Christoph Rochlitz

ORCID: 0000-0001-7808-2497
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About
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Research Areas
  • Cancer Genomics and Diagnostics
  • Cancer Treatment and Pharmacology
  • DNA Repair Mechanisms
  • Lung Cancer Treatments and Mutations
  • Breast Cancer Treatment Studies
  • HER2/EGFR in Cancer Research
  • Cancer Cells and Metastasis
  • Angiogenesis and VEGF in Cancer
  • Advanced Breast Cancer Therapies
  • Virus-based gene therapy research
  • Genetic factors in colorectal cancer
  • Monoclonal and Polyclonal Antibodies Research
  • Pancreatic and Hepatic Oncology Research
  • Bone health and treatments
  • Cancer-related Molecular Pathways
  • Colorectal Cancer Treatments and Studies
  • Immunotherapy and Immune Responses
  • Cancer Research and Treatments
  • CAR-T cell therapy research
  • Lung Cancer Research Studies
  • Neuroblastoma Research and Treatments
  • Cancer, Hypoxia, and Metabolism
  • Neuroendocrine Tumor Research Advances
  • Nanoparticle-Based Drug Delivery
  • Oral and Maxillofacial Pathology

University Hospital of Basel
2015-2025

University of Basel
2006-2023

Swiss Group For Clinical Cancer Research
2003-2023

Breast Center
2015

Stiftung Tumorforschung Kopf-Hals
2013

McMaster University
2011-2012

University of California, Los Angeles
2012

Hospital Base
2007-2010

University Hospital of Bern
2007-2009

Kantonsspital Aarau
2009

The ability of circulating tumor cells (CTCs) to form clusters has been linked increased metastatic potential. Yet biological features and vulnerabilities CTC remain largely unknown. Here, we profile the DNA methylation landscape single CTCs from breast cancer patients mouse models on a genome-wide scale. We find that binding sites for stemness- proliferation-associated transcription factors are specifically hypomethylated in clusters, including OCT4, NANOG, SOX2, SIN3A, paralleling...

10.1016/j.cell.2018.11.046 article EN cc-by-nc-nd Cell 2019-01-01

To investigate response, survival, and safety profile of the somatostatin-based radiopeptide (90)yttrium-labeled tetraazacyclododecane-tetraacetic acid modified Tyr-octreotide ([(90)Y-DOTA]-TOC) in neuroendocrine cancers.In a clinical phase II single-center open-label trial, patients with cancers were treated repeated cycles [(90)Y-DOTA]-TOC. Each cycle consisted single intravenous injection 3.7GBq/m(2) body-surface Additional withheld case tumor progression and/or permanent...

10.1200/jco.2010.33.7873 article EN Journal of Clinical Oncology 2011-05-10

Abstract Background Insulin-like growth factor-1 (IGF-I) signalling is important for cancer initiation and progression. Given the emerging evidence role of stroma in these processes, we aimed to characterize effects IGF-I on cells stromal separately. Methods We used an ex vivo culture model measured gene expression changes after stimulation with cDNA microarrays. In vitro data were correlated findings by comparing results published datasets human biopsies. Results Upon IGF-I, breast...

10.1186/1741-7015-8-1 article EN cc-by BMC Medicine 2010-01-05

Circulating tumor cells (CTCs) are shed from solid cancers in the form of single or clustered cells, and latter display an extraordinary ability to initiate metastasis. Yet, biological phenomena that trigger shedding CTC clusters a primary cancerous lesion poorly understood. Here, when dynamically labeling breast cancer along progression, we observe majority undergoing hypoxia, while CTCs largely normoxic. Strikingly, find vascular endothelial growth factor (VEGF) targeting leads shrinkage,...

10.1016/j.celrep.2020.108105 article EN cc-by-nc-nd Cell Reports 2020-09-01

Abstract The presence of circulating tumor cell (CTC) clusters is associated with disease progression and reduced survival in a variety cancer types. In breast cancer, preclinical studies showed that inhibitors the Na + /K ATPase suppress CTC block metastasis. Here we conducted prospective, open-label, proof-of-concept study women metastatic where primary objective was to determine whether treatment inhibitor digoxin could reduce mean cluster size. An analysis nine patients treated daily...

10.1038/s41591-024-03486-6 article EN cc-by Nature Medicine 2025-01-24

PURPOSE: To study the additional benefit from adenoviral p53 gene therapy in patients undergoing first-line chemotherapy for advanced non–small-cell lung cancer (NSCLC). PATIENTS AND METHODS: Twenty-five with nonresectable NSCLC were enrolled an open-label, multicenter phase II of three cycles regimen A, carboplatin (area under curve, 6; day 1) plus paclitaxel (175 mg/m 2 , 1), or B, cisplatin (100 vinorelbine (25 days 1, 8, 15, and 22) combination intratumoral injection 7.5 × 10 12...

10.1200/jco.2001.19.6.1750 article EN Journal of Clinical Oncology 2001-03-15

Radiopeptide therapy is commonly performed with a single radioisotope. We aimed to compare the effectiveness of somatostatin-based radiopeptide versus combination radioisotopes.In cohort study, patients metastasized neuroendocrine cancer were treated repeated cycles (90)yttrium-labeled tetraazacyclododecane-tetraacetic acid modified Tyr-octreotide ([(90)Y-DOTA]-TOC) or alternating between [(90)Y-DOTA]-TOC and (177)lutetium-labeled DOTA-TOC ([(177)Lu-DOTA]-TOC) until tumor progression...

10.1200/jco.2011.37.2151 article EN Journal of Clinical Oncology 2012-03-06

We aimed to explore the efficacy of (90)Yttrium-1,4,7,10-tetra-azacyclododecane N,N',N'',N-'''-tetraacetic acid ((90)Y-DOTA)-Tyr(3)-octreotide (TOC) therapy in advanced medullary thyroid cancer.In a phase II trial, we investigated response, survival, and long-term safety profile systemic [(90)Y-DOTA]-TOC treatment metastasized cancer. Adverse events were assessed according criteria National Cancer Institute. Survival analyses done using multiple regression models.Thirty-one patients...

10.1158/1078-0432.ccr-07-0935 article EN Clinical Cancer Research 2007-11-15
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

Purpose Luminal breast cancer has a long natural history, with recurrences continuing beyond 10 years after diagnosis. We analyzed long-term follow-up (LTFU) of efficacy outcomes and adverse events in the Breast International Group (BIG) 1-98 study reported median 12.6 years. Patients Methods BIG is four-arm, phase III, double-blind, randomized trial comparing adjuvant letrozole versus tamoxifen (either treatment received for 5 years) their sequences (2 one plus 3 other) postmenopausal women...

10.1200/jco.18.00440 article EN Journal of Clinical Oncology 2018-11-26

Abstract Background The MUC1 protein is a highly glycosylated mucin normally found at the apical surface of mucin‐secreting epithelial cells in many types tissues. expressed, but heavily underglycosylated, different human tumors. TG4010 viral suspension recombinant vaccinia vector (MVA) containing DNA sequences coding for antigen and interleukin‐2 (IL‐2). This product was developed use as vaccine cancer patients whose tumors express antigen. objective present study to determine safety define...

10.1002/jgm.397 article EN The Journal of Gene Medicine 2003-03-17

Mutations of the tumor suppressor gene p53 are most common genetic alterations observed in human cancer. Loss wild-type function impairs cell cycle arrest as well repair mechanisms involved response to DNA damage. Further, apoptotic pathways induced by radio- or chemotherapy also abrogated. Gene transfer was shown reverse these deficiencies and induce apoptosis vitro preclinical vivo models. A phase I dose escalation study a single intratumoral injection replication-defective adenoviral...

10.1089/hum.1998.9.14-2075 article EN Human Gene Therapy 1998-09-20

CEACAM6, CEACAM1, and human carcinoembryonic antigen (CEA) are coexpressed in normal colorectal epithelia, but show deregulated expression cancers (CRC). Upregulation of CEACAM6 hyperplastic polyps early adenomas represents one the earliest observable molecular events leading to tumors. The aim our study was evaluate prognostic relevance CEA tissue patients with CRC.Immunohistochemical analysis carried out on microarrays from 243 paraffin-embedded biopsies a randomized controlled clinical...

10.1200/jco.2003.55.135 article EN Journal of Clinical Oncology 2003-09-25

Angiogenesis is a key process in tumor progression. By binding VEGF, VEGF receptor-2 (VEGFR2) main signaling transducer tumor-associated angiogenesis. Accordingly, therapeutic approaches against the VEGF/VEGFR2 axis have been designed. However, an efficient and specific chemotherapeutic targeting of endothelial cells has not yet achieved.We employed anti-VEGFR2 antibodies covalently linked to pegylated liposomal doxorubicin (PLD) specifically ablate Rip1Tag2 mouse model insulinoma, MMTV-PyMT...

10.1158/1078-0432.ccr-11-1102 article EN Clinical Cancer Research 2011-11-08

Advanced triple negative breast cancer (TNBC) is an aggressive, but initially chemo-sensitive disease. The prognosis poor and more than three quarters of patients experience progression 12 months after the initiation conventional first-line chemotherapy. Approximately two thirds TNBC express epidermal growth factor receptor 1 (EGFR). We have developed anti-EGFR targeted nanocontainer drug by inserting antibody fragments into membrane pegylated liposomes (anti-EGFR-ILs-dox). payload consists...

10.1038/s41598-023-30950-z article EN cc-by Scientific Reports 2023-03-06
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