature.com
Nature Medicine, Published online: 06 January 2025; doi:10.1038/s41591-024-03398-5
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MDL

Genomic and transcriptomic signatures of sequential carcinogenesis from papillary neoplasm to biliary tract cancer
Papillary neoplasms of the biliary tree, including intraductal papillary neoplasms (IPN) and intracholecystic papillary neoplasms (ICPN), are recognized as precancerous lesions. However, the genetic characteristics underlying sequential carcinogenesis remain unclear.
Genomic and transcriptomic signatures of sequential carcinogenesis from papillary neoplasm to biliary tract cancer
Papillary neoplasms of the biliary tree, including intraductal papillary neoplasms (IPN) and intracholecystic papillary neoplasms (ICPN), are recognized as precancerous lesions. However, the genetic characteristics underlying sequential carcinogenesis remain unclear.
Clinical outcomes and treatment patterns of maintenance avelumab in locally advanced or metastatic urothelial carcinoma: a multicenter collaborative study
academic.oup.com
AbstractBackgroundThe JAVELIN Bladder 100 trial demonstrated improved overall survival (OS) with maintenance avelumab in patients with locally advanced or metastatic urothelial carcinoma UC (la/mUC) who achieved disease control following first-line platinum-based chemotherapy (1 L-PBC). However, real-world data on eligibility, utilization, and outcomes of maintenance avelumab therapy remain limited.MethodsThis retrospective study included patients with la/mUC who received 1 L-PBC. Eligibility for maintenance avelumab therapy was determined based on the best overall response to 1 L-PBC, with patients who achieved stable disease or a partial or complete response considered eligible. Survival outcomes were analyzed using the Kaplan–Meier method. Multivariate Cox regression analysis was used to identify prognostic factors among patients with la/mUC who received maintenance avelumab.ResultsOf 161 prospective patients, 67.1% were eligible for maintenance avelumab therapy, and 46.3% of eligible patients received the treatment. The median progression-free survival (PFS) following avelumab initiation was 10.2 months, whereas the median OS was not reached. Prognostic factors associated with PFS included the presence of liver metastases, elevated C-reactive protein (> 1.0 g/dL), and administration of more than five cycles of 1 L-PBC. Adverse events occurred in 60% of patients treated with avelumab, with 16% experiencing grade 3–4 adverse events.ConclusionWe emphasize the real-world applicability of maintenance avelumab for Japanese patients with la/mUC. Maintenance avelumab demonstrated favorable survival outcomes, consistent with clinical trial data. Identifying prognostic factors and optimizing treatment sequencing are essential strategies for improving outcomes in this patient population.
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Pediatrie

Mortality after cancer diagnosis among children with congenital heart disease in Denmark and Sweden
academic.oup.com
AbstractBackgroundRecent decades have witnessed tangible improvements in childhood cancer survival. However, the prognosis for children with congenital heart disease (CHD), the most prevalent birth defect, remains unclear. Due to improved survival of CHD and childhood cancer, evaluating outcomes within this intersection is important for clinical practice. We aimed to assess mortality post-cancer diagnosis among children with CHD.MethodsWe conducted a study on the population of Denmark and Sweden, born 1970–2014, with a cancer diagnosis before age 20 in the national cancer registers (end of follow-up 2015; n?=?20,665). CHD diagnoses (n?=?397) and recorded deaths were retrieved from national health registers. We evaluated the effect of CHD on five-year mortality post-cancer diagnosis fitting Cox proportional hazards regression.ResultsWhen excluding children with Down syndrome, children with CHD had a higher five-year mortality post-cancer diagnosis compared to children without (HR 1.48, 95% CI 1.18–1.86). This was particularly notable in children with lymphoma (HR 2.17, 95% CI 1.11–4.25) and neuroblastoma (HR 2.39, 95% CI 1.11–5.15). In more recent decades (post-1990), children with CHD had similar five-year mortality as their counterparts without, except for children diagnosed with lymphoma, where mortality remained elevated (HR 3.37, 95% CI 1.65–6.89).ConclusionsIn this large, register-based cohort study, children with CHD fared worse post-cancer diagnosis—particularly lymphoma and neuroblastoma. While a more positive trend emerged in recent years, lymphoma-related mortality remained disproportionately high among children with CHD, underscoring the need for continued research and interventions to improve outcomes for this vulnerable group.
Norgine submits MAA to EMA for eflornithine in high?risk neuroblastoma
pharmabiz.com
Norgine, a uniquely positioned, specialty pharmaceutical and consumer healthcare company, announced that it completed its marketing authorisation application filing to European Medicines Agency (EMA) for
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Sarcoom

Researchers uncover what drives aggressive bone cancer
sciencedaily.com
Study identifies a novel mechanism driving osteosarcoma and provides insights to help predict patient outcomes.
US FDA grants breakthrough therapy designation to GSK's B7─H3─targeted ADC, GSK'227 to treat relapsed or refractory osteosarcoma
pharmabiz.com
GSK plc announced that the US Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation for GSK5764227 (GSK'227), its B7─H3─targeted antibody─drug conjugate (ADC) being evaluated for the treatment of adult patients with relapsed or refractory osteosarcoma
Novel Antibody-Drug Conjugate Gets Breakthrough Tx Designation for R/R Osteosarcoma
empr.com
The Breakthrough Therapy designation is supported by data from the open-label, phase 2 ARTEMIS-002 trial.
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