Publications by authors named "Turja Chakrabarti"

Purpose: To assess the safety and efficacy of the third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor osimertinib as neoadjuvant therapy in patients with surgically resectable stage I-IIIA -mutated non-small cell lung cancer (NSCLC).

Patients And Methods: This was a multi-institutional phase II trial of neoadjuvant osimertinib for patients with surgically resectable stage I-IIIA (American Joint Committee on Cancer [AJCC] V7) -mutated (L858R or exon 19 deletion) NSCLC (ClinicalTrials.gov identifier: NCT03433469).

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The phenomenon of mixed/heterogenous treatment responses to cancer therapies within an individual patient presents a challenging clinical scenario. Furthermore, the molecular basis of mixed intra-patient tumor responses remains unclear. Here, we show that patients with metastatic lung adenocarcinoma harbouring co-mutations of EGFR and TP53, are more likely to have mixed intra-patient tumor responses to EGFR tyrosine kinase inhibition (TKI), compared to those with an EGFR mutation alone.

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Article Synopsis
  • A study analyzed 424 patients with KRASG12C-mutant non-small cell lung cancer (NSCLC) and identified key genomic alterations (in KEAP1, SMARCA4, and CDKN2A) that lead to worse outcomes with KRASG12C inhibitors (KRASG12Ci).
  • These alterations allowed researchers to classify patients into different prognostic groups, indicating nearly 50% of those who experienced early disease progression.
  • The research suggests potential pathways not only associated with poor response (like PI3K/AKT/MTOR) but also hints that certain DNA damage response issues might improve KRASG12Ci effectiveness, paving the way for personalized treatment strategies.
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Background: Definitive chemoradiation with consolidative immunotherapy offers the best chance for cure in patients with unresectable, locally advanced non-small cell lung cancer (NSCLC). However, treatment-related lymphopenia (TRL) may negatively impact outcomes.

Methods: Patients definitively treated with chemoradiation and immunotherapy from 2015 to 2019 at a single tertiary academic center were identified.

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