(National Institute of Neurological Disorders and Stroke (R01NS100782))
(R01 CA255840) Támogató: OOI
(TKP2021-NKTA-47)
(TKCS-2021/32)
Nemzeti Kardiovaszkuláris Laboratórium(RRF-2.3.1-21-2022-00003) Támogató: NKFIH
Nemzeti Gyógyszerkutatási és Fejlesztési Laboratórium (PharmaLab)(RRF-2.3.1-21-2022-00015)
Támogató: NKFIH
(135784) Támogató: NKFIH
(101004093/EUniWell/EAC-A02- 2019/EAC-A02-2019-1)
(EKÖP-2024–2) Támogató: New National Excellence Program
(EKÖP-2024-9)
Delaying the initiation of cancer treatment increases the risk of mortality, particularly
in colorectal cancer (CRC), which is among the most common and deadliest malignancies.
This study aims to explore the impact of treatment delays on mortality in CRC. A systematic
literature search was conducted in PubMed, Web of Science, and Scopus for studies
published between 2000 and 2025. Meta-analyses were performed using random-effects
models with inverse variance method to calculate hazard ratios (HRs) for both overall
and cancer-specific survival at 4-, 8-, and 12-week treatment delay intervals, with
heterogeneity assessed through I2-statistics and publication bias evaluated using
funnel plots and Egger's test. A total of 20 relevant studies were included in the
meta-analysis. The analyses of all patients demonstrated a progressively increasing
risk of 12-39% with longer treatment delays (4 weeks, HR = 1.12; 95% CI, 1.08-1.16;
8 weeks, HR = 1.24; 95% CI, 1.16-1.34; 12 weeks, HR = 1.39; 95% CI, 1.25-1.55). In
particular, incrementally higher hazard ratios were observed for all-cause mortality
at 4 weeks (HR = 1.14; 95% CI, 1.09-1.18), 8 weeks (HR = 1.29; 95% CI, 1.20-1.39),
and 12 weeks (HR = 1.47; 95% CI, 1.31-1.64). In contrast, cancer-specific survival
analysis showed a similar trend but did not reach statistical significance (4 weeks,
HR = 1.07; 95% CI, 0.98-1.18; 8 weeks, HR = 1.15; 95% CI, 0.95-1.39; 12 weeks, HR
= 1.23; 95% CI, 0.93-1.63). Treatment delays in colorectal cancer patients were associated
with progressively worsening overall survival, with each 4-week delay increment leading
to a substantially higher mortality risk. This study suggests that timely treatment
initiation should be prioritized in clinical practice, as these efforts can lead to
substantial improvements in survival rates.