The Gastrointestinal Stromal Tumor: the first systematic, comprehensive and professional journal for gastrointestinal stromal tumor
Foreword

The Gastrointestinal Stromal Tumor: the first systematic, comprehensive and professional journal for gastrointestinal stromal tumor

Gastrointestinal stromal tumors (GISTs) originate from mesenchymal tissue and have a potential malignant tendency. The incidence rate is 1–2/10 million. These tumors occur in the entire digestive tract, and most commonly in the stomach (approximately 60%), and the parameters of immunohistochemical expression are CD34, CD117 and Dog 1 (1-3). Since the mutation of c-kit gene in GIST was discovered by Japanese scholars in 1998 (4) and the first case of tyrosine kinase inhibitors in the treatment of metastatic GIST occurred in 2001 (5), GIST has attracted the attention of doctors and gradually become a model of targeted therapy (6).

The understanding of GIST is expanding, while more challenging clinical issues of GIST are emerging, such as, the resistance to molecular therapy, discussions in laparoscopy and robotic surgery, treatment of rare gene mutations, the management of malignant small GISTs and metastatic GISTs, etc. Although many GIST-related issues have been reported and published, there is not a platform to systemically discuss and timely present the state of the art on GIST. Therefore, cooperating with Prof. Yong Li (who has profound research in the standardized treatment of gastrointestinal stromal tumor in Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China), we are going to launch a brand-new journal Gastrointestinal Stromal Tumor to keep publishing up-to-date findings, knowledge, skills, experience, and valued ideas in the exploring of GIST, to help the clinicians and researchers always update their skills and knowledge in the field of GIST.

The journal Gastrointestinal Stromal Tumor will cover all aspects of GIST, from epidemiology, molecular biology, imaging to pathogenesis, diagnosis and treatment (including but not limited to).

We will spare no effort to build the journal Gastrointestinal Stromal Tumor an international reader-friendly platform for learning and education, communication and cooperation for clinical practice and medical science in the field of GIST. To achieve this, we warmly welcome the GIST researchers and clinicians, colleagues and friends across the globe to join our effort to push the field forward and ultimately help our patients live longer and better.


References

  1. Valsangkar N, Sehdev A, Misra S, et al. Current management of gastrointestinal stromal tumors: Surgery, current biomarkers, mutations, and therapy. Surgery 2015;158:1149-64. [Crossref] [PubMed]
  2. Søreide K, Sandvik OM, Søreide JA, et al. Global epidemiology of gastrointestinal stromal tumours (GIST): A systematic review of population-based cohort studies. Cancer Epidemiol 2016;40:39-46. [Crossref] [PubMed]
  3. Zhao X, Yue C. Gastrointestinal stromal tumor. J Gastrointest Oncol 2012;3:189-208. [PubMed]
  4. Hirota S, Isozaki K, Moriyama Y, et al. Gain-of-function mutations of c-kit in human gastrointestinal stromal tumors. Science 1998;279:577-80. [Crossref] [PubMed]
  5. Joensuu H, Roberts PJ, Sarlomo-Rikala M, et al. Effect of the tyrosine kinase inhibitor STI571 in a patient with a metastatic gastrointestinal stromal tumor. N Engl J Med 2001;344:1052-6. [Crossref] [PubMed]
  6. Cioffi A, Maki RG. GI Stromal Tumors: 15 Years of Lessons from a Rare Cancer. J Clin Oncol 2015;33:1849-54. [Crossref] [PubMed]

GIST Editorial Office

AME Publishing Company, Guangzhou 510000, China.
(Email: gist@amegroups.com)

doi: 10.21037/gist.2018.08.01

Conflicts of Interest: The author has no conflicts of interest to declare.

doi: 10.21037/gist.2018.08.01
Cite this article as: GIST Editorial Office. The Gastrointestinal Stromal Tumor: the first systematic, comprehensive and professional journal for gastrointestinal stromal tumor. Gastrointest Stromal Tumor 2018;1:1.