Nick Pavlakis

ORCID: 0000-0002-1738-0316
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About
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Research Areas
  • Lung Cancer Treatments and Mutations
  • Pancreatic and Hepatic Oncology Research
  • Colorectal Cancer Treatments and Studies
  • Neuroendocrine Tumor Research Advances
  • Lung Cancer Research Studies
  • Cancer Genomics and Diagnostics
  • Gastric Cancer Management and Outcomes
  • Cancer Immunotherapy and Biomarkers
  • Occupational and environmental lung diseases
  • Neuroblastoma Research and Treatments
  • Cancer Treatment and Pharmacology
  • Lung Cancer Diagnosis and Treatment
  • Pleural and Pulmonary Diseases
  • Cancer Research and Treatments
  • Renal cell carcinoma treatment
  • Genetic factors in colorectal cancer
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Metastasis and carcinoma case studies
  • Fibroblast Growth Factor Research
  • Radiopharmaceutical Chemistry and Applications
  • Cancer, Hypoxia, and Metabolism
  • Medical Imaging Techniques and Applications
  • Pancreatitis Pathology and Treatment
  • Medical Imaging and Pathology Studies
  • Gastrointestinal Tumor Research and Treatment

Royal North Shore Hospital
2016-2025

The University of Sydney
2016-2025

Northern Sydney Local Health District
2016-2024

Westmead Hospital
2024

St. Leonards Hospital
2024

Sydney Local Health District
2024

Northern Cancer Institute
2015-2023

North Shore Hospital
2010-2022

Hudson Institute
2021-2022

Genesis HealthCare
2022

Purpose Human epidermal growth factor receptor 2 ( HER2, ERBB2)-activating mutations occur in 2% of lung cancers. We assessed the activity ado-trastuzumab emtansine, a HER2-targeted antibody-drug conjugate, cohort patients with HER2-mutant cancers as part phase II basket trial. Patients and Methods received emtansine at 3.6 mg/kg intravenously every 3 weeks until progression. The primary end point was overall response rate using Response Evaluation Criteria Solid Tumors (RECIST) version 1.1....

10.1200/jco.2018.77.9777 article EN Journal of Clinical Oncology 2018-07-10

Asbestos-induced chronic inflammation is implicated in the pathogenesis of malignant mesothelioma (MM). We have investigated blood neutrophil-to-lymphocyte ratio (NLR), an index systemic inflammation, as a prognostic factor MM patients.Patients with who had therapy at participating institutes were studied. Potential factors such age, gender, performance status, histologic subtype, and baseline laboratory parameters, including NLR, analyzed. Overall survival from commencement was determined...

10.1158/1078-0432.ccr-10-2245 article EN Clinical Cancer Research 2010-10-19

The study aims to investigate the prognostic value of lymphocyte-to-monocyte ratio (LMR) in patients with colorectal cancer (CRC) undergoing curative resection and compare it established biomarkers including neutrophil-to-lymphocyte (NLR), platelet-to-lymphocyte (PLR), modified Glasgow score (mGPS), combined BRAF-mismatch repair (MMR) status.The significance systemic inflammatory markers CRC such as NLR, PLR, mGPS has been well defined. Commonly used genetic BRAF-MMR status have also found...

10.1097/sla.0000000000001743 article EN Annals of Surgery 2016-04-19

Abstract Accurately identifying patients with high-grade serous ovarian carcinoma (HGSOC) who respond to poly(ADP-ribose) polymerase inhibitor (PARPi) therapy is of great clinical importance. Here we show that quantitative BRCA1 methylation analysis provides new insight into PARPi response in preclinical models and cancer patients. The 12 HGSOC patient-derived xenografts (PDX) the rucaparib was assessed, variable dose-dependent responses observed chemo-naive BRCA1/2 -mutated PDX, no PDX...

10.1038/s41467-018-05564-z article EN cc-by Nature Communications 2018-09-24

Background: PET scans using FDG and somatostatin receptor imaging agents have both been used to study neuroendocrine tumours.Most reports documented the sensitivity specificity of each radiopharmaceutical independently, even suggested superiority one over other for different grades disease.Aim: The aim this work was develop a grading scheme that describes joint results in staging subjects with tumours single combined parameter.The has developed is referred as NETPET grade.Methods: This...

10.7150/thno.18068 article EN cc-by Theranostics 2017-01-01

Personalized medicine strategies using genomic profiling are particularly pertinent for pancreas cancer. The Individualized Molecular Pancreatic Cancer Therapy (IMPaCT) trial was initially designed to exploit results from genome sequencing of pancreatic cancer under the auspices International Genome Consortium (ICGC) in Australia. Sequencing revealed small subsets patients with aberrations their tumor that could be targeted currently available therapies.

10.1158/1078-0432.ccr-15-0426 article EN Clinical Cancer Research 2015-04-21

Purpose We evaluated the activity of regorafenib, an oral multikinase inhibitor, in advanced gastric adenocarcinoma. Patients and Methods conducted international (Australia New Zealand, South Korea, Canada) randomized phase II trial which patients were randomly assigned at a two-to-one ratio stratified by lines prior chemotherapy for disease (one v two) region. Eligible received best supportive care plus regorafenib 160 mg or matching placebo orally on days 1 to 21 each 28-day cycle until...

10.1200/jco.2015.65.1901 article EN Journal of Clinical Oncology 2016-06-21
Margaret A. Tempero Uwe Pelzer Eileen M. O’Reilly Jordan M. Winter Do‐Youn Oh and 95 more Chung‐Pin Li Giampaolo Tortora Heung-Moon Chang Charles D. Lopez Tanios Bekaii‐Saab Andrew H. Ko Armando Santoro Joon Oh Park Marcus Smith Noel Giovanni Luca Frassineti Yan‐Shen Shan Andrew Dean Hanno Riess Eric Van Cutsem Jordan Berlin Philip Philip Malcolm J. Moore David Goldstein Josep Tabernero Mingyu Li Stefano Ferrara Yvan Le Bruchec George Zhang Brian Lu Andrew V. Biankin Michele Reni Richard A. Epstein Paul L. Vasey Jeremy Shapiro Matthew Burge Yu Jo Chua Marion Harris Nick Pavlakis Niall C. Tebbutt Gerald W. Prager Christian Dittrich Alois Lang Kathrin Philipp‐Abbrederis Richard Greil Herbert Stöger Michael Girschikofsky Thomas Kuehr Jean–Luc Van Laethem Stéphanie Laurent Neesha C. Dhani Yoo Joung Ko Scot Dowden Petr Kavan Mustapha Édouard Tehfe Eugen Kubala Milan Kohoutek Per Pfeiffer Mette Yilmaz Vibeke Parner Tapio Salminen Leena‐Maija Soveri Eija Korkeila Pia Österlund Julien Taı̈eb David Tougeron Pascal Artru François‐Xavier Caroli‐Bosc Rosine Guimbaud Anthony Turpin Thomas Walter Jean‐Baptiste Bachet Volker Kunzmann Florian Kreth Andreas De Block Marino Venerito Helmut Oettle Meinolf Karthaus Jörg Trojan Gunnar Folprecht Markus M. Lerch Frank Kullmann Marcel Reiser Volker Heinemann Marcus‐Alexander Wörns H. Schulz Benjamin Garlipp Thomas Yau Lam Stephen Chan Balázs Juhász László Landherr Tamàs Pintér G. Bodoky Zsuzsanna Kahán Ray McDermott Derek G. Power Luca Gianni Salvatore Siena Michèle Milella Alfredo Falcone Rossana Berardi

This randomized, open-label trial compared the efficacy and safety of adjuvant

10.1200/jco.22.01134 article EN cc-by-nc-nd Journal of Clinical Oncology 2022-12-15
Jessica L. Chitty Michelle Yam Lara Perryman Amelia L. Parker Joanna N. Skhinas and 95 more Yordanos F. Setargew Ellie T. Y. Mok Emmi Tran Rhiannon D. Grant Sharissa L. Latham Brooke A. Pereira Shona Ritchie Kendelle J. Murphy Michael Trpceski Alison D. Findlay Pauline Mélénec Elysse C. Filipe Audrey Nadalini Sipiththa Velayuthar Gretel Major Kaitlin Wyllie Michael Papanicolaou Shivanjali Ratnaseelan Phoebe A. Phillips George Sharbeen Janet Youkhana Alice G. Russo Antonia Blackwell Jordan F. Hastings Morghan C. Lucas Cecilia R. Chambers Daniel A. Reed Janett Stoehr Claire Vennin Ruth Pidsley Anaiis Zaratzian Andrew M. Da Silva Michael Tayao Brett Charlton David Herrmann Max Nobis Susan J. Clark Andrew V. Biankin Amber L. Johns David R. Croucher Adnan Nagrial Anthony J. Gill Sean M. Grimmond Lorraine A. Chantrill Angela Chou Tanya Dwarte Xanthe L. Metcalf Gloria Jeong Lara Kenyon Nicola Waddell John V. Pearson Ann-Marie Patch Kátia Nones Felicity Newell Pamela Mukhopadhyay Venkateswar Addala Stephen H. Kazakoff Oliver Holmes Conrad Leonard Scott Wood Oliver Hofmann Jaswinder S. Samra Nick Pavlakis Jennifer Arena Hilda High Ray Asghari Neil D. Merrett Amitabha Das Peter H. Cosman Kasim Ismail Alina Stoita David B. Williams Allan Spigellman Duncan McLeo Judy Kirk James G. Kench Peter Grimison Charbel Sandroussi Annabel Goodwin R. Scott Mead Katherine L. Tucker Lesley Andrews Michael Texler Cindy Forrest Mo Ballal David Fletcher Maria Beilin Kynan Feeney Krishna Epari Sanjay Mukhedkar Nikolajs Zeps Nan Q. Nguyen Andrew Ruszkiewicz Chris Worthley John Chen

Abstract The lysyl oxidase family represents a promising target in stromal targeting of solid tumors due to the importance this crosslinking and stabilizing fibrillar collagens its known role tumor desmoplasia. Using small-molecule drug-design approaches, we generated validated PXS-5505, first-in-class highly selective potent pan-lysyl inhibitor. We demonstrate vitro vivo that inhibition decreases chemotherapy-induced pancreatic desmoplasia stiffness, reduces cancer cell invasion metastasis,...

10.1038/s43018-023-00614-y article EN cc-by Nature Cancer 2023-08-28

PURPOSE Although checkpoint inhibitors have improved first-line treatment for non–small cell lung cancer (NSCLC), a therapeutic need remains patients whose disease does not respond or who experience progression after anti–PD-L1/PD-1 immunotherapy. CONTACT-01 (ClinicalTrials.gov identifier: NCT04471428 ) evaluated atezolizumab plus cabozantinib versus docetaxel in with metastatic NSCLC developed concurrent sequential and platinum-containing chemotherapy. METHODS This multicenter, open-label,...

10.1200/jco.23.02166 article EN cc-by-nc-nd Journal of Clinical Oncology 2024-03-29

Mobocertinib is an oral epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor that targets EGFR exon 20 insertion (ex20ins) mutations in non-small cell lung cancer (NSCLC). This open-label, phase III trial (EXCLAIM-2: ClinicalTrials.gov identifier: NCT04129502) compared mobocertinib versus platinum-based chemotherapy as first-line treatment of ex20ins+ advanced/metastatic NSCLC. Patients with treatment-naive locally NSCLC were randomly assigned 1:1 to 160 mg once daily or...

10.1200/jco-24-01269 article EN Journal of Clinical Oncology 2025-01-29

BackgroundSubstantial numbers of cancer patients use complementary medicine therapies, even without a supportive evidence base. This study aimed to evaluate in randomized controlled trial, the Medical Qigong (MQ) compared with usual care improve quality life (QOL) patients.Patients and methodsOne hundred sixty-two range cancers were recruited. QOL fatigue measured by Functional Assessment Cancer Therapy—General Therapy—Fatigue, respectively, mood status Profile Mood State. The inflammatory...

10.1093/annonc/mdp479 article EN cc-by-nc Annals of Oncology 2009-10-31

BACKGROUND Pulmonary toxicity reported with gemcitabine is usually mild and self-limiting. The authors report a series of three patients who had life-threatening pulmonary after receiving gemcitabine. METHODS presented to two major teaching hospitals significant dysfunction while Case data were obtained from patient records. A review the literature was done seek reports cytosine arabinoside (ara-C). RESULTS common features respiratory illnesses in this study tachypnea, marked hypoxemia, an...

10.1002/(sici)1097-0142(19970715)80:2<286::aid-cncr17>3.0.co;2-q article EN Cancer 1997-07-15
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