Efficacy of Sirolimus Treatment in PEComa–10 Years of Practice Perspective

Perivascular epithelioid cell tumors (PEComa) represent a family of rare mesenchymal tumors resultant from deregulation in mTOR pathway activity. The aim of this study is to evaluate the long-term efficacy of targeted PEComa treatment. We reviewed all consecutive patients with PEComa who started sys...

Full description

Bibliographic Details
Main Authors: Tomasz Świtaj, Aleksandra Sobiborowicz, Paweł Teterycz, Anna Klimczak, Donata Makuła, Michał Wągrodzki, Anna Szumera-Ciećkiewicz, Piotr Rutkowski, Anna M. Czarnecka
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/10/16/3705
id doaj-8cefaa9ce1f24307a2d642510aae4263
record_format Article
spelling doaj-8cefaa9ce1f24307a2d642510aae42632021-08-26T13:55:57ZengMDPI AGJournal of Clinical Medicine2077-03832021-08-01103705370510.3390/jcm10163705Efficacy of Sirolimus Treatment in PEComa–10 Years of Practice PerspectiveTomasz Świtaj0Aleksandra Sobiborowicz1Paweł Teterycz2Anna Klimczak3Donata Makuła4Michał Wągrodzki5Anna Szumera-Ciećkiewicz6Piotr Rutkowski7Anna M. Czarnecka8Department of Soft Tissue/Bone, Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, PolandDepartment of Soft Tissue/Bone, Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, PolandDepartment of Soft Tissue/Bone, Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, PolandDepartment of Soft Tissue/Bone, Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, PolandDepartment of Radiology I, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, PolandDepartment of Pathology and Laboratory Diagnostics, Maria Skłodowska-Curie Institute-Oncology Center, 02-781 Warsaw, PolandDepartment of Pathology and Laboratory Diagnostics, Maria Skłodowska-Curie Institute-Oncology Center, 02-781 Warsaw, PolandDepartment of Soft Tissue/Bone, Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, PolandDepartment of Soft Tissue/Bone, Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781 Warsaw, PolandPerivascular epithelioid cell tumors (PEComa) represent a family of rare mesenchymal tumors resultant from deregulation in mTOR pathway activity. The aim of this study is to evaluate the long-term efficacy of targeted PEComa treatment. We reviewed all consecutive patients with PEComa who started systemic treatment with sirolimus in our reference sarcoma center between January 2011 and August 2020. Histopathology of PEComa was reviewed and confirmed in all cases by a designated sarcoma pathologist. Any surviving progression-free patients were censored at the last follow-up (31 March 2021). Survival curves were calculated according to Kaplan–Meier method and compared with the log-rank test or a Cox proportional hazard model. Fifteen (12 females and 3 males) consecutive PEComa patients were treated. The median age of patients treated systemically was 50 years. Median progression-free survival (PFS) was 4.9 months (95% CI: 3.8-NA) for first-line chemotherapy and was not reached (95% CI: 42.0-NA) for sirolimus as first-line therapy. There was one objective response (OR) in the chemotherapy group. The OR rate reached 73% (11/15 cases) for sirolimus regardless of the treatment line. All patients archived disease control. Three patients died due to disease progression after 55, 32, and 32 months since metastatic disease diagnosis. After a median follow-up of 55.7 (range: 3.2–220) months, the 5 yr OS was 65% (CI 95% 39–100). Our study is the largest single-institution report on PEComa systemic targeted therapy and fills the gap in the field of advanced PEComa care since the FDA/EMEA approval of sirolimus.https://www.mdpi.com/2077-0383/10/16/3705perivascular epithelioid cell tumorPEComalymphangioleiomyomatosissarcomasirolimusmTOR inhibitors
collection DOAJ
language English
format Article
sources DOAJ
author Tomasz Świtaj
Aleksandra Sobiborowicz
Paweł Teterycz
Anna Klimczak
Donata Makuła
Michał Wągrodzki
Anna Szumera-Ciećkiewicz
Piotr Rutkowski
Anna M. Czarnecka
spellingShingle Tomasz Świtaj
Aleksandra Sobiborowicz
Paweł Teterycz
Anna Klimczak
Donata Makuła
Michał Wągrodzki
Anna Szumera-Ciećkiewicz
Piotr Rutkowski
Anna M. Czarnecka
Efficacy of Sirolimus Treatment in PEComa–10 Years of Practice Perspective
Journal of Clinical Medicine
perivascular epithelioid cell tumor
PEComa
lymphangioleiomyomatosis
sarcoma
sirolimus
mTOR inhibitors
author_facet Tomasz Świtaj
Aleksandra Sobiborowicz
Paweł Teterycz
Anna Klimczak
Donata Makuła
Michał Wągrodzki
Anna Szumera-Ciećkiewicz
Piotr Rutkowski
Anna M. Czarnecka
author_sort Tomasz Świtaj
title Efficacy of Sirolimus Treatment in PEComa–10 Years of Practice Perspective
title_short Efficacy of Sirolimus Treatment in PEComa–10 Years of Practice Perspective
title_full Efficacy of Sirolimus Treatment in PEComa–10 Years of Practice Perspective
title_fullStr Efficacy of Sirolimus Treatment in PEComa–10 Years of Practice Perspective
title_full_unstemmed Efficacy of Sirolimus Treatment in PEComa–10 Years of Practice Perspective
title_sort efficacy of sirolimus treatment in pecoma–10 years of practice perspective
publisher MDPI AG
series Journal of Clinical Medicine
issn 2077-0383
publishDate 2021-08-01
description Perivascular epithelioid cell tumors (PEComa) represent a family of rare mesenchymal tumors resultant from deregulation in mTOR pathway activity. The aim of this study is to evaluate the long-term efficacy of targeted PEComa treatment. We reviewed all consecutive patients with PEComa who started systemic treatment with sirolimus in our reference sarcoma center between January 2011 and August 2020. Histopathology of PEComa was reviewed and confirmed in all cases by a designated sarcoma pathologist. Any surviving progression-free patients were censored at the last follow-up (31 March 2021). Survival curves were calculated according to Kaplan–Meier method and compared with the log-rank test or a Cox proportional hazard model. Fifteen (12 females and 3 males) consecutive PEComa patients were treated. The median age of patients treated systemically was 50 years. Median progression-free survival (PFS) was 4.9 months (95% CI: 3.8-NA) for first-line chemotherapy and was not reached (95% CI: 42.0-NA) for sirolimus as first-line therapy. There was one objective response (OR) in the chemotherapy group. The OR rate reached 73% (11/15 cases) for sirolimus regardless of the treatment line. All patients archived disease control. Three patients died due to disease progression after 55, 32, and 32 months since metastatic disease diagnosis. After a median follow-up of 55.7 (range: 3.2–220) months, the 5 yr OS was 65% (CI 95% 39–100). Our study is the largest single-institution report on PEComa systemic targeted therapy and fills the gap in the field of advanced PEComa care since the FDA/EMEA approval of sirolimus.
topic perivascular epithelioid cell tumor
PEComa
lymphangioleiomyomatosis
sarcoma
sirolimus
mTOR inhibitors
url https://www.mdpi.com/2077-0383/10/16/3705
work_keys_str_mv AT tomaszswitaj efficacyofsirolimustreatmentinpecoma10yearsofpracticeperspective
AT aleksandrasobiborowicz efficacyofsirolimustreatmentinpecoma10yearsofpracticeperspective
AT pawełteterycz efficacyofsirolimustreatmentinpecoma10yearsofpracticeperspective
AT annaklimczak efficacyofsirolimustreatmentinpecoma10yearsofpracticeperspective
AT donatamakuła efficacyofsirolimustreatmentinpecoma10yearsofpracticeperspective
AT michałwagrodzki efficacyofsirolimustreatmentinpecoma10yearsofpracticeperspective
AT annaszumeracieckiewicz efficacyofsirolimustreatmentinpecoma10yearsofpracticeperspective
AT piotrrutkowski efficacyofsirolimustreatmentinpecoma10yearsofpracticeperspective
AT annamczarnecka efficacyofsirolimustreatmentinpecoma10yearsofpracticeperspective
_version_ 1721192311670439936