Browsing by author "O'Brien, Mary"
Now showing items 1-20 of 24
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The changing diagnostic pathway for lung cancer patients in Shanghai, China.
Jiang, T; Ren, S; Li, X; Su, C; Zhou, C; O'Brien, M (2017-10)Accumulating evidence suggest that patients with advanced non-small-cell lung cancer (NSCLC) and specific genomic alterations including epidermal growth factor receptor and microtubule-associated protein-like 4 anaplastic ... -
Characterisation of the Phosphatidylinositol 3-Kinase Pathway in Non-Small Cell Lung Cancer Cells Isolated from Pleural Effusions.
Puglisi, M; Stewart, A; Thavasu, P; Frow, M; Carreira, S; Minchom, A; Punwani, R; Bhosle, J; Popat, S; Ratoff, J; de Bono, J; Yap, TA; O''Brien, M; Banerji, U (2016-01)<h4>Objectives</h4>We hypothesised that it was possible to quantify phosphorylation of important nodes in the phosphatidylinositol 3-kinase (PI3K) pathway in cancer cells isolated from pleural effusions of patients with ... -
Clinical outcomes and prognostic factors of patients with advanced mesothelioma treated in a phase I clinical trials unit.
Papadatos-Pastos, D; Roda, D; De Miguel Luken, MJ; Petruckevitch, A; Jalil, A; Capelan, M; Michalarea, V; Lima, J; Diamantis, N; Bhosle, J; Molife, LR; Banerji, U; de Bono, JS; Popat, S; O'Brien, MER; Yap, TA (2017-04)<h4>Background</h4>We have previously reported a prognostic score for patients in phase I trials in the Drug Development Unit, treated at the Royal Marsden Hospital (RPS). The RPS is an objective tool used in patient ... -
Concurrent once-daily versus twice-daily chemoradiotherapy in patients with limited-stage small-cell lung cancer (CONVERT): an open-label, phase 3, randomised, superiority trial.
Faivre-Finn, C; Snee, M; Ashcroft, L; Appel, W; Barlesi, F; Bhatnagar, A; Bezjak, A; Cardenal, F; Fournel, P; Harden, S; Le Pechoux, C; McMenemin, R; Mohammed, N; O'Brien, M; Pantarotto, J; Surmont, V; Van Meerbeeck, JP; Woll, PJ; Lorigan, P; Blackhall, F; CONVERT Study Team (2017-08)<h4>Background</h4>Concurrent chemoradiotherapy is the standard of care in limited-stage small-cell lung cancer, but the optimal radiotherapy schedule and dose remains controversial. The aim of this study was to establish ... -
Development and responses of brain metastases during treatment with trastuzumab emtansine (T-DM1) for HER2 positive advanced breast cancer: A single institution experience.
Okines, A; Irfan, T; Khabra, K; Smith, I; O'Brien, M; Parton, M; Noble, J; Stanway, S; Somaiah, N; Ring, A; Johnston, S; Turner, N (2018-05)Ado-trastuzumab emtansine (T-DM1) is an antibody-drug conjugate that does not cross an intact blood-brain barrier. In the EMILIA trial of T-DM1 vs capecitabine/lapatinib for HER2 positive advanced breast cancer, all patients ... -
Development of molecularly targeted agents and immunotherapies in small cell lung cancer.
Sharp, A; Bhosle, J; Abdelraouf, F; Popat, S; O'Brien, M; Yap, TA (2016-06)Small cell lung cancer (SCLC) is a smoking-induced malignancy with multiple toxin-associated mutations, which accounts for 15% of all lung cancers. It remains a clinical challenge with a rapid doubling time, early dissemination ... -
Differences in Signaling Patterns on PI3K Inhibition Reveal Context Specificity in <i>KRAS</i>-Mutant Cancers.
Stewart, A; Coker, EA; Pölsterl, S; Georgiou, A; Minchom, AR; Carreira, S; Cunningham, D; O'Brien, ME; Raynaud, FI; de Bono, JS; Al-Lazikani, B; Banerji, U (2019-08)It is increasingly appreciated that drug response to different cancers driven by the same oncogene is different and may relate to differences in rewiring of signal transduction. We aimed to study differences in dynamic ... -
Efficient Genotyping of KRAS Mutant Non-Small Cell Lung Cancer Using a Multiplexed Droplet Digital PCR Approach.
Pender, A; Garcia-Murillas, I; Rana, S; Cutts, RJ; Kelly, G; Fenwick, K; Kozarewa, I; Gonzalez de Castro, D; Bhosle, J; O'Brien, M; Turner, NC; Popat, S; Downward, J (2015-01)Droplet digital PCR (ddPCR) can be used to detect low frequency mutations in oncogene-driven lung cancer. The range of KRAS point mutations observed in NSCLC necessitates a multiplex approach to efficient mutation detection ... -
Evaluation of diffusion-weighted MRI and (18F) fluorothymidine-PET biomarkers for early response assessment in patients with operable non-small cell lung cancer treated with neoadjuvant chemotherapy.
Carlin, D; Weller, A; Kramer, G; Liu, Y; Waterton, JC; Chiti, A; Sollini, M; Joop de Langen, A; O'Brien, MER; Urbanowicz, M; Jacobs, BK; deSouza, NObjective:To correlate changes in the apparent diffusion coefficient (ADC) from diffusion-weighted (DW)-MRI and standardised uptake value (SUV) from fluorothymidine (18FLT)-PET/CT with histopathological estimates of response ... -
Health-related quality-of-life results for pembrolizumab versus chemotherapy in advanced, PD-L1-positive NSCLC (KEYNOTE-024): a multicentre, international, randomised, open-label phase 3 trial.
Brahmer, JR; Rodríguez-Abreu, D; Robinson, AG; Hui, R; Csőszi, T; Fülöp, A; Gottfried, M; Peled, N; Tafreshi, A; Cuffe, S; O'Brien, M; Rao, S; Hotta, K; Zhang, J; Lubiniecki, GM; Deitz, AC; Rangwala, R; Reck, M (2017-12)<h4>Background</h4>In the phase 3 KEYNOTE-024 trial, treatment with pembrolizumab conferred longer progression-free survival than did platinum-based therapy in patients with treatment-naive, advanced non-small-cell lung ... -
An investigation of the prevalence of swallowing difficulties and impact on quality of life in patients with advanced lung cancer.
Brady, GC; Roe, JWG; O' Brien, M; Boaz, A; Shaw, C (2018-02)<h4>Background</h4>Dysphagia can occur in advanced lung cancer due to direct tumour invasion or nerve compression. Anti-cancer treatments and co-morbid conditions may also cause or compound dysphagic symptoms. Speech and ... -
Looking back and to the future: Are we improving 'cure' in non-small cell lung cancer?
Walder, D; O'Brien, M (2017-04)In surgical series, cancer-free survival at 5 years is often referred to as a cure. In recent years, attempts to improve cure rates in non-small cell lung cancer (NSCLC) have focussed on earlier diagnosis through cost-effective ... -
Mechanism and non-mechanism based imaging biomarkers for assessing biological response to treatment in non-small cell lung cancer.
Weller, A; O'Brien, MER; Ahmed, M; Popat, S; Bhosle, J; McDonald, F; Yap, TA; Du, Y; Vlahos, I; deSouza, NM (2016-05)Therapeutic options in locally advanced non-small cell lung cancer (NSCLC) have expanded in the past decade to include a palate of targeted interventions such as high dose targeted thermal ablations, radiotherapy and growing ... -
Molecular Adequacy of Image-Guided Rebiopsies for Molecular Retesting in Advanced Non-Small Cell Lung Cancer: A Single-Center Experience.
Tokaca, N; Barth, S; O'Brien, M; Bhosle, J; Fotiadis, N; Wotherspoon, A; Thompson, L; Popat, S (2018-01)<h4>Introduction</h4>In the era of biomarker-driven systemic therapy for advanced NSCLC, the role of routine repeated biopsies for decision making outside EGFR-mutant disease remains unproven. We report our center's ... -
Molecular and immunological features of a prolonged exceptional responder with malignant pleural mesothelioma treated initially and rechallenged with pembrolizumab.
Minchom, A; Yuan, W; Crespo, M; Gurel, B; Figueiredo, I; Wotherspoon, A; Miranda, S; Riisnaes, R; Ferreira, A; Bertan, C; Pereira, R; Clarke, M; Baker, C; Ang, JE; Fotiadis, N; Tunariu, N; Carreira, S; Popat, S; O'Brien, M; Banerji, U; de Bono, J; Lopez, J (2020-03)<h4>Background</h4>This case represents an exceptional response to pembrolizumab in a patient with epithelioid mesothelioma with a further response on rechallenge.<h4>Case presentation</h4>A 77-year-old woman with advanced ... -
Phase I clinical trials in patients with advanced non-small cell lung cancer treated within a Drug Development Unit: What have we learnt?
Capelan, M; Roda, D; Geuna, E; Rihawi, K; Bodla, S; Kaye, SB; Bhosle, J; Banerji, U; O'Brien, M; de Bono, JS; Popat, S; Yap, TA (2017-09)<h4>Objectives</h4>Despite advances in novel drug development for patients with advanced non-small cell lung cancer (NSCLC), there are still only a limited number of approved treatments. We therefore evaluated the clinical ... -
A phase I study to assess afatinib in combination with carboplatin or with carboplatin plus paclitaxel in patients with advanced solid tumors.
O'Brien, MER; Sarker, D; Bhosle, J; Thillai, K; Yap, TA; Uttenreuther-Fischer, M; Pemberton, K; Jin, X; Wiebe, S; de Bono, J; Spicer, J (2018-11)<h4>Purpose</h4>Afatinib, an irreversible ErbB family blocker, has demonstrated preclinical antitumor activity with chemotherapy.<h4>Methods</h4>As part of a phase I trial in patients with advanced solid tumors (NCT00809133; ... -
A prospective observational study of on-treatment plasma homocysteine levels as a biomarker of toxicity, depression and vitamin supplementation lead-in time pre pemetrexed, in patients with non-small cell lung cancer and malignant mesothelioma.
Minchom, A; Mak, D; Gunapala, R; Walder, D; Kumar, R; Yousaf, N; Hodgkiss, A; Bhosle, J; Popat, S; O'Brien, MER<h4>Objectives</h4>Vitamin supplementation reduces pemetrexed toxicity. Raised plasma homocysteine reflects deficiency in vitamin B12 and folate, and is suppressed by supplementation. This observational study of 112 patients ... -
Radiological evaluation of malignant pleural mesothelioma - defining distant metastatic disease.
Collins, DC; Sundar, R; Constantidinou, A; Dolling, D; Yap, TA; Popat, S; O'Brien, ME; Banerji, U; de Bono, JS; Lopez, JS; Tunariu, N; Minchom, A (2020-12-09)<h4>Background</h4>Malignant pleural mesothelioma (MPM) is traditionally characterized by local destructive spread of the pleura and surrounding tissues. Patient outcomes in MPM with distant metastatic dissemination are ... -
A randomised assessment of the use of a quality of life questionnaire with or without intervention in patients attending a thoracic cancer clinic.
Nimako, K; Ayite, B; Priest, K; Severn, J; Fries, HM; Gunapala, R; Bhosle, J; Popat, S; O'Brien, M (2017-07)The study examined the impact of using a quality of life (QoL) questionnaire during a clinic to identify QoL issues and to improve QoL. 138 patients were randomised (1:1:1) to either (1) an Intervention group that completed ...