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

被引:0
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作者
Guven, Deniz Can [1 ,13 ]
Aykan, Musa Baris [2 ]
Muglu, Harun [3 ]
Bayram, Ertugrul [4 ]
Helvaci, Kaan [5 ]
Dursun, Bengue [6 ]
Celayir, Melisa [7 ]
Chelebiyev, Elvin [1 ]
Nayir, Erdinc [8 ]
Erman, Mustafa [1 ]
Sezer, Ahmet [9 ]
Urun, Yuksel [6 ]
Demirci, Umut [5 ]
Er, Ozlem [7 ]
Disel, Umut [10 ]
Bilici, Ahmet [3 ]
Arslan, Cagatay [11 ]
Karadurmus, Nuri [2 ]
Kilickap, Saadettin [12 ]
机构
[1] Hacettepe Univ, Canc Inst, Dept Med Oncol, Ankara, Turkiye
[2] Univ Hlth Sci, Gulhane Sch Med, Dept Med Oncol, Ankara, Turkiye
[3] Istanbul Medipol Univ, Fac Med, Istanbul, Turkiye
[4] Cukurova Univ, Dept Med Oncol, Adana, Turkiye
[5] Mem Ankara Hosp, Ankara, Turkiye
[6] Ankara Univ, Dept Med Oncol, Ankara, Turkiye
[7] MAA Acıbadem Univ, Dept Med Oncol, Istanbul, Turkiye
[8] Mersin Med Pk Hosp, Dept Med Oncol, Mersin, Turkiye
[9] Baskent Univ, Adana Hosp, Adana, Turkiye
[10] Acibadem Adana Hosp, Dept Med Oncol, Adana, Turkiye
[11] Izmir Econ Univ, Med Pk Hosp, Sch Med, Dept Med Oncol, Izmir, Turkiye
[12] Istinye Univ, Fac Med, Dept Med Genet, Istanbul, Turkiye
[13] Hacettepe Univ, Canc Inst, Dept Med Oncol, TR-06100 Ankara, Turkiye
来源
CANCER MEDICINE | 2024年 / 13卷 / 01期
关键词
immune checkpoint inhibitor; immunotherapy; rare tumor; sarcoma; OPEN-LABEL; SINGLE-ARM; CANCER-RESEARCH; SOLID TUMORS; PEMBROLIZUMAB; MULTICENTER; CHALLENGES; NIVOLUMAB; SARCOMA; ADULTS;
D O I
10.1002/cam4.6869
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: 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.
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页数:9
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