V isceral crisis (VC), as defined most recently, refers to disease progression and serious organ dysfunction accompanied by clinical symptoms and laboratory findings. Hepatic visceral crisis (HVC) is defined by rapidly increasing bilirubin levels >1.5 × the upper limit of normal laboratory range, without Gilbert's syndrome or bile duct obstruction. [1] VC associated with malignancies can stem from widespread organ metastases or may be secondary to the primary pathophysiology of the disease and paraneoplastic causes. In cases of VC with intense metastases affecting vital organs and posing a life-threatening condition, the primary goal is to mitigate rapid clinical deterioration. For prompt symptom relief and disease control, the current approach for these patients should preferably involve combination chemotherapies. [1] Liver metastases refer to tumors that originate from cancers in other parts of the body and spread to the liver. They are most commonly seen as secondary tumors resulting from colorectal cancer (CRC), pancreatic cancer, breast cancer, melanoma, and lung cancer. [2] Worldwide, lung cancer and CRC are the leading causes of cancer-related deaths, with stomach cancer ranking third. Stomach cancer often Objectives: The aim of the study is to investigate the impact of the timing of chemotherapy (CT) initiation and CT protocol on overall survival (OS) in patients with hepatic visceral crisis (HVC). Methods: The study evaluated the timing of starting CT and the contribution of the initiated CT protocol to OS in patients with hepatic visceral crisis (HVC) who have clinical symptoms due to tumor burden characterized by liver metastasis and hyperbilirubinemia ≥1.5 times the upper limit, along with elevated at least one of ALT/AST values. Results: Between November 2007 and July 2021, analyzed 233 patients in HVC. 60 individuals were able to receive CT and divided into two groups based on the timing of initiating CT during HVC. CT initiated patients within 7 days were observed to have longer median OS (mOS) compared to patients initiated CT after 7 days (3.88 vs 2.99 months; p=0.04). Furthermore single-agent CT exhibited a significantly mOS compared to patients unable to undergo CT (1.70 months vs 1.08 months; p=0.03) Additionally patients who received combination CT had longer mOS compared to those who received monotherapy (4.27 months vs 1.70 months; p=0.03).
Conclusion:Initiating early CT during HVC in eligible patients has a positive impact on OS.