203 research outputs found

    Long-term incidence of lung cancer in the TARGIT-A randomised trial of targeted intraoperative radiotherapy for breast cancer

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    Background: With improvement in survival after breast cancer, the burden and longer-term side effects of treatment are increasingly relevant. Today, most patients can avoid a mastectomy, but having a breast conserving surgery is traditionally followed by external beam whole breast radiotherapy (EBRT), which can be onerous and leads to inevitable and potentially carcinogenic irradiation of nearby vital organs such as the lungs. The results of the TARGIT-A randomised trial found that TARGIT-IORT during the initial lumpectomy is as effective as EBRT in controlling breast cancer, and has several benefits to the patient including reduced pain, improved cosmetic outcome and quality of life, and significantly fewer deaths from non-breast-cancer causes, leading to an overall survival benefit in patients with grade 1 or 2 cancers with a 12-year mortality reduction from 15% to 10.5%. / Material and methods: We collected long term data about health status and new cancer diagnoses of UK patients from the TARGIT-A randomised trial, using direct patient contact, & NHS Digital data. We compared lung cancer incidence between patients randomised to TARGIT-IORT vs EBRT. / Results: The length of follow up of UK patients (n=714) increased to a median of 14 years (IQR 13 to 16) There were significantly more lung cancer diagnoses in the EBRT arm compared with TARGIT-IORT arm; HR 3.3 (95%CI 1.1 – 10.2). The 16-year incidences were: EBRT: 7.2% (95%CI 3.7 – 13.7) and TARGIT: 1.8% (95%CI 0.6-5.2), difference 5.38% (95%CI 0.3 -10.5), log rank p=0.0266. An estimated 920000 breast cancer patients worldwide are suitable for TARGIT-IORT annually. Using the 5.38% reduction in lung cancer risk that we have observed, if TARGIT-IORT were to be made accessible to these patients, then 49496 (95%CI 5500-134320) of these patients would be spared the diagnosis of a lung cancer during their follow up. / Conclusions: With very long-term follow data from of a large TARGIT-A randomised trial, we found a substantial increase in lung cancer incidence with EBRT compared with TARGIT-IORT. It is a tragedy when women who outlive breast cancer then succumb to this frequently lethal radiation-induced lung cancer, which is avoidable by using TARGIT-IORT during lumpectomy instead of post-operative EBRT. These new data further mandate full discussion about benefits of TARGIT-IORT with patients, including reduction in lung cancer incidence, before their surgery

    A pilot study combining individual-based smoking cessation counseling, pharmacotherapy, and dental hygiene intervention

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    BACKGROUND: Dentists are in a unique position to advise smokers to quit by providing effective counseling on the various aspects of tobacco-induced diseases. The present study assessed the feasibility and acceptability of integrating dentists in a medical smoking cessation intervention. METHODS: Smokers willing to quit underwent an 8-week smoking cessation intervention combining individual-based counseling and nicotine replacement therapy and/or bupropion, provided by a general internist. In addition, a dentist performed a dental exam, followed by an oral hygiene treatment and gave information about chronic effects of smoking on oral health. Outcomes were acceptability, global satisfaction of the dentist's intervention, and smoking abstinence at 6-month. RESULTS: 39 adult smokers were included, and 27 (69%) completed the study. Global acceptability of the dental intervention was very high (94% yes, 6% mostly yes). Annoyances at the dental exam were described as acceptable by participants (61% yes, 23% mostly yes, 6%, mostly no, 10% no). Participants provided very positive qualitative comments about the dentist counseling, the oral exam, and the resulting motivational effect, emphasizing the feeling of oral cleanliness and health that encouraged smoking abstinence. At the end of the intervention (week 8), 17 (44%) participants reported smoking abstinence. After 6 months, 6 (15%, 95% CI 3.5 to 27.2) reported a confirmed continuous smoking abstinence. DISCUSSION: We explored a new multi-disciplinary approach to smoking cessation, which included medical and dental interventions. Despite the small sample size and non-controlled study design, the observed rate was similar to that found in standard medical care. In terms of acceptability and feasibility, our results support further investigations in this field. TRIAL REGISTRATION NUMBER: ISRCTN67470159

    Enabling Universal Memory by Overcoming the Contradictory Speed and Stability Nature of Phase-Change Materials

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    The quest for universal memory is driving the rapid development of memories with superior all-round capabilities in non-volatility, high speed, high endurance and low power. Phase-change materials are highly promising in this respect. However, their contradictory speed and stability properties present a key challenge towards this ambition. We reveal that as the device size decreases, the phase-change mechanism changes from the material inherent crystallization mechanism (either nucleation- or growth-dominated), to the hetero-crystallization mechanism, which resulted in a significant increase in PCRAM speeds. Reducing the grain size can further increase the speed of phase-change. Such grain size effect on speed becomes increasingly significant at smaller device sizes. Together with the nano-thermal and electrical effects, fast phase-change, good stability and high endurance can be achieved. These findings lead to a feasible solution to achieve a universal memory

    CRISPR Recognition Tool (CRT): a tool for automatic detection of clustered regularly interspaced palindromic repeats

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    <p>Abstract</p> <p>Background</p> <p>Clustered Regularly Interspaced Palindromic Repeats (CRISPRs) are a novel type of direct repeat found in a wide range of bacteria and archaea. CRISPRs are beginning to attract attention because of their proposed mechanism; that is, defending their hosts against invading extrachromosomal elements such as viruses. Existing repeat detection tools do a poor job of identifying CRISPRs due to the presence of unique spacer sequences separating the repeats. In this study, a new tool, CRT, is introduced that rapidly and accurately identifies CRISPRs in large DNA strings, such as genomes and metagenomes.</p> <p>Results</p> <p>CRT was compared to CRISPR detection tools, Patscan and Pilercr. In terms of correctness, CRT was shown to be very reliable, demonstrating significant improvements over Patscan for measures precision, recall and quality. When compared to Pilercr, CRT showed improved performance for recall and quality. In terms of speed, CRT proved to be a huge improvement over Patscan. Both CRT and Pilercr were comparable in speed, however CRT was faster for genomes containing large numbers of repeats.</p> <p>Conclusion</p> <p>In this paper a new tool was introduced for the automatic detection of CRISPR elements. This tool, CRT, showed some important improvements over current techniques for CRISPR identification. CRT's approach to detecting repetitive sequences is straightforward. It uses a simple sequential scan of a DNA sequence and detects repeats directly without any major conversion or preprocessing of the input. This leads to a program that is easy to describe and understand; yet it is very accurate, fast and memory efficient, being O(<it>n</it>) in space and O(<it>nm</it>/<it>l</it>) in time.</p

    Improved accuracy of multiple ncRNA alignment by incorporating structural information into a MAFFT-based framework

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    <p>Abstract</p> <p>Background</p> <p>Structural alignment of RNAs is becoming important, since the discovery of functional non-coding RNAs (ncRNAs). Recent studies, mainly based on various approximations of the Sankoff algorithm, have resulted in considerable improvement in the accuracy of pairwise structural alignment. In contrast, for the cases with more than two sequences, the practical merit of structural alignment remains unclear as compared to traditional sequence-based methods, although the importance of multiple structural alignment is widely recognized.</p> <p>Results</p> <p>We took a different approach from a straightforward extension of the Sankoff algorithm to the multiple alignments from the viewpoints of accuracy and time complexity. As a new option of the MAFFT alignment program, we developed a multiple RNA alignment framework, X-INS-i, which builds a multiple alignment with an iterative method incorporating structural information through two components: (1) pairwise structural alignments by an external pairwise alignment method such as SCARNA or LaRA and (2) a new objective function, Four-way Consistency, derived from the base-pairing probability of every sub-aligned group at every multiple alignment stage.</p> <p>Conclusion</p> <p>The BRAliBASE benchmark showed that X-INS-i outperforms other methods currently available in the sum-of-pairs score (SPS) criterion. As a basis for predicting common secondary structure, the accuracy of the present method is comparable to or rather higher than those of the current leading methods such as RNA Sampler. The X-INS-i framework can be used for building a multiple RNA alignment from any combination of algorithms for pairwise RNA alignment and base-pairing probability. The source code is available at the webpage found in the Availability and requirements section.</p
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