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Survival in patients with high-risk neuroblastoma treated without autologous stem cell transplant or dinutuximab beta.
Jain, Richa; Trehan, Amita; Menon, Prema; Kapoor, Rakesh; Kakkar, Nandita; Radhika, Srinivasan; Saxena, Akshay Kumar; Mittal, Bhagwant Rai; Varma, Neelam; Samujh, Ram; Bansal, Deepak.
Afiliação
  • Jain R; Pediatric Hematology-Oncology Unit, Department of Pediatrics, Advanced Pediatrics Center, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Trehan A; Pediatric Hematology-Oncology Unit, Department of Pediatrics, Advanced Pediatrics Center, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Menon P; Department of Pediatric Surgery, Advanced Pediatrics Center, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Kapoor R; Department of Radiotherapy, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Kakkar N; Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Radhika S; Department of Cytopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Saxena AK; Department of Radiodiagnosis and Imaging, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Mittal BR; Department of Nuclear Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Varma N; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Samujh R; Department of Pediatric Surgery, Advanced Pediatrics Center, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Bansal D; Pediatric Hematology-Oncology Unit, Department of Pediatrics, Advanced Pediatrics Center, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Pediatr Hematol Oncol ; 38(4): 291-304, 2021 May.
Article em En | MEDLINE | ID: mdl-33622164
ABSTRACT
The majority of patients with high-risk neuroblastoma (HR-NB) in low- and middle-income countries (LMIC) do not have access to autologous stem cell transplant (ASCT) and dinutuximab. Consolidation with nonmyeloablative chemotherapy is not well-defined, and the outcomes are variable. We report a single-center outcome of patients with HR-NB, treated with nonmyeloablative consolidation. A tabulated compilation of similar reports is included. A retrospective chart review of patients with HR-NB was performed from January 2009 till June 2016. Patients were treated on the backbone of HR-NBL1/SIOPEN protocol. Treatment included induction with rapid-COJEC, surgery, followed by consolidation. Consolidation involved 4 cycles of topotecan, vincristine, and doxorubicin (TVD) instead of ASCT. Infusion of vincristine and doxorubicin were modified for ease and to enable administration in the clinic. Subsequent treatment included radiotherapy to the primary tumor and differentiation therapy with isotretinoin. Over 7½ years, 28 patients with HR-NB were treated. Two (7%) patients had therapy-related mortality. A relapse or disease progression occurred in 11 (39%) patients at a median duration of 17 months (IQR 5, 18). Treatment abandonment was observed in 4 (14%) patients. The median follow-up of disease-free patients was 49 months (IQR 45, 79). Patients with relapse were not treated further. A 4-year EFS of 29.3% was observed when 4-cycles of TVD were administered instead of ASCT in patients with HR-NB. The study and the review will aid decision-making for care of patients in LMIC while considering the options of treatment for HR-NB if access to ACST and dinutuximab is lacking.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vincristina / Protocolos de Quimioterapia Combinada Antineoplásica / Doxorrubicina / Topotecan / Neuroblastoma Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vincristina / Protocolos de Quimioterapia Combinada Antineoplásica / Doxorrubicina / Topotecan / Neuroblastoma Idioma: En Ano de publicação: 2021 Tipo de documento: Article