Published online Jun 6, 2022. doi: 10.12998/wjcc.v10.i16.5253
Peer-review started: December 30, 2021
First decision: March 7, 2022
Revised: March 9, 2022
Accepted: April 22, 2022
Article in press: April 22, 2022
Published online: June 6, 2022
Processing time: 153 Days and 11.1 Hours
Malignant gastrointestinal obstruction is an important issue in advanced cancer and occurs in approximately 30% of patients with gastrointestinal cancer. Gastrointestinal obstruction causes oral intake impairment, nausea, vomiting, and abdominal pain and increases the risk of gastrointestinal perforation. Primary therapy involves fasting and decompression, and subsequently complete surgical resection is performed for resectable malignant gastrointestinal obstruction; palliative surgery includes bypass and stoma surgery or self-expandable metal stent (SEMS) placement.
The impacts of chemotherapy on patients with malignant gastrointestinal obstructions remain unclear, and multicenter evidence is lacking.
We performed a large multicenter cohort study to evaluate the effectiveness and safety of chemotherapy after palliative surgery or SEMS placement compared with best supportive care (BSC) in patients with unresectable malignant gastrointestinal obstructions. In addition, we aimed to identify the optimal population for chemotherapy after palliative surgery or SEMS placement.
We conducted a multicenter retrospective cohort study that compared the chemotherapy group who received any chemotherapeutics after interventions, including palliative surgery or self-expandable metal stent placement, for unresectable malignant gastrointestinal obstruction vs BSC group between 2014 and 2019 in nine hospitals. The primary outcome was overall survival, and the secondary outcomes were patency duration and adverse events, including gastrointestinal perforation and gastrointestinal bleeding.
In total, 470 patients in the chemotherapy group and 652 patients in the BSC group were analyzed. During the follow-up period of 54.1 mo, the median overall survival durations were 19.3 mo in the chemotherapy group and 5.4 mo in the BSC group (log-rank test, P < 0.01). The median patency durations were 9.7 mo [95% confidence interval (CI): 7.7-11.5 mo] in the chemotherapy group and 2.5 mo (95%CI: 2.0-2.9 mo) in the BSC group (log-rank test, P < 0.01). The perforation rate was 1.3% (6/470) in the chemotherapy group and 0.9% (6/652) in the BSC group (P = 0.567). The gastrointestinal bleeding rate was 1.5% (7/470) in the chemotherapy group and 0.5% (3/652) in the BSC group (P = 0.105).
Chemotherapy after interventions for unresectable malignant gastrointestinal obstruction was associated with increased overall survival and patency duration.
Our results showed that chemotherapy may be more beneficial in cases of pancreatic cancer and gastroduodenal obstruction. These findings will help guide future research on treatment approaches and precision medicine. In the near future, these precision medicine methods are expected to contribute to cancer therapies including molecular targeted anti-cancer drugs, monoclonal antibody therapy, and antibiotic therapies.