person

Marta O. S.

Country
Poland
Department
NA

Research Overview

Data & Insights

medical_services
Primary Speciality
Main therapeutic area

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Return Partnerships
Recurring site collaborations
11
Sites with multiple studies

Has run more than one trial at 11 of 120 partner sites.

Specializations

Hormone Receptor‑Positive Breast Cancer

Investigation of advanced hormone receptor‑positive breast cancer with emphasis on endocrine‑resistant disease and biomarker‑guided therapeutic combinations.

  • CDK4/6 inhibitor combinations
  • PIK3CA‑mutated disease strategies
  • Post‑chemotherapy maintenance approaches
  • Adjuvant endocrine optimization

Integration of molecular profiling to refine patient selection for novel agents.

Non‑Small Cell Lung Cancer

Focused on targeted and immune‑based interventions for non‑small cell lung cancer, including molecularly defined subgroups.

  • EGFR exon 20 insertion therapies
  • KRAS‑G12C targeted agents
  • PD‑L1 high disease regimens
  • ALK‑positive disease management

Collaborative trials conducted through the National Oncology Institute in Warsaw.

Hematologic Malignancies

Clinical programs addressing acute leukemias and lymphoid cancers, with a strong focus on genetic drivers and cellular therapies.

  • Acute myeloid leukemia with NPM1 mutation
  • CAR‑T cell approaches in lymphoma
  • Maintenance strategies post‑stem cell transplant
  • Targeted agents in chronic lymphocytic leukemia

Application of next‑generation sequencing to personalize treatment pathways.

Gastrointestinal and Hepatobiliary Cancers

Exploration of biomarker‑driven therapies across gastrointestinal malignancies, including liver and biliary tract cancers.

  • MSI‑high colorectal cancer interventions
  • FGFR2b‑positive gastric cancer targeting
  • KRAS‑mutated pancreatic cancer trials
  • BRAF‑mutated cholangiocarcinoma approaches

Emphasis on integrating molecular diagnostics into trial eligibility.

Immunotherapy and Targeted Therapy in Solid Tumors

Broad program evaluating checkpoint inhibition and novel targets across diverse solid tumors.

  • PD‑1 refractory melanoma strategies
  • VEGF‑targeted renal cell carcinoma regimens
  • BAP1‑deficient mesothelioma studies
  • TIGIT inhibition in solid tumors

Combination designs aim to enhance response durability and overcome resistance.

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