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Ifosfamide, Carboplatin, and Etoposide (ICE) in Combination with Regional Hyperthermia as Salvage Therapy in Patients with Locally Advanced Nonmetastatic and Metastatic Soft-Tissue Sarcoma

Patients with localized relapse of soft-tissue sarcoma (STS) after anthracycline-based chemotherapy have a dismal prognosis, particularly when surgery is not possible. To facilitate resection and improve long-term tumor control, we applied an intensified perioperative treatment consisting of ICE (if...

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Autores principales: Bücklein, Veit, Limmroth, Christina, Kampmann, Eric, Schuebbe, Gesa, Issels, Rolf, Roeder, Falk, Angele, Martin, Dürr, Hans Roland, Knösel, Thomas, Abdel-Rahman, Sultan, Di Gioia, Dorit, Lindner, Lars H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068144/
https://www.ncbi.nlm.nih.gov/pubmed/32189990
http://dx.doi.org/10.1155/2020/6901678
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author Bücklein, Veit
Limmroth, Christina
Kampmann, Eric
Schuebbe, Gesa
Issels, Rolf
Roeder, Falk
Angele, Martin
Dürr, Hans Roland
Knösel, Thomas
Abdel-Rahman, Sultan
Di Gioia, Dorit
Lindner, Lars H.
author_facet Bücklein, Veit
Limmroth, Christina
Kampmann, Eric
Schuebbe, Gesa
Issels, Rolf
Roeder, Falk
Angele, Martin
Dürr, Hans Roland
Knösel, Thomas
Abdel-Rahman, Sultan
Di Gioia, Dorit
Lindner, Lars H.
author_sort Bücklein, Veit
collection PubMed
description Patients with localized relapse of soft-tissue sarcoma (STS) after anthracycline-based chemotherapy have a dismal prognosis, particularly when surgery is not possible. To facilitate resection and improve long-term tumor control, we applied an intensified perioperative treatment consisting of ICE (ifosfamide 6 g/m(2), carboplatin 400 mg/m(2), and etoposide 600 mg/m(2)) in combination with regional hyperthermia (RHT) to maximize local control. Here, we retrospectively evaluate the safety and efficacy of this strategy. Patients aged ≥18 years with locally advanced high-risk STS, either with or without metastasis, treated with ICE + RHT after the failure of first-line anthracycline-based chemotherapy were included in this analysis. Radiographic response, toxicity, progression-free survival (PFS), and overall survival (OS) were assessed. Between 1996 and 2018, 213 sarcoma patients received ICE at our centre. Of these, 110 patients met the selection criteria (progressive disease, suitable high-grade STS histology, anthracycline pretreatment, RHT treatment) for this analysis. Fifty-four patients had locally advanced disease without metastases (LA-STS), and 56 patients had additional metastatic disease (M-STS). Disease control was achieved in 59% of LA-STS patients and in 47% of M-STS patients. For LA-STS, 21% of the patients achieved radiographic response, facilitating resection in 4 patients (7%), compared with 11% of the M-STS patients, facilitating resection in 5 patients (9%). PFS was significantly longer in LA-STS than in M-STS (10 vs. 4 months, p < 0.0001). Median OS was 26 months in LA-STS and 12 months in M-STS. Disease control was the only independent prognostic factor for improved OS in multivariate analysis. Toxicity was high with neutropenic fever occurring in 25% of the patients and three therapy-related deaths (3%). ICE + RHT demonstrated activity in high-risk STS and facilitated resection in selected patients after anthracycline failure. Disease control was associated with improved OS. Based on the observed toxicities, the dose should be reduced to 75%.
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spelling pubmed-70681442020-03-18 Ifosfamide, Carboplatin, and Etoposide (ICE) in Combination with Regional Hyperthermia as Salvage Therapy in Patients with Locally Advanced Nonmetastatic and Metastatic Soft-Tissue Sarcoma Bücklein, Veit Limmroth, Christina Kampmann, Eric Schuebbe, Gesa Issels, Rolf Roeder, Falk Angele, Martin Dürr, Hans Roland Knösel, Thomas Abdel-Rahman, Sultan Di Gioia, Dorit Lindner, Lars H. Sarcoma Research Article Patients with localized relapse of soft-tissue sarcoma (STS) after anthracycline-based chemotherapy have a dismal prognosis, particularly when surgery is not possible. To facilitate resection and improve long-term tumor control, we applied an intensified perioperative treatment consisting of ICE (ifosfamide 6 g/m(2), carboplatin 400 mg/m(2), and etoposide 600 mg/m(2)) in combination with regional hyperthermia (RHT) to maximize local control. Here, we retrospectively evaluate the safety and efficacy of this strategy. Patients aged ≥18 years with locally advanced high-risk STS, either with or without metastasis, treated with ICE + RHT after the failure of first-line anthracycline-based chemotherapy were included in this analysis. Radiographic response, toxicity, progression-free survival (PFS), and overall survival (OS) were assessed. Between 1996 and 2018, 213 sarcoma patients received ICE at our centre. Of these, 110 patients met the selection criteria (progressive disease, suitable high-grade STS histology, anthracycline pretreatment, RHT treatment) for this analysis. Fifty-four patients had locally advanced disease without metastases (LA-STS), and 56 patients had additional metastatic disease (M-STS). Disease control was achieved in 59% of LA-STS patients and in 47% of M-STS patients. For LA-STS, 21% of the patients achieved radiographic response, facilitating resection in 4 patients (7%), compared with 11% of the M-STS patients, facilitating resection in 5 patients (9%). PFS was significantly longer in LA-STS than in M-STS (10 vs. 4 months, p < 0.0001). Median OS was 26 months in LA-STS and 12 months in M-STS. Disease control was the only independent prognostic factor for improved OS in multivariate analysis. Toxicity was high with neutropenic fever occurring in 25% of the patients and three therapy-related deaths (3%). ICE + RHT demonstrated activity in high-risk STS and facilitated resection in selected patients after anthracycline failure. Disease control was associated with improved OS. Based on the observed toxicities, the dose should be reduced to 75%. Hindawi 2020-02-27 /pmc/articles/PMC7068144/ /pubmed/32189990 http://dx.doi.org/10.1155/2020/6901678 Text en Copyright © 2020 Veit Bücklein et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bücklein, Veit
Limmroth, Christina
Kampmann, Eric
Schuebbe, Gesa
Issels, Rolf
Roeder, Falk
Angele, Martin
Dürr, Hans Roland
Knösel, Thomas
Abdel-Rahman, Sultan
Di Gioia, Dorit
Lindner, Lars H.
Ifosfamide, Carboplatin, and Etoposide (ICE) in Combination with Regional Hyperthermia as Salvage Therapy in Patients with Locally Advanced Nonmetastatic and Metastatic Soft-Tissue Sarcoma
title Ifosfamide, Carboplatin, and Etoposide (ICE) in Combination with Regional Hyperthermia as Salvage Therapy in Patients with Locally Advanced Nonmetastatic and Metastatic Soft-Tissue Sarcoma
title_full Ifosfamide, Carboplatin, and Etoposide (ICE) in Combination with Regional Hyperthermia as Salvage Therapy in Patients with Locally Advanced Nonmetastatic and Metastatic Soft-Tissue Sarcoma
title_fullStr Ifosfamide, Carboplatin, and Etoposide (ICE) in Combination with Regional Hyperthermia as Salvage Therapy in Patients with Locally Advanced Nonmetastatic and Metastatic Soft-Tissue Sarcoma
title_full_unstemmed Ifosfamide, Carboplatin, and Etoposide (ICE) in Combination with Regional Hyperthermia as Salvage Therapy in Patients with Locally Advanced Nonmetastatic and Metastatic Soft-Tissue Sarcoma
title_short Ifosfamide, Carboplatin, and Etoposide (ICE) in Combination with Regional Hyperthermia as Salvage Therapy in Patients with Locally Advanced Nonmetastatic and Metastatic Soft-Tissue Sarcoma
title_sort ifosfamide, carboplatin, and etoposide (ice) in combination with regional hyperthermia as salvage therapy in patients with locally advanced nonmetastatic and metastatic soft-tissue sarcoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7068144/
https://www.ncbi.nlm.nih.gov/pubmed/32189990
http://dx.doi.org/10.1155/2020/6901678
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