Regardless of improvement in cure of Rhabdomyosarcoma (RMS), the results in treatment of advanced stage of RMS in children are still dismal. Recently, high-dose chemotherapy followed by autologous peripheral blood stem cell transplantation (HDC/APBSCT) has been tried to manage the advanced high-risk RMS patients. We investigated the effectiveness of HDC/APBSCT by reviewing the clinical records of high-risk pediatric RMS patients in single institute database. Over twenty years, 37 patients were diagnosed as RMS with high-risk at the time of first diagnosis. These patients were classified as two groups according to treatment method. The first group was HDC/APBSCT and the other was conventional multi-agent chemotherapy group. Differences of cl...
This therapeutic trial deals with 81 patients with stage III rhabdomyosarcoma (RMS), from different ...
Introduction: From 2002 to 2011, the Italian Soft Tissue Sarcoma Committee explored a combination of...
INTRODUCTION: From 2002 to 2011, the Italian Soft Tissue Sarcoma Committee explored a combination o...
Rhabdomyosarcoma (RMS), the most common soft-tissue sarcoma in children, is cured with conventional ...
Patients with metastatic rhabdomyosarcoma (RMS) have a poor prognosis. The aim of this systematic re...
AIM: The RMS4.99 study was designed to explore the role of multiple sequential high-dose chemotherap...
PurposeWe performed a pilot study to determine the benefit of high-dose chemotherapy and autologous ...
Soft tissue sarcomas (STS) are highly malignant tumours that constitute 5–6% of all malignant childh...
Simple Summary The major challenge in pediatric oncology is the optimal adaptation of therapy burden...
Introduction: Patients with metastatic rhabdomyosarcoma (RMS) have a poor prognosis. The aim of this...
BACKGROUND In childhood cancer, consolidation treatment with chemotherapy followed by autologous hem...
Recent development of stratified chemotherapeutic regimens has rapidly improved the survival rate of...
© 2013 The Cochrane Collaboration. Background: Soft tissue sarcomas (STS) are a highly heterogeneous...
Recent development of stratified chemotherapeutic regimens has rapidly improved the survival rate of...
Background and Objective: Neuroblastoma is the most common extracranial solid tumor found in pediatr...
This therapeutic trial deals with 81 patients with stage III rhabdomyosarcoma (RMS), from different ...
Introduction: From 2002 to 2011, the Italian Soft Tissue Sarcoma Committee explored a combination of...
INTRODUCTION: From 2002 to 2011, the Italian Soft Tissue Sarcoma Committee explored a combination o...
Rhabdomyosarcoma (RMS), the most common soft-tissue sarcoma in children, is cured with conventional ...
Patients with metastatic rhabdomyosarcoma (RMS) have a poor prognosis. The aim of this systematic re...
AIM: The RMS4.99 study was designed to explore the role of multiple sequential high-dose chemotherap...
PurposeWe performed a pilot study to determine the benefit of high-dose chemotherapy and autologous ...
Soft tissue sarcomas (STS) are highly malignant tumours that constitute 5–6% of all malignant childh...
Simple Summary The major challenge in pediatric oncology is the optimal adaptation of therapy burden...
Introduction: Patients with metastatic rhabdomyosarcoma (RMS) have a poor prognosis. The aim of this...
BACKGROUND In childhood cancer, consolidation treatment with chemotherapy followed by autologous hem...
Recent development of stratified chemotherapeutic regimens has rapidly improved the survival rate of...
© 2013 The Cochrane Collaboration. Background: Soft tissue sarcomas (STS) are a highly heterogeneous...
Recent development of stratified chemotherapeutic regimens has rapidly improved the survival rate of...
Background and Objective: Neuroblastoma is the most common extracranial solid tumor found in pediatr...
This therapeutic trial deals with 81 patients with stage III rhabdomyosarcoma (RMS), from different ...
Introduction: From 2002 to 2011, the Italian Soft Tissue Sarcoma Committee explored a combination of...
INTRODUCTION: From 2002 to 2011, the Italian Soft Tissue Sarcoma Committee explored a combination o...