P. Huber
University Hospital Heidelberg
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Featured researches published by P. Huber.
BMC Cancer | 2006
Alexandra D. Jensen; Marc W. Münter; Helge Bischoff; Renate Haselmann; Carmen Timke; Robert Krempien; Florian Sterzing; Simeon Nill; S. Heeger; A. Hoess; Uwe Haberkorn; P. Huber; Martin Steins; Michael Thomas; Juergen Debus; Klaus Herfarth
BackgroundEven today, treatment of Stage III NSCLC still poses a serious challenge. So far, surgical resection is the treatment of choice. Patients whose tumour is not resectable or who are unfit to undergo surgery are usually referred to a combined radio-chemotherapy. However, combined radio-chemotherapeutic treatment is also associated with sometimes marked side effects but has been shown to be more efficient than radiation therapy alone.Nevertheless, there is a significant subset of patients whose overall condition does not permit administration of chemotherapy in a combined-modality treatment.It could be demonstrated though, that NSCLCs often exhibit over-expression of EGF-receptors hence providing an excellent target for the monoclonal EGFR-antagonist cetuximab (Erbitux®) which has already been shown to be effective in colorectal as well as head-and-neck tumours with comparatively mild side-effects.Methods/designThe NEAR trial is a prospective phase II feasibility study combining a monoclonal EGF-receptor antibody with loco-regional irradiation in patients with stage III NSCLC. This trial aims at testing the combinations efficacy and rate of development of distant metastases with an accrual of 30 patients.Patients receive weekly infusions of cetuximab (Erbitux®) plus loco-regional radiation therapy as intensity-modulated radiation therapy. After conclusion of radiation treatment patients continue to receive weekly cetuximab for 13 more cycles.DiscussionThe primary objective of the NEAR trial is to evaluate toxicities and feasibility of the combined treatment with cetuximab (Erbitux®) and IMRT loco-regional irradiation.Secondary objectives are remission rates, 3-year-survival and local/systemic progression-free survival.
Radiation Oncology | 2012
Michael Schwarz; Kristina Giske; Armin Stoll; Simeon Nill; P. Huber; Jürgen Debus; Rolf Bendl; Eva Maria Stoiber
BackgroundTo evaluate the impact of image-guided radiation therapy (IGRT) versus non-image-guided radiation therapy (non-IGRT) on the dose to the clinical target volume (CTV) and the cervical spinal cord during fractionated intensity-modulated radiation therapy (IMRT) for head-and-neck cancer (HNC) patients.Material and MethodsFor detailed investigation, 4 exemplary patients with daily control-CT scans (total 118 CT scans) were analyzed. For the IGRT approach a target point correction (TPC) derived from a rigid registration focused to the high-dose region was used. In the non-IGRT setting, instead of a TPC, an additional cohort-based safety margin was applied. The dose distributions of the CTV and spinal cord were calculated on each control-CT and the resulting dose volume histograms (DVHs) were compared with the planned ones fraction by fraction. The D50 and D98 values for the CTV and the D5 values of the spinal cord were additionally reported.ResultsIn general, the D50 and D98 histograms show no remarkable difference between both strategies. Yet, our detailed analysis also reveals differences in individual dose coverage worth inspection. Using IGRT, the D5 histograms show that the spinal cord less frequently receives a higher dose than planned compared to the non-IGRT setting. This effect is even more pronounced when looking at the curve progressions of the respective DVHs.ConclusionsBoth approaches are equally effective in maintaining CTV coverage. However, IGRT is beneficial in spinal cord sparing. The use of an additional margin in the non-IGRT approach frequently results in a higher dose to the spinal cord than originally planned. This implies that a margin reduction combined with an IGRT correction helps to maintain spinal cord dose sparing best as possible. Yet, a detailed analysis of the dosimetric consequences dependent on the used strategy is required, to detect single fractions with unacceptable dosimetric deviations.
Archive | 1995
Michael V. Knopp; Stefan Delorme; Antonia Dimitrakopoulou-Strauss; R. Engenhart; Jürgen Debus; P. Huber; Peter Bachert; Thomas Heß
Die Radiologie ist eines der wichtigsten Fachgebiete fur die Erkennung, Behandlung und Verlaufskontrolle von Krebserkrankungen. Die Fachbezeichnung Radiologie schliest heute neben den bekannten rontgenologischen Diagnose- und Therapieverfahren auch jene neuen Methoden ein, bei denen nichtionisierende Strahlen zum Einsatz kommen.
Radiotherapy and Oncology | 2013
Eva Maria Stoiber; Michael Schwarz; Jürgen Debus; P. Huber; Rolf Bendl; Kristina Giske
PURPOSEnTo present a new method that assesses the delivered maximum dose of different spinal cord sections in head-and-neck cancer treated with intensity-modulated radiation therapy (IMRT). This allows a more accurate estimation of the remaining cord dose tolerance in case of a later re-irradiation treatment planning.nnnMATERIALS AND METHODSnThe suggested workflow is demonstrated using daily acquired kilo-voltage control-CTs of four head-and-neck cancer patients (118 control-CTs). The local maximum dose inside different cord levels is determined and accumulated for the planning situation and over the treatment course for an IGRT and a non-IGRT approach.nnnRESULTSnThe approach is suitable to accurately detect and document the delivered maximum dose dependent on the cord levels. The delivered maximum dose differed up to 13% from the planned one in all sections due to setup uncertainties and the applied correction strategy.nnnCONCLUSIONnThe presented approach facilitates later re-irradiation treatment planning due to detailed documentation of the delivered maximum dose to the spinal cord levels in the primary IMRT. The method also facilitates the interpretation of complex 3D dose information by reducing it to its essentials. This 2D illustration is an aid to orientation for the physician in the re-irradiation planning process.
Physica Medica | 2011
Alexandra D. Jensen; Simeon Nill; Nathalie Rochet; Rolf Bendl; Wolfgang Harms; P. Huber; Jürgen Debus; Marc W. Münter
INTRODUCTIONnDespite enormous efforts to improve therapeutic strategies for patients with advanced ovarian carcinoma, outcome remains poor even with the advent cisplatinum-based chemotherapy regimen or taxanes with over 70% of patients developing local failure. Several trials were able to establish the potential benefit of adjuvant whole abdominal RT (WAI) though at the cost of sometimes marked side-effects. New technologies like IMRT have the potential of sparing normal tissues thus also potentially limiting treatment-related toxicity, hence a phase I trial was initiated to evaluate potential clinical benefit of WAI with IMRT. We intended to demonstrate that whole-abdominal IMRT is feasible and can be used in a routine clinical setting.nnnMETHODSnA water-equivalent phantom containing OARs was created simulating organ shape of the upper abdomen to investigate the necessary number of beams for the upper abdominal target irrespective of the number of segments and hence treatment times. We prescribed a total dose of 30xa0Gy in 1.5xa0Gy fractions to the median of the target. IMRT treatment plans for three patients with advanced ovarian cancer were created using 2 isocentres and between 12 and 14 beams while restricting the number of segments so as to restrict treatment times to less than 45xa0min. Dose to OARs such as kidneys and liver was strictly limited even below established maxima.nnnRESULTSnIn the phantom plans, no clear indication as to the optimum number of beams could be shown though there seems to be a slight trend toward a higher number of beams yielding better results. Examples demonstrating clinically inacceptable dose distributions for plans using only 9 beams. Acceptable treatment plans for real patients could be achieved using 12-14 beams and 2 isocentres. Treatment plans consisted of 264-286 segments resulting in an overall treatment time of approximately 37-45xa0min. Mean doses to the kidneys could be limited to 29.3% [23.1-33.2%] (right), and 26.8% [21-30.4%] (left). 50% of the liver received less than 72.4% [61-83%].nnnCONCLUSIONnIMRT for whole abdominal irradiation in patients with advanced ovarian carcinoma is applicable and feasible though treatment planning is complex and time-consuming. There is a significant reduction of dose to critical organs by using IMRT while maintaining target volume coverage.
Archive | 1995
Michael V. Knopp; Stefan Delorme; Antonia Dimitrakopolou-Strauss; R. Engenhart; Jürgen Debus; P. Huber; Peter Bachert; Thomas Hess
Radiology is one of the most important specializations in medicine for the detection, treatment, and follow-up of cancer diseases. Today, radiology not only encompasses conventional radiological methods of diagnosis and therapy, but also advanced techniques that make use of non-ionizing forms of radiation.
Radiotherapy and Oncology | 2012
Eva Maria Stoiber; Michael Schwarz; Jürgen Debus; P. Huber; Rolf Bendl; Kristina Giske
Radiotherapy and Oncology | 2011
Eva Maria Stoiber; Michael Schwarz; Kristina Giske; P. Huber; Jürgen Debus; Rolf Bendl
Fuel and Energy Abstracts | 2010
David P. Schmitt; Simeon Nill; Klaus Herfarth; Marc W. Münter; Jurgen Pfitzenmaier; Angelika Zabel-du Bois; Falk Röder; P. Huber; Uwe Oelfke
Radiotherapy and Oncology | 2007
Zahra Taheri-Kadkhoda; Simeon Nill; Jan J. Wilkens; Uwe Oelfke; Thomas Björk-Eriksson; P. Huber; Marc W. Münter