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    <title>Zee, J. van der</title>
    <link>http://repub.eur.nl/res/aut/9323/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Prognostic Markers in Pancreatic Cancer: the tumor and its environment (Doctoral Thesis)</title>
      <link>http://repub.eur.nl/res/pub/38920/</link>
      <pubDate>2012-12-06T00:00:00Z</pubDate>
      <description>Incidence
Pancreatic cancer is not one of the most common types of cancer; however it is
most certainly one of the most devastating types, ranking fourth in the list of cancer
related deaths with a 5-year survival of only 6%. In 2010 there were an estimated
43.140 new cases whereas 36.800 patients were expected to die from this
disease in the United States. Worldwide, the expected numbers were 278.684
new cases and 266.669 deaths. In the Netherlands 2481 patients died of pancreatic
cancer in 2010. Interestingly, whereas for most cancers, death rates have
decreased over the years, those of pancreatic cancer have remained relatively
stable.
Pathogenesis
In order to effectively diagnose, prevent and treat pancreatic cancer, a detailed
understanding of the molecular biology of this disease is required. Like many
other cancers, pancreatic cancer results from the accumulation of genetic alterations.
It originates in the ductal epithelium and evolves from non-invasive precursor
lesions of which pancreatic intraepithelial neoplasias (PanINs) are the
best characterized. The progression from minimally dysplastic epithelium (PanIN
grade 1) to more severe dysplasia (PanIN grades 2 and 3) and finally to invasive
carcinoma is paralleled by the successive accumulation of genetic alterations of
which some appear earlier than others (figure 1).
A brief overview of the molecular mechanisms underlying the biology of pancreatic
cancer is given in chapter 2.</description>
    </item> <item>
      <title>Angiogenesis: A prognostic determinant in pancreatic cancer? (Article)</title>
      <link>http://repub.eur.nl/res/pub/34008/</link>
      <pubDate>2011-11-01T00:00:00Z</pubDate>
      <description>Angiogenesis has been associated with disease progression in many solid tumours, however the statement that tumours need angiogenesis to grow, invade and metastasise seems no longer applicable to all tumours or to all tumour subtypes. Prognostic studies in pancreatic cancer are conflicting. In fact, pancreatic cancer has been suggested an example of a tumour in which angiogenesis is less essential for tumour progression. The aim of the present study was therefore to measure angiogenesis in two anatomically closely related however prognostically different types of pancreatic cancer, pancreatic head and periampullary cancer, and investigate its relation with outcome. Vessels were stained by CD31 on original paraffin embedded tissue from 206 patients with microscopic radical resection (R0) of pancreatic head (n = 98) or periampullary cancer (n = 108). Angiogenesis was quantified by microvessel density (MVD) and measured by computerised image analysis of three randomly selected fields and investigated for associations with recurrence free survival (RFS), cancer specific survival (CSS), overall survival (OS) and conventional prognostic factors. MVD was heterogeneous both between and within tumours. A higher MVD was observed in periampullary cancers compared with pancreatic head cancers (p &lt;.01). Furthermore, MVD was associated with lymph node involvement in pancreatic head (p =.014), but not in periampullary cancer (p =.55). Interestingly, MVD was not associated with RFS, CSS or with OS. In conclusion, angiogenesis is higher in periampullary cancer and although associated with nodal involvement in pancreatic head cancer, pancreatic cancer prognosis seems indeed angiogenesis independent. </description>
    </item> <item>
      <title>Differential expression and prognostic value of HMGA1 in pancreatic head and periampullary cancer (Article)</title>
      <link>http://repub.eur.nl/res/pub/21004/</link>
      <pubDate>2010-12-01T00:00:00Z</pubDate>
      <description>The high mortality rate and minimal progress made in the treatment of pancreatic cancer over the last few decades, warrant an alternative approach. Treatment protocols should be individualised to the patient guided by prognostic markers. A particularly interesting target would be the architectural transcription factor high mobility group A1 (HMGA1), that is low or undetectable in normal tissue, induced during neoplastic transformation and consequently often exceptionally high in cancer. The aim of the current study was therefore to determine the differential expression of HMGA1 in pancreatic head and periampullary cancer and investigate its relation with outcome. HMGA1 expression was determined by immunohistochemistry on original paraffin embedded tissue from 99 pancreatic head- and 112 periampullary cancers (with R0). Expression was investigated for associations with recurrence free (RFS), cancer specific (CSS) and overall survival (OS) and conventional prognostic factors. HMGA1 was expressed in 47% and 26% of pancreatic head- and periampullary cancer, respectively and associated with poor RFS, CSS and OS in periampullary cancer. CSS 5 years following surgery was 25% and 44% for patients with tumours which were positive or negative for HMGA1 protein, respectively. HMGA1 expression was not associated with survival in pancreatic head cancer. In conclusion HMGA1 was identified as an independent prognostic marker predicting poor outcome in periampullary cancer. Although expressed to a higher extent as compared to periampullary cancer, HMGA1 was not associated with survival in pancreatic head cancer.</description>
    </item> <item>
      <title>Reirradiation combined with hyperthermia in breast cancer recurrences: Overview of experience in Erasmus MC (Article)</title>
      <link>http://repub.eur.nl/res/pub/27889/</link>
      <pubDate>2010-10-01T00:00:00Z</pubDate>
      <description>For superficial hyperthermia a custom-built multi-applicator multi-amplifier superficial hyperthermia system operating at 433 MHz is utilised. Up to 6 Lucite Cone applicators can be used simultaneously to treat an area of 600 cm2. Temperatures are measured continuously with fibre optic multi-sensor probes. For patients with non-standard clinical problems, hyperthermia treatment planning is used to support decision making with regard to treatment strategy. In 74 of our patients with recurrent breast cancer treated with a reirradiation scheme of 8 fractions of 4 Gy in 4 weeks, combined with 4 or 8 hyperthermia treatments, a complete response is achieved, approximately twice as high as the CR rate following the same reirradation alone. The CR rate in tumours smaller than 30 mm is 8090, for larger tumours it is 65. Hyperthermia appears beneficial for patients with microscopic residual tumour as well. To achieve high CR rates it is important to heat the whole radiotherapy field, and to use an adequate heating technique. </description>
    </item> <item>
      <title>FUS pathology defines the majority of tau-and TDP-43-negative frontotemporal lobar degeneration (Article)</title>
      <link>http://repub.eur.nl/res/pub/20260/</link>
      <pubDate>2010-07-01T00:00:00Z</pubDate>
      <description>Through an international consortium, we have collected 37 tau-and TAR DNA-binding protein 43 (TDP-43)-negative frontotemporal lobar degeneration (FTLD) cases, and present here the first comprehensive analysis of these cases in terms of neuropathology, genetics, demographics and clinical data. 92% (34/37) had fused in sarcoma (FUS) protein pathology, indicating that FTLD-FUS is an important FTLD subtype. This FTLD-FUS collection specifically focussed on aFTLD-U cases, one of three recently defined subtypes of FTLD-FUS. The aFTLD-U subtype of FTLD-FUS is characterised clinically by behavioural variant frontotemporal dementia (bvFTD) and has a particularly young age of onset with a mean of 41 years. Further, this subtype had a high prevalence of psychotic symptoms (36% of cases) and low prevalence of motor symptoms (3% of cases). We did not find FUS mutations in any aFTLD-U case. To date, the only subtype of cases reported to have ubiquitin-positive but tau-, TDP-43-and FUS-negative pathology, termed FTLD-UPS, is the result of charged multivesicular body protein 2B gene (CHMP2B) mutation. We identified three FTLD-UPS cases, which are negative for CHMP2B mutation, suggesting that the full complement of FTLD pathologies is yet to be elucidated.</description>
    </item> <item>
      <title>The clinical feasibility of deep hyperthermia treatment in the head and neck (Article)</title>
      <link>http://repub.eur.nl/res/pub/20697/</link>
      <pubDate>2010-04-06T00:00:00Z</pubDate>
      <description>To apply high-quality hyperthermia treatment to tumours at deep locations in the head and neck (H&amp;N), we have designed and built a site-specific phased-array applicator. Earlier, we demonstrated its features in parameter studies, validated those by phantom measurements and clinically introduced the system. In this paper we will critically reviewour first clinical experiences and demonstrate the pivotal role of hyperthermia treatment planning (HTP). Three representative patient cases (thyroid, oropharynx and nasal cavity) are selected and discussed. Treatment planning, the treatment, interstitially measured temperatures and their interrelation are analysed from a physics point of view. Treatments lasting 1 h were feasible and well tolerated and no acute treatment-related toxicity has been observed. Maximum temperatures measured are in the range of those obtained during deep hyperthermia treatments in the pelvic region but mean temperatures are still to be improved. Further, we found that simulated power absorption correlated well with measured temperatures illustrating the validity of our treatment approach of using energy profile
optimizations to arrive at higher  temperatures. This is the first data proving
that focussed heating of tumours in the H&amp;N is feasible. Further, HTP proved
a valuable tool in treatment optimization. Items to improve are (1) the transfer
of HTP settings into the clinic and (2) the registration of the thermal dose,
i.e. dosimetry.</description>
    </item> <item>
      <title>Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions (Article)</title>
      <link>http://repub.eur.nl/res/pub/19229/</link>
      <pubDate>2010-03-01T00:00:00Z</pubDate>
      <description>Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The predominant neuropathology is FTLD with TAR DNA-binding protein (TDP-43) inclusions (FTLD-TDP). FTLD-TDP is frequently familial, resulting from mutations in GRN (which encodes progranulin). We assembled an international collaboration to identify susceptibility loci for FTLD-TDP through a genome-wide association study of 515 individuals with FTLD-TDP. We found that FTLD-TDP associates with multiple SNPs mapping to a single linkage disequilibrium block on 7p21 that contains TMEM106B. Three SNPs retained genome-wide significance following Bonferroni correction (top SNP rs1990622, P = 1.08 × 10 11; odds ratio, minor allele (C) 0.61, 95% CI 0.53-0.71). The association replicated in 89 FTLD-TDP cases (rs1990622; P = 2 × 10 4). TMEM106B variants may confer risk of FTLD-TDP by increasing TMEM106B expression. TMEM106B variants also contribute to genetic risk for FTLD-TDP in individuals with mutations in GRN. Our data implicate variants in TMEM106B as a strong risk factor for FTLD-TDP, suggesting an underlying pathogenic mechanism.</description>
    </item> <item>
      <title>Clinical implementation of hyperthermia treatment planning guided steering: A cross over trial to assess its current contribution to treatment quality (Article)</title>
      <link>http://repub.eur.nl/res/pub/19243/</link>
      <pubDate>2010-02-26T00:00:00Z</pubDate>
      <description>Purpose: To assess the current feasibility of online hyperthermia treatment planning guided steering (HGS) and its current contribution to treatment quality in deep hyperthermia for locally advanced cervical cancer. Materials and methods: 36 patients were randomized to receive either their second and fourth (arm A) or their third and fifth (arm B) hyperthermia treatment of the series with the aid of HGS. The other treatments were conducted according to the Rotterdam Empirical Steering Guidelines (RESG). Results: During period I (second and third treatment of the series) similar results were found for HGS and RESG with a slight, non-significant difference found in favour of HGS. The average temperature T50 was 40.3°C for both (p=0.409) and the dose parameter CEM43T90 was 0.64 for RESG and 0.63 for HGS (p=0.154). However, during period II (fourth and fifth treatment of the series) HGS performed less well, with significant lower thermal dose parameters, minimum, mean and maximum intraluminal temperatures, tolerance measures and net integrated power. T50 was 40.4°C after RESG and 40°C after HGS (p=0.001) and CEM43T90 0.57 and 0.38 (p=0.01) respectively. Conclusion: We found that the procedure of online treatment planning guided steering is feasible. For maximal exploitation of its possibilities, however, better control and understanding of several patient, tumour and technical parameters is required. This study has been very helpful in identifying some of the challenges and flaws that warrant further investigation in the near future, such as patient positioning and the prevention of hotspot-related complaints.</description>
    </item> <item>
      <title>The clinical feasibility of deep hyperthermia treatment in the head and neck (Article)</title>
      <link>http://repub.eur.nl/res/pub/20698/</link>
      <pubDate>2010-01-01T00:00:00Z</pubDate>
      <description>To apply high-quality hyperthermia treatment to tumours at deep locations in the head and neck (H&amp;N), we have designed and built a site-specific phased-array applicator. Earlier, we demonstrated its features in parameter studies, validated those by phantom measurements and clinically introduced the system. In this paper we will critically reviewour first clinical experiences and demonstrate the pivotal role of hyperthermia treatment planning (HTP). Three representative patient cases (thyroid, oropharynx and nasal cavity) are selected and discussed. Treatment planning, the treatment, interstitially measured temperatures and their interrelation are analysed from a physics point of view. Treatments lasting 1 h were feasible and well tolerated and no acute treatment-related toxicity has been observed. Maximum temperatures measured are in the range of those obtained during deep hyperthermia treatments in the pelvic region but mean temperatures are still to be improved. Further, we found that simulated power absorption correlated well with measured temperatures illustrating the validity of our treatment approach of using energy profile
optimizations to arrive at higher  temperatures. This is the first data proving
that focussed heating of tumours in the H&amp;N is feasible. Further, HTP proved
a valuable tool in treatment optimization. Items to improve are (1) the transfer
of HTP settings into the clinic and (2) the registration of the thermal dose,
i.e. dosimetry.</description>
    </item> <item>
      <title>Concomitant hyperthermia and radiation therapy for treating locally advanced rectal cancer (Article)</title>
      <link>http://repub.eur.nl/res/pub/26898/</link>
      <pubDate>2009-09-15T00:00:00Z</pubDate>
      <description>Background: Surgery has been the treatment of choice for patients with rectal cancer. For locally advanced cancer results were poor, with high rates of locoregional recurrences and poor overall survival data. Adding (chemo)radiotherapy upfront improved results mainly in locoregional control. Adding hyperthermia to radiotherapy preoperatively might have an equivalent beneficial effect. Objectives: To quantify the potential beneficial effect of thermo radiation compared to chemo-radiation with respect to pathological complete responses, overall survival and toxicity in rectal cancer therapy. Search strategy: We identified the relevant phase II and III randomised controlled trials in any language trough electronic searches May 2007 of the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 1, 2007), the Cochrane Colorectal Cancer Groups Specialised Register, MEDLINE (from 1966), EMBASE (from 1974), CINAHL (from 1982). Furthermore, various trial databases were searched for the identification of recent completed and ongoing trials (meta Register of Controlled Trials, Cancer Research UK, Cancer.gov, The Eastern Cooperative Oncology Group Trials Database). All studies identified until May 2007 were considered for inclusion in the present study. Selection criteria: Only phase II and III randomised controlled clinical trials were included in the analysis. Data collection and analysis: All identified studies were assessed by two independent reviewers. A weighted estimate of the treatment effect was computed for 2, 3, 4 and 5-year survival, for local tumour recurrence, severe acute and late toxicity and complete tumour response (CR). CR was defined either clinically by disappearance of all pretreatment signs of local tumour or pathologically by microscopically free margins. The risk ratio (RR) and hazard ratio (HR) were used. Analyses were performed with the Reference Manager (RevMan). Main results: Six RCTs published between 1990 and 2007 were identified. A total number of 520 patients was treated, 258 in the radiotherapy only arm (RT) and 262 in the radiotherapy-hyperthermia arm (RHT). Four studies (424 patients) reported overall survival (OS) rates. After 2 years, OS was significantly better in the RHT group (HR 2.06; 95% CI 1.33-3.17; p=.001), but this difference disappeared after a longer period (3, 4 and 5 year OS). All but one studies reported CR rates. A significant higher CR rate was observed in the RHT group (RR 2.81; 95% CI 1.22-6.45; p=.01). Only 2 studies reported on acute toxicity. In these 2 studies no significant differences were observed between the RT and the RHT group. Late toxicity data were not reported. Authors' conclusions: Further studies are needed to compare chemoradiation versus thermoradiation versus chemoradiation plus hyperthermia in well selected/conducted and quality controlled randomised trials. Copyright </description>
    </item> <item>
      <title>Radiotherapy and Hyperthermia for Treatment of Primary Locally Advanced Cervix Cancer: Results in 378 Patients (Article)</title>
      <link>http://repub.eur.nl/res/pub/25044/</link>
      <pubDate>2009-01-01T00:00:00Z</pubDate>
      <description>Purpose: To report response rate, pelvic tumor control, survival, and late toxicity after treatment with combined radiotherapy and hyperthermia (RHT) for patients with locally advanced cervical carcinoma (LACC) and compare the results with other published series. Methods and Materials: From 1996 to 2005, a total of 378 patients with LACC (International Federation of Gynecology and Obstetrics Stage IB2-IVA) were treated with RHT. External beam radiotherapy (RT) was applied to 46-50.4 Gy and combined with brachytherapy. The hyperthermia (HT) was prescribed once weekly. Primary end points were complete response (CR) and local control. Secondary end points were overall survival, disease-specific survival, and late toxicity. Patient, tumor, and treatment characteristics predictive for the end points were identified in univariate and multivariate analyses. Results: Overall, a CR was achieved in 77% of patients. At 5 years, local control, disease-specific survival, and incidence of late toxicity Common Terminology Criteria for Adverse Events Grade 3 or higher were 53%, 47%, and 12%, respectively. In multivariate analysis, number of HT treatments emerged as a predictor of outcome in addition to commonly identified prognostic factors. Conclusions: The CR, local control, and survival rates are similar to previously observed results of RHT in the randomized Dutch Deep Hyperthermia Trial. Reported treatment results for currently applied combined treatment modalities (i.e., RT with chemotherapy and/or HT) do not permit definite conclusions about which combination is superior. The present results confirm previously shown beneficial effects from adding HT to RT and justify the application of RHT as first-line treatment in patients with LACC as an alternative to chemoradiation. </description>
    </item> <item>
      <title>Steering in locoregional deep hyperthermia: Evaluation of common practice with 3D-planning (Article)</title>
      <link>http://repub.eur.nl/res/pub/29540/</link>
      <pubDate>2008-12-22T00:00:00Z</pubDate>
      <description>Purpose: In Rotterdam, fifteen years of clinical experience with deep hyperthermia has sublimated in empirical treatment guidelines. In this paper, a hyperthermia treatment planning system (HTPS) is employed to investigate the effect of these guidelines on global power distribution, their effectiveness and the rationale behind each guideline. Materials and methods: Four guidelines were investigated. The first two prescribe steering actions for balancing intraluminal temperatures and alleviating complaints of deep-seated pain or pressure. The third guideline handles superficial complaints of pain or heat sensation. The last guideline states that frequency should be increased from 77 MHz upwards in case of multiple, opposite, painful regions uncontrollable by the previous steering actions. For all steering actions it is assumed that input power is increased until complaints occur. Sigma Hyperplan was used to calculate specific absorption rate (SAR) distributions for five patient models with locally advanced cervical cancer. Absorbed power ratios of different regions of interest were evaluated to illustrate steering efficacy and complaint reduction. Results and conclusions: Phase steering is effective in shifting the central power distribution to the periphery, and is an appropriate method to balance temperatures or to handle deep-seated complaints. Reduction of amplitude is the proper action to alleviate superficial complaints of heat or pressure. Compression of the SAR distribution, mainly in the lateral direction, is predicted with increasing frequency. Hence, for complaints in the lower back or on the sides, a frequency increase should be considered. We conclude that the results of the HTPS are in close agreement with the empirical steering guidelines.</description>
    </item> <item>
      <title>Prevention of work-related airway allergies; summary of the advice from the Health Council of the Netherlands (Article)</title>
      <link>http://repub.eur.nl/res/pub/14255/</link>
      <pubDate>2008-12-01T00:00:00Z</pubDate>
      <description>The Health Council of the Netherlands published a report in which the best procedure and method for recommending health-based occupational exposure limits (OELs) for inhaled allergens were identified by evaluating the scientific state of the art. Many respiratory disorders in the workplace arise from inhalation of substances which can cause allergy. To protect workers against respiratory allergy, various preventive measures are taken, one of them being reduction of exposure by setting legally binding standards. These are based on health-based OELs that specify a level of exposure to an airborne substance, a threshold level, below which it may reasonably be expected that there is no risk of adverse health effects. The Council is of the opinion that an OEL should prevent against allergic sensitization, as sensitization plays a crucial biological role and is a prerequisite for the development of allergy. Furthermore, the Council considers it most likely that the exposure level below which no allergic sensitization develops for most allergens is so low, that OELs are difficult to set with the current knowledge and technical feasibilities. An alternative approach is to accept exposure, which carries a small predefined risk in developing allergic sensitization. In addition, it is worth considering periodic screening of exposed workers on allergic sensitization, because timely intervention can prevent worse. The feasibility of periodic screening and what else is needed to comply with the most important criteria, should however be judged case-by-case.</description>
    </item> <item>
      <title>Incidence of acute peripheral neurotoxicity after deep regional hyperthermia of the pelvis (Article)</title>
      <link>http://repub.eur.nl/res/pub/29470/</link>
      <pubDate>2008-06-01T00:00:00Z</pubDate>
      <description>Background: After observing rather severe acute neurotoxicity in a few patients following deep hyperthermia treatment for a pelvic tumour, we evaluated the incidence of neurotoxicity in all patients treated with deep hyperthermia of the pelvis between June 1990 and April 2004. Materials and methods: Hyperthermia treatment registrations and hospital charts of all 736 patients were reviewed. Differences between the incidence of neurotoxicity in subgroups of patients were evaluated by 2×2 exact tests. Results: Grade 2 or 3 acute neurotoxicity occurred in 2.3% of patients, grade 3 in 0.7%. The duration of symptoms was longer than 3 months in 6 patients (0.8%). Neurological examination in 5 patients showed that the most commonly involved structures are the sacral and lower lumbar nerve roots and the sacral plexus. Acute neurotoxicity occurred only after November 1999 and only in patients treated for primary cervical cancer. Comparison of applied powers and achieved temperatures in patients developing neurotoxicity did not show differences between treatment sessions which resulted in neurotoxicity and sessions not resulting in neurotoxicity. Conclusion: Acute neurotoxicity following hyperthermia for pelvic tumours is a rare complication, but can result in symptoms affecting the activities of daily life. We found no patient, tumour or treatment characteristics predictive for a risk of neurotoxicity.</description>
    </item> <item>
      <title>Long-Term Improvement in Treatment Outcome After Radiotherapy and Hyperthermia in Locoregionally Advanced Cervix Cancer: An Update of the Dutch Deep Hyperthermia Trial (Article)</title>
      <link>http://repub.eur.nl/res/pub/29714/</link>
      <pubDate>2008-03-15T00:00:00Z</pubDate>
      <description>Purpose: The local failure rate in patients with locoregionally advanced cervical cancer is 41-72% after radiotherapy (RT) alone, whereas local control is a prerequisite for cure. The Dutch Deep Hyperthermia Trial showed that combining RT with hyperthermia (HT) improved 3-year local control rates of 41-61%, as we reported earlier. In this study, we evaluate long-term results of the Dutch Deep Hyperthermia Trial after 12 years of follow-up. Methods and Materials: From 1990 to 1996, a total of 114 women with locoregionally advanced cervical carcinoma were randomly assigned to RT or RT + HT. The RT was applied to a median total dose of 68 Gy. The HT was given once weekly. The primary end point was local control. Secondary end points were overall survival and late toxicity. Results: At the 12-year follow-up, local control remained better in the RT + HT group (37% vs. 56%; p = 0.01). Survival was persistently better after 12 years: 20% (RT) and 37% (RT + HT; p = 0.03). World Health Organization (WHO) performance status was a significant prognostic factor for local control. The WHO performance status, International Federation of Gynaecology and Obstetrics (FIGO) stage, and tumor diameter were significant for survival. The benefit of HT remained significant after correction for these factors. European Organization for Research and Treatment of Cancer Grade 3 or higher radiation-induced late toxicities were similar in both groups. Conclusions: For locoregionally advanced cervical cancer, the addition of HT to RT resulted in long-term major improvement in local control and survival without increasing late toxicity. This combined treatment should be considered for patients who are unfit to receive chemotherapy. For other patients, the optimal treatment strategy is the subject of ongoing research. </description>
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      <title>Kadota Fund International Forum 2004. Application of thermal stress for the improvement of health, 15-18 June 2004, Awaji Yumebutai International Conference Center, Awaji Island, Hyogo, Japan. Final Report (Article)</title>
      <link>http://repub.eur.nl/res/pub/29499/</link>
      <pubDate>2008-03-01T00:00:00Z</pubDate>
      <description></description>
    </item> <item>
      <title>The Kadota Fund International Forum 2004 - Clinical group consensus (Article)</title>
      <link>http://repub.eur.nl/res/pub/29526/</link>
      <pubDate>2008-03-01T00:00:00Z</pubDate>
      <description>The results from experimental studies indicate that hyperthermia is both an effective complementary treatment to, and a strong sensitiser of, radiotherapy and many cytotoxic drugs. Since the first international hyperthermia conference in 1975, Washington DC, techniques to increase tumour temperature have been developed and tested clinically. Hyperthermia can be applied by several methods: local hyperthermia by external or internal energy sources, perfusion hyperthermia of organs, limbs, or body cavities, and whole body hyperthermia. The clinical value of hyperthermia in combination with other treatment modalities has been shown by randomised trials. Significant improvement in clinical outcome has been demonstrated for tumours of the head and neck, breast, brain, bladder, cervix, rectum, lung, oesophagus, for melanoma and sarcoma. The addition of hyperthermia resulted in remarkably higher (complete) response rates, accompanied by improved local tumour control rates, better palliative effects, and/or better overall survival rates. Toxicity from hyperthermia cannot always be avoided, but is usually of limited clinical relevance. In spite of these good clinical results, hyperthermia has received little attention. Problems with acceptance concern the limited availability of equipment, the lack of awareness concerning clinical results, and the lack of financial resources. In this paper the most relevant literature describing the clinical effects of hyperthermia is reviewed and discussed, and means to overcome the lack of awareness and use of this modality is described.</description>
    </item> <item>
      <title>RF-power and temperature data analysis of 444 patients with primary cervical cancer: Deep hyperthermia using the Sigma-60 applicator is reproducible (Article)</title>
      <link>http://repub.eur.nl/res/pub/35887/</link>
      <pubDate>2007-12-01T00:00:00Z</pubDate>
      <description>Treatment reproducibility is important to guarantee reproducible treatment-outcome, a low-complication rate and efficient treatment procedures. This study evaluated the performance of loco-regional deep hyperthermia with four BSD-2000 configurations during 1990-2005 using the direct available parameters, i.e., temperature and power. Primary cervical cancer patients (n = 444) were all treated within the Sigma-60. Patients were grouped in three weight-groups: &lt;61 kg, 61-70 kg, &lt;70 kg. Different temperature and power indices were extensively analyzed per BSD configuration, per weight-group, and over the time-period. No substantial variations were found for temperature/power indices over the four BSD configurations or for the temperature doses in similar weight-groups. The 'bare' power indices were increased with weight; however, the derivative power-related (W/kg, W/cm2) and temperature indices decreased. Large variations were found in the power-related parameters during 1991-1996 (1st time-period), whereas they were much smaller during 1997-2005 (2nd time-period). The most relevant change noted was the adaptation of the treatment strategy with respect to power modulation. The average frequency of switched-off was 3.4 and 8.9 times/treatment session for the 1st and 2nd time-period, respectively, while the average duration of each switched-off time was 78.2 vs. 38.3 s. The yearly average of vagina T50 was in the range of 39.3-40.2°C (1st time-period) and 40.0-40.5°C (2nd time-period). In 40% of the patients, a positive correlation was found between normalized net integrated power per pelvic area and vagina T50. Good reproducible heating is achieved with the BSD-2000 Sigma-60 irrespective of the regular technological upgrades of the system and variation of trained staff-members.</description>
    </item> <item>
      <title>The HYPERcollar: A novel applicator for hyperthermia in the head and neck (Article)</title>
      <link>http://repub.eur.nl/res/pub/20653/</link>
      <pubDate>2007-11-01T00:00:00Z</pubDate>
      <description>The purpose of this work was to define all features, and show the potential, of the novel HYPERcollar applicator system for
hyperthermia treatments in the head and neck region. The HYPERcollar applicator consists of (1) an antenna ring, (2) a
waterbolus system and (3) a positioning system. The specific absorption rate (SAR) profile of this applicator was investigated by performing infra-red measurements in a cylindrical phantom. Mandatory patient-specific treatment planning was performed as an object lesson to a patient with a laryngeal tumour and an artificial lymph node metastasis. Comfort tests with healthy volunteers have revealed that the applicator provides sufficient comfort to maintain in treatment position for an hour: the standard hyperthermia treatment duration in our centre. By phantom measurements, we established that a central focus in the neck can be obtained, with 50% iso-SAR lengths of 3.5 cm in transversal directions (x/y) and 9–11 cm in the axial direction (z). Using treatment planning by detailed electromagnetic simulations, we showed that the SAR pattern can be optimised to enable simultaneous encompassing of a primary laryngeal tumour and a lymph node metastasis at the 25% iso-SAR level. This study shows that the applicator enables a good control, and sufficient possibilities for optimisation, of the SAR pattern. In an ongoing clinical feasibility study, we will investigate the possibilities of heating various target regions in the neck with this apparatus.</description>
    </item> <item>
      <title>Comparison of intratumor and intraluminal temperatures during locoregional deep hyperthermia of pelvic tumors (Article)</title>
      <link>http://repub.eur.nl/res/pub/35739/</link>
      <pubDate>2007-09-01T00:00:00Z</pubDate>
      <description>Purpose: To investigate whether intraluminal thermometry provides sufficient information to apply high quality deep hyperthermia in pelvic tumors. Patients and Methods: The intratumor and intraluminal temperatures of 48 patients were analyzed per cancer type: rectum (21 male, 14 female), cervix (n = 8), and bladder (n = 5). Temperature-dose parameters were calculated, temperature curves within each treatment session were compared, and correlation between intratumor and intraluminal temperatures was analyzed. Results: Intratumor and intraluminal temperatures at the same time points during individual treatments were highly correlated (mean correlation coefficient: 0.93). However, the quantitative level differed from 0.1 to 1.1°C and the differences of the timetemperature graphs varied per tumor group. Average intratumor and intraluminal temperatures were not different in the four groups. Intratumor thermometry was found not superior over intraluminal thermometry to improve tumor temperature level and homogeneity by SAR steering. Conclusion: Intraluminal thermometry provides sufficient information to apply deep hyperthermia to individual patients with centrally located rectum, cervix or bladder cancer. </description>
    </item> <item>
      <title>Benefits of superficial hyperthermia treatment planning: Five case studies (Article)</title>
      <link>http://repub.eur.nl/res/pub/35920/</link>
      <pubDate>2007-08-01T00:00:00Z</pubDate>
      <description>Purpose: To demonstrate the benefits of treatment planning in superficial hyperthermia. Materials and methods: Five patient cases are presented, in which treatment planning was applied to troubleshoot treatment-limiting hotspots, to select the optimum applicator type and orientation, to assess the risk associated with metallic implants, to assess the feasibility of heating a deeper seated tumour, and to analyse the effective SAR coverage resulting from arrays of multiple incoherent applicators. FDTD simulation tools were used to investigate treatment options, either based on segmented or simplified anatomies. Results: The background, approach and model implementation are presented per case. SAR cross-sections, profiles and isosurfaces are visualized to predict the effective SAR coverage of the target and the location of the maximum power absorption. In addition, the followed treatment strategy and the implications for the clinical treatment are given: for example, higher temperatures, relief of treatment limiting hot-spots or increased power input. Conclusions: Treatment planning in superficial hyperthermia can be applied to improve clinical routine. Its application supports the selection of the optimum technique in non-standard cases, leading to direct benefits for the patient. In addition, treatment planning has shown to be an excellent tool for education and training for hyperthermia technicians and physicians.</description>
    </item> <item>
      <title>Concomitant radiotherapy and hyperthermia for primary carcinoma of the vagina: A cohort study (Article)</title>
      <link>http://repub.eur.nl/res/pub/36062/</link>
      <pubDate>2007-07-01T00:00:00Z</pubDate>
      <description>Objective: To evaluate the supplementary value of adding hyperthermia to radiotherapy in patients with primary vaginal cancer. Study design: Cohort of 44 patients diagnosed with primary vaginal cancer between 1990 and 2002 was assessed. Survival rates and median survival of patients with primary vaginal cancer undergoing radiotherapy with and without hyperthermia were compared. Hyperthermia was solely added to radiotherapy in case of a tumor size &gt;4 cm in diameter for FIGO stage III disease. Results: The calculated overall 5-year survival of primary vaginal cancer was 63%. In comparison to histologic high grade tumors, higher survival rates for histologic low grade tumors were calculated. For FIGO stage III of disease, the addition of hyperthermia to radiotherapy for tumors &gt;4 cm in diameter resulted similar survival rates and median survival when compared to those achieved by radiotherapy as monotherapy in tumors of &lt;4 cm in diameter. Conclusions: The addition of hyperthermia to radiotherapy might result in better survival rates in primary vaginal cancer for tumors &gt;4 cm in diameter. The supplementary effect of hyperthermia to radiotherapy may be a feasible and beneficial approach in the treatment of vaginal cancer. </description>
    </item> <item>
      <title>On heating head and neck tumours using the novel clinical em applicator: the HYPERcollar (Article)</title>
      <link>http://repub.eur.nl/res/pub/20654/</link>
      <pubDate>2007-05-01T00:00:00Z</pubDate>
      <description>Abstract
Purpose: Definition of all features and the potential of the novel HYPERcollar applicator system for hyperthermia treatments in the head and neck (H&amp;N) region.
Methods and Materials: The HYPERcollar applicator consists of 1) an antenna ring, 2) a waterbolus system and 3) a positioning system. The specific absorption rate (SAR) profile of this applicator is investigated by performing infra-red (IR) measurements in a cylindrical phantom. Mandatory patient-specific treatment planning is performed as an object lesson to a patient with a laryngeal tumour and an artificial lymph node metastasis.
Results: The comfort tests with healthy volunteers have revealed that the applicator provides su±cient comfort to maintain in treatment position for an hour: in our center the standard hyperthermia treatment duration. We further established that a central focus in the neck can be obtained, with 50% iso-SAR lengths of 3.5cm in transversal directions and 9-11cm in the axial direction (z). Using treatment planning by detailed electromagnetic simulations, we showed that the SAR pattern can be optimized to enable simultaneous encompassing a primary laryngeal tumour and a lymph node metastasis at the 25% iso-SAR level.
Conclusions: A site-specific H&amp;N applicator was designed that enables good control and sufficient possibilities for optimizing the SAR pattern. In an ongoing clinical feasibility study we will investigate the possibilities of heating various target regions in the neck with this apparatus.</description>
    </item> <item>
      <title>Assessment of the local SAR Distortion by Major Anatomical Structures in a Cylindrical Neck Phantom (Article)</title>
      <link>http://repub.eur.nl/res/pub/10495/</link>
      <pubDate>2005-03-01T00:00:00Z</pubDate>
      <description>The objective of this work is to gain insight in the distortions on the local SAR distribution by various major anatomical structures in the neck. High resolution 3D FDTD calculations based on a variable grid are made for a semi-3D generic phantom based on average dimensions obtained from CT-derived human data and in which simplified structures representing trachea, cartilage, spine and spinal cord are inserted. In addition, phantoms with dimensions equal to maximum and minimum values within the CT-derived data are also studied. In all cases, the phantoms are exposed to a circular coherent array of eight dipoles within a water bolus and driven at 433 MHz. Comparisons of the SAR distributions due to individual structures or a combination of structures are made relative to a cylindrical
phantom with muscle properties. The calculations predict a centrally located region of high SAR within all neck phantoms. This focal region, expressed as contours at either 50% or 75% of the peak SAR, changes from a circular cross-section in the case of the muscle phantom to a doughnut
shaped region when the anatomical structures are present. The presence of the spine causes the greatest change in the SAR distribution, followed closely by the trachea. Global changes in the mean SAR relative to the uniform phantom are &lt;11%, whilst local changes are as high as 2.7-fold. There is little difference in the focal dimensions between the average and smallest phantoms, but a decrease in the focal region is seen in the case of the largest phantom. This study presents a first step towards understanding of the complex influences of the various parameters on the SAR pattern
which will facilitate the design of a site-specific head and neck hyperthermia applicator.</description>
    </item> <item>
      <title>Heating the patient: a promising approach? (Article)</title>
      <link>http://repub.eur.nl/res/pub/9955/</link>
      <pubDate>2002-01-01T00:00:00Z</pubDate>
      <description>There is a clear rationale for using hyperthermia in cancer treatment.
      Treatment at temperatures between 40 and 44 degrees C is cytotoxic for
      cells in an environment with a low pO(2) and low pH, conditions that are
      found specifically within tumour tissue, due to insufficient blood
      perfusion. Under such conditions radiotherapy is less effective, and
      systemically applied cytotoxic agents will reach such areas in lower
      concentrations than in well perfused areas. Therefore, the addition of
      hyperthermia to radiotherapy or chemotherapy will result in at least an
      additive effect. Furthermore, the effects of both radiotherapy and many
      drugs are enhanced at an increased temperature. Hyperthermia can be
      applied by several methods: local hyperthermia by external or internal
      energy sources, regional hyperthermia by perfusion of organs or limbs, or
      by irrigation of body cavities, and whole body hyperthermia. The use of
      hyperthermia alone has resulted in complete overall response rates of 13%.
      The clinical value of hyperthermia in addition to other treatment
      modalities has been shown in randomised trials. Significant improvement in
      clinical outcome has been demonstrated for tumours of the head and neck,
      breast, brain, bladder, cervix, rectum, lung, oesophagus, vulva and
      vagina, and also for melanoma. Additional hyperthermia resulted in
      remarkably higher (complete) response rates, accompanied by improved local
      tumour control rates, better palliative effects and/or better overall
      survival rates. Generally, when combined with radiotherapy, no increase in
      radiation toxicity could be demonstrated. Whether toxicity from
      chemotherapy is enhanced depends on sequence of the two modalities, and on
      which tissues are heated. Toxicity from hyperthermia cannot always be
      avoided, but is usually of limited clinical relevance. Recent developments
      include improvements in heating techniques and thermometry, development of
      hyperthermia treatment planning models, studies on heat shock proteins and
      an effect on anti-cancer immune responses, drug targeting to tumours, bone
      marrow purging, combination with drugs targeting tumour vasculature, and
      the role of hyperthermia in gene therapy. The clinical results achieved to
      date have confirmed the expectations raised by results from experimental
      studies. These findings justify using hyperthermia as part of standard
      treatment in tumour sites for which its efficacy has been proven and,
      furthermore, to initiate new studies with other tumours. Hyperthermia is
      certainly a promising approach and deserves more attention than it has
      received until now.</description>
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