Comparison of Long-Term Outcome between Doublet and Triplet Neoadjuvant Chemotherapy in Non-Metastatic Osteosarcoma of the Extremity

Objective: This study compared outcomes between doublet (AP) and triplet (IAP) neoadjuvant chemotherapy for nonmetastatic osteosarcoma of the extremity. Methods: A total of 124 patients were enrolled. In the AP group, a doublet regimen of intraarterial cisplatin and intravenous doxorubicin was given...

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Veröffentlicht in:Oncology 2011-06, Vol.80 (1-2), p.107-117
Hauptverfasser: Hong, Soojung, Shin, Sang Joon, Jung, Minkyu, Jeong, Jaeheon, Lee, Young Joo, Shin, Kyoo-Ho, Roh, Jae Kyung, Rha, Sun Young
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container_end_page 117
container_issue 1-2
container_start_page 107
container_title Oncology
container_volume 80
creator Hong, Soojung
Shin, Sang Joon
Jung, Minkyu
Jeong, Jaeheon
Lee, Young Joo
Shin, Kyoo-Ho
Roh, Jae Kyung
Rha, Sun Young
description Objective: This study compared outcomes between doublet (AP) and triplet (IAP) neoadjuvant chemotherapy for nonmetastatic osteosarcoma of the extremity. Methods: A total of 124 patients were enrolled. In the AP group, a doublet regimen of intraarterial cisplatin and intravenous doxorubicin was given to 77 patients from 1991 to 1999. In the IAP group, a triplet regimen of additional intravenous ifosfamide was given to 47 patients from 2000 to 2007. After completion of 3 cycles of chemotherapy, patients underwent surgery. We assessed tumor response according to pathologic tumor necrosis, and treated patients with further adjuvant chemotherapy. Results: The overall pathologic response was excellent with more than 90% tumor necrosis in 74.8% of patients. Total necrosis of tumors was also found in 46 (37.4%) patients. There was no difference between the 2 groups in pathologic response (75.3 vs. 72.3%; p = 0.52) or other clinicopathologic parameters. There was no difference between the 2 groups in recurrence rate (31.2 vs. 31.9%; p = 0.17) or lung metastasis (28.6 vs. 23.4%; p = 0.53). Moreover, there were no statistical differences in median disease-free survival and overall survival between the groups. There was more hematologic toxicity in the IAP group (neutropenia, p = 0.002; thrombocytopenia, p = 0.001; febrile neutropenia, p < 0.001). Conclusions: The addition of ifosfamide to doxorubicin and cisplatin in neoadjuvant chemotherapy did not show improved outcomes in this study. Further trials are required to elucidate optimal neoadjuvant chemotherapy and effective salvage regimens.
doi_str_mv 10.1159/000327216
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Methods: A total of 124 patients were enrolled. In the AP group, a doublet regimen of intraarterial cisplatin and intravenous doxorubicin was given to 77 patients from 1991 to 1999. In the IAP group, a triplet regimen of additional intravenous ifosfamide was given to 47 patients from 2000 to 2007. After completion of 3 cycles of chemotherapy, patients underwent surgery. We assessed tumor response according to pathologic tumor necrosis, and treated patients with further adjuvant chemotherapy. Results: The overall pathologic response was excellent with more than 90% tumor necrosis in 74.8% of patients. Total necrosis of tumors was also found in 46 (37.4%) patients. There was no difference between the 2 groups in pathologic response (75.3 vs. 72.3%; p = 0.52) or other clinicopathologic parameters. There was no difference between the 2 groups in recurrence rate (31.2 vs. 31.9%; p = 0.17) or lung metastasis (28.6 vs. 23.4%; p = 0.53). Moreover, there were no statistical differences in median disease-free survival and overall survival between the groups. There was more hematologic toxicity in the IAP group (neutropenia, p = 0.002; thrombocytopenia, p = 0.001; febrile neutropenia, p &lt; 0.001). Conclusions: The addition of ifosfamide to doxorubicin and cisplatin in neoadjuvant chemotherapy did not show improved outcomes in this study. Further trials are required to elucidate optimal neoadjuvant chemotherapy and effective salvage regimens.</description><identifier>ISSN: 0030-2414</identifier><identifier>EISSN: 1423-0232</identifier><identifier>DOI: 10.1159/000327216</identifier><identifier>PMID: 21677455</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Adjuvants ; Adolescent ; Adult ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Bone cancer ; Bone Neoplasms - drug therapy ; Bone Neoplasms - pathology ; Bone Neoplasms - surgery ; Chemotherapy ; Child ; Child, Preschool ; Cisplatin ; Cisplatin - administration &amp; dosage ; Clinical outcomes ; Clinical Study ; Clinical trials ; Comparative studies ; Disease-Free Survival ; Diseases of the osteoarticular system ; Doxorubicin ; Doxorubicin - administration &amp; dosage ; Extremities - pathology ; Female ; Humans ; IAP protein ; Ifosfamide ; Ifosfamide - administration &amp; dosage ; Intravenous administration ; Kaplan-Meier Estimate ; Long term ; Lung ; Lung Neoplasms - secondary ; Male ; Medical sciences ; Metastases ; Middle Aged ; Necrosis ; Neoadjuvant Therapy ; Neoplasm Recurrence, Local ; Neutropenia ; Neutropenia - chemically induced ; Osteosarcoma ; Osteosarcoma - drug therapy ; Osteosarcoma - pathology ; Osteosarcoma - surgery ; Retrospective Studies ; Statistics ; Surgery ; Survival ; Survival Rate ; Thrombocytopenia ; Thrombocytopenia - chemically induced ; Toxicity ; Treatment Outcome ; Tumors ; Tumors of striated muscle and skeleton ; Young Adult</subject><ispartof>Oncology, 2011-06, Vol.80 (1-2), p.107-117</ispartof><rights>2011 S. Karger AG, Basel</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 S. Karger AG, Basel.</rights><rights>Copyright (c) 2011 S. 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Methods: A total of 124 patients were enrolled. In the AP group, a doublet regimen of intraarterial cisplatin and intravenous doxorubicin was given to 77 patients from 1991 to 1999. In the IAP group, a triplet regimen of additional intravenous ifosfamide was given to 47 patients from 2000 to 2007. After completion of 3 cycles of chemotherapy, patients underwent surgery. We assessed tumor response according to pathologic tumor necrosis, and treated patients with further adjuvant chemotherapy. Results: The overall pathologic response was excellent with more than 90% tumor necrosis in 74.8% of patients. Total necrosis of tumors was also found in 46 (37.4%) patients. There was no difference between the 2 groups in pathologic response (75.3 vs. 72.3%; p = 0.52) or other clinicopathologic parameters. There was no difference between the 2 groups in recurrence rate (31.2 vs. 31.9%; p = 0.17) or lung metastasis (28.6 vs. 23.4%; p = 0.53). Moreover, there were no statistical differences in median disease-free survival and overall survival between the groups. There was more hematologic toxicity in the IAP group (neutropenia, p = 0.002; thrombocytopenia, p = 0.001; febrile neutropenia, p &lt; 0.001). Conclusions: The addition of ifosfamide to doxorubicin and cisplatin in neoadjuvant chemotherapy did not show improved outcomes in this study. Further trials are required to elucidate optimal neoadjuvant chemotherapy and effective salvage regimens.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>21677455</pmid><doi>10.1159/000327216</doi><tpages>11</tpages></addata></record>
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source MEDLINE; Karger Journals; Alma/SFX Local Collection
subjects Adjuvants
Adolescent
Adult
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Bone cancer
Bone Neoplasms - drug therapy
Bone Neoplasms - pathology
Bone Neoplasms - surgery
Chemotherapy
Child
Child, Preschool
Cisplatin
Cisplatin - administration & dosage
Clinical outcomes
Clinical Study
Clinical trials
Comparative studies
Disease-Free Survival
Diseases of the osteoarticular system
Doxorubicin
Doxorubicin - administration & dosage
Extremities - pathology
Female
Humans
IAP protein
Ifosfamide
Ifosfamide - administration & dosage
Intravenous administration
Kaplan-Meier Estimate
Long term
Lung
Lung Neoplasms - secondary
Male
Medical sciences
Metastases
Middle Aged
Necrosis
Neoadjuvant Therapy
Neoplasm Recurrence, Local
Neutropenia
Neutropenia - chemically induced
Osteosarcoma
Osteosarcoma - drug therapy
Osteosarcoma - pathology
Osteosarcoma - surgery
Retrospective Studies
Statistics
Surgery
Survival
Survival Rate
Thrombocytopenia
Thrombocytopenia - chemically induced
Toxicity
Treatment Outcome
Tumors
Tumors of striated muscle and skeleton
Young Adult
title Comparison of Long-Term Outcome between Doublet and Triplet Neoadjuvant Chemotherapy in Non-Metastatic Osteosarcoma of the Extremity
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