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Poster session 03

859P - The influence of hematologic malignancies on response to immune checkpoint inhibition in patients with advanced melanoma

Date

10 Sep 2022

Session

Poster session 03

Topics

Immunotherapy

Tumour Site

Melanoma;  Haematological Malignancies

Presenters

Olivier van Not

Citation

Annals of Oncology (2022) 33 (suppl_7): S356-S409. 10.1016/annonc/annonc1059

Authors

O.J. van Not1, F. Van Den Eertwegh2, J.B.A.G. Haanen3, R.S. van Rijn4, M. Aarts5, F. Van den Berkmortel6, C.U. Blank3, M. Boers-Sonderen7, J.W.B. de Groot8, G. Hospers9, E. Kapiteijn10, M.M. De Meza3, D. Piersma11, M. Stevense-den Boer12, A.A.M. Van der Veldt13, G. Vreugdenhil14, M. Wouters3, W.A.M. Blokx15, K.P.M. Suijkerbuijk1

Author affiliations

  • 1 Medical Oncology Dept, UMC-University Medical Center Utrecht, 3584 CX - Utrecht/NL
  • 2 Medical Oncology, Amsterdam UMC - Vrije University Medical Centre (VUmc), 1081 HV - Amsterdam/NL
  • 3 Medical Oncology Dept, NKI-AVL - Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital, 1066 CX - Amsterdam/NL
  • 4 Hematology Department, MCL - Medisch Centrum Leeuwarden, 8934 AD - Leeuwarden/NL
  • 5 Department Of Medical Oncology, Grow-school For Oncology And Reproduction, Maastricht University Medical Centre+, 6229 HX - Maastricht/NL
  • 6 Medical Oncology, Zuyderland Medical Center, 6419 PC - Heerlen/NL
  • 7 Medical Oncology Department, Radboud University Medical Center, Nijmegen, 6525 GA - Nijmegen/NL
  • 8 Oncology Center Department, Isala ziekenhuis, 8025 AB - Zwolle/NL
  • 9 University Medical Centre Groningen, UMCG - University Medical Center Groningen, 9700 RB - Groningen/NL
  • 10 Medical Oncology Dept., Leiden University Medical Center (LUMC), 2300 RC - Leiden/NL
  • 11 Internal Medicine, Medisch Spectrum Twente (MST) - Radiology, 7513 ER - Enschede/NL
  • 12 Internal Medicine, Amphia Ziekenhuis-location Molengracht, 4818 CK - Breda/NL
  • 13 Medical Oncology Department, Erasmus MC - University Medical Center, 3015 CE - Rotterdam/NL
  • 14 Internal Medicine Dept., Maxima Medisch Centrum -Veldhoven, 5500 MB - Veldhoven/NL
  • 15 Pathology, UMC - University Medical Center Utrecht, 3508 GA - Utrecht/NL

Resources

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Abstract 859P

Background

Patients diagnosed with hematologic malignancies (HM) have a higher risk of developing subsequent solid tumors, such as melanoma. Patients with HM were mostly excluded from clinical trials but could derive less benefit from immune checkpoint inhibition due to disease or treatment-related T- or B-cell dysfunction.

Methods

All advanced stage IIIc and IV melanoma patients treated with anti-PD-1 or ipilimumab-nivolumab between 2015 and 2021 were included from the prospective nationwide Dutch Melanoma Treatment Registry. Progression-free survival (PFS), overall survival (OS), and melanoma-specific survival (MSS) were analyzed for patients with HM (HM+) and without HM (HM-). A cox model was used to account for confounders associated with PFS and OS.

Results

Fifty-seven HM+ patients and 2506 HM- patients were included. Twenty-two patients were diagnosed with leukemia, 26 with malignant lymphoma, three with multiple myeloma, and six had a different type of HM. Forty-four percent received curative treatment for their HM. In the anti-PD-1 cohort, median PFS was 2.8 months for HM+ and 9.9 months for HM- (p=0.01). MSS was 41.2 months for HM+ and 58.1 months for HM- (p=0.00086). In multivariable analysis, the presence of a HM was significantly associated with a higher risk of melanoma progression (HRadj 1.68; 95%CI 1.24-2.29; p<0.001) and death (HRadj 1.76; 95%CI 1.25-2.47; p<0.001). Median PFS, OS, and MSS for anti-PD-1 and ipilimumab-nivolumab can be seen in the table. Table: 859P

Median progression-free survival, overall survival, and melanoma-specific survival in months, stratified by hematologic malignancy and treatment type

Median PFS in months (95% CI) Median OS in months (95% CI) Median MSS in months (95% CI)
Anti-PD-1 and HM+ (n=46) 2.8 (2.6-7.3) 12.8 (6.2-NR) 41.2 (12.8-NR)
Anti-PD-1 and HM (n=1717) 9.9 (8.6-11.8) 31.0 (28.5-35.0) 58.1 (47.5-NR)
Ipilimumab-nivolumab and HM+ (n=11) 2.3 (2.0-NR) 4.6 (2.4-NR) 4.6 (2.4-NR)
Ipilimumab-nivolumab and HM- (n=789) 6.9 (5.5-9.2) 31.7 (22.1-39.0) 46.1 (33.4-NR)

Conclusions

Patients with hematologic malignancy and advanced melanoma show significantly worse melanoma-related survival than patients with advanced melanoma alone. Larger numbers of patients are needed to look into the different subtypes of HM.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

For the Dutch Melanoma Treatment Registry (DMTR), the Dutch Institute for Clinical Auditing foundation received a start-up grant from governmental organization The Netherlands Organization for Health Research and Development (ZonMW, project number 836002002). The DMTR is structurally funded by Bristol Myers Squibb, Merck Sharpe & Dohme, Novartis, and Roche Pharma. Roche Pharma stopped funding in 2019, and Pierre Fabre started funding the DMTR in 2019. For this work, no funding was granted.

Disclosure

F. Van Den Eertwegh: Non-Financial Interests, Advisory Role: Amgen, BMS, Roche, Novartis, MSD, Pierre Fabre, Sanofi, Pfizer, Ipsen, Merck; Non-Financial Interests, Research Grant: Sanofi, Roche, BMS, Idera, TEVA; Non-Financial Interests, Other, travel expenses: MSD Oncology, Roche, Pfizer, Sanofi; Non-Financial Interests, Invited Speaker: BMS, Novartis. J.B.A.G. Haanen: Non-Financial Interests, Advisory Role: Aimm, Achilles Therapeutics, Amgen, AstraZeneca, Bayer, BMS, BioNTech, GSK, Immunocore, Ipsen, MSD, Merck Serono, Molecular Partners, Novartis, Neogene Therapeutics, Pfizer, Roche/Genetech, Sanofi, Seattle Genetics, Third Rock Ventures, Vaximm; Non-Financial Interests, Research Grant: Amgen, BMS, MSD, BioNTech, Neogene Therapeutics, Novartis. R.S. van Rijn: Non-Financial Interests, Advisory Role: Pfizer; Non-Financial Interests, Other, Expert meeting fee: Roche. M. Aarts: Non-Financial Interests, Advisory Role: Amgen, BMS, Novartis, MSD-Merck, Merck-Pfizer, Pierre Fabre, Sanofi, Astellas, Bayer; Non-Financial Interests, Research Grant: Merck-Pfizer. C.U. Blank: Financial Interests, Institutional, Advisory Board: BMS, MSD, Roche, Novartis, GSK, AZ, Pfizer, Lilly, GenMab, Pierre Fabre; Financial Interests, Personal, Expert Testimony: Third Rock Ventures; Financial Interests, Personal, Stocks/Shares: Uniti Cars, co-founder Immagene BV; Financial Interests, Institutional, Invited Speaker: BMS, Novartis, NanoString, 4SC. M. Boers-Sonderen: Non-Financial Interests, Advisory Role: Pierre Fabre, MSD, Novartis. J.W.B. de Groot: Non-Financial Interests, Advisory Role: BMS, Pierre Fabre, Servier, MSD, Novartis. G. Hospers: Non-Financial Interests, Advisory Role: Amgen, BMS, Roche, MSD, Pfizer, Novartis, Pierre Fabre; Non-Financial Interests, Research Grant: BMS, Seerave. E. Kapiteijn: Financial Interests, Institutional, Advisory Board: BMS, Novartis, Pierre Fabre, Merck, Delcath, Bayer; Financial Interests, Institutional, Invited Speaker: BMS. A.A.M. Van der Veldt: Non-Financial Interests, Advisory Role: BMS, MSD, Roche, Novartis, Pierre Fabre, Pfizer, Sanofi, Ipsen, Eisai, Merck. K.P.M. Suijkerbuijk: Non-Financial Interests, Advisory Role: BMS, Novartis, MSD, Pierre Fabre, AbbVie; Non-Financial Interests, Other, honoraria: Novartis, MSD, Roche. All other authors have declared no conflicts of interest.

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