Survival outcomes of patients with oligometastatic non-small cell lung cancer who were treated with radical therapy: a multicenter analysis

dc.contributor.authorid0000-0002-1273-1674
dc.contributor.coauthorAçikgöz, Özgür
dc.contributor.coauthorBilici, Ahmet
dc.contributor.coauthorTataroğlu Özyükseler, Deniz
dc.contributor.coauthorGöktaş Aydin, Sabin
dc.contributor.coauthorRzazade, Rashad
dc.contributor.coauthorÖlmez, Ömer Fatih
dc.contributor.coauthorBaşak Çağlar, Hale
dc.contributor.departmentN/A
dc.contributor.kuauthorSelçukbiricik, Fatih
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.yokid202015
dc.date.accessioned2025-01-19T10:34:26Z
dc.date.issued2023
dc.description.abstractBackground/aim: Oligometastatic disease for nonsmall cell lung cancer (NSCLC) patients is generally thought to represent a better prognosis with a quieter biology, limited number of disease sites and long-term disease control. In this study, we aimed to determine the efficacy of radical treatment options for patients with oligometastatic NSCLC. Materials and methods: This retrospective trial included totally 134 patients with oligometastatic NSCLC. The presence of oncodriver mutation, tumor stages and nodal status, the number of metastases and involved metastatic site, treatment of primary tumor and oligometastasis, response rate, overall survival (OS) and progression-free survival (PFS) were evaluated. Results: Of 134 patients 66.4% were defined as adenocarcinoma, 26.1% were squamous cell carcinoma and 7.5% of patients were in other histology. Based on the treatment of primary tumor, in 36 patients (26.9%) curative surgery has undergone, in addition, 19 (14.2%) patients were received chemotherapy, 73 (54.5%) were treated with chemoradiotherapy, while immunotherapy and targeted therapy were used in 1 (0.7%) and 2 (1.4%), respectively. The preferred treatment for oligometastatic lesions were SBRT in 72.4% of patients, surgery in 10.5%, and both SBRT and surgery in 17.1% of patients. At the median follow up of 31.3 months (range: 9.5–48.5), the median PFS and OS times were 17 and 24.4 months, respectively. Moreover, OS-2 after progression was also 7.2 months. Conclusion: Based on our real-life experience, we demonstrated a significant correlation between good response to first treatment and survival in oligometastatic disease, we also understand that local ablative treatment modalities prolong and also delay both OS and PFS in oligometastatic NSCLC patients OS-2. © TÜBİTAK.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.indexedbyTR Dizin
dc.description.issue4
dc.description.openaccessAll Open Access; Bronze Open Access
dc.description.publisherscopeInternational
dc.description.volume62
dc.identifier.doi10.55730/1300-0144.5659
dc.identifier.eissn1303-6165
dc.identifier.issn13000144
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85168797683
dc.identifier.urihttps://doi.org/10.55730/1300-0144.5659
dc.identifier.urihttps://hdl.handle.net/20.500.14288/26770
dc.identifier.wos1166710900012
dc.keywordsNonsmall cell lung cancer
dc.keywordsOligometastasis
dc.keywordsRadical treatment
dc.keywordsTargeted therapy
dc.languageen
dc.publisherTurkiye Klinikleri
dc.sourceTurkish Journal of Medical Sciences
dc.subjectMedicine
dc.titleSurvival outcomes of patients with oligometastatic non-small cell lung cancer who were treated with radical therapy: a multicenter analysis
dc.typeJournal Article

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