Background: Since the introduction of 3-D conformal radiotherapy (CRT) doses of = 70 Gy have been used in many European countries. In this analysis, the impact of a short-term neoadjuvant hormonal treatment in combination with CRT to a moderate dose level of 66 Gy was examined.
Patients And Methods: From January 1994 to February 1999 397 patients were treated for carcinoma of the prostate. In 279 patients a definitive curative treatment (T1 = 38, T2 = 165, T3 = 50, Tx = 11) with or without androgen deprivation was performed. 164 patients with radiotherapy of the prostate +/- seminal vesicles to a total dose of 66 Gy (n = 109) alone or in combination with a short-term hormonal treatment (n = 55) were included in this analysis. Biochemical relapse was defined as three rising PSA values or reintroduction of hormonal treatment. A low-risk subgroup was defined for patients with maximum serum PSA level = 10 and cT=2 and G=2, all other patients were summarized as high-risk patients.
Results: The median follow-up of alive patients was 40 months (12-72 months). There was a total of 29/164 deaths, two were cause-specific and 27 were considered unrelated to prostate cancer. The 4-year rates of no biochemical evidence of disease for all patients was 58%. For the high-risk group the 4-year rates could be improved with borderline significance from 35% to 66% (p = 0.057) by additional neoadjuvant hormonal treatment. In contrast for the low-risk group no significant improvement was observed: 73% and 82%, respectively (p = 0.5).
Conclusion: Especially in high-risk patients doses = 70 Gy for radiotherapy alone seem not to be sufficient for curative treatment. Additional hormonal treatment and doses >/= 70 Gy should be considered. As a consequence of our earlier analysis a prospective multicenter treatment optimization protocol has been initiated in 1999. The protocol includes a risk-adapted dose increase from 70 Gy in low-risk patients to 74 Gy in high-risk patients including short-term androgen ablation.
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http://dx.doi.org/10.1007/s00066-002-0963-2 | DOI Listing |
Indian J Cancer
January 2024
Surgical Oncology, Cancer Research Institute, Himalayan Institute of Medical Sciences, Swami Rama Himalayan University, Dehradun, Uttarakhand, India.
Introduction: Radiation-induced lung toxicity (RILT) is a major concern in patients who receive radiation to thorax. The purpose of the study was to evaluate the changes of pulmonary function tests (PFTs) in lung carcinoma patients treated with three-dimensional conformal radiation therapy (3-D CRT) and relation RILT with dosimetric and nondosimetric factors.
Methods: This was a prospective observational study which included 65 patients of lung carcinoma treated with 3-D CRT.
Protein Pept Lett
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Botany and Microbiology Department, Faculty of Science, Damietta University, Damietta, Egypt.
Adv Mater
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Department of Mechanical Engineering, Division of Materials Science and Engineering, Department of Chemistry, Boston University, 110 Cummington Mall, Boston, MA, 02215, USA.
Natural systems, synthetic materials, and devices almost always feature interphases that control the flow of mass and energy or stabilize interfaces between incompatible materials. With technologies transitioning to non-planar and 3D mesoscale architectures, novel deposition methods for realizing ultrathin coatings and interphases are required. Polymer networks are of particular interest for their tunable chemical and physical properties combined with their structural integrity.
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August 2024
Department of Mathematics, Sunamgonj Science and Technology University, Bangladesh.
In this work, we study the Chafee-Infante model with conformable fractional derivative. This model describes the energy balance between equator and pole of solar system, which transmit energy via heat diffusion. To explore the multi soliton solutions and their interaction, we implemented the new modified simple equation (NMSE) scheme.
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Department of Biological Sciences, Bose Institute, EN-80 Sector V, Salt Lake, Unified Campus, Kolkata 700091, India. Electronic address:
ORAI1 is an intrinsic component of store-operated calcium entry (SOCE) that strictly regulates Ca influx in most non-excitable cells. ORAI1 is overexpressed in a wide variety of cancers, and its signal transduction has been associated with chemotherapy resistance. There is extensive proteomic interaction of ORAI1 with other channels and effectors, resulting in various altered phenotypes.
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