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Oxaliplatin-associated shock in stage III colorectal cancer patients: real-world evidence in Taiwan.
Wang, Ling-Yi; Hsieh, Hui-Hsia; Chu, Sung-Chao; Chang, Wei-Chuan; Kuo, Yi-Ting; Wu, Tien-Yuan.
Afiliação
  • Wang LY; Graduate Institute of Clinical Pharmacy, Tzu Chi University, Hualien, Taiwan.
  • Hsieh HH; Department of Pharmacy, Buddhist Tzu Chi General Hospital, Hualien, Taiwan.
  • Chu SC; Department of Pharmacy, Taichung Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Taichung City, Taiwan.
  • Chang WC; Department of Hematology and Oncology, Buddhist Tzu Chi General Hospital, Hualien City, Taiwan.
  • Kuo YT; School of Medicine, Tzu Chi University, Hualien, Taiwan.
  • Wu TY; Epidemiology and Biostatistics Consulting Center, Department of Medical Research, Buddhist Tzu Chi General Hospital, Hualien City, Taiwan.
Ther Adv Drug Saf ; 15: 20420986241266439, 2024.
Article em En | MEDLINE | ID: mdl-39086615
ABSTRACT

Background:

Oxaliplatin-associated shock (referred to as shock) is a rare but life-threatening adverse event.

Objectives:

This pioneering cohort study aimed to quantitatively investigate the association between oxaliplatin use and shock in patients with stage III colorectal cancer (CRC), identify potential independent risk factors for shock, and assess the cycle-to-shock during oxaliplatin treatment.

Design:

The study utilized a nested case-control (NCC) design to assess the association between oxaliplatin and shock and employed a case-crossover approach to address unmeasured confounders.

Methods:

All newly diagnosed stage III CRC patients were identified from the CRC Health Database (2012-2016). Conditional logistic regression was used to calculate odds ratios (OR) and 95% confidence intervals (CIs) for oxaliplatin's link to shock incidence.

Results:

Among 6932 oxaliplatin recipients, 331 suffered shock. In all, 3309 controls were selected via risk-set sampling for the shock cases. Oxaliplatin use is associated with a doubled risk of shock (adjusted OR 2.08, 95% CI 1.23-3.52). Two independent risk factors were male sex (adjusted OR 1.33, 95% CI 1.05-1.69) and heart diseases (adjusted OR 1.65, 95% CI 1.17-2.32). The case-crossover analysis revealed a more than fourfold risk (OR 4.4, 95% CI 1.67-11.62). In total, 22 of 331 shock cases were exposed to oxaliplatin within 2 days of shock onset, with a median cycle-to-shock time at the seventh cycle.

Conclusion:

Oxaliplatin use significantly increased shock risk in stage III CRC patients. Male sex and heart disease are two independent risk factors.
This pioneering study identified potential independent risk factors and the cycle-to-shock of oxaliplatin-associated shock which is a rare but life-threatening adverse event Why was the study done? Oxaliplatin-induced anaphylactic shock (referred to as shock) is a rare but life-threatening adverse event which is a harmful and undesirable experience associated with medical care in a patient. What did the researchers do? This pioneering cohort study aimed to quantitatively investigate the association between oxaliplatin use and shock in patients with stage III colorectal cancer (CRC), identify potential independent risk factors for shock and assess the cycle-to-shock during oxaliplatin treatment. All newly diagnosed stage III CRC patients were identified from the CRC Health Database (2012­2016). The study utilized a nested case-control (NCC) design to assess the association between oxaliplatin and shock and employed a case-crossover approach to address unmeasured confounders. Conditional logistic regression was used to quantify the association between oxaliplatin and shock incidence. What did the researchers find? Among 6,932 oxaliplatin recipients, 331 suffered shock. 3,309 controls were selected via risk-set sampling for the shock cases. Oxaliplatin use is associated with a doubled risk of shock. Independent risk factors were male sex and heart diseases. The risk of shock was 33% higher for males and 65% higher for people with heart diseases compared to females and those without heart diseases. The case-crossover analysis revealed a more than four-fold risk of shock of oxaliplatin. Twenty-two of 331 shock cases were exposed to oxaliplatin within two days before the shock onset. The median cycle-to-shock time is at the seventh cycle. What do the findings mean? Oxaliplatin use significantly increased shock risk in stage III CRC patients. Male sex and having heart diseases are two independent risk factors.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article