Blerina Resuli

ORCID: 0000-0003-2024-2771
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About
Contact & Profiles
Research Areas
  • Colorectal Cancer Treatments and Studies
  • Lung Cancer Treatments and Mutations
  • Genetic factors in colorectal cancer
  • Chronic Lymphocytic Leukemia Research
  • Advanced Breast Cancer Therapies
  • Chromatin Remodeling and Cancer
  • Computational Drug Discovery Methods
  • Cancer Mechanisms and Therapy
  • Melanoma and MAPK Pathways
  • Cancer Genomics and Diagnostics
  • Mechanisms of cancer metastasis
  • Lung Cancer Research Studies
  • HER2/EGFR in Cancer Research
  • PI3K/AKT/mTOR signaling in cancer
  • Enzyme function and inhibition
  • Brain Metastases and Treatment
  • Peptidase Inhibition and Analysis
  • Ovarian cancer diagnosis and treatment
  • Synthesis and biological activity
  • Acute Myeloid Leukemia Research
  • Cancer-related Molecular Pathways
  • Cancer Immunotherapy and Biomarkers
  • Multiple and Secondary Primary Cancers
  • Cancer therapeutics and mechanisms
  • Lung Cancer Diagnosis and Treatment

German Center for Lung Research
2024-2025

LMU Klinikum
2023-2025

Ludwig-Maximilians-Universität München
2023-2025

München Klinik
2024

Istituti Fisioterapici Ospitalieri
2023

Fondazione IRCCS Istituto Nazionale dei Tumori
2023

Istituti di Ricovero e Cura a Carattere Scientifico
2023

Molecular modifiers of KRASG12C inhibitor (KRASG12Ci) efficacy in advanced KRASG12C-mutant NSCLC are poorly defined. In a large unbiased clinicogenomic analysis 424 patients with non-small cell lung cancer (NSCLC), we identified and validated coalterations KEAP1, SMARCA4, CDKN2A as major independent determinants inferior clinical outcomes KRASG12Ci monotherapy. Collectively, comutations these three tumor suppressor genes segregated into distinct prognostic subgroups captured ∼50% those early...

10.1158/2159-8290.cd-22-1420 article EN Cancer Discovery 2023-04-17

Evaluating patients and treatment decisions in a multidisciplinary tumor board has led to better quality of care longer survival cancer patients. The aim this study was evaluate recommendations for thoracic oncology regarding guideline adherence transferal into clinical practice.We evaluated the at Ludwig-Maximilians University (LMU) Hospital Munich between 2014 2016. We compared patient characteristics guideline-adherent non-guideline-adherent recommendations, as well transferred...

10.1007/s00432-023-05025-1 article EN cc-by Journal of Cancer Research and Clinical Oncology 2023-07-05

BackgroundDocetaxel alone or in combination with ramucirumab nintedanib is recommended as second-line treatment metastatic non-small cell lung cancer (NSCLC) patients after progression on first-line platinum-base chemotherapy immune-checkpoint inhibitors (ICI). The purpose of our study was to compare the toxicity profile and efficacy docetaxel paclitaxel- pemetrexed-platinum ICI.Patients und MethodsMetastatic NSCLC treated pemetrexed paclitaxel-platinum without ICI were included...

10.1177/10732748251328618 article EN cc-by-nc Cancer Control 2025-03-01

<title>Abstract</title> Anaplastic lymphoma kinase tyrosine inhibitors (ALK TKIs) show robust activity in patients with non-small-cell lung cancer (NSCLC) harboring an ALK-rearrangement. Rare but serious side effects, such as pneumonitis can occur ALK TKIs. We here report a case of patient NSCLC echinoderm microtubule-associated protein-like 4-anaplastic (EML4- ALK) translocation who tolerated brigatinib following alectinib-induced pneumonitis. The was notable for diffuse ground-glass...

10.21203/rs.3.rs-4650153/v1 preprint EN cc-by Research Square (Research Square) 2024-08-09

&lt;p&gt;A) ORR (left), PFS (middle) and OS (right) in patients with ECOG-PS 0 or 1, at least 1 prior line of therapy for metastatic disease without untreated brain metastases; B) Survival outcomes treated metastases to starting KRAS G12Ci; C) according PD-L1 status (TPS: tumor proportion score); D) survival immune checkpoint inhibitor therapy.&lt;/p&gt;

10.1158/2159-8290.27025406 preprint EN 2024-09-16

&lt;p&gt;A) ORR (left), PFS (middle) and OS (right) in patients with ECOG-PS 0 or 1, at least 1 prior line of therapy for metastatic disease without untreated brain metastases; B) Survival outcomes treated metastases to starting KRAS G12Ci; C) according PD-L1 status (TPS: tumor proportion score); D) survival immune checkpoint inhibitor therapy.&lt;/p&gt;

10.1158/2159-8290.27025406.v1 preprint EN 2024-09-16
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