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 09

633P - Determining the prognostic value of end of treatment (EOT) 18F-choline positron emission tomography (PET) in patients treated with primary central nervous system lymphoma (PCNSL) who respond to first-line therapy: A single centre retrospective study at the Royal Marsden Hospital (RMH)

Date

10 Sep 2022

Session

Poster session 09

Topics

Radiological Imaging;  Nuclear Medicine and Clinical Molecular Imaging

Tumour Site

Lymphomas;  Central Nervous System Malignancies

Presenters

Su Li

Citation

Annals of Oncology (2022) 33 (suppl_7): S283-S294. 10.1016/annonc/annonc1055

Authors

S. Li1, B. Sharma2, Y. Du2, D. El-Sharkawi2, S. Iyengar3, E. Nicholson3, M. Potter4, M. Ethell4, C. Arias3, S. Easdale3, E. Alexander5, D. Cunningham1, I. Chau6

Author affiliations

  • 1 Medical Oncology Department, The Royal Marsden Hospital - NHS Foundation Trust, SW3 6JJ - London/GB
  • 2 Department Of Radiology, The Royal Marsden Hospital (Sutton), SM2 5PT - Sutton/GB
  • 3 Department Of Haematology, The Royal Marsden Hospital (Sutton), SM2 5PT - Sutton/GB
  • 4 Department Of Haematology, The Royal Marsden Hospital (Sutton), SM1 5PT - Sutton/GB
  • 5 Department Of Medicine  , The Royal Marsden Hospital (Sutton), SM1 5PT - Sutton/GB
  • 6 Deaprtment Of Medicine  , The Institute of Cancer Research/Royal Marsden NHS Foundation Trust, SM1 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 633P

Background

PCNSL response assessments rely upon contrast enhanced magnetic resonance imaging (MRI) for the evaluation of response. EOT MRI is not fully accurate in anticipating cure or relapse as patients (pts) in complete response (CR) will recur while some patients in partial response (PR) will not. We aimed to determine the prognostic value of EOT 18F-choline PET as novel adjunctive study at the RMH for pts with PR and CR at EOT MRI following first line (1L) treatment.

Methods

Clinical data was collected from pts treated at RMH for PCNSL between August 2009 and March 2020. Kaplan Meier survival analysis for progression free survival (PFS) and overall survival (OS) was performed for pts who were in PR (residual contrast visible) or CR (no residual contrast) on their EOT MRI. PFS and OS was also calculated for pts with residual choline (PET-PR) vs no residual choline uptake (PET-CR) on PET. PFS is calculated from time from 1st treatment to progression/death. OS is calculated from time from 1st treatment to death of any cause.

Results

70 pts were treated for PCNSL. 40/70 pts completed all intended induction treatment. The majority that did not complete treatment was due to progression/death. 7 pts that completed intended treatment were excluded from evaluation as 3 had progressive disease (PD) on their EOT MRI and EOT MRI was not available for 4. All 3 patients with PD had choline uptake on their EOT scan. For the remaining 33 evaluable pts the table below summarises their outcomes. After this EOT timepoint, 17 of these 33 patients proceeded to consolidation with either whole brain radiotherapy or autologous stem cell transplant following 1L chemotherapy. Table: 633P

(n)= Number of pts. (*)=Omitting pts where no PET performed. (+)= Unable to calculate upper bound due to insufficient number of events
Response category n Median PFS (years) (95% CI) p-value Median OS (years) (95% CI) p-value n receiving consolidation after 1L therapy
All pts 33 2.2 (1.2, 7.0) 5.0 (2.0, +) 17
EOT MRI outcome CR 17 1.6 (0.6, 5.7) 0.08 5.0 (1.2, +) 0.40 6
PR 16 5.2 (1.6, +) 6.0 (1.8, +) 11
EOT PET outcome* CR 19 1.9 (0.8, 7.0) 0.98 5.0 (1.8, +) 0.73 7
PR 5 2.2 (0.8, +) 4.8 (1.5, +) 3

Conclusions

Patients achieving PR on MR or PET had similar OS to those with CR. This could be attributed to higher proportion of pts with PR receiving consolidation therapy.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

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.