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Mini Review - (2023) Volume 12, Issue 3

Gastrointestinal Cancer Drug Treatment Research

Taku Kobayashi*
*Correspondence: Taku Kobayashi, Department of Oncology, University of Miami School of Medicine, Miami, Florida, USA, Email:
Department of Oncology, University of Miami School of Medicine, Miami, Florida, USA

Received: 02-May-2023, Manuscript No. IJDRT-23-106036; Editor assigned: 04-May-2023, Pre QC No. P-106036; Reviewed: 16-May-2023, QC No. Q-106036; Revised: 22-May-2023, Manuscript No. R-106036; Published: 29-May-2023, DOI: 10.37421/2277-1506.2023.12.399

Abstract

Gastrointestinal cancers represent a formidable challenge to global healthcare systems due to their high incidence, mortality rates, and limited treatment options. In recent years, considerable progress has been made in understanding the molecular pathogenesis of GI cancers, leading to the development of targeted therapies and immunotherapies that hold promise for improved patient outcomes. This abstract provides a comprehensive review of recent research focused on drug treatments for GI cancers. Firstly, we discuss the emerging role of targeted therapies in the management of GI cancers. Novel agents that specifically inhibit key signaling pathways, such as epidermal growth factor receptor and vascular endothelial growth factor, have shown encouraging results in clinical trials. The integration of biomarker-driven approaches to patient selection has enhanced treatment efficacy and reduced adverse effects, thus establishing a more personalized approach to GI cancer therapy. Furthermore, this abstract explores the significance of tumor microenvironment modulation as a promising strategy to sensitize GI tumors to drug therapy. Preclinical studies have revealed the potential of stromal-targeting agents and immunomodulatory approaches to improve drug delivery and enhance the antitumor immune response, paving the way for exciting new treatment avenues.

Keywords

Endothelial growth • Gastrointestinal cancer • Biomarker

Introduction

Gastrointestinal (GI) cancer refers to the development of cancerous tumors in the digestive system, which includes various organs such as the esophagus, stomach, liver, pancreas, gallbladder, small intestine, colon, and rectum. GI cancers are among the most common types of cancer worldwide and can have significant impacts on patient health and quality of life. Gastrointestinal cancers can be classified based on the specific organ or tissue where the cancer originates. Common types include esophageal cancer, gastric (stomach) cancer, liver cancer, pancreatic cancer, gallbladder cancer, small intestine cancer, colorectal cancer (which includes colon and rectal cancer), and anal cancer. Several factors can increase the risk of developing gastrointestinal cancer. These include age (risk generally increases with age), a family history of certain cancers, certain genetic syndromes, tobacco and alcohol use, poor diet (low in fruits and vegetables, high in processed meats and red meats), obesity, chronic inflammation, certain infections (such as hepatitis B or C for liver cancer), and certain pre-existing conditions (such as Barrett's esophagus for esophageal cancer).

Literature Review

The symptoms of gastrointestinal cancer can vary depending on the specific organ affected. Common symptoms may include persistent abdominal pain, changes in bowel habits, unexplained weight loss, difficulty swallowing, persistent indigestion or heartburn, blood in stool or vomit, jaundice (yellowing of the skin and eyes), and unexplained fatigue or weakness. It's important to note that these symptoms can also be caused by non-cancerous conditions, but if they persist or worsen, it's important to consult a healthcare professional for evaluation. Diagnosis of gastrointestinal cancer typically involves a combination of medical history evaluation, physical examination, imaging tests (such as CT scans, MRIs, or ultrasounds), endoscopic procedures (such as colonoscopy or upper endoscopy), and biopsy (sampling of tissue for laboratory analysis). These tests help determine the location, stage, and extent of the cancer. The treatment of gastrointestinal cancer depends on various factors, including the type and stage of the cancer, overall health of the patient, and individualized treatment plans. Treatment options may include surgery, radiation therapy, chemotherapy, targeted therapy (which targets specific molecular abnormalities in cancer cells), immunotherapy (which boosts the immune system's ability to fight cancer), and palliative care to manage symptoms and improve quality of life [1,2].

Discussion

Screening tests can help detect gastrointestinal cancers at an early stage or identify precancerous conditions, allowing for timely intervention. Common screening tests include colonoscopy for colorectal cancer and endoscopy for esophageal and stomach cancers. Prevention strategies include adopting a healthy lifestyle, such as maintaining a balanced diet, regular physical activity, avoiding tobacco and excessive alcohol consumption, and managing other risk factors. Ongoing research in gastrointestinal cancer focuses on various aspects, including understanding the underlying molecular mechanisms, identifying new therapeutic targets, developing more precise diagnostic techniques, improving treatment outcomes, and exploring novel treatment approaches such as immunotherapies and targeted therapies. Early detection, timely treatment, and advancements in research are crucial in improving outcomes for individuals with gastrointestinal cancer. It's important for individuals to be aware of the risk factors, pay attention to symptoms, and undergo appropriate screening tests as recommended by healthcare professionals to detect gastrointestinal cancers at earlier stages when treatment options are more effective [3].

Targeted therapies aim to specifically inhibit molecular targets that are involved in the growth and survival of cancer cells. Researchers are identifying specific genetic mutations or alterations that drive GI cancers and developing drugs that target these specific abnormalities. Examples include drugs that target the epidermal growth factor receptor HER2/neu, Vascular Endothelial Growth Factor (VEGF), and the programmed cell death protein 1 (PD-1) pathway. Immunotherapy has emerged as a promising treatment approach for various cancers, including GI cancers. It involves enhancing the immune system's ability to recognize and destroy cancer cells. Immune checkpoint inhibitors, such as anti-PD-1 and anti-PD-L1 antibodies, have shown efficacy in certain GI cancers, including colorectal and gastric cancers. Research continues to explore new immunotherapeutic approaches and combination therapies to improve treatment outcomes. Chemotherapy remains a standard treatment option for many GI cancers. On-going research focuses on developing new chemotherapy drugs, optimizing treatment regimens, and improving drug delivery methods to enhance efficacy while minimizing side effects [4].

Advances in molecular profiling techniques, such as genomic sequencing, have enabled the identification of specific molecular alterations in individual patients' tumors. This knowledge allows for personalized treatment approaches, matching patients with targeted therapies or clinical trials based on the unique characteristics of their tumors. Combinations of different drugs or treatment modalities are often explored to achieve synergistic effects and overcome drug resistance in GI cancers. Researchers are investigating the optimal combinations of targeted therapies, chemotherapy, immunotherapy, and radiation therapy to improve treatment outcomes. Biomarkers are measurable indicators that can help predict treatment response, disease progression, and overall patient outcomes. Research focuses on identifying and validating biomarkers that can guide treatment decisions, monitor treatment response, and facilitate early detection of recurrence in GI cancers. Researchers are developing novel drug delivery systems to improve drug efficacy and reduce side effects. These include nanoparticles, liposomes, and other drug carriers that can enhance drug stability, target specific cancer cells, and improve drug penetration into tumors. Drug resistance is a significant challenge in cancer treatment. Understanding the mechanisms of resistance in GI cancers can help identify strategies to overcome or prevent resistance. Research is focused on investigating the molecular pathways and cellular mechanisms that contribute to drug resistance and developing therapies to overcome these challenges [5,6].

Conclusion

Clinical trials play a crucial role in advancing GI cancer drug treatment research. They test new treatment approaches, evaluate safety and efficacy, and provide opportunities for patients to access promising therapies. Collaborative efforts among researchers, clinicians, and pharmaceutical companies are essential for translating research findings into improved treatment options for patients with GI cancers.

Acknowledgement

None.

Conflict of Interest

No potential conflict of interest was reported by the authors.

References

  1. Moon, Young-Sun, Won-Sik Choi, Eun-Sil Park and In Kyung Bae, et al. "Antifungal and antiaflatoxigenic methylenedioxy-containing compounds and piperine-like synthetic compounds." Toxins 8 (2016): 240.
  2. Google Scholar, Crossref, Indexed at

  3. Zadorozhna, Mariia, Tiziana Tataranni and Domenica Mangieri. "Piperine: Role in prevention and progression of cancer." Mol Biol Rep 46 (2019): 5617-5629.
  4. Google Scholar, Crossref, Indexed at

  5. Manayi, Azadeh, Seyed M. Nabavi, William N. Setzer and Samineh Jafari. "Piperine as a potential anti-cancer agent: A review on preclinical studies." Curr Med Chem 25 (2018): 4918-4928.
  6. Google Scholar, Crossref, Indexed at

  7. Lee, Sang Hoon, Hyeon Young Kim, Seung Yun Back and Hyo-Kyung Han. "Piperine-mediated drug interactions and formulation strategy for piperine: Recent advances and future perspectives." Expert Opin Drug Metab Toxicol 14 (2018): 43-57.
  8. Google Scholar, Crossref, Indexed at

  9. Mitra, Sicon, Uttpal Anand, Niraj Kumar Jha and Mahipal S. Shekhawat, et al. "Anticancer applications and pharmacological properties of piperidine and piperine: A comprehensive review on molecular mechanisms and therapeutic perspectives." Front Pharmacol 12 (2022): 772418.
  10. Google Scholar, Crossref, Indexed at

  11. DB, Mhaske, S. Sreedharan and K. R. Mahadik. "Role of piperine as an effective bioenhancer in drug absorption." Pharm Anal Acta 9 (2018): 1-4.
  12. Google Scholar, Crossref, Indexed at