» Articles » PMID: 27647984

Optimal Duration of a First-line Palliative Chemotherapy in Disseminated Colorectal Cancer - a Review of the Literature from a Developing Country Perspective

Overview
Publisher Termedia
Specialty Oncology
Date 2016 Sep 21
PMID 27647984
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

We still do not know whether the presently used protocol of the first-line palliative treatment of disseminated colorectal cancer (FOLFOX/FOLFIRI protocol) allows maximization of therapeutic response and minimization of side effects. No-one has verified whether continuation of the first-line chemotherapy despite the lack of progression is reflected by improved prognosis or significant risk of toxicity. This issue is of vital importance in the case of developing countries where targeted therapies are not available due to financial shortages. We have identified three potential strategies of the palliative therapy of disseminated colorectal cancer: 1) discontinuation of chemotherapy after a fixed number of cycles with its restart on progression (stop-and-go strategy), 2) intermittent protocol of chemotherapy, and 3) continuation of chemotherapy with discontinuation of the most toxic agent. None of the studies proved the superiority of the most commonly used standard, i.e. 12 cycles of the FOLFOX or FOLFIRI regimen. Although longer duration of this treatment may be associated with higher response rates and longer progression-free survival, these improvements frequently prove insignificant on statistical analysis.

Citing Articles

Selective Antibacterial and Antiproliferative Effects of Ethanolic Extracts from Cambodian and Philippine Plants Used in Folk Medicine for Diarrhea Treatment.

Kudera T, Fiserova B, Korytakova M, Doskocil I, Salmonova H, Tulin E Front Pharmacol. 2021; 12:746808.

PMID: 34899301 PMC: 8661004. DOI: 10.3389/fphar.2021.746808.


Carbon nanotube/polyurethane modified hollow fiber-pencil graphite electrode for in situ concentration and electrochemical quantification of anticancer drugs Capecitabine and Erlotinib.

Eshaghi Z, Moeinpour F Eng Life Sci. 2020; 19(4):302-314.

PMID: 32625010 PMC: 6999328. DOI: 10.1002/elsc.201800167.


Salidroside could enhance the cytotoxic effect of L‑OHP on colorectal cancer cells.

Shi X, Zhao W, Yang Y, Wu S, Lv B Mol Med Rep. 2017; 17(1):51-58.

PMID: 29115408 PMC: 5780144. DOI: 10.3892/mmr.2017.7846.

References
1.
Lokich J, Ahlgren J, Cantrell J, HEIM W, WAMPLER G, Gullo J . A prospective randomized comparison of protracted infusional 5-fluorouracil with or without weekly bolus cisplatin in metastatic colorectal carcinoma. A Mid-Atlantic Oncology Program study. Cancer. 1991; 67(1):14-9. DOI: 10.1002/1097-0142(19910101)67:1<14::aid-cncr2820670104>3.0.co;2-m. View

2.
Sobrero A, Herrmann R, Rischin D, Zalcberg J . Does biomodulation of 5-fluorouracil improve results?. Eur J Cancer. 1999; 35(2):186-94. DOI: 10.1016/s0959-8049(98)00362-1. View

3.
Elonen E, Almqvist A, Hanninen A, Jansson S, JARVENTIE G, Koistinen P . Comparison between four and eight cycles of intensive chemotherapy in adult acute myeloid leukemia: a randomized trial of the Finnish Leukemia Group. Leukemia. 1998; 12(7):1041-8. DOI: 10.1038/sj.leu.2401068. View

4.
Therasse P, Arbuck S, Eisenhauer E, Wanders J, Kaplan R, Rubinstein L . New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst. 2000; 92(3):205-16. DOI: 10.1093/jnci/92.3.205. View

5.
. Duration and intensity of maintenance chemotherapy in acute lymphoblastic leukaemia: overview of 42 trials involving 12 000 randomised children. Lancet. 1996; 347(9018):1783-8. DOI: 10.1016/s0140-6736(96)91615-3. View