Following colorectal cancer
surgery, longer delay to beginning chemotherapy associated with worse
survival
An analysis of data from previously published
studies indicates that longer time to beginning adjuvant chemotherapy
after surgery for colorectal cancer is associated with worse survival,
according to a study presented at the ASCO 2011 Annual Meeting and
published in the June 8 issue of JAMA, a theme issue on cancer.
The study is being published early online to coincide with its presentation
at the American Society of Clinical Oncology 2011 Annual Meeting.
"Colorectal cancer (CRC) is the third leading cause of cancer
mortality in the Western world. While surgical resection remains
the cornerstone of management for patients with stage I-III disease,
a considerable proportion of patients will ultimately relapse and
die from their disease," according to background information
in the article. "Adjuvant chemotherapy [AC] improves survival
among patients with resected colorectal cancer. However, the optimal
timing from surgery to initiation of AC is unknown." There
is also a question of the benefit of beginning chemotherapy after
a certain time period, typically believed to be 12 weeks.
James J. Biagi, M.D., of Queen's University, Kingston, Ontario,
Canada, and colleagues conducted a review and meta-analysis of studies
that assessed the relationship between time to AC and survival in
CRC. Studies were only included if relevant prognostic factors were
adequately described and either comparative groups were balanced
or results adjusted for these prognostic factors. The researchers
identified 10 eligible studies involving 15,410 patients (7 published
articles, 3 abstracts) that met study criteria for inclusion. Nine
of the studies were cohort or population based and 1 was a secondary
analysis from a randomized trial of chemotherapy.
The researchers found that meta-analysis indicated that a 4-week
increase in time to AC was associated with a significant decrease
(14 percent) in both overall survival and disease-free survival.
There was no significant heterogeneity among included studies. Results
remained significant after adjustment for potential publication
bias and when the analysis was repeated to exclude studies of largest
weight.
"The effect of AC on survival is thought to be eradication
of micro-metastatic deposits in a proportion of patients who would
otherwise be destined to have cancer recurrence. There is a substantial
theoretical rationale to initiate AC promptly after curative surgery,"
the authors write.
Regarding the question of after what time period would beginning
chemotherapy appear to be of limited benefit, the authors found
that their results indicate survival of 48 percent if chemotherapy
is administered at 12 weeks instead of 4 weeks, suggesting there
may be some benefit to chemotherapy beyond a 12-week window, and
that a reasonable limit may be more in the order of 4 to 5 months.
These findings suggest that timing of AC plays a critical role
in the management and outcomes of patients with CRC and that it
would be prudent for clinicians and jurisdictions to avoid delays
in access to chemotherapy, the researchers write. "Our results
indicate that at a population level, the effect of delays might
be substantial. With approximately 140,000 new cases of CRC diagnosed
in the United States in 2009, of which roughly 35 percent or 49,000
had stage III disease, the population at risk is sizeable."
"In conclusion, our results demonstrate a significant adverse
association between time to AC and survival in CRC, supporting a
position that clinicians and jurisdictions need to optimize patient
flow logistics to minimize time to AC," the authors write.
"Our results provide further validation of the intuitive concept
of early time to AC. Physicians may need to more carefully consider
timing when discussing AC with patients."
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