Safety and efficacy of pazopanib as a second-line treatment and beyond for soft tissue sarcomas: A real-life tertiary-center experience in the MENA region

dc.contributor.authorAbdul Halim, Nour
dc.contributor.authorEl Sayed, Rola
dc.contributor.authorAlameh, Ibrahim A.
dc.contributor.authorKhoury, Jessica
dc.contributor.authorNakib, Clara El
dc.contributor.authorZerdan, Maroun Bou
dc.contributor.authorCharafeddine, Maya A.
dc.contributor.authorFarhat, Fadi Sami
dc.contributor.authorEl-Karak, Fadi
dc.contributor.authorAssi, Hazem I.
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:43:06Z
dc.date.available2025-01-24T11:43:06Z
dc.date.issued2021
dc.description.abstractIntroduction: Sarcomas are uncommon malignancies. No advances have been recently achieved despite multiple efforts. Pazopanib is a safe and effective tyrosine kinase inhibitor used in managing soft tissue sarcomas (STS) after chemotherapy failure. However, its use is limited in developing countries and no efficacy data exist from our region. We aimed to study the efficacy of pazopanib in our population, characterized by response rates of patients with chemotherapy-refractory advanced STS receiving pazopanib. Secondary endpoints included progression-free survival (PFS), overall survival (OS) and toxicity profile. Materials and Methods: 15 patients (age≥18 year) diagnosed with advanced STS, refractory to first-line chemotherapy, receiving pazopanib as ≥second-line therapy in one tertiary center in Lebanon were included between January 1st, 2014 and October 31st, 2018. Patient and disease characteristics, disease evaluation, as well as tolerance to treatment, were extracted from charts retrospectively. Statistical analysis was done using SPSS version 24. Results: The mean age was 48.6 [19–66] years. Eleven patients (73.3%) received pazopanib in second-line, whereas four patients (26.7%) received it in third-line. Thirteen patients (86.7%) progressed, and two patients (13.3%) had stable disease. The median PFS was three months [1–19] and the mean OS was 25.4 months [17.2–33.6]. Five patients required dose-reductions due to poor tolerance. Conclusion: Conclusions cannot be drawn due to small patient numbers. However, given the 3-month PFS, 13% of patients maintaining stable disease, and tolerable safety profile, it is reasonable to incorporate pazopanib in STS treatment. More focused studies with larger patient populations need to be done in Lebanon. © 2020
dc.identifier.doihttps://doi.org/10.1016/j.ctarc.2020.100275
dc.identifier.eid2-s2.0-85097799076
dc.identifier.pmid33340905
dc.identifier.urihttp://hdl.handle.net/10938/30203
dc.language.isoen
dc.publisherElsevier Ltd
dc.relation.ispartofCancer Treatment and Research Communications
dc.sourceScopus
dc.subjectAdverse events
dc.subjectOutcomes
dc.subjectPazopanib
dc.subjectSafety
dc.subjectSoft tissue sarcoma
dc.subjectAdult
dc.subjectAged
dc.subjectAppetite
dc.subjectFatigue
dc.subjectFemale
dc.subjectHumans
dc.subjectIndazoles
dc.subjectLebanon
dc.subjectMale
dc.subjectMiddle aged
dc.subjectNeoplasm staging
dc.subjectProgression-free survival
dc.subjectProtein kinase inhibitors
dc.subjectPyrimidines
dc.subjectRetrospective studies
dc.subjectSarcoma
dc.subjectSulfonamides
dc.subjectTertiary care centers
dc.subjectYoung adult
dc.subjectCisplatin
dc.subjectCyclophosphamide
dc.subjectDocetaxel
dc.subjectDoxorubicin
dc.subjectEtoposide
dc.subjectGemcitabine
dc.subjectIfosfamide
dc.subjectOlaratumab
dc.subjectVincristine
dc.subjectIndazole derivative
dc.subjectProtein kinase inhibitor
dc.subjectPyrimidine derivative
dc.subjectSulfonamide
dc.subjectArticle
dc.subjectCancer chemotherapy
dc.subjectCancer growth
dc.subjectCardiotoxicity
dc.subjectClinical article
dc.subjectDrug dose reduction
dc.subjectDrug efficacy
dc.subjectDrug safety
dc.subjectFollow up
dc.subjectHistology
dc.subjectHuman
dc.subjectLiver toxicity
dc.subjectLoss of appetite
dc.subjectMalaise
dc.subjectOverall survival
dc.subjectProgression free survival
dc.subjectRetrospective study
dc.subjectCancer staging
dc.subjectDrug effect
dc.subjectMortality
dc.subjectTertiary care center
dc.titleSafety and efficacy of pazopanib as a second-line treatment and beyond for soft tissue sarcomas: A real-life tertiary-center experience in the MENA region
dc.typeArticle

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