The University of Southampton
University of Southampton Institutional Repository

Standard or high dose chemoradiotherapy, with or without the protease inhibitor nelfinavir, in patients with locally advanced pancreatic cancer: the phase 1/randomised phase 2 SCALOP-2 trial

Standard or high dose chemoradiotherapy, with or without the protease inhibitor nelfinavir, in patients with locally advanced pancreatic cancer: the phase 1/randomised phase 2 SCALOP-2 trial
Standard or high dose chemoradiotherapy, with or without the protease inhibitor nelfinavir, in patients with locally advanced pancreatic cancer: the phase 1/randomised phase 2 SCALOP-2 trial
Background: the multi-centre two-stage SCALOP-2 trial (ISRCTN50083238) assessed whether dose escalation of consolidative chemoradiotherapy (CRT) or concurrent sensitization using the protease inhibitor nelfinavir improve outcomes in locally advanced pancreatic cancer (LAPC) following four cycles of gemcitabine/nab-paclitaxel.

Methods: in stage 1, the maximum tolerated dose (MTD) of nelfinavir concurrent with standard-dose CRT (50.4 Gy in 28 fractions) was identified from a cohort of 27 patients. In stage 2, 159 patients were enrolled in an open-label randomized controlled comparison of standard versus high dose (60 Gy in 30 fractions) CRT, with or without nelfinavir at MTD. Primary outcomes following dose escalation and nelfinavir use were respectively overall survival (OS) and progression free survival (PFS). Secondary endpoints included health-related quality of life (HRQoL).

Results: high dose CRT did not improve OS (16.9 (60 % confidence interval, CI 16.2–17.7) vs. 15.6 (60 %CI 14.3–18.2) months; adjusted hazard ratio, HR 1.13 (60 %CI 0.91–1.40; p = 0.68)). Similarly, median PFS was not improved by nelfinavir (10.0 (60 %CI 9.9–10.2) vs. 11.1 (60 %CI 10.3–12.8) months; adjusted HR 1.71 (60 %CI 1.38–2.12; p = 0.98)). Local progression at 12 months was numerically lower with high-dose CRT than with standard dose CRT (n = 11/46 (23.9 %) vs. n = 15/45 (33.3 %)). Neither nelfinavir nor radiotherapy dose escalation impacted on treatment compliance or grade 3/4 adverse event rate. There were no sustained differences in HRQoL scores between treatment groups over 28 weeks post-treatment.

Conclusions: dose-escalated CRT may improve local tumour control and is well tolerated when used as consolidative treatment in LAPC but does not impact OS. Nelfinavir use does not improve PFS.
Chemoradiotherapy, Dose escalation, Health-related quality of life, Nelfinavir, Outcomes, Pancreatic cancer, Survival, Toxicity
0959-8049
Mukherjee, Somnath
81b82408-8d54-4983-a412-81969f5edfdd
Qi, Cathy
becf7b18-4600-4e34-a31c-a2376958d89e
Shaw, Rachel
e13d32cd-9fe8-4ccf-aedc-1973950db8bf
Jones, Christopher M.
1859a414-71a6-4bf9-897c-81d00c80bf77
Bridgewater, John A.
22a97d4c-b9df-4f88-b413-d3193d2d14b7
Radhakrishna, Ganesh
9f1b2cb2-3fbe-4cb6-ada9-d8a3c120c937
Patel, Neel
c222e69f-5076-4686-b790-31565a044928
Holmes, Jane
cae8db15-fb4a-473f-a5f8-5008dc4c8991
Virdee, Pradeep S.
7b32d7e6-5a66-4f9b-a944-c8166e6b09c2
Tranter, Bethan
e7de6aab-6e5f-4ef2-bf1e-cb9b99ebdedf
Parsons, Philip
48a6af49-b049-446e-86a9-d07395f14ee9
Falk, Stephen
6bda4f5d-d5b0-4558-89d3-9e32cacf202a
Wasan, Harpreet S.
b3e99d74-5de4-4ae4-9721-8c639f6adbdb
Ajithkumar, Thankamma V.
721f6fa3-f47f-4a56-9c68-c7f7f5d218fc
Holyoake, Daniel
7de47192-264d-4b77-810d-ae22852beeda
Roy, Rajarshi
7de1069c-55ef-4dd8-89e3-1ae379e5c6e5
Scott-Brown, Martin
a11781a3-f887-4db7-9b92-ceff24c7b90b
Hurt, Christopher N.
bf8b37a0-8f08-4b47-b3f3-6fc65f7ab87f
O’Neill, Eric
e07a61b5-078a-466f-a369-7a621da27653
Sebag-Montefiore, David
7cd6f558-4265-4adb-b8dd-771f47ab8343
Maughan, Tim S.
2ff5497d-063a-4788-a620-23fc6473f08b
Hawkins, Maria A.
fe46c6fb-a77c-4308-8861-48b34a65c2f3
Corrie, Pippa
3db0646e-eb17-4b5e-b13f-d02dd449cddb
Mukherjee, Somnath
81b82408-8d54-4983-a412-81969f5edfdd
Qi, Cathy
becf7b18-4600-4e34-a31c-a2376958d89e
Shaw, Rachel
e13d32cd-9fe8-4ccf-aedc-1973950db8bf
Jones, Christopher M.
1859a414-71a6-4bf9-897c-81d00c80bf77
Bridgewater, John A.
22a97d4c-b9df-4f88-b413-d3193d2d14b7
Radhakrishna, Ganesh
9f1b2cb2-3fbe-4cb6-ada9-d8a3c120c937
Patel, Neel
c222e69f-5076-4686-b790-31565a044928
Holmes, Jane
cae8db15-fb4a-473f-a5f8-5008dc4c8991
Virdee, Pradeep S.
7b32d7e6-5a66-4f9b-a944-c8166e6b09c2
Tranter, Bethan
e7de6aab-6e5f-4ef2-bf1e-cb9b99ebdedf
Parsons, Philip
48a6af49-b049-446e-86a9-d07395f14ee9
Falk, Stephen
6bda4f5d-d5b0-4558-89d3-9e32cacf202a
Wasan, Harpreet S.
b3e99d74-5de4-4ae4-9721-8c639f6adbdb
Ajithkumar, Thankamma V.
721f6fa3-f47f-4a56-9c68-c7f7f5d218fc
Holyoake, Daniel
7de47192-264d-4b77-810d-ae22852beeda
Roy, Rajarshi
7de1069c-55ef-4dd8-89e3-1ae379e5c6e5
Scott-Brown, Martin
a11781a3-f887-4db7-9b92-ceff24c7b90b
Hurt, Christopher N.
bf8b37a0-8f08-4b47-b3f3-6fc65f7ab87f
O’Neill, Eric
e07a61b5-078a-466f-a369-7a621da27653
Sebag-Montefiore, David
7cd6f558-4265-4adb-b8dd-771f47ab8343
Maughan, Tim S.
2ff5497d-063a-4788-a620-23fc6473f08b
Hawkins, Maria A.
fe46c6fb-a77c-4308-8861-48b34a65c2f3
Corrie, Pippa
3db0646e-eb17-4b5e-b13f-d02dd449cddb

Mukherjee, Somnath, Qi, Cathy, Shaw, Rachel, Jones, Christopher M., Bridgewater, John A., Radhakrishna, Ganesh, Patel, Neel, Holmes, Jane, Virdee, Pradeep S., Tranter, Bethan, Parsons, Philip, Falk, Stephen, Wasan, Harpreet S., Ajithkumar, Thankamma V., Holyoake, Daniel, Roy, Rajarshi, Scott-Brown, Martin, Hurt, Christopher N., O’Neill, Eric, Sebag-Montefiore, David, Maughan, Tim S., Hawkins, Maria A. and Corrie, Pippa (2024) Standard or high dose chemoradiotherapy, with or without the protease inhibitor nelfinavir, in patients with locally advanced pancreatic cancer: the phase 1/randomised phase 2 SCALOP-2 trial. European Journal of Cancer, 209, [114236]. (doi:10.1016/j.ejca.2024.114236).

Record type: Article

Abstract

Background: the multi-centre two-stage SCALOP-2 trial (ISRCTN50083238) assessed whether dose escalation of consolidative chemoradiotherapy (CRT) or concurrent sensitization using the protease inhibitor nelfinavir improve outcomes in locally advanced pancreatic cancer (LAPC) following four cycles of gemcitabine/nab-paclitaxel.

Methods: in stage 1, the maximum tolerated dose (MTD) of nelfinavir concurrent with standard-dose CRT (50.4 Gy in 28 fractions) was identified from a cohort of 27 patients. In stage 2, 159 patients were enrolled in an open-label randomized controlled comparison of standard versus high dose (60 Gy in 30 fractions) CRT, with or without nelfinavir at MTD. Primary outcomes following dose escalation and nelfinavir use were respectively overall survival (OS) and progression free survival (PFS). Secondary endpoints included health-related quality of life (HRQoL).

Results: high dose CRT did not improve OS (16.9 (60 % confidence interval, CI 16.2–17.7) vs. 15.6 (60 %CI 14.3–18.2) months; adjusted hazard ratio, HR 1.13 (60 %CI 0.91–1.40; p = 0.68)). Similarly, median PFS was not improved by nelfinavir (10.0 (60 %CI 9.9–10.2) vs. 11.1 (60 %CI 10.3–12.8) months; adjusted HR 1.71 (60 %CI 1.38–2.12; p = 0.98)). Local progression at 12 months was numerically lower with high-dose CRT than with standard dose CRT (n = 11/46 (23.9 %) vs. n = 15/45 (33.3 %)). Neither nelfinavir nor radiotherapy dose escalation impacted on treatment compliance or grade 3/4 adverse event rate. There were no sustained differences in HRQoL scores between treatment groups over 28 weeks post-treatment.

Conclusions: dose-escalated CRT may improve local tumour control and is well tolerated when used as consolidative treatment in LAPC but does not impact OS. Nelfinavir use does not improve PFS.

Text
SCALOP2_Manuscript_FinalWorkingdraft-FINAL_CMJ_clean - Accepted Manuscript
Restricted to Repository staff only until 26 July 2025.
Request a copy
Text
Tables_FinalWorkingDraft_CMJ
Restricted to Repository staff only
Request a copy
Text
Figures_FinalWorkingDraft-FINAL
Restricted to Repository staff only
Request a copy
Text
Appendix 2 - Supplementary information_CMJ_clean
Restricted to Repository staff only
Request a copy

More information

e-pub ahead of print date: 23 July 2024
Published date: 26 July 2024
Keywords: Chemoradiotherapy, Dose escalation, Health-related quality of life, Nelfinavir, Outcomes, Pancreatic cancer, Survival, Toxicity

Identifiers

Local EPrints ID: 495193
URI: http://eprints.soton.ac.uk/id/eprint/495193
ISSN: 0959-8049
PURE UUID: 4b753690-f1ac-42d8-b27f-ed24378e4090
ORCID for Christopher N. Hurt: ORCID iD orcid.org/0000-0003-1206-8355

Catalogue record

Date deposited: 31 Oct 2024 17:40
Last modified: 01 Nov 2024 03:07

Export record

Altmetrics

Contributors

Author: Somnath Mukherjee
Author: Cathy Qi
Author: Rachel Shaw
Author: Christopher M. Jones
Author: John A. Bridgewater
Author: Ganesh Radhakrishna
Author: Neel Patel
Author: Jane Holmes
Author: Pradeep S. Virdee
Author: Bethan Tranter
Author: Philip Parsons
Author: Stephen Falk
Author: Harpreet S. Wasan
Author: Thankamma V. Ajithkumar
Author: Daniel Holyoake
Author: Rajarshi Roy
Author: Martin Scott-Brown
Author: Christopher N. Hurt ORCID iD
Author: Eric O’Neill
Author: David Sebag-Montefiore
Author: Tim S. Maughan
Author: Maria A. Hawkins
Author: Pippa Corrie

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.

×