Corina J. van den Hurk
Leiden University Medical Center
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Featured researches published by Corina J. van den Hurk.
Journal of Clinical Oncology | 2013
Floortje Mols; Tonneke Beijers; Valery Lemmens; Corina J. van den Hurk; Gerard Vreugdenhil; Lonneke V. van de Poll-Franse
PURPOSE To gain insight into the prevalence and severity of chemotherapy-induced neuropathy and its influence on health-related quality of life (HRQOL) in a population-based sample of colorectal cancer (CRC) survivors 2 to 11 years after diagnosis. METHODS All alive individuals diagnosed with CRC between 2000 and 2009 as registered by the Dutch population-based Eindhoven Cancer Registry were eligible for participation. Eighty-three percent (n = 1,643) of patients filled out the European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire (QLQ) C30 and the EORTC QLQ Chemotherapy-Induced Peripheral Neuropathy 20. RESULTS The five neuropathy subscale-related symptoms that bothered patients with CRC the most during the past week were erectile problems (42% of men), trouble hearing (11%), trouble opening jars or bottles (11%), tingling toes/feet (10%), and trouble walking stairs or standing up (9%). Additionally, patients who received oxaliplatin more often reported tingling (29% v 8%; P = .001), numbness (17% v 5%; P = .005), and aching or burning pain (13% v 6%; P = .03) in toes/feet compared with those not treated with chemotherapy. They also more often reported tingling toes/feet (29% v 14%; P = .0127) compared with those treated with chemotherapy without oxaliplatin. Those with many neuropathy symptoms (eg, upper 10%) reported statistically significant and clinically relevant worse HRQOL scores on all EORTC QLQ-C30 subscales (all P < .01). CONCLUSION Two to 11 years after diagnosis of CRC, neuropathy-related symptoms are still reported, especially sensory symptoms in the lower extremities among those treated with oxaliplatin. Because neuropathy symptoms have a negative influence on HRQOL, these should be screened for and alleviated. Future studies should focus on prevention and relief of chemotherapy-induced neuropathy.
European Journal of Cancer | 2013
Ariana Znaor; Corina J. van den Hurk; Maja Primic-Zakelj; Dominic Agius; Daniela Coza; Anna Demetriou; Nadia Dimitrova; Sultan Eser; Hulya Karakilinc; Snezana Zivkovic; Freddie Bray; J.W.W. Coebergh
INTRODUCTION Cancer registration coverage and cancer control programmes in South Eastern (SE) Europe, embracing about six new EU member states, remain thin, despite a relatively high incidence and mortality burden from avoidable cancers, particularly in males. We assembled the most recent cancer registry data to estimate the burden of the 17 most common cancers in the region, from Slovenia to Cyprus and Malta. METHODS Data were made available for analysis from Bulgaria, Croatia, Cyprus, Malta, Romania (Cluj County), Serbia, Slovenia and Turkey (Antalya and Izmir provinces). We analysed incidence and mortality of the 17 most common cancers (counts and age-standardised rates, for the most recent year available and for the period 1999-2008). We used Joinpoint regression to quantify recent trends. FINDINGS For much of SE Europe, there were no marked declines in overall cancer mortality rates during 1999-2008. In men, lung cancer incidence and mortality rates were high compared to other European countries (age-standardised rates (ASRW) of incidence being 50-60/100,000 in most of the countries), and still increasing in Bulgaria, Serbia and Turkey. Prostate cancer incidence rapidly increased throughout the region by 3-12% annually, largely without any clear declines in mortality. Colorectal cancer incidence increased throughout the region, as did mortality especially in Croatia, Serbia and Bulgaria (average annual percentage change (AAPC) 1.5-2%). In women, breast cancer mortality significantly declined in Slovenia, Croatia and Malta (Average Annual Percentage of Change [AAPC] -2%, -1% and -5%, respectively), but not elsewhere. Cervical cancer incidence rates remained very high in Romania, Serbia and Bulgaria (ASRW>20/100,000). INTERPRETATION Our data confirmed the North West to South East Europe gradient of increasing incidence and mortality rates of tobacco-related cancers, as well as increasing mortality rates of screen-detectable cancers. The lack of decline in overall cancer mortality also indicates suboptimal levels of cancer control in the region.
Psycho-oncology | 2009
Corina J. van den Hurk; Floortje Mols; A.J.J.M. Vingerhoets; W.P.M. Breed
Objective: Chemotherapy‐induced alopecia, a common and distressing side effect of chemotherapy, may be prevented by scalp cooling, which reduces toxicity of cytostatics in hair root cells. This is the first study designed to assess the effect of scalp cooling on well‐being.
Oncologist | 2013
M.M.C. Komen; Carolien H. Smorenburg; Corina J. van den Hurk; Johan W. R. Nortier
The success of scalp cooling in preventing or reducing chemotherapy-induced alopecia (CIA) is highly variable between patients and chemotherapy regimens. The outcome of hair preservation is often unpredictable and depends on various factors. Methods. We performed a structured search of literature published from 1970 to February 2012 for articles that reported on factors influencing the effectiveness of scalp cooling to prevent CIA in patients with cancer. Results. The literature search identified 192 reports, of which 32 studies were considered relevant. Randomized studies on scalp cooling are scarce and there is little information on the determinants of the result. The effectiveness of scalp cooling for hair preservation depends on dose and type of chemotherapy, with less favorable results at higher doses. Temperature seems to be an important determinant. Various studies suggest that a subcutaneous scalp temperature less than 22 °C is required for hair preservation. Conclusions. The effectiveness of scalp cooling for hair preservation varies by chemotherapy type and dose, and probably by the degree and duration of cooling.
European Journal of Cancer | 2015
Jan Willem Coebergh; Corina J. van den Hurk; Marieke W. Louwman; Harry Comber; Stefano Rosso; Roberto Zanetti; Lidia Sacchetto; Hans H. Storm; Evert Ben Van Veen; Sabine Siesling; Janny Van Den Eijnden-Van Raaij
Currently about 160 population-based cancer registries (CRs) in Europe have extensive experience in generating valid information on variation in cancer risk and survival with time and place. Most CRs cover all cancers, but some are confined to specific cancers or to children. They cover 15-55% of the populations in all of the larger member states of the European Union (EU), except the United Kingdom (UK), and 100% coverage in 80% of those with populations below 20 million. The EU FP 7 EUROCOURSE project, which operated in 2009-2013, explored the essential role of CRs in cancer research and public health, and also focused attention on their programme owners (POs) and stakeholders (e.g. cancer societies, oncological professionals, cancer patient groups, and planners, providers and evaluators of cancer care and mass screening). Generally, all CRs depended on their regional and/or national oncological context and were increasingly involved in population-based studies of quality of cancer care, long-term prognosis and quality of life, one third being very active. Within the public health domain, CRs, in addition to describing the variety of environmental and lifestyle-related cancer epidemics, have also contributed actively to aetiologic research by a European databases that showed wide discrepancies in cancer risk and survival across the EU, and in more depth by follow-up of cohorts and recruitment for case-control studies. CRs were also actively contributing to independent evaluation of mass screening as an intervention which affects quality of care and cancer mortality. The potential of CRs for clinical evaluation has grown substantially through interaction with clinical stakeholders and more incidentally biobanks, also with greater involvement of patient groups - with a special focus on elderly patients who generally do not take part in clinical trials. Whereas 25-35% of CRs are active in a range of cancer research areas, the rest have a low profile and usually provide only incidence and survival data. If they are unable to do so because POs and stakeholders do not demand it, they might also be inhibited by data protection restrictions, especially in German and French speaking countries. The value of population-based studies of quality of oncologic care and mass screening and the flawless reputation with regard to data protection of intensively used CRs in the northwest of Europe offered a sharp contrast, although they also follow the 1995 EU guideline on data protection. CRs thus offer a perfect example of what can be done with sensitive and minimal data, also when enriched by linkages to other databases. Intensive use of the data has allowed CR research departments to take on a visible expertise-based profile but a neutral in many public controversies in preventive oncology. Their management and fundability also appeared to benefit from externally classifying the wide array of tumour- or tract-specific intelligence and research activities for the various users in oncology and public health and also patients - who are the source of the data - are better informed. Transparency on what CRs enable may also improve through programmes of research have been deemed essential to our funding POs (ministries, cancer charities, cancer centres or public health institutes) who might benefit from some guidance to - often suboptimal -governance. Therefore, a metaphoric RegisTree has been developed for self-assessment and to clarify CR working methods and domain-specific performance to stakeholders and funding agencies, showing much room for development in many CRs. All in all, CRs are likely to remain unique sources of independent expert information on the burden of cancer, indispensable for cancer surveillance, with increased attention to cancer survivors, up to 4% of the population. Investments in the expanding CR network across Europe offer an excellent way forward for comparative future cancer surveillance with so many epidemiologic and clinical changes ahead.
Acta Oncologica | 2014
Corina J. van den Hurk; M. Elske van den Akker-van Marle; W.P.M. Breed; Lonneke V. van de Poll-Franse; Johan W. R. Nortier; J.W.W. Coebergh
Abstract Background. Alopecia is a frequently occurring side effect of chemotherapy that often can be prevented by cooling the scalp during the infusion. This study compared effects and costs of scalp cooling with usual general oncological care, i.e. purchasing a wig or head cover. Material and methods. Scalp-cooled patients (n = 160) were compared with non-scalp-cooled patients (n = 86) at 15 Dutch hospitals. Patients were enrolled prior to anthracycline and/or taxane-based chemotherapy for several types of cancer between 2007 and 2008. Cost-effectiveness of scalp cooling compared with that of usual care was determined by the ratio of costs to quality adjusted life years (QALYs). Costs for scalp cooling (machines and nursing time), hair dressers, wigs and head covers were estimated from a societal perspective. QALYs were measured using the Short Form-36. Results. Scalp cooling reduced the use of a wig or head cover by 40%, but wigs were still purchased unnecessarily by 38% of scalp-cooled patients. Average societal costs decreased therefore only by €269 per patient due to scalp cooling (p = 0.02). Given the eligibility for scalp cooling at the time, the insignificant difference in QALYs resulted from a balance of the benefits for those patients with successful scalp cooling and those without success. For the Dutch, given the generally accepted threshold of willingness to pay for a QALY (between €20 000 and €40 000), scalp cooling was cost-effective, therefore justifying the choice of scalp cooling or purchasing a wig or head cover. Conclusion. Given the right indication, cost-effectiveness might be improved further by postponing wig and head cover purchases, by improving scalp cooling efficacy, as well as using the scalp cooling capacity more intensively.
Dermatologic Surgery | 2012
Maria A.E. Hendriks; Paulus A.F. Geerts; Marcus W. Dercksen Md; Corina J. van den Hurk; W.P.M. Breed
Background Until now, there has been no reliable, simple method available for measuring hair quantity that is suitable in clinical practice. Recently, the cross‐section trichometer by Cohen has been introduced. This study was designed to test its clinical utility. Methods The hair mass index (HMI) is ratio of the cross‐sectional area of an isolated bundle of hair and the premeasured area of skin from which it was taken using the trichometer device. The intra‐ and interobserver reproducibility of measurements at the same location and after relocation were evaluated. Results For intraobserver reproducibility, the HMI ranged from 3 to 120 (mean difference .2, 95% confidence interval [CI] = −4.7–5.1, correlation coefficient [r] = .99. For interobserver reproducibility, the HMI ranged from 18 to 119 (mean difference –.4, 95% CI = −8,0–7,2, r = .98). With relocation, the HMI ranged from 2 to 113 (mean difference –1.0, 95% CI = −10.1–8.1, r = .97). Measurements took 5–10 minutes per area. Conclusion Measurements were simple to perform, and the data showed high reproducibility. The trichometer is a promising technology for hair quantity measurements and has multiple clinical and research applications.
Asia-Pacific Journal of Oncology Nursing | 2015
Mijke Peerbooms; Corina J. van den Hurk; W.P.M. Breed
Objective: Scalp cooling (SC) is applied to reduce chemotherapy-induced alopecia (CIA). The aim of this study was to investigate patients′ familiarity and opinions and oncological professionals′ attitude and knowledge about SC in the Netherlands. Methods: Ex breast cancer patients, nurses and medical oncologists (MDs) from SC and non-SC hospitals filled out questionnaires. Results: The majority of MDs and nurses were satisfied with the results of SC, as were SC patients. Over 33% of MDs and nurses perceived their knowledge level insufficient to inform patients about effectiveness, which was over 43% for information about safety. MDs main reason to not apply SC was doubt about effectiveness and safety. Nurses generally offered SC to a minority of eligible patients. Patients were frequently unfamiliar with SC before diagnosis. Seventy percent of SC patients with insufficient results (20/52) reported to mind it very much. With expected success rates of 35% and 50%, respectively, 36% and 54% of patients would use SC again. Conclusion: Room for improvement has been shown for both patients′ familiarity and oncological professionals′ knowledge about SC. Sharing knowledge about results, safety and patients′ experiences will improve patient counseling and SC availability. The results of this survey led to the development of a national standard on CIA and SC.
Handbook of hair in health and disease | 2012
Corina J. van den Hurk; W.P.M. Breed; Floortje Mols
Chemotherapy-induced alopecia (CIA) is a common side effect of chemotherapy and its incidence and severity depends most on the type and dose of cytostatics. Rapid proliferating hair follicle cells, i.e. in the anagen phase, are affected by the cytostatics, as are rapid proliferating cancer cells. CIA occurs within a few weeks after the first chemotherapy cycle and is often extensive. The underlying molecular mechanisms of hair follicle apoptosis by chemotherapy is poorly understood, but several signalling pathways are involved. CIA is usually temporary. Hair regrowth usually starts within several months following the last chemotherapy cycle, but there is often a transient change in structure or color. The impact of CIA is underestimated by nurses and medical doctors. Patients rank it among the most feared and experienced side effects. The impact of CIA is also shown by the number of patients that want to camouflage their baldness; most patients purchase a wig or other head covering. Psychological distress caused by CIA is high, in which men’s experiences have been largely ignored. In addition, CIA may seriously affect one’s body image, which has impact on self-esteem and self-confidence. However, anticipatory adaptation and wig use may mitigate experiences of hair loss. Before the start of chemotherapy, patients have to be prepared for potential hair loss to minimize its impact on quality of life. CIA prevention comprises attempts of using pharmacological agents and mechanical strategies, however scalp cooling is the only effective method until now. The majority of patients tolerate scalp cooling very well and it is cost-effective compared to purchasing wigs and head covers. If patients preserve their hair during chemotherapy, hairs are minimally damaged, as shown by diminished hair shaft diameters.
Acta Oncologica | 2016
Antoinetta J. M. Beijers; Floortje Mols; Corina J. van den Hurk; Art Vreugdenhil
ANTOINETTA J. M. BEIJERS, FLOORTJE MOLS, CORINA J. VAN DEN HURK & ART VREUGDENHIL Department of Internal Medicine, Máxima Medical Center, Eindhoven and Veldhoven, the Netherlands, CoRPS – Centre of Research on Psychology in Somatic diseases, Department of Medical and Clinical Psychology, Tilburg University, Tilburg, The Netherlands, Netherlands Comprehensive Cancer Organisation (IKNL), Utrecht, The Netherlands and Department of Medical Oncology, Maastricht University Medical Centre, Maastricht, The Netherlands