Introduction: Bevacizumab is a recombinant humanized monoclonal antibody against human vascular endothelial growth factor (VEGF), which inhibits angiogenesis in tumor tissues by blocking VEGF activity. Although rare, bevacizumab-induced gastrointestinal perforation (BIGP) can reduce patients' quality of life and even lead to death. We aimed to evaluate the time to BIGP onset according to the indication, its outcome, and the effect of bevacizumab in combination with various anticancer agents.
Method: Adverse events in the Japanese Adverse Drug Reaction Reports (JADER) database were defined according to the Medical Dictionary for Regulatory Activities, and "gastrointestinal perforation (SMQ 'standardized MedDRA inquiry' 20000107)" was extracted. Reasons for use were categorized by seven indications, and other diseases were classified as "other" and were evaluated for time-to-onset analysis and outcomes. Association rule mining was used to assess the risk of BIGP associated with the administration of bevacizumab combined with various anticancer agents.
Results: The JADER database includes 887,704 reports submitted between April 2004 and March 2024, including 2,112 reports of BIGP. The times to BIGP onset (quartile range) for non-small cell lung, colorectal, and ovarian cancers were 46.0 (11.0-122.0), 77.0 (29.0-196.0), and 67.0 (23.0-203.0) days, respectively. The log-rank test demonstrated that BIGP occurred earlier in patients with non-small cell lung cancer than in patients with colorectal (P < 0.0001) or ovarian (P = 0.0033) cancer. Association rule mining results showed that for the consequent (right-hand side) "1-100 days onset," drugs used to treat non-small cell lung cancer were at the top. However, for "101-200 days onset," irinotecan and drugs for colorectal cancer were at the top of the association rule. BIGP outcomes in the JADER report were 64.7% "improvement" and 35.3% "no improvement."
Conclusion: In non-small cell lung cancer, the time to BIGP onset is earlier than that in colorectal and ovarian cancers. This finding suggests that healthcare providers can detect and intervene BIGP at early stages.
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http://dx.doi.org/10.7759/cureus.78585 | DOI Listing |
AJR Am J Roentgenol
March 2025
Professor of Radiology, Mayo Clinic College of Medicine and Science, Consultant Radiologist, Division of Cardiothoracic Imaging, Mayo Clinic Florida, 4500 San Pablo Road, Jacksonville, FL 32224.
Cancer Rep (Hoboken)
March 2025
Thoracic and Vascular Surgery Research Center, Shiraz University of Medical Science, Shiraz, Iran.
Introduction: Globally, lung cancer is one of the most commonly diagnosed cancers and continues to take the lead in cancer-related mortality rates. This study aims to provide the latest statistics on the clinical, histopathological, and epidemiological features of lung cancer patients who underwent surgical resection in referral hospitals in Southern Iran.
Method: In this retrospective study, records of all patients with operable primary and secondary lung cancer who underwent surgical resection of the lung in Shiraz hospitals, located in Southern Iran from November 2009 to May 2022 were screened.
Front Oncol
February 2025
Department of Oncology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
[This corrects the article DOI: 10.3389/fonc.2024.
View Article and Find Full Text PDFFront Oncol
February 2025
Department of Radiation Oncology, Shandong Cancer Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Osimertinib combined with chest radiotherapy has a high incidence of pneumonia, dacomitinib is widely used in clinical practice, but there are no studies reporting the pulmonary safety of dacomitinib in combinating with radiotherapy. Here we report a case of radiation pneumonitis occurring by dacomitinib and thoracic radiotherapy (TRT). The patient was a 55-year-old woman with lung adenocarcinoma.
View Article and Find Full Text PDFFront Oncol
February 2025
Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, China.
Anaplastic lymphoma kinase (ALK) inhibitors have shown efficacy in treating ALK-positive advanced non-small cell lung cancer (NSCLC) patients. However, the effectiveness of ensartinib neoadjuvant therapy remains ambiguous. Herein, we reported that preoperative systemic treatment with the ALK inhibitor ensartinib can be beneficial for treating initially inoperable tumors.
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