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The efficacy of immunotherapy and chemoimmunotherapy in patients with advanced rare tumors: A Turkish oncology group (TOG) study

dc.contributor.authorGuven, Deniz Can
dc.contributor.authorAykan, Musa Baris
dc.contributor.authorMuglu, Harun
dc.contributor.authorBayram, Ertugrul
dc.contributor.authorHelvaci, Kaan
dc.contributor.authorDursun, Bengue
dc.contributor.authorCelayir, Melisa
dc.contributor.authorChelebiyev, Elvin
dc.contributor.authorNayir, Erdinc
dc.contributor.authorErman, Mustafa
dc.contributor.authorSezer, Ahmet
dc.contributor.authorUrun, Yuksel
dc.contributor.authorDemirci, Umut
dc.contributor.authorEr, Ozlem
dc.contributor.authorDisel, Umut
dc.contributor.authorBilici, Ahmet
dc.contributor.authorArslan, Cagatay
dc.contributor.authorKaradurmus, Nuri
dc.contributor.authorKilickap, Saadettin
dc.date.accessioned2026-11-05T11:04:44Z
dc.date.issued2024
dc.description.abstractIntroduction: The advances in immune checkpoint inhibitors (ICIs) were relatively slow in rare tumors. Therefore, we conducted a multi-center study evaluating the efficacy of ICI monotherapy and the combination of ICIs with chemotherapy (CT) in patients with advanced rare tumors.Methods: In this retrospective cohort study, we included 93 patients treated with ICIs for NCI-defined rare tumors from the 12 cancer centers in Turkey. The primary endpoints were the overall response (ORR) and disease control rate (DCR).Results: The cohort's median age was 56, and 53.8% of the patients were male. The most frequent diagnosis was sarcoma (29%), and 81.7% of the patients were previously treated with at least one line of systemic therapy in the advanced stage. The ORR and DCR were 36.8% and 63.2%, respectively. The germ cell tumors had the lowest ORR (0%), while the Merkel cell carcinoma had the highest ORR to ICIs (57.1%). Patients treated with ICI + ICI or ICI plus chemotherapy combinations had higher ORR (55.2% vs. 27.6%, p = 0.012) and DCR (82.8% vs. 53.4%, p = 0.008). The median OS was 13.47 (95% CI: 7.79-19.15) months, and the six and 12-month survival rates were 71% and 52%. The median duration of response was 16.59 months, and the 12-month progression-free survival rate was 66% in responders. The median time-to-treatment failure was 5.06 months (95% CI: 3.42-6.71). Three patients had high-grade irAEs with ICIs (grade 3 colitis, grade 3 gastritis, and grade 3 encephalitis in one patient each).Results: The cohort's median age was 56, and 53.8% of the patients were male. The most frequent diagnosis was sarcoma (29%), and 81.7% of the patients were previously treated with at least one line of systemic therapy in the advanced stage. The ORR and DCR were 36.8% and 63.2%, respectively. The germ cell tumors had the lowest ORR (0%), while the Merkel cell carcinoma had the highest ORR to ICIs (57.1%). Patients treated with ICI + ICI or ICI plus chemotherapy combinations had higher ORR (55.2% vs. 27.6%, p = 0.012) and DCR (82.8% vs. 53.4%, p = 0.008). The median OS was 13.47 (95% CI: 7.79-19.15) months, and the six and 12-month survival rates were 71% and 52%. The median duration of response was 16.59 months, and the 12-month progression-free survival rate was 66% in responders. The median time-to-treatment failure was 5.06 months (95% CI: 3.42-6.71). Three patients had high-grade irAEs with ICIs (grade 3 colitis, grade 3 gastritis, and grade 3 encephalitis in one patient each).Conclusion: We observed over 30% ORR and a 13-month median OS in patients with rare cancers treated with ICI monotherapy or ICI plus CT combinations. The response rates to ICIs or ICIs plus CT significantly varied across different tumor types. Responding patients had over 2 years of survival, highlighting a need for further trials with ICIs for patients with rare tumors.
dc.description.issue1
dc.description.volume13
dc.identifier.doi10.1002/cam4.6869
dc.identifier.issn2045-7634
dc.identifier.urihttps://doi.org/10.1002/cam4.6869
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/11225
dc.identifier.wosWOS:001129651900001
dc.language.isoen
dc.publisherWILEY
dc.relation.hasversion10.1002/cam4.6869
dc.relation.ispartofCANCER MEDICINE
dc.subjectimmune checkpoint inhibitor
dc.subjectimmunotherapy
dc.subjectrare tumor
dc.subjectsarcoma
dc.subjectOPEN-LABEL
dc.subjectSINGLE-ARM
dc.subjectCANCER-RESEARCH
dc.subjectSOLID TUMORS
dc.subjectPEMBROLIZUMAB
dc.subjectMULTICENTER
dc.subjectCHALLENGES
dc.subjectNIVOLUMAB
dc.subjectADULTS
dc.subjectOncology
dc.titleThe efficacy of immunotherapy and chemoimmunotherapy in patients with advanced rare tumors: A Turkish oncology group (TOG) study
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.issue1
oaire.citation.volume13
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