Shane White

ORCID: 0009-0003-6030-2801
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Cancer Treatment and Pharmacology
  • HER2/EGFR in Cancer Research
  • Lung Cancer Treatments and Mutations
  • Immunotherapy and Immune Responses
  • Cancer Immunotherapy and Biomarkers
  • Lung Cancer Research Studies
  • Colorectal Cancer Treatments and Studies
  • Advanced Breast Cancer Therapies
  • Neuroendocrine Tumor Research Advances
  • SARS-CoV-2 and COVID-19 Research
  • Glycosylation and Glycoproteins Research
  • Breast Cancer Treatment Studies
  • Estrogen and related hormone effects
  • Cancer Genomics and Diagnostics
  • COVID-19 Clinical Research Studies
  • Long-Term Effects of COVID-19
  • Lung Cancer Diagnosis and Treatment
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Monoclonal and Polyclonal Antibodies Research
  • Prostate Cancer Treatment and Research
  • Cancer therapeutics and mechanisms
  • Global Cancer Incidence and Screening
  • Cancer Risks and Factors
  • Cancer Research and Treatments
  • Vaccine Coverage and Hesitancy

Olivia Newton-John Cancer Wellness & Research Centre
2013-2024

Austin Health
2009-2024

Austin Hospital
2006-2024

The University of Melbourne
2009-2024

Cedars-Sinai Medical Center
2022-2023

Footscray Hospital
2019-2023

Northern Health
2012-2017

St Vincent's Hospital
2016

Northern Hospital
1984-2016

The University of Notre Dame Australia
2016

Abstract Purpose: Tumor antigen-loaded dendritic cells show promise for cancer immunotherapy. This phase I study evaluated immunization with autologous pulsed mannan-MUC1 fusion protein (MFP) to treat patients advanced malignancy. Experimental Design: Eligible had adenocarcinoma expressing MUC1, were of performance status 0 1, no autoimmune disease. Patients underwent leukapheresis generate by culture ex vivo granulocyte macrophage colony-stimulating factor and interleukin 4 5 days....

10.1158/1078-0432.ccr-05-1574 article EN Clinical Cancer Research 2006-02-01
Marco Colleoni Weixiu Luo Per Karlsson Jacquie Chirgwin Stefan Aebi and 95 more Guy Jérusalem Patrick Neven Erika Hitre Marie-Pascale Graas Edda Simoncini Claus Kamby Alastair M. Thompson Sibylle Loibl Joaquín Gavilá Katsumasa Kuroi Christian Marth Bettina Müller Séamus O’Reilly Vincenzo Di Lauro Andrea Gombos Thomas Ruhstaller Harold J. Burstein Karin Ribi Jürg Bernhard Giuseppe Viale Rudolf Maibach Manuela Rabaglio Richard D. Gelber Alan S. Coates Angelo Di Leo Meredith M. Regan Aron Goldhirsch A. Vandebroek Martine Berlière C. Mitine Peter Vuylsteke Marleen Borms Randal D’hondt Philippe Glorieux Jeroen Mebis Didier Verhoeven Michael Coibion Frédéric Forget Lionel Duck Didier Verhoeven Wim Wyendaele Annelore Barbeaux Jean-Paul Salmon Patrick Berteloot Joanna Vermeij Vincent R. Richard Saverio Cinieri Lorenzo Gianni Mario Clerico Graziella Pinotti Antônio Bernardo Laura Biganzoli Alessandra Gennari Claudio Graiff Dino Amadori Rodolfo Passalacqua John Forbes Prudence A. Francis Serene S. Foo Frances Boyle Andrew Redfern André van der Westhuizen Craig Lewis Sharad Sharma Philip Beale Ian Byard Stephen Begbie Frank Sardelic Ehtesham Abdi D.D. Clark Aaron Chindewere Stephen Della‐Fiorentina Ray Asghari Mohammed Islam Lee Na Teo Shane White Linda Gilbert Katherine Gardner Catarina Uhlmann Daniel Rauch Meinrad Mannhart Katharina Buser Konstantin J. Dedes Andreas Mueller Christoph Rageth Stephanie von Orelli Hans Joerg Senn Olivia Pagani A Pedrazzini Christoph Rochlitz Alexandre Bodmer Sandro Anchisi Khalil Zaman Roger von Moos Daniel Betticher

10.1016/s1470-2045(17)30715-5 article EN The Lancet Oncology 2017-11-17

Abstract Purpose: To evaluate a triplet regimen combining immune checkpoint blockade, AKT pathway inhibition, and (nab-) paclitaxel as first-line therapy for locally advanced/metastatic triple-negative breast cancer (mTNBC). Patients Methods: The single-arm CO40151 phase Ib study (NCT03800836), the signal-seeking cohort of IPATunity130 (NCT03337724), randomized III IPATunity170 trial (NCT04177108) enrolled patients with previously untreated mTNBC. Triplet comprised intravenous atezolizumab...

10.1158/1078-0432.ccr-23-2084 article EN cc-by-nc-nd Clinical Cancer Research 2023-12-07

Intravaginal testosterone (IVT) is a potential treatment of vulvovaginal atrophy (VVA) associated with aromatase inhibitor (AI) use.To investigate the effects IVT on sexual satisfaction, vaginal symptoms, and urinary incontinence (UI) AI use.Double-blind, randomized, placebo-controlled trial.Academic clinical research center.Postmenopausal women taking an VVA symptoms.IVT cream (300 μg per dose) or identical placebo, self-administered daily for 2 weeks then thrice weekly 24 weeks.The primary...

10.1210/jc.2018-01345 article EN The Journal of Clinical Endocrinology & Metabolism 2018-09-14

Abstract Purpose: Recent randomized trials in advanced TNBC have demonstrated improved efficacy with the addition of atezo to 1L nab-PAC patients (pts) PD-L1+ tumors (IMpassion130 [Schmid 2018]), and oral AKT inhibitor IPAT PAC, particularly pts PIK3CA/AKT1/PTEN-altered (LOTUS [Kim 2017]). Loss PTEN, a negative regulator AKT, has emerged as potential mechanism for resistance checkpoint therapy; inhibiting PI3K/AKT pathway led reversal T-cell-mediated immunotherapy [Peng 2016]. We report...

10.1158/1538-7445.am2019-ct049 article EN Cancer Research 2019-07-01

Background Cancer-Testis Antigens (CTAs) are immunogenic proteins that poor prognostic markers in non-small cell lung cancer (NSCLC). We investigated expression of CTAs NSCLC and their association with response to chemotherapy, genetic mutations survival. Methods studied 199 patients pathological N2 treated neoadjuvant chemotherapy (NAC; n = 94), post-operative observation (n 49), adjuvant 47) or unknown 9). Immunohistochemistry for NY-ESO-1, MAGE-A MAGE-C1 was performed. Clinicopathological...

10.1371/journal.pone.0067876 article EN cc-by PLoS ONE 2013-07-23

Abstract Context Menopause is associated with changes in musculoskeletal, body composition, and metabolic parameters that may be amplified premenopausal women receiving estradiol suppression for breast cancer. Denosumab offsets deleterious skeletal effects of has been reported to have on composition preclinical observational studies, but evidence from double-blind randomized controlled trials limited. Objective To assess the effect denosumab parameters. Methods In a prespecified secondary...

10.1210/clinem/dgae003 article EN cc-by The Journal of Clinical Endocrinology & Metabolism 2024-01-04

<h3>Background</h3> Mucin 1 antigen, highly expressed by epithelial ovarian cancer (EOC), is a potential target for immunotherapy. A previous successful phase trial was conducted in patients with adenocarcinoma who were injected Cvac, autologous monocyte-derived dendritic cells (DCs) incubated mannosylated mucin protein (M-FP). The present study 2 of Cvac advanced EOC. <h3>Methods</h3> Eligible had EOC progressive disease, defined as an increase CA125 ≥ 25% 1&nbsp;month. primary endpoint...

10.1186/2051-1426-2-16 article EN cc-by Journal for ImmunoTherapy of Cancer 2014-06-18

Summary Background We investigated whether metformin prevents tamoxifen‐induced endometrial changes and insulin resistance ( IR ) after a diagnosis of breast cancer. Methods This was single‐centre, randomized, double‐blind, placebo‐controlled, parallel group trial. Postmenopausal women with hormone receptor‐positive cancer taking tamoxifen were randomly allocated to 850 mg or identical placebo, twice daily, for 52 weeks. Outcome measures included double thickness ET measured by transvaginal...

10.1111/cen.13830 article EN Clinical Endocrinology 2018-08-14

PURPOSE Suppression of ovarian function and aromatase inhibition (AI) increases disease-free survival in premenopausal women with estrogen receptor (ER)–positive early-stage breast cancer but accelerates bone loss. We therefore hypothesized that suppressing remodeling using denosumab (DMAB) would prevent loss these women. METHODS In a 12-month double-blind randomized trial, 68 ER-positive commencing suppression AI were randomly assigned to 60 mg DMAB (n = 34) or placebo (PBO; n once every 6...

10.1200/jco.23.02309 article EN Journal of Clinical Oncology 2024-07-02

BACKGROUND Information on the effect of chemotherapy in a group patients with poor prognosis, performance status small cell lung carcinoma (SCLC) is scarce. A randomized study comparing single-agent carboplatin combination this largely unreported population SCLC was undertaken. METHODS One hundred nineteen were allocated to four cycles either cyclophosphamide, doxorubicin, and vincristine (CAV) or carboplatin. Patients had Karnofsky score ≤ 50 and/or prognostic indicative 1-year survival...

10.1002/1097-0142(20010801)92:3<601::aid-cncr1360>3.0.co;2-k article EN Cancer 2001-01-01

Abstract Concurrent chemoradiotherapy ( CCRT ) has become the standard of care for patients with unresectable stage III non–small cell lung cancer NSCLC ). The comparative merits two widely used regimens: carboplatin/paclitaxel PC and cisplatin/etoposide PE ), each concurrent radiotherapy, remain largely undefined. Records consecutive treated or ≥60 Gy chest radiotherapy between 2000 2011 were reviewed outcomes toxicity. Survival was estimated using Kaplan–Meier method Cox modeling Wald...

10.1002/cam4.142 article EN cc-by Cancer Medicine 2013-10-16

8514 Background: Early phase trials of anti-programmed death 1 (PD-1) antibodies have demonstrated important responses in malignant mesothelioma (MM). Expression the ligand, PD-L1, is a potential biomarker for PD-1 directed therapy use and expressed significant proportion MM. We present results cohort treated with inhibitory assessed PD-L1 expression. Methods: Patients (pts) unresectable pleural or peritoneal mm anti-PD-1 were included. Data was collected retrospectively. Radiological...

10.1200/jco.2017.35.15_suppl.8514 article EN Journal of Clinical Oncology 2017-05-20

Abstract Background The safety of a third dose SARS-CoV-2 mRNA vaccination in patients with inflammatory bowel disease is unknown. Methods We compared symptoms following vaccine after the second IBD. Results study group included 594 (70% female, 58% BNT162b2). Overall, 41% reported dose. Symptom frequency and severity were lower relative to for every organ system, except gastrointestinal which marginally worse. Conclusion are generally similar or milder than most systems.

10.1093/ibd/izac174 article EN Inflammatory Bowel Diseases 2022-08-23

Aim The potential beneficial interaction between erlotinib and chemotherapy may require sequencing or pharmacodynamic separation. aim of this study was to evaluate the efficacy tolerance sequential gemcitabine versus monotherapy as first-line therapy in elderly ECOG PS-2 patients with advanced non-small cell lung carcinoma. Methods primary objective multicenter randomized Phase II progression-free survival (PFS). Secondary objectives were overall response rate (ORR), disease control rate,...

10.1111/ajco.12178 article EN Asia-Pacific Journal of Clinical Oncology 2014-02-27

This study determined the efficacy and safety of a modified FOLFOX regimen that improved patient convenience without compromising oxaliplatin dose intensity. A total 62 patients with previously untreated metastatic colorectal cancer were enrolled to receive, entirely as outpatients, 2-weekly cycles 100 mg m−2 i.v. over 2 h, together leucovorin 400 5-fluorouracil (5-FU) m−2, bolus, followed by 46-h infusion 5-FU at 2.4 g m−2. Treatment was given until progression or unmanageable toxicity. In...

10.1038/sj.bjc.6602426 article EN cc-by-nc-sa British Journal of Cancer 2005-03-01
Coming Soon ...