Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster session 05

1614P - Integrated palliative care for patients referred for Chimeric Antigen Receptor T-cell (CAR-T) therapy: A service evaluation

Date

21 Oct 2023

Session

Poster session 05

Topics

Supportive Care and Symptom Management;  End-of-Life Care;  Cell-Based Therapy

Tumour Site

Lymphomas

Presenters

Rebekah Williams

Citation

Annals of Oncology (2023) 34 (suppl_2): S887-S894. 10.1016/S0923-7534(23)01267-X

Authors

R. Williams1, J.M. Droney1, E. Nicholson2, C. Arias2, R. Ellard2, N. Bradley2, C. Maycock2, A. Halley1

Author affiliations

  • 1 Symptom Control And Palliative Care Department, The Royal Marsden Hospital - Chelsea, SW3 6JJ - London/GB
  • 2 Haematology, The Royal Marsden Hospital (Sutton), SM2 5PT - Sutton/GB

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 1614P

Background

CAR-T therapy is potentially lifesaving for patients with certain types of refractory or relapsed lymphoma. However, patients face uncertainty about treatment outcomes and are at risk of severe toxicity. A novel integrated service was developed at our cancer centre offering patients with lymphoma being considered for CAR-T therapy a review by the Palliative Care team. The aims of this study were to describe the uptake of this service and the nature of the palliative care interventions.

Methods

Health record data was analysed for all patients with lymphoma referred for consideration of CAR-T therapy at a tertiary referral cancer centre between January 2020 and March 2022. Outcomes were recorded up to 1 year. This service evaluation was approved by the local Committee for Clinical Research.

Results

37 patient records were included. 83.8% (n=31) proceeded with CAR-T therapy. All patients had 2 or more previous lines of systemic treatment. 97.3% had an ECOG performance status of 0-1 at time of referral and median age was 66 years. Post CAR-T therapy, 35.5% had disease progression or relapse. 35.5% developed a grade 3 or 4 toxicity. 5 patients (16.1%) died, 4 due to disease progression and 4 of whom were seen by palliative care. The median time between first palliative care review and death was 133 days (range 78 - 309). Of the patients who did not proceed with CAR-T therapy, 100% (n=6) died, all due to disease progression, of whom 5 were seen by palliative care. The median time between first palliative care review and death was 18 days (range 1 - 99). In total 25 patients (67.6%) were seen by the palliative care team, of whom 40% had more than 1 consultation. The most frequent interventions were information provision (n=25), symptom control (n=13), communication (n=10) and advance care planning (n=9). Pain was the most common symptom, followed by constipation, nausea and vomiting and anxiety.

Conclusions

An integrated palliative care service is feasible within a CAR-T oncology service and is an opportunity to provide patients with information about palliative care. Development of an earlier and more integrated service can be explored. Specialist palliative care input may be required to support symptom control and advance care planning.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The Royal Marsden NHS Foundation Trust.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.