Third- and Late Line Treatments of Metastatic Gastric Cancer: Still More to Be Done.

Curr Oncol

Clinical Oncology Unit, Department of Experimental Oncology, Mediterranean Institute of Oncology, 95029 Catania, Italy.

Published: September 2022

AI Article Synopsis

  • Recent advances in anticancer therapies for metastatic gastric cancer (mGC) have improved survival rates and patient conditions, leading to better treatment options.
  • Treatment choices depend on factors like performance status, age, disease stage, and specific tumor characteristics, such as microsatellite instability and HER2 overexpression.
  • Despite having more third-line treatment options, effectiveness is still limited after two prior lines of therapy; however, several agents like TAS-102 and pembrolizumab show promise for managing refractory mGC patients.

Article Abstract

In recent years, advances of anticancer and supportive therapies have determined a gradual improvement in survival rates and patients' general conditions in metastatic gastric cancer (mGC), allowing them to receive further treatments. The choice of treatment is driven by performance status, age, stage of disease, number of metastatic sites and time from the first to third line of treatment. Targets such as microsatellite instability, PD-L1 expression, and HER2 overexpression or amplification may be addressed to personalise treatment and prolong survival. Despite a growing number of third line options that have provided clinicians with greater opportunities to customise treatments, up to date few agents have been demonstrated as effective after two standard lines for mGC; for these reasons, chemotherapy, immunotherapy, and targeted therapy were all widely investigated in both phase II and phase III studies. Overall, TAS-102, apatinib, regorafenib, nilotinib, trastuzumab, and pembrolizumab were demonstrated to be valid options in the third line scenario for mGC patient refractory to at least two lines of therapy. A multimodal approach based on chemotherapy, immunotherapy, targeted agents, a personalised nutritional programme as well as the research of new predictive biomarkers may pave the way to new strategies to identify the best treatment for each patient.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9497544PMC
http://dx.doi.org/10.3390/curroncol29090506DOI Listing

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