Different strategies of sequential and combination chemotherapy for patients with poor prognosis advanced colorectal cancer (MRC FOCUS): a randomised controlled trial
Different strategies of sequential and combination chemotherapy for patients with poor prognosis advanced colorectal cancer (MRC FOCUS): a randomised controlled trial
BACKGROUND: In the non-curative setting, the sequence in which anticancer agents are used, singly or in combination, may be important if patients are to receive the maximum period of disease control with the minimum of adverse effects. We compared sequential and combination chemotherapy strategies in patients with unpretreated advanced or metastatic colorectal cancer, who were regarded as not potentially curable irrespective of response.
METHODS: We studied patients with advanced colorectal cancer, starting treatment with non-curative intent. 2135 unpretreated patients were randomly assigned to three treatment strategies in the ratio 1:1:1. Strategy A (control group) was single-agent fluorouracil (given with levofolinate over 48 h every 2 weeks) until failure, then single-agent irinotecan. Strategy B was fluorouracil until failure, then combination chemotherapy. Strategy C was combination chemotherapy from the outset. Within strategies B and C, patients were randomly assigned to receive, as the combination regimen, fluorouracil plus irinotecan (groups B-ir and C-ir) or fluorouracil plus oxaliplatin (groups B-ox and C-ox). The primary endpoint was overall survival, analysed by intention to treat. This study is registered as an International Standard Randomised Controlled Trial, number ISRCTN 79877428.
RESULTS: Median survival of patients allocated to control strategy A was 13.9 months. Median survival of each of the other groups was longer (B-ir 15.0, B-ox 15.2, C-ir 16.7, and C-ox 15.4 months). However, log-rank comparison of each group against control showed that only C-ir--the first-line combination strategy including irinotecan--satisfied the statistical test for superiority (p=0.01). Overall comparison of strategy B with strategy C was within the predetermined non-inferiority boundary of HR=1.18 or less (HR=1.06, 90% CI 0.97-1.17).
INTERPRETATION: Our data challenge the assumption that, in this non-curative setting, maximum tolerable treatment must necessarily be used first-line. The staged approach of initial single-agent treatment upgraded to combination when required is not worse than first-line combination, and is an alternative option for discussion with patients.
Aged, Antineoplastic Combined Chemotherapy Protocols, Camptothecin, Colorectal Neoplasms, Drug Administration Schedule, Female, Fluorouracil, Humans, Leucovorin, Male, Middle Aged, Organoplatinum Compounds, Prognosis, Survival Analysis, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
143-52
Seymour, Matthew T
398287ed-4467-487d-b851-b43ceefc2c5e
Maughan, Timothy S
fb224abb-9c96-44d2-ad18-464c74271955
Ledermann, Jonathan A
d0779a51-47a1-4a53-bf0e-5a4cce8d930c
Topham, Clare
e5964f21-95c5-4336-b0d9-dc8298669d2d
James, Roger
15099c0b-7241-4bfc-8980-b34d92b3358d
Gwyther, Stephen J
dee39928-a4cc-4962-ae6d-d832d47c3890
Smith, David B
217b19f1-7588-4d54-a062-8394eea6dea1
Shepherd, Stephen
09fabe4c-b70d-4425-bf48-7abe13ffb4dd
Maraveyas, Anthony
d3b63674-d174-461a-b4d3-c561f9666440
Ferry, David R
75fb0004-e9d9-47db-8cde-5b9c48e8d737
Meade, Angela M
157e7055-92ac-4c89-ab51-3e9039b0d904
Thompson, Lindsay
c17054fe-dbf1-4989-919e-7bc3658c89b9
Griffiths, Gareth O
7fd300c0-d279-4ff6-842d-aa1f2b9b864d
Parmar, Mahesh K B
5574463d-506e-499e-9381-6130f1ef7dbe
Stephens, Richard J
f792b135-01d0-4ca3-82f5-bd6da92fe82e
FOCUS Trial Investigators
14 July 2007
Seymour, Matthew T
398287ed-4467-487d-b851-b43ceefc2c5e
Maughan, Timothy S
fb224abb-9c96-44d2-ad18-464c74271955
Ledermann, Jonathan A
d0779a51-47a1-4a53-bf0e-5a4cce8d930c
Topham, Clare
e5964f21-95c5-4336-b0d9-dc8298669d2d
James, Roger
15099c0b-7241-4bfc-8980-b34d92b3358d
Gwyther, Stephen J
dee39928-a4cc-4962-ae6d-d832d47c3890
Smith, David B
217b19f1-7588-4d54-a062-8394eea6dea1
Shepherd, Stephen
09fabe4c-b70d-4425-bf48-7abe13ffb4dd
Maraveyas, Anthony
d3b63674-d174-461a-b4d3-c561f9666440
Ferry, David R
75fb0004-e9d9-47db-8cde-5b9c48e8d737
Meade, Angela M
157e7055-92ac-4c89-ab51-3e9039b0d904
Thompson, Lindsay
c17054fe-dbf1-4989-919e-7bc3658c89b9
Griffiths, Gareth O
7fd300c0-d279-4ff6-842d-aa1f2b9b864d
Parmar, Mahesh K B
5574463d-506e-499e-9381-6130f1ef7dbe
Stephens, Richard J
f792b135-01d0-4ca3-82f5-bd6da92fe82e
Seymour, Matthew T, Maughan, Timothy S, Ledermann, Jonathan A, Topham, Clare, James, Roger, Gwyther, Stephen J, Smith, David B, Shepherd, Stephen, Maraveyas, Anthony, Ferry, David R, Meade, Angela M, Thompson, Lindsay, Griffiths, Gareth O, Parmar, Mahesh K B and Stephens, Richard J
,
FOCUS Trial Investigators
(2007)
Different strategies of sequential and combination chemotherapy for patients with poor prognosis advanced colorectal cancer (MRC FOCUS): a randomised controlled trial.
The Lancet, 370 (9582), .
(doi:10.1016/S0140-6736(07)61087-3).
Abstract
BACKGROUND: In the non-curative setting, the sequence in which anticancer agents are used, singly or in combination, may be important if patients are to receive the maximum period of disease control with the minimum of adverse effects. We compared sequential and combination chemotherapy strategies in patients with unpretreated advanced or metastatic colorectal cancer, who were regarded as not potentially curable irrespective of response.
METHODS: We studied patients with advanced colorectal cancer, starting treatment with non-curative intent. 2135 unpretreated patients were randomly assigned to three treatment strategies in the ratio 1:1:1. Strategy A (control group) was single-agent fluorouracil (given with levofolinate over 48 h every 2 weeks) until failure, then single-agent irinotecan. Strategy B was fluorouracil until failure, then combination chemotherapy. Strategy C was combination chemotherapy from the outset. Within strategies B and C, patients were randomly assigned to receive, as the combination regimen, fluorouracil plus irinotecan (groups B-ir and C-ir) or fluorouracil plus oxaliplatin (groups B-ox and C-ox). The primary endpoint was overall survival, analysed by intention to treat. This study is registered as an International Standard Randomised Controlled Trial, number ISRCTN 79877428.
RESULTS: Median survival of patients allocated to control strategy A was 13.9 months. Median survival of each of the other groups was longer (B-ir 15.0, B-ox 15.2, C-ir 16.7, and C-ox 15.4 months). However, log-rank comparison of each group against control showed that only C-ir--the first-line combination strategy including irinotecan--satisfied the statistical test for superiority (p=0.01). Overall comparison of strategy B with strategy C was within the predetermined non-inferiority boundary of HR=1.18 or less (HR=1.06, 90% CI 0.97-1.17).
INTERPRETATION: Our data challenge the assumption that, in this non-curative setting, maximum tolerable treatment must necessarily be used first-line. The staged approach of initial single-agent treatment upgraded to combination when required is not worse than first-line combination, and is an alternative option for discussion with patients.
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More information
Published date: 14 July 2007
Keywords:
Aged, Antineoplastic Combined Chemotherapy Protocols, Camptothecin, Colorectal Neoplasms, Drug Administration Schedule, Female, Fluorouracil, Humans, Leucovorin, Male, Middle Aged, Organoplatinum Compounds, Prognosis, Survival Analysis, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
Organisations:
Medical Education, Clinical Trials Unit
Identifiers
Local EPrints ID: 406326
URI: http://eprints.soton.ac.uk/id/eprint/406326
ISSN: 0140-6736
PURE UUID: 419c06a9-6f7b-4fb4-b8b3-ada22ec0f781
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Date deposited: 10 Mar 2017 10:44
Last modified: 16 Aug 2024 01:48
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Contributors
Author:
Matthew T Seymour
Author:
Timothy S Maughan
Author:
Jonathan A Ledermann
Author:
Clare Topham
Author:
Roger James
Author:
Stephen J Gwyther
Author:
David B Smith
Author:
Stephen Shepherd
Author:
Anthony Maraveyas
Author:
David R Ferry
Author:
Angela M Meade
Author:
Lindsay Thompson
Author:
Mahesh K B Parmar
Author:
Richard J Stephens
Corporate Author: FOCUS Trial Investigators
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