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 07

2196P - PET-CT detects response to treatment with ipilimumab and nivolumab in malignant mesothelioma far better than CT

Date

21 Oct 2023

Session

Poster session 07

Topics

Immunotherapy

Tumour Site

Mesothelioma

Presenters

Daniel C. Christoph

Citation

Annals of Oncology (2023) 34 (suppl_2): S1135-S1144. 10.1016/S0923-7534(23)01269-3

Authors

D.C.C. Christoph1, M. Metzenmacher2, S. Bölükbas3, J. Volmerig4, G. Nilius5, D. Moka6, H. Hautzel7

Author affiliations

  • 1 Medical Oncology, KEM | Evang. Kliniken Essen-Mitte gGmbH, 45136 - Essen/DE
  • 2 Medical Oncology, WTZ - Westdeutsches Tumorzentrum Essen, 45147 - Essen/DE
  • 3 Department Of Thoracic Surgery And Endoscopy, West German Cancer Center, University Medicine Essen - Ruhrlandklinik, University Duisburg-Essen, 45239 - Essen/DE
  • 4 Thoracic Surgery, KEM | Evang. Kliniken Essen-Mitte gGmbH, 45136 - Essen/DE
  • 5 Pneumology, KEM | Evang. Kliniken Essen-Mitte gGmbH, 45136 - Essen/DE
  • 6 Nuclear Medicine Centre, Nuclear Medicine Centre, 45136 - Essen/DE
  • 7 Nuclear Medicine, Universitätsklinikum Essen, 45147 - Essen/DE

Resources

Login to get immediate access to this content.

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

Abstract 2196P

Background

Checkpoint-Inhibition with Ipilimumab and Nivolumab is standard-of-care for first-line treatment of patients with unresectable malignant mesothelioma. However, response assessment by conventional CT using modified RECIST might miss detection of response and result in premature treatment discontinuation. PET-CT based assessment might recognize more patients benefitting from this therapy.

Methods

A retrospective analysis of patients suffering from unresectable malignant mesothelioma who were treated with first-line nivolumab and ipilimumab was performed. Patients got therapy in the Department of Medical Oncology (at the Evang. Kliniken Essen-Mitte or the University Hospital Essen) and underwent PET-CT. Patients received PET-CT scan at their initial diagnosis to clarify resectability (baseline PET-CT). PET-CT scans were repeated after every 12 weeks of treatment. ORR was calculated by using RECIST v1.1, mRECIST, PERCISTSULpeak and PERCISTMTV were used separately to categorize responders in CT and PET imaging studies.

Results

27 patients (19 male (70.4%) and 8 female patients (29.6%) received a baseline PET-CT and underwent therapy with ipilimumab (1mg/kg, q1, q6w) and nivolumab (360 mg abs., d1+22, q6w). Due to clinical progression and/or adverse events, a follow-up PET-CT was performed only in 18 patients (while 3 patients have recently started therapy). In 2 patients (7.4%), CT scan based response assessment showed progressive disease, However, both patients continued treatment due to metabolic response detected in additional PET-CT follow-up scans. Another patient showed progression after 2 cycles, continued therapy due to clinical benefit and responded well after 4 cycles (pseudo-progression). According to follow-up PET-CT scan, 8 patients responded (42.1%), 7 patients achieved diseases stabilization (36.8%) and 4 patients showed progression (21.1%). Median PFS/OS was 8.5/17.3 months. Detailed response assessment with RECIST v1.1, mRECIST, PERCISTSULpeak and PERCISTMTV will be reported at the meeting.

Conclusions

PET-CT scans based response assessment identifies mesothelioma patients responding to ipilimumab and nivolumab better than CT scans.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

D.C.C. Christoph.

Funding

Has not received any funding.

Disclosure

D.C.C. Christoph: Financial Interests, Personal, Speaker, Consultant, Advisor: AstraZeneca, Boehringer-Ingelheim, Bristol Myers Squibb, Chugai, MSD Merck, Sharp & Dohme, Novartis, Novocure, Pfizer, Roche, Sanofi, Takeda. M. Metzenmacher: Financial Interests, Personal, Advisory Board: AstraZeneca, Bristol Myers Squibb, MSD Merck, Sharp & Dohme, Novartis, Novocure, Pfizer, Roche, Takeda. S. Bölükbas: Financial Interests, Personal, Advisory Board: AstraZeneca, BD; Financial Interests, Personal, Speaker’s Bureau: AstraZeneca, Bristol Myers Squibb, KLS Martin, Roche. All other 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.