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  1. Article: Interview mit Roger von Moos

    Mühlebach, T. / von Moos, Roger

    Schweizer Krebs-Bulletin

    2016  Volume 36, Issue 2, Page(s) 123–124

    Language English ; French ; German
    Document type Article
    ZDB-ID 1340924-4
    Database Current Contents Medicine

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  2. Article ; Online: Olaparib not cost-effective as maintenance therapy for platinum-sensitive, BRCA1/2 germline-mutated metastatic pancreatic cancer.

    Mehra, Tarun / Lupatsch, Judith E / Kössler, Thibaud / Dedes, Konstantin / Siebenhüner, Alexander Reinhard / von Moos, Roger / Wicki, Andreas / Schwenkglenks, Matthias E

    PloS one

    2024  Volume 19, Issue 4, Page(s) e0301271

    Abstract: Objective: To assess the cost-effectiveness and budget impact of olaparib as a maintenance therapy in platinum-responsive, metastatic pancreatic cancer patients harboring a germline BRCA1/2 mutation, using the Swiss context as a model.: Methods: ... ...

    Abstract Objective: To assess the cost-effectiveness and budget impact of olaparib as a maintenance therapy in platinum-responsive, metastatic pancreatic cancer patients harboring a germline BRCA1/2 mutation, using the Swiss context as a model.
    Methods: Based on data from the POLO trial, published literature and local cost data, we developed a partitioned survival model of olaparib maintenance including full costs for BRCA1/2 germline testing compared to FOLFIRI maintenance chemotherapy and watch-and-wait. We calculated the incremental cost-effectiveness ratio (ICER) for the base case and several scenario analyses and estimated 5-year budget impact.
    Results: Comparing olaparib with watch-and wait and maintenance chemotherapy resulted in incremental cost-effectiveness ratios of CHF 2,711,716 and CHF 2,217,083 per QALY gained, respectively. The 5-year costs for the olaparib strategy in Switzerland would be CHF 22.4 million, of which CHF 11.4 million would be accounted for by germline BRCA1/2 screening of the potentially eligible population. This would amount to a budget impact of CHF 15.4 million (USD 16.9 million) versus watch-and-wait.
    Conclusions: Olaparib is not a cost-effective maintenance treatment option. Companion diagnostics are an equally important cost driver as the drug itself.
    MeSH term(s) Female ; Humans ; BRCA1 Protein/genetics ; Ovarian Neoplasms/genetics ; Platinum/therapeutic use ; BRCA2 Protein/genetics ; Phthalazines/therapeutic use ; Pancreatic Neoplasms/drug therapy ; Pancreatic Neoplasms/genetics ; Pancreatic Neoplasms/pathology ; Germ Cells/pathology ; Cost-Benefit Analysis ; Piperazines
    Chemical Substances BRCA1 protein, human ; BRCA1 Protein ; olaparib (WOH1JD9AR8) ; Platinum (49DFR088MY) ; BRCA2 protein, human ; BRCA2 Protein ; Phthalazines ; Piperazines
    Language English
    Publishing date 2024-04-04
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0301271
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: RE: Real-World Use of Bone Modifying Agents in Metastatic Castration-Sensitive Prostate Cancer.

    Mark, Michael / von Moos, Roger / Cathomas, Richard / Stoffel, Sandro / Gillessen, Silke

    Journal of the National Cancer Institute

    2021  Volume 114, Issue 4, Page(s) 635–636

    MeSH term(s) Bone Neoplasms/drug therapy ; Bone Neoplasms/secondary ; Castration ; Humans ; Male ; Prostatic Neoplasms/drug therapy ; Prostatic Neoplasms/pathology ; Prostatic Neoplasms/surgery ; Prostatic Neoplasms, Castration-Resistant/drug therapy ; Prostatic Neoplasms, Castration-Resistant/pathology
    Language English
    Publishing date 2021-11-25
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 2992-0
    ISSN 1460-2105 ; 0027-8874 ; 0198-0157
    ISSN (online) 1460-2105
    ISSN 0027-8874 ; 0198-0157
    DOI 10.1093/jnci/djab216
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Completion and publication of clinical trials in a cooperative group: a cohort study of trials of the Swiss Group for Clinical Cancer Research (SAKK).

    Hayoz, Stefanie / Kasenda, Benjamin / Schenker, Annina Lea / Kopp, Christoph / Schär, Sämi / Thürlimann, Beat / von Moos, Roger / Pless, Miklos

    BMJ open

    2023  Volume 13, Issue 4, Page(s) e068490

    Abstract: Background: Premature trial discontinuation and non-publication of trial results are still major issues negatively affecting reliable evidence generation.: Objectives: To investigate trial completion and publication rate of cancer trials conducted ... ...

    Abstract Background: Premature trial discontinuation and non-publication of trial results are still major issues negatively affecting reliable evidence generation.
    Objectives: To investigate trial completion and publication rate of cancer trials conducted within the Swiss Group for Clinical Cancer Research (SAKK).
    Design: Cohort study of clinical trials.
    Setting: Cohort of interventional cancer trials conducted in Switzerland with accrual closure between 1986 and 2021 identified from the SAKK trial management system.
    Outcomes: Premature trial discontinuation and publication in peer-reviewed journal.
    Results: We included 261 trials; median number of recruited patients was 150.5 (range 1-8028). Most trials (67.0%) were randomised. Overall, 76 of 261 (29.1%) trials were prematurely closed for accrual. The three main reasons for premature closure were insufficient accrual in 28 trials, followed by stopping for futility in 17 or efficacy in 8 trials. We included 240 trials for the publication status (21 excluded, because 8 still in follow-up, for 10 the primary completion date was less than a year ago and for 3 the manuscript was submitted, but to accepted yet). 216 of 240 (90.0%) were published as a full article, 14 were published in other formats, leading to an overall publication rate of 95.8%. The rate of premature discontinuation declined over time, with 34.2%, 27.8% and 23.5% in trials activated before 2000, between 2000 and 2009, and since 2010, respectively. We observed an increasing publication rate in peer-reviewed journals over time: 79.2% (closed before 2000), 95.7% (closed between 2000 and 2009) and 93.2% (closed after 2010).
    Conclusion: Insufficient patient recruitment is still the major reason for premature trial discontinuation. SAKK has continuously improved its quality management of trial conduct over time leading to increased successful trial completion and publication. However, there is still room for improvement to increase the number of trials reaching their target sample size.
    MeSH term(s) Humans ; Cohort Studies ; Neoplasms/therapy ; Research Design ; Patient Selection ; Ethnicity
    Language English
    Publishing date 2023-04-18
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2022-068490
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: First-line durvalumab in patients with PD-L1 positive, advanced non-small cell lung cancer (NSCLC) with a performance status of 2 (PS2). Primary analysis of the multicenter, single-arm phase II trial SAKK 19/17.

    Mark, Michael / Froesch, Patrizia / Gysel, Katrin / Rothschild, Sacha I / Addeo, Alfredo / Ackermann, Christoph J / Chiquet, Sabrina / Schneider, Martina / Ribi, Karin / Maranta, Angela Fischer / Bastian, Sara / von Moos, Roger / Joerger, Markus / Früh, Martin

    European journal of cancer (Oxford, England : 1990)

    2024  Volume 200, Page(s) 113600

    Abstract: Introduction: The safety and efficacy of first-line durvalumab in PS2 patients with advanced NSCLC is unknown. Here, we present the primary analysis of first-line durvalumab in PS2 patients, unsuitable for combination chemotherapy.: Methods: In this ... ...

    Abstract Introduction: The safety and efficacy of first-line durvalumab in PS2 patients with advanced NSCLC is unknown. Here, we present the primary analysis of first-line durvalumab in PS2 patients, unsuitable for combination chemotherapy.
    Methods: In this single-arm, multicenter, phase II trial patients with PD-L1 positive (tumor proportional score ≥25%), advanced NSCLC with PS2, received four-weekly durvalumab 1500 mg. The primary endpoint was overall survival (OS) at 6 months.
    Results: Forty-eight patients were included. Median follow-up was 23.3 months (95% CI: 14.3-28.6). OS at 6 months was 60% (95% CI: 45-74%). Median OS was 8.5 months (95%CI: 4.4-16.7). Objective response rate and median progression free survival were 17% (95% CI: 8-30%) and 2.5 months (95% CI: 1.8-7.1), respectively. Thirty-three deaths were observed at the time point of the analysis. Seven early fatal events considered not treatment-related occurred during the first 5 weeks of treatment. Four out of the first 7 early fatal events (4/7; 57%) were respiratory failure in patients with advanced symptomatic primary lung tumors. Three more early fatal events occurred after exclusion of patients with grade ≥ 3 dyspnea. Treatment-related AEs ≥G3 were reported in 9 patients (19%) and included colonic perforation in one patient (grade 5), colitis in 4 patients (8%), increased lipase in 3 patients (6%), and hepatitis in 2 patients (4%).
    Conclusions: First-line durvalumab in PS2 patients with advanced PD-L1 positive NSCLC results in a high number of early fatal events. When patients with grade ≥ 3 dyspnea are excluded a promising 6-month OS with an acceptable toxicity profile can be observed. Durvalumab could be an option instead of single agent chemotherapy for PS2 patients who are not candidates for platinum doublet chemotherapy provided they are well selected.
    MeSH term(s) Humans ; Carcinoma, Non-Small-Cell Lung/pathology ; Lung Neoplasms/pathology ; B7-H1 Antigen/metabolism ; Dyspnea ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Antibodies, Monoclonal
    Chemical Substances durvalumab (28X28X9OKV) ; B7-H1 Antigen ; Antibodies, Monoclonal
    Language English
    Publishing date 2024-02-05
    Publishing country England
    Document type Clinical Trial, Phase II ; Multicenter Study ; Journal Article
    ZDB-ID 82061-1
    ISSN 1879-0852 ; 0277-5379 ; 0959-8049 ; 0964-1947
    ISSN (online) 1879-0852
    ISSN 0277-5379 ; 0959-8049 ; 0964-1947
    DOI 10.1016/j.ejca.2024.113600
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Safety and anti-tumor activity of lisavanbulin administered as 48-hour infusion in patients with ovarian cancer or recurrent glioblastoma: a phase 2a study.

    Joerger, Markus / Hundsberger, Thomas / Haefliger, Simon / von Moos, Roger / Hottinger, Andreas F / Kaindl, Thomas / Engelhardt, Marc / Marszewska, Michalina / Lane, Heidi / Roth, Patrick / Stathis, Anastasios

    Investigational new drugs

    2023  Volume 41, Issue 2, Page(s) 267–275

    Abstract: Purpose: Lisavanbulin (BAL101553) is the prodrug of avanbulin (BAL27862), a microtubule-destabilizing agent. The goal of this study (NCT02895360) was to characterize the safety, tolerability and antitumor activity of lisavanbulin administered as a 48- ... ...

    Abstract Purpose: Lisavanbulin (BAL101553) is the prodrug of avanbulin (BAL27862), a microtubule-destabilizing agent. The goal of this study (NCT02895360) was to characterize the safety, tolerability and antitumor activity of lisavanbulin administered as a 48-hour intravenous (IV) infusion at the recommended Phase 2 dose (RP2D) of 70 mg/m
    MeSH term(s) Humans ; Female ; Glioblastoma ; Neoplasm Recurrence, Local/drug therapy ; Ovarian Neoplasms/drug therapy ; Ovarian Neoplasms/pathology
    Chemical Substances lisavanbulin
    Language English
    Publishing date 2023-02-16
    Publishing country United States
    Document type Multicenter Study ; Clinical Trial, Phase II ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 604895-x
    ISSN 1573-0646 ; 0167-6997
    ISSN (online) 1573-0646
    ISSN 0167-6997
    DOI 10.1007/s10637-023-01336-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Initiation of bone-targeted agents in patients with bone metastases and breast or castrate-resistant prostate cancer actively treated in routine clinical practice in Europe.

    von Moos, Roger / Lewis, Katie / Massey, Lucy / Marongiu, Andrea / Rider, Alex / Seesaghur, Anouchka

    Bone

    2021  Volume 154, Page(s) 116243

    Abstract: Background: Guidelines recommend starting bone-targeted agents (BTA), such as zoledronic acid and denosumab, as soon as bone metastases (BMs) are definitively diagnosed in all patients with breast cancer (BC) or castration-resistant prostate cancer ( ... ...

    Abstract Background: Guidelines recommend starting bone-targeted agents (BTA), such as zoledronic acid and denosumab, as soon as bone metastases (BMs) are definitively diagnosed in all patients with breast cancer (BC) or castration-resistant prostate cancer (CRPC) whether they are symptomatic or not.
    Methods: Data were analyzed from 1364 patients with BC and 1161 patients with CRPC who had BMs and were receiving anti-cancer therapy in hospitals across six European countries (Belgium, France, Germany, Italy, Spain and the UK). The 731 physicians (medical oncologists or urologists) provided insights in the decision-making factors driving their management of bone health for these patients, and the patient medical records indicated how these decisions were reflected in routine clinical practice.
    Results: Within three months of a BM diagnosis, 74% of BC and 51% of CRPC patients had initiated treatment with a BTA. Around 12% of BC and 23% of CRPC patients did not receive a BTA following BM diagnosis. Irrespective of the tumour type (BC or CRPC), most physicians prescribed either denosumab or zoledronic acid as first BTA therapy. Physicians reported bone pain as a major decision-making factor to initiate a BTA. The presence of bone complications at BM diagnosis and bone pain at BM diagnosis were found to be significant predictive factors for a BTA initiation, irrespective of tumour type.
    Conclusions: Despite European Society for Medical Oncology (ESMO) guidance on bone protection irrespective of symptomatic disease, not all patients with BMs received a BTA following a BM diagnosis. This suggests that clinical judgements and patients' communication of their pain to their physicians contributed to the decision to prescribe bone protection therapy in cancer patients.
    MeSH term(s) Bone Density Conservation Agents/therapeutic use ; Bone Neoplasms/drug therapy ; Bone Neoplasms/secondary ; Breast Neoplasms/drug therapy ; Breast Neoplasms/pathology ; Germany ; Humans ; Male ; Prostatic Neoplasms/pathology ; Zoledronic Acid/therapeutic use
    Chemical Substances Bone Density Conservation Agents ; Zoledronic Acid (6XC1PAD3KF)
    Language English
    Publishing date 2021-10-29
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 632515-4
    ISSN 1873-2763 ; 8756-3282
    ISSN (online) 1873-2763
    ISSN 8756-3282
    DOI 10.1016/j.bone.2021.116243
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Completion and publication of clinical trials in a cooperative group

    Benjamin Kasenda / Miklos Pless / Beat Thürlimann / Stefanie Hayoz / Annina Lea Schenker / Christoph Kopp / Sämi Schär / Roger von Moos

    BMJ Open, Vol 13, Iss

    a cohort study of trials of the Swiss Group for Clinical Cancer Research (SAKK)

    2023  Volume 4

    Abstract: Background Premature trial discontinuation and non-publication of trial results are still major issues negatively affecting reliable evidence generation.Objectives To investigate trial completion and publication rate of cancer trials conducted within the ...

    Abstract Background Premature trial discontinuation and non-publication of trial results are still major issues negatively affecting reliable evidence generation.Objectives To investigate trial completion and publication rate of cancer trials conducted within the Swiss Group for Clinical Cancer Research (SAKK).Design Cohort study of clinical trials.Setting Cohort of interventional cancer trials conducted in Switzerland with accrual closure between 1986 and 2021 identified from the SAKK trial management system.Outcomes Premature trial discontinuation and publication in peer-reviewed journal.Results We included 261 trials; median number of recruited patients was 150.5 (range 1–8028). Most trials (67.0%) were randomised. Overall, 76 of 261 (29.1%) trials were prematurely closed for accrual. The three main reasons for premature closure were insufficient accrual in 28 trials, followed by stopping for futility in 17 or efficacy in 8 trials. We included 240 trials for the publication status (21 excluded, because 8 still in follow-up, for 10 the primary completion date was less than a year ago and for 3 the manuscript was submitted, but to accepted yet). 216 of 240 (90.0%) were published as a full article, 14 were published in other formats, leading to an overall publication rate of 95.8%. The rate of premature discontinuation declined over time, with 34.2%, 27.8% and 23.5% in trials activated before 2000, between 2000 and 2009, and since 2010, respectively. We observed an increasing publication rate in peer-reviewed journals over time: 79.2% (closed before 2000), 95.7% (closed between 2000 and 2009) and 93.2% (closed after 2010).Conclusion Insufficient patient recruitment is still the major reason for premature trial discontinuation. SAKK has continuously improved its quality management of trial conduct over time leading to increased successful trial completion and publication. However, there is still room for improvement to increase the number of trials reaching their target sample size.
    Keywords Medicine ; R
    Subject code 610
    Language English
    Publishing date 2023-04-01T00:00:00Z
    Publisher BMJ Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Quality of life, effectiveness, and safety of aflibercept plus FOLFIRI in older patients with metastatic colorectal cancer: An analysis of the prospective QoLiTrap study.

    Piringer, Gudrun / Thaler, Josef / Anchisi, Sandro / Geffriaud-Ricouard, Christine / Gueldner, Max / Scholten, Felicitas / Derigs, Hans-Günter / Bohanes, Pierre / Grünberger, Birgit / Schwarz, Leonora / von Moos, Roger / Hofheinz, Ralf-Dieter

    Journal of geriatric oncology

    2023  Volume 14, Issue 8, Page(s) 101638

    Abstract: Introduction: Colorectal cancer (CRC) mainly affects older patients. The pivotal VELOUR phase III trial of aflibercept plus FOLFIRI in metastatic CRC (mCRC) included only 5.9% of patients aged ≥75 years. Herein, we report a preplanned analysis from ... ...

    Abstract Introduction: Colorectal cancer (CRC) mainly affects older patients. The pivotal VELOUR phase III trial of aflibercept plus FOLFIRI in metastatic CRC (mCRC) included only 5.9% of patients aged ≥75 years. Herein, we report a preplanned analysis from QoLiTrap, a large prospective observational study evaluating the impact of age on quality of life (QoL), effectiveness, and safety of aflibercept plus FOLFIRI in daily clinical practice in Europe.
    Materials and methods: Enrolled patients had progressive mCRC, had failed a prior oxaliplatin-based regimen, and had received aflibercept (4 mg/kg) plus FOLFIRI every two weeks until disease progression, death, unacceptable toxicity, or physician/patient decision. Analyses were performed by age classes (<60, 60-64, 65-69, 70-74, and ≥ 75 years). The primary endpoint was the percentage of patients whose global health status (GHS) of the European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) was maintained (i.e., no worsening from baseline by at least 5% over a 12-week treatment). Secondary endpoints included tumor objective response rate (ORR), progression-free survival (PFS), overall survival (OS), and safety.
    Results: Overall, 1277 patients (<60 years, n = 327; 60-64 years, n = 231; 65-69 years, n = 227; 70-74 years, n = 259; and ≥ 75 years, n = 233) were treated, of whom 872 were evaluable for QoL. GHS was maintained in 36.5%, 41.6%, 38.9%, 41.8%, and 44.8% of patients aged <60, 60-64, 65-69, 70-74, and ≥ 75 years, respectively. Age did not influence PFS (median 7.8 months), OS (median 14.4 months), or ORR (20.8%). Number of cycles, dose delays for any cause, and dose reductions for adverse events (AEs) were comparable between age classes. Grade ≥ 3 AEs occurred in 47.7%, 51.9%, 51.5%, 55.2%, and 55.8% of patients aged <60, 60-64, 65-69, 70-74, and ≥ 75 years, respectively. The main grade ≥ 3 AEs were hypertension (11.2%) and diarrhea (9%) in patients aged ≥75 years.
    Discussion: The results suggest that aflibercept plus FOLFIRI maintains QoL and retains its activity, including a high objective tumor response, regardless of age and treatment line. In fit older patients, the safety profile seems manageable, with no new safety signals.
    MeSH term(s) Humans ; Aged ; Colorectal Neoplasms/pathology ; Quality of Life ; Prospective Studies ; Fluorouracil/adverse effects ; Camptothecin/adverse effects ; Receptors, Vascular Endothelial Growth Factor ; Colonic Neoplasms/drug therapy ; Rectal Neoplasms/drug therapy ; Recombinant Fusion Proteins/adverse effects ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Leucovorin/adverse effects ; Bevacizumab/therapeutic use
    Chemical Substances aflibercept (15C2VL427D) ; Fluorouracil (U3P01618RT) ; Camptothecin (XT3Z54Z28A) ; Receptors, Vascular Endothelial Growth Factor (EC 2.7.10.1) ; Recombinant Fusion Proteins ; Leucovorin (Q573I9DVLP) ; Bevacizumab (2S9ZZM9Q9V)
    Language English
    Publishing date 2023-09-28
    Publishing country Netherlands
    Document type Observational Study ; Journal Article
    ZDB-ID 2556813-9
    ISSN 1879-4076 ; 1879-4068
    ISSN (online) 1879-4076
    ISSN 1879-4068
    DOI 10.1016/j.jgo.2023.101638
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Effects of CTLA-4 Single Nucleotide Polymorphisms on Toxicity of Ipilimumab-Containing Regimens in Patients With Advanced Stage Melanoma.

    de Joode, Karlijn / Mora, Alfonso Rojas / van Schaik, Ron H N / Zippelius, Alfred / van der Veldt, Astrid / Gerard, Camille Léa / Läubli, Heinz / Michielin, Olivier / von Moos, Roger / Joerger, Markus / Levesque, Mitchell P / Aeppli, Stefanie / Mangana, Johanna / Mangas, Cristina / Trost, Nadine / Meyer, Stefan / Parvex, Sandra Leoni / Mathijssen, Ron / Metaxas, Yannis

    Journal of immunotherapy (Hagerstown, Md. : 1997)

    2024  

    Abstract: Single nucleotide polymorphisms (SNPs) in the cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) gene, an inhibitor of T-cell priming, are associated with auto and alloimmunity. Studies implied a role for these SNPs as surrogate markers for ... ...

    Abstract Single nucleotide polymorphisms (SNPs) in the cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) gene, an inhibitor of T-cell priming, are associated with auto and alloimmunity. Studies implied a role for these SNPs as surrogate markers for immunotherapy-outcome in patients with melanoma. However, no predictive SNPs are defined to date. We analyzed different CTLA-4 SNPs in a large multicenter cohort of patients with ipilimumab-treated melanoma and investigated possible correlations with treatment-related outcomes. Archival blood and/or tumor tissue samples were collected from 361 patients with advanced-stage ipilimumab-treated (±nivolumab) in 6 Swiss and Dutch hospitals. Matrix-assisted laser desorption/ionization-time of flight mass spectrometry based DNA genotyping was performed for 10 different CTLA-4 SNPs: 49A>G, CT60G>A, Jo27T>C, Jo30G>A, Jo31G>T, -658C>T, -1722T>C, -1661A>G, 318C>T, and C>T rs1863800. Associations between different allele genotypes and occurrence of grade ≥3 adverse events (AEs) and survival were tested using univariable logistic regressions or Cox proportional hazard models. 262/361 (73%) patients could be analyzed; 65% of those were males, the median age was 58 years, 39% showed a partial or complete response, and 65% had ≥1 AEs. A TT-genotype of -1722T>C SNP was significantly associated with a lower incidence of grade ≥3 AEs (P = 0.049), whereas the GG-genotype of CT60G>A correlated with a higher incidence of grade ≥3 AEs (P = 0.026). The TT-genotype of Jo27T>C SNP (P = 0.056) and GG-genotype of Jo31G>T (P = 0.046) were associated with overall survival. CTLA-4 SNPs might predict treatment-related outcomes in patients with melanoma receiving ipilimumab. Confirmatory studies are needed to fully exploit those findings as predictive biomarkers for ipilimumab AEs.
    Language English
    Publishing date 2024-02-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1064067-8
    ISSN 1537-4513 ; 1053-8550 ; 1524-9557
    ISSN (online) 1537-4513
    ISSN 1053-8550 ; 1524-9557
    DOI 10.1097/CJI.0000000000000506
    Database MEDical Literature Analysis and Retrieval System OnLINE

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