Abstract

Simple SummaryGallbladder cancer is distinct type of biliart tract cancer that is rare, aggressive and with limited treatment options aside from surgical resection. As of now in year 2022, systemic chemotherapy remains as the mainstay treatment option for patients with advanced staged gallbladder cancer. Despite decades of scientific research, new treatment options have been struggling to succeed. Furthermore, almost all clinical studies on gallbladder cancer have included other tyes of biliary tract cancers, raising the need to specifically inspect the outcomes of these clinical trial regimens on gallbladder cancer. In this article, we summarized all seminal literature and the most recent advances in scientific discoveries and clinical trials on gallbladder cancer. We provide a succinct update on current understanding, treatment landscape and therapeutic challenges in gallbladder cancer, as well as future prospects in the management of this disease.Gallbladder cancer (GBC) is a biological, anatomical, and clinically distinct subset of biliary tract cancers (BTC), which also include extra- and intra-hepatic cholangiocarcinoma. The advent of next-generation sequencing (NGS) clearly shows that GBC is genetically different from cholangiocarcinoma. Although GBC is a relatively rare cancer, it is highly aggressive and carries a grave prognosis. To date, complete surgical resection remains the only path for cure but is limited to patients with early-stage disease. The majority of the patients are diagnosed at an advanced, inoperable stage when systemic treatment is administered as an attempt to enable surgery or for palliation. Gemcitabine and platinum-based chemotherapies have been the main treatment modality for unresectable, locally advanced, and metastatic gallbladder cancer. However, over the past decade, the treatment paradigm has evolved. These include the introduction of newer chemotherapeutic strategies after progression on frontline chemotherapy, incorporation of targeted therapeutics towards driver mutations of genes including HER2, FGFR, BRAF, as well as approaches to unleash host anti-tumor immunity using immune checkpoint inhibitors. Notably, due to the rarity of BTC in general, most clinical trials included both GBC and cholangiocarcinomas. Here, we provide a review on the pathogenesis of GBC, past and current systemic treatment options focusing specifically on GBC, clinical trials tailored towards its genetic mutations, and emerging treatment strategies based on promising recent clinical studies.

Highlights

  • Genomic studies have clearly shown that biliary tract cancers (BTC) are a heterogeneous group of cancers biologically and that cholangiocarcinomas and Gallbladder cancer (GBC) have distinct genetic alterations

  • More and more actionable mutations are being treated for BTCs as a group, but success in GBC remains limited, as clearly discerned by subgroup analysis of these clinical trials

  • In the year 2022, combination chemotherapies continue to be the backbone of treatment for most patients in the frontline, second line, and adjuvant settings

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Summary

Introduction

Gallbladder cancer (GBC) is a rare but deadly malignancy, with an estimated 5-year survival rate of 2% in metastatic disease. Prognosis is poor in older patients and racial minorities [1]. The incidence of GBC varies significantly based on geographic location. Incidence rates are very high in South America, high in Japan and Korea, moderate in Eastern and Central Europe, and low in North America. In the United States, GBC is a relatively rare cancer. In 2022, an estimated 12,130 GBC and other biliary cancers are expected to be diagnosed, and 4400 will die from these diseases [2]. We review the risk factors for developing GBC, its pathophysiology, current systemic treatments, and ongoing clinical trials with a focus on targeted therapy for GBCs

Risk Factors
Pathogenesis
Genomics
Treatment Options
Neoadjuvant Therapy for BTCs
Adjuvant Therapy
Systemic Therapy
Targeted Therapy
HER2/neu Pathway
FGFR Pathway
BRAF/MEK Pathway
PD-1 Pathway
Future Directions
Findings
Conclusions
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