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Review
. 2024 Jul 20;16(14):2597.
doi: 10.3390/cancers16142597.

Chemotoxicity and Associated Risk Factors in Colorectal Cancer: A Systematic Review and Meta-Analysis

Affiliations
Review

Chemotoxicity and Associated Risk Factors in Colorectal Cancer: A Systematic Review and Meta-Analysis

Claire J Han et al. Cancers (Basel). .

Abstract

Background: Colorectal cancer (CRC) patients experience multiple types of chemotoxicity affecting treatment compliance, survival, and quality of life (QOL). Prior research shows clinician-reported chemotoxicity (i.e., grading scales or diagnostic codes) predicts rehospitalization and cancer survival. However, a comprehensive synthesis of clinician-reported chemotoxicity is still lacking.

Objectives: We conducted a systematic review and meta-analysis to determine chemotoxicity's prevalence and risk factors in CRC.

Methods: A systematic search from 2009 to 2024 yielded 30 studies for review, with 25 included in the meta-analysis.

Results: Pooled prevalences of overall, non-hematological, and hematological moderate-to-severe toxicities were 45.7%, 39.2%, and 25.3%, respectively. The most common clinician-reported chemotoxicities were gastrointestinal (GI) toxicity (22.9%) and neuropathy or neutropenia (17.9%). Significant risk factors at baseline were malnutritional status, frailty, impaired immune or hepato-renal functions, short telomere lengths, low gut lactobacillus levels, age, female sex, aggressive chemotherapy, and low QOL. Age was associated with neutropenia (β: -1.44) and GI toxicity (β:1.85) (p-values < 0.01). Older adults (>65 y.o.) had higher prevalences of overall (OR: 1.14) and GI (OR: 1.65) toxicities, but a lower prevalence of neutropenia (OR: 0.65) than younger adults (p-values < 0.05).

Conclusions: Our findings highlight the importance of closely monitoring and managing chemotoxicity in CRC patients receiving chemotherapy.

Keywords: chemotoxicity; colorectal cancer; prevalence; review; risk factors.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
The PRISMA 2020 flow diagram.
Figure 2
Figure 2
Funnel plot of publication bias (based on the 17 articles reporting prevalences of overall moderate-to-severe chemotoxicity data).
Figure 3
Figure 3
Forest plots for pooled prevalences of moderate-to-severe chemotoxicity (overall, non-hematological, and hematological toxicities) [7,30,31,32,33,34,35,39,40,41,43,44,45,46,47,48,49,50,52,53,54,55,56,58].
Figure 4
Figure 4
Forest plots for pooled prevalences of mild chemotoxicity (overall, non-hematological, and hematological toxicities) [7,31,32,49,50,52,54].

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