Cited by 662Colorectal Cancer Treatments and StudiesColorectal Cancer Surgical TreatmentsIntraperitoneal and Appendiceal Malignancies

Palliative chemotherapy for advanced colorectal cancer: systematic review and meta-analysis

Open access
Colorectal Cancer Collaborative Group·2000·BMJ

Abstract

OBJECTIVES: To determine the benefits and harms of palliative chemotherapy in patients with locally advanced or metastatic colorectal cancer and to compare the outcomes for elderly and younger patients. DESIGN: Meta-analysis of individual patient data and published summary statistics from trials for which individual patient data could not be obtained from the investigators. STUDIES: All randomised controlled trials comparing palliative chemotherapy with supportive care in patients with advanced colorectal cancer that were identified by computerised and hand searches of the literature, scanning references, and contacting investigators. MAIN OUTCOME MEASURES: Survival, disease progression, quality of life, and toxicity. RESULTS: 13 randomised controlled trials including a total of 1365 patients met the inclusion criteria. Meta-analysis of seven trials that provided individual patient data (866 patients) showed that palliative chemotherapy was associated with a 35% reduction in the risk of death (95% confidence interval 24% to 44%). This translates into an absolute improvement in survival of 16% at both six and 12 months and an improvement in median survival of 3.7 months. No age related differences were found in the effectiveness of chemotherapy, but elderly patients were under represented in trials. The overall quality of evidence relating to treatment toxicity, symptom control, and quality of life was poor. CONCLUSIONS: Chemotherapy is effective in prolonging time to disease progression and survival in patients with advanced colorectal cancer. The survival benefit may be underestimated in this analysis as some patients in the control arms received chemotherapy.

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Crossref · 10.1136/bmj.321.7260.531

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  • Randomized controlled trials involving PS 0 to PS 2 patients have shown that chemotherapy groups have a significantly longer survival time than BSC groups that did not receive anticancer drugs.

    “Randomized controlled trials involving PS 0 to PS 2 patients have shown that chemotherapy groups have a significantly longer survival time than BSC groups that did not receive anticancer drugs [54–56].”

    From Japanese Society for Cancer of the Colon and Rectum (JSCCR) guidelines 2016 for the treatment of colorectal cancer (2018) · cites this paper as [55]

    The Survival section reports significantly longer survival for the chemotherapy group in a pooled analysis of randomized trials. However, the paper does not establish that the patients were restricted to PS 0–2, and the Description of studies and Discussion note that some supportive-care patients subsequently received chemotherapy. The claim’s absolute description of the control groups is therefore not supported. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • Chemotherapy has improved overall survival from approximately 6 months in untreated historical cohorts to 16-20 months for FOLFOX and FOLFIRI combination therapy within clinical trials.

    “So far, chemotherapy has improved overall survival from approximately 6 months in untreated historical cohorts18 to 16–20 months for the doublet chemotherapy regimen with intravenous fluorouracil/leucovorin and oxaliplatin (FOLFOX)19 and doublet chemotherapy regimen with intravenous fluorouracil/leucovorin and irinotecan (FOLFIRI)20 combination therapy within clinical trials.”

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Research works printed but not linked: 4

  1. [10]10. Beretta G, Bollina R, Cozzi C, Morabito A. Should we consider the weekly chemotherapy with fluorouracil + racemic folic acid a standard treatment for advanced/metastatic carcinoma of the digestive tract in elderly patients? Proc Am Soc Clin Oncol 1997;16:A920.
  2. [11]11. Gerard A, Buyse M, Pector JC, Bleiberg H, Arnaud JP, Willems G, et al. Hepatic artery ligation with and without portal infusion of 5-FU. A rand- omized study in patients with unresectable liver metastases from colorec- tal carcinoma. The EORTC Gastrointestinal Cancer Cooperative Group (GI group). Eur J Surg Oncol 1991;17:289-94.
  3. [12]12. Hafstrom L, Engaras B, Holmberg SB, Gustavsson B, Jonsson P, Linder P, et al. Treatment of liver metastases from colorectal cancer with hepatic artery occlusion, intraportal 5-fluouracil infusion, and oral allopurinol. Cancer 1994;74:2749-56.
  4. [19]19. Chisholm E, Malhotra A, Giles GR. Quadruple chemotherapy for advanced colorectal cancer. Clin Oncol 1983;9:185-6.

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Authors
Colorectal Cancer Collaborative Group
Affiliations
Southampton General Hospital (GB)
Corresponding author
Colorectal Cancer Collaborative Group
Venue
BMJ
Publisher
BMJ
Published
2000-09-02
Volume
321
Issue
7260
Pages
531-535
ISSN
  • 0007-1447 (ISSN-L)
  • 0959-8138
  • 1468-5833
OpenAlex
W141482010
Cited by
662
References
22
Citations by year
2026: 5 · 2025: 5 · 2024: 3 · 2023: 9 · 2022: 5 · 2021: 11 · 2020: 16 · 2019: 17 · 2018: 8 · 2017: 19 · 2016: 17 · 2015: 26 · 2014: 26 · 2013: 16 · 2012: 22
FWCI
2.10
Type
journal article
Language
en
Open access
Locations
  • BMJ (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Oncology › Colorectal Cancer Treatments and Studies
  • Health Sciences › Medicine › Oncology › Colorectal Cancer Surgical Treatments
  • Health Sciences › Medicine › Surgery › Intraperitoneal and Appendiceal Malignancies
Keywords
palliative chemotherapy, advanced colorectal cancer, metastatic colorectal cancer, survival, disease progression, quality of life, chemotherapy toxicity, elderly patients, supportive care
MeSH terms
Aged, Antimetabolites, Antineoplastic, Fluorouracil, Humans, Middle Aged, Palliative Care, Colorectal Neoplasms, Proportional Hazards Models, Odds Ratio, Survival Analysis, Randomized Controlled Trials as Topic, Databases, Bibliographic, Treatment Outcome, Disease Progression

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