The University of Southampton
University of Southampton Institutional Repository

Gemcitabine alone or in combination with cisplatin in patients with advanced or metastatic cholangiocarcinomas or other biliary tract tumours: a multicentre randomised phase II study - the UK ABC-01 study

Gemcitabine alone or in combination with cisplatin in patients with advanced or metastatic cholangiocarcinomas or other biliary tract tumours: a multicentre randomised phase II study - the UK ABC-01 study
Gemcitabine alone or in combination with cisplatin in patients with advanced or metastatic cholangiocarcinomas or other biliary tract tumours: a multicentre randomised phase II study - the UK ABC-01 study
Background: we assessed the activity of gemcitabine (G) and cisplatin/gemcitabine (C/G) in patients with locally advanced (LA) or metastatic (M) (advanced) biliary cancers (ABC) for whom there is no standard chemotherapy.
Methods: patients, aged greater than or equal to18 years, with pathologically confirmed ABC, Karnofsky performance (KP) greater than or equal to60, and adequate haematological, hepatic and renal function were randomised to G 1000?mg?m?2 on D1, 8, 15 q28d (Arm A) or C 25?mg?m?2 followed by G 1000?mg?m?2 D1, 8 q21d (Arm B) for up to 6 months or disease progression.
Results: in total, 86 patients (A/B, n=44/42) were randomised between February 2002 and May 2004. Median age (64/62.5 years), KP, primary tumour site, earlier surgery, indwelling biliary stent and disease stage (LA: 25/38%) are comparable between treatment arms. Grade 3–4 toxicity included (A/B, % patients) anaemia (4.5/2.4), leukopenia (6.8/4.8), neutropenia (13.6/14.3), thrombocytopenia (9.1/11.9), lethargy (9.1/28.6), nausea/vomiting (0/7.1) and anorexia (2.3/4.8). Responses (WHO criteria, % of evaluable patients: A n=31 vs B n=36): no CRs; PR 22.6 vs 27.8%; SD 35.5 vs 47.1% for a tumour control rate (CR+PR+SD) of 58.0 vs 75.0%. The median TTP and 6-month progression-free survival (PFS) (the primary end point) were greater in the C/G arm (4.0 vs 8.0 months and 45.5 vs 57.1% in arms A and B, respectively).
Conclusion: both regimens seem active in ABC. C/G is associated with an improved tumour control rate, TTP and 6-month PFS. The study has been extended (ABC-02 study) and powered to determine the effect on overall survival and the quality of life
cholangiocarcinoma, gallbladder cancer, biliary tract, chemotherapy, gemcitabine, cisplatin
0007-0920
621-627
Valle, J.W.
6c843c8f-08ba-40c9-b8e9-a29affa03aec
Wasan, H.
164ed21f-3e69-441e-b840-3a12cd8d19d4
Johnson, P.
f908ae86-60e0-4157-b387-26df76ff956b
Jones, E.
52e90d30-403c-44c5-9cb4-238fb75641d3
Dixon, L.
6d208aac-e596-4b61-97d4-69f783cf5216
Swindell, R.
4449ab53-e6c3-4416-a097-bc1bfbe9c1c8
Baka, S.
e2c19dac-ca2d-48a8-b081-06b8c55eff6e
Maraveyas, A.
97566f81-6f85-466e-a26e-dd1deab52867
Corrie, P.
e7c55e64-c126-43f8-bff5-dd38ecaf6c01
Falk, S.
027429c5-5570-414e-a8ca-b6ecf6e2ae06
Golins, S.
0f6d1c80-db50-4965-8726-c1debd1ebfff
Lofts, F.
5ae80cd9-3103-4052-9704-a8dffeb7caa8
Evans, L.
70b368ef-5cbe-40e2-97b1-c4f89da2d049
Meyer, T.
8ac918a9-e659-4d8e-8ada-7c0b205b54e6
Anthoney, A.
1d07dea6-703a-412d-a35e-5c37ca9d238d
Iveson, T.
867cb6c5-ea9a-4521-a4cc-4cd4d2503b3a
Highley, M.
bc89d697-9cf4-428b-9abe-099aca8743f7
Osborne, R.
e9f373c1-48aa-4cec-8fce-da201cc63187
Bridgewater, J.
a9612e28-f0c0-4792-8be5-e14b2cd07408
Valle, J.W.
6c843c8f-08ba-40c9-b8e9-a29affa03aec
Wasan, H.
164ed21f-3e69-441e-b840-3a12cd8d19d4
Johnson, P.
f908ae86-60e0-4157-b387-26df76ff956b
Jones, E.
52e90d30-403c-44c5-9cb4-238fb75641d3
Dixon, L.
6d208aac-e596-4b61-97d4-69f783cf5216
Swindell, R.
4449ab53-e6c3-4416-a097-bc1bfbe9c1c8
Baka, S.
e2c19dac-ca2d-48a8-b081-06b8c55eff6e
Maraveyas, A.
97566f81-6f85-466e-a26e-dd1deab52867
Corrie, P.
e7c55e64-c126-43f8-bff5-dd38ecaf6c01
Falk, S.
027429c5-5570-414e-a8ca-b6ecf6e2ae06
Golins, S.
0f6d1c80-db50-4965-8726-c1debd1ebfff
Lofts, F.
5ae80cd9-3103-4052-9704-a8dffeb7caa8
Evans, L.
70b368ef-5cbe-40e2-97b1-c4f89da2d049
Meyer, T.
8ac918a9-e659-4d8e-8ada-7c0b205b54e6
Anthoney, A.
1d07dea6-703a-412d-a35e-5c37ca9d238d
Iveson, T.
867cb6c5-ea9a-4521-a4cc-4cd4d2503b3a
Highley, M.
bc89d697-9cf4-428b-9abe-099aca8743f7
Osborne, R.
e9f373c1-48aa-4cec-8fce-da201cc63187
Bridgewater, J.
a9612e28-f0c0-4792-8be5-e14b2cd07408

Valle, J.W., Wasan, H., Johnson, P., Jones, E., Dixon, L., Swindell, R., Baka, S., Maraveyas, A., Corrie, P., Falk, S., Golins, S., Lofts, F., Evans, L., Meyer, T., Anthoney, A., Iveson, T., Highley, M., Osborne, R. and Bridgewater, J. (2009) Gemcitabine alone or in combination with cisplatin in patients with advanced or metastatic cholangiocarcinomas or other biliary tract tumours: a multicentre randomised phase II study - the UK ABC-01 study. British Journal of Cancer, 101 (4), 621-627. (doi:10.1038/sj.bjc.6605211).

Record type: Article

Abstract

Background: we assessed the activity of gemcitabine (G) and cisplatin/gemcitabine (C/G) in patients with locally advanced (LA) or metastatic (M) (advanced) biliary cancers (ABC) for whom there is no standard chemotherapy.
Methods: patients, aged greater than or equal to18 years, with pathologically confirmed ABC, Karnofsky performance (KP) greater than or equal to60, and adequate haematological, hepatic and renal function were randomised to G 1000?mg?m?2 on D1, 8, 15 q28d (Arm A) or C 25?mg?m?2 followed by G 1000?mg?m?2 D1, 8 q21d (Arm B) for up to 6 months or disease progression.
Results: in total, 86 patients (A/B, n=44/42) were randomised between February 2002 and May 2004. Median age (64/62.5 years), KP, primary tumour site, earlier surgery, indwelling biliary stent and disease stage (LA: 25/38%) are comparable between treatment arms. Grade 3–4 toxicity included (A/B, % patients) anaemia (4.5/2.4), leukopenia (6.8/4.8), neutropenia (13.6/14.3), thrombocytopenia (9.1/11.9), lethargy (9.1/28.6), nausea/vomiting (0/7.1) and anorexia (2.3/4.8). Responses (WHO criteria, % of evaluable patients: A n=31 vs B n=36): no CRs; PR 22.6 vs 27.8%; SD 35.5 vs 47.1% for a tumour control rate (CR+PR+SD) of 58.0 vs 75.0%. The median TTP and 6-month progression-free survival (PFS) (the primary end point) were greater in the C/G arm (4.0 vs 8.0 months and 45.5 vs 57.1% in arms A and B, respectively).
Conclusion: both regimens seem active in ABC. C/G is associated with an improved tumour control rate, TTP and 6-month PFS. The study has been extended (ABC-02 study) and powered to determine the effect on overall survival and the quality of life

This record has no associated files available for download.

More information

Published date: 18 August 2009
Keywords: cholangiocarcinoma, gallbladder cancer, biliary tract, chemotherapy, gemcitabine, cisplatin

Identifiers

Local EPrints ID: 79356
URI: http://eprints.soton.ac.uk/id/eprint/79356
ISSN: 0007-0920
PURE UUID: 495953f3-091f-498f-89b1-282d21add0a0
ORCID for T. Iveson: ORCID iD orcid.org/0000-0002-4681-2712

Catalogue record

Date deposited: 15 Mar 2010
Last modified: 14 Mar 2024 02:41

Export record

Altmetrics

Contributors

Author: J.W. Valle
Author: H. Wasan
Author: P. Johnson
Author: E. Jones
Author: L. Dixon
Author: R. Swindell
Author: S. Baka
Author: A. Maraveyas
Author: P. Corrie
Author: S. Falk
Author: S. Golins
Author: F. Lofts
Author: L. Evans
Author: T. Meyer
Author: A. Anthoney
Author: T. Iveson ORCID iD
Author: M. Highley
Author: R. Osborne
Author: J. Bridgewater

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×