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

2191P - Real-world outcomes of patients with malignant pleural mesothelioma (MPM) treated with combination nivolumab and ipilimumab in the first- or later line setting

Date

21 Oct 2023

Session

Poster session 07

Topics

Immunotherapy

Tumour Site

Mesothelioma

Presenters

Sabine Schmid

Citation

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

Authors

S. Schmid1, L. Holer2, M. Frueh3, K. Koster4, S.I. Rothschild5, C. Britschgi6, L. Boos7, L. Frehner8, S. Cardoso Almeida9, Y. Metaxas10, M.T. Mark11, P.R. Froesch12, W. Janthur13, A.T. Allemann14, C. Waibel15, C. Vonder Mühll-Schill16, F.W.F. Cerciello17, L.A. Mauti18

Author affiliations

  • 1 Oncology And Haematology Department, Inselspital - Universitatsklinik fur Medizinische Onkologie, 3010 - Bern/CH
  • 2 -, SAKK - Swiss Group for Clinical Cancer Research, 3008 - Bern/CH
  • 3 Medical Oncology, Kantonsspital St. Gallen, 9007 - St. Gallen/CH
  • 4 Department Of Medical Oncology And Hematology, Kantonsspital St. Gallen, 9007 - St. Gallen/CH
  • 5 Medical Oncology Department, Universitätsspital Basel, 4031 - Basel/CH
  • 6 Department Of Medical Oncology And Hematology, USZ - University Hospital Zürich, 8091 - Zurich/CH
  • 7 Medical Oncology, University Hospital Zürich, 8091 - Zurich/CH
  • 8 Medical Oncology, University of Bern, 3012 - Bern/CH
  • 9 Medical Oncology, KSW - Kantonsspital Winterthur, 8401 - Winterthur/CH
  • 10 Oncology/hematology Department, Spital Thurgau AG - Kantonsspital Muensterlingen, 8596 - Muensterlingen/CH
  • 11 Oncology/hematology Department, KSGR - Kantonsspital Graubünden, 7000 - Chur/CH
  • 12 Medical Oncology Department, EOC - Ospedale Regionale di Locarno - Istituto Oncologico Svizzera Italiana (IOSI), 6600 - Locarno/CH
  • 13 Medical Oncology, Kantonsspital Aarau, 5001 - Aarau/CH
  • 14 Medical Oncology Department, Luzerner Kantonsspital, 6210 - Sursee/CH
  • 15 Medical Oncology, Kantonsspital Baden, 5404 - Baden/CH
  • 16 Medical Oncology, St. Claraspital AG, 4058 - Basel/CH
  • 17 Medical Oncology Dept., Inselspital - Universitatsklinik fur Medizinische Onkologie, 3010 - Bern/CH
  • 18 Medical Oncology Department, KSW - Kantonsspital Winterthur, 8401 - Winterthur/CH

Resources

Login to get immediate access to this content.

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

Abstract 2191P

Background

Based on the positive results of the CheckMate-743 trial, first-line (1L) treatment of MPM with ipilimumab in combination with nivolumab (ipi/nivo) has become a standard 1L treatment in patients (pts) with non-epithelioid MPM and epithelioid MPM. Pts who received 1L platinum-pemetrexed are often considered for further-line treatment with ipi/nivo based on the MAPS2 trial results. Here we report on real-world survival outcomes and toxicity with ipi/nivo for treatment of MPM in Switzerland.

Methods

This was a retrospective multicenter analysis in 12 Swiss centers including all pts treated with ipi/nivo for MPM; data cut-off was on May 1, 2023. Pts’ characteristics including age, sex, histology, PD-L1, ECOG and previous/subsequent treatments were collected. Efficacy and safety outcomes were assessed by local investigators.

Results

Of 109 patients with MPM (75% epithelioid, 9% biphasic, 16% sarcomatoid) treated with ipi/nivo (start of treatment November 2017-March 2023) median age was 72 years, 91% were males, and 83% had ECOG 0-1 at start of ipi/nivo. Ipi/nivo was given as 1L treatment in 43%, as 2L or further line in 57% of pts. 2 year-completion rate of ipi/nivo was 0%; treatment is ongoing in 16 pts (15%). Median follow-up from start of ipi/nivo was 16.6 months (mo). Efficacy outcomes for ipi/nivo are shown in the table. Highest-grade adverse events (AE) were as follows: 14% G1, 22% G2, 21% G3, 2% G4 and 3% G5 (1 colitis, 2 pneumonitis). Treatment discontinuation rate due to toxicity was 19%.

Table: 2191P

Outcomes

total (n=109) 1L (n=47) Further line (n=62)
ORR (95% CI) 17 % (11-26%) 21% (11-36%) 15% (7-26%)
DCR (95% CI) 46% (36-56%) 62% (46-76%) 34% (22-47%)
mPFS (95% CI), mo 3.4 (2.9-5.0) 6.5 (3.5-10.6) 2.8 (2.3-3.4)
mOS (95% CI), mo 10.6 (6.1-12.2) 12.6 (6.5-16.5) 6.9 (4.5-11.6)
OS at 6 mo (95% CI) 62% (52-71%) 70% (53-81%) 57% (44-68%)
OS at 12 mo (95% CI) 42% (32-52%) 55% (38-69%) 34% (22-46%)

Conclusions

In this real-world cohort of MPM pts treated with ipi/nivo efficacy outcomes were inferior to those reported in the CM743 and MAPS2 trials, while safety outcomes were similar. Subgroup analyses by histology, PD-L1 expression, age and ECOG will be presented at the meeting.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

S. Schmid: Financial Interests, Institutional, Advisory Board: AstraZeneca, MSD, BMS, Merck; Financial Interests, Institutional, Funding: Janssen, BMS, AstraZeneca; Financial Interests, Personal, Other, Congress travel support: Takeda, MSD, Amgen; Financial Interests, Institutional, Speaker, Consultant, Advisor: MSD. M. Frueh: Financial Interests, Institutional, Advisory Board: BMS, AstraZeneca, MSD, Takeda, Roche, Lilly, Boehringer Ingelheim, Novartis, Amgen; Financial Interests, Institutional, Funding: BMS. K. Koster: Financial Interests, Institutional, Other, Travel support: Takeda, Janssen. S.I. Rothschild: Financial Interests, Institutional, Other, Honoraria: Roche, AstraZeneca, BMS, Boehringer Ingelheim, MSD, Novartis, Amgen, Lilly, Eisai, Merck. Pfizer, Takeda, Bayer, Janssen, Otsuka, PharmaMar, Sanofi; Financial Interests, Institutional, Advisory Board: AstraZeneca, Boehringer Ingelheim, BMS, Pfizer, Eisai, Lilly, Merck, MSD, Novartis, Roche, Takeda, Amgen, Otsuka, PharaMar; Financial Interests, Institutional, Other, Speakers Bureau: Roche, Sanofi/Aventis, Amgen, AstraZeneca, Takeda; Financial Interests, Institutional, Funding: AbbVie, BMS, AstraZeneca, Boehringer Ingelheim, Merck, Roche; Financial Interests, Institutional, Other, Travel support etc: Sanofi, Roche, BMS, MSD, AstraZeneca, Takeda, Boehringer Ingelheim, Amgen; Financial Interests, Personal, Other: Federal Drug Commission of the Federal Office of public Health; Financial Interests, Institutional, Other: SAKK. C. Britschgi: Financial Interests, Personal, Advisory Board: AstraZeneca, Pfizer, Roche, Takeda, Janssen, Boehringer Ingelheim, Roche, Merck, Sanofi; Financial Interests, Personal, Other, Travel support: AstraZeneca, Takeda, Amgen. M.T. Mark: Financial Interests, Institutional, Advisory Board: AstraZeneca, Merck, MSD, Sanofi, BMS, Roche, Takeda; Financial Interests, Personal, Other, Travel grants: Takeda, Sanofi, Roche; Financial Interests, Institutional, Funding: Gilead, Swiss Cancer Foundation. P.R. Froesch: Financial Interests, Institutional, Advisory Board: Roche, Takeda, Janssen, Pfizer, Novartis, Lilly, Sanofi. W. Janthur: Financial Interests, Personal, Advisory Board: Astra, Roche, Pfizer, BI, MSD, Takeda; Financial Interests, Personal, Other, Travel Grant: Astra, Roche. A.T. Allemann: Financial Interests, Institutional, Advisory Board: Janssen; Financial Interests, Personal, Other, Travel support: Janssen; Financial Interests, Institutional, Speaker, Consultant, Advisor: Janssen, AstraZeneca. F.W.F. Cerciello: Financial Interests, Institutional, Advisory Board: BMS, PharmaMar. L.A. Mauti: Financial Interests, Personal, Other, Honoraria: Takeda, Amgen, MSD, Astra; Financial Interests, Personal, Advisory Board: MSD, BMS, Astra, Merck, Roche, Pfizer, Novartis, Sanofi, Takeda; Financial Interests, Institutional, Funding: AstraZeneca; Financial Interests, Personal, Expert Testimony: MSD, Merck; Financial Interests, Personal, Other, Travel support: Roche, Sanofi, Takeda, Astra. 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.