Pediatric sarcoma in Central America

Outcomes, challenges, and plans for improvement

Authors

  • Paola Friedrich MD,

    Corresponding author
    1. Department of Pediatric Hematology-Oncology, Dana-Farber/Children's Hospital Cancer Center, Boston, USA
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    • Dana-Farber Cancer Institute, 450 Brookline Avenue D322A, Boston, MA 02115

    Search for more papers by this author
    • Fax: (617) 632-5710

  • Roberta Ortiz MD,

    1. Department of Pediatric Oncology, “La Mascota” Children's Hospital, Managua, Nicaragua
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    Search for more papers by this author
  • Kelly Strait MS,

    1. Department of Pediatric Hematology-Oncology, Dana-Farber/Children's Hospital Cancer Center, Boston, USA
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    Search for more papers by this author
  • Soad Fuentes MD,

    1. Department of Pediatric Oncology, Benjamin Bloom National Children's Hospital, San Salvador, El Salvador
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    Search for more papers by this author
  • Yéssica Gamboa MD,

    1. Department of Pediatric Oncology, National Children's Hospital, San Jose, Costa Rica
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    Search for more papers by this author
  • Ingrid Arambú MD,

    1. Department of Pediatric Oncology, Maternal and Child Hospital, Tegucigalpa, Honduras
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    Search for more papers by this author
  • María Ah-Chu-Sanchez MD,

    1. Department of Pediatric Oncology, Children's Hospital, Panama City, Panama
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    Search for more papers by this author
  • Wendy London PhD,

    1. Department of Pediatric Hematology-Oncology, Dana-Farber/Children's Hospital Cancer Center, Boston, USA
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    Search for more papers by this author
  • Carlos Rodríguez-Galindo MD,

    1. Department of Pediatric Hematology-Oncology, Dana-Farber/Children's Hospital Cancer Center, Boston, USA
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    Search for more papers by this author
  • Federico Antillón-Klussmann MD,

    1. Department of Pediatric Oncology, Benjamin Bloom National Children's Hospital, San Salvador, El Salvador
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    Search for more papers by this author
  • Fulgencio Báez MD,

    1. Department of Pediatric Oncology, “La Mascota” Children's Hospital, Managua, Nicaragua
    2. Department of Pediatric Oncology, National Pediatric Oncology Unit, Guatemala City, Guatemala
    Search for more papers by this author
  • for the Central American Association of Pediatric Hematologists Oncologists (AHOPCA)

    1. Department of Pediatric Hematology-Oncology, Dana-Farber/Children's Hospital Cancer Center, Boston, USA
    Search for more papers by this author

Abstract

BACKGROUND:

Children with cancer in middle-income countries have inferior outcomes compared with similar children in high-income countries. The magnitude and drivers of this survival gap are not well understood. In the current report, the authors sought to describe patterns of clinical presentation, magnitude of treatment abandonment, and survival in children with sarcoma in Central America.

METHODS:

A retrospective review was conducted of hospital-based registries from national pediatric oncology referral centers. Patients with newly diagnosed osteosarcoma, Ewing sarcoma, rhabdomyosarcoma (RMS), and soft tissue sarcoma (STS) between January 1, 2000 and December 31, 2009 were included. Survival analyses were performed first using standard definitions of overall survival (OS) and event-free survival (EFS) and then with abandonment included as an event (abandonment-sensitive OS and abandonment-sensitive EFS).

RESULTS:

In total, 785 new cases of pediatric sarcoma were reported (264 diagnoses of osteosarcoma, 175 diagnoses of Ewing sarcoma, 240 diagnoses of RMS, and 106 diagnoses of STS). The rate of metastatic disease at presentation was high (osteosarcoma, 38%; Ewing sarcoma, 39%; RMS, 29%; and STS, 21%). The treatment abandonment rate also was high, particularly among patients with extremity bone sarcomas (osteosarcoma, 30%; Ewing sarcoma, 15%; RMS, 25%; and STS, 15%). Of 559 patients who experienced a first event, 59% had either recurrent or progressive disease. The 4-year OS rate (±standard error) was 40% ± 3%, and the EFS rate was 30% ± 2%; however, these rates decreased further to 31% ± 2% and 24% ± 2%, respectively, when abandonment was taken into account.

CONCLUSIONS:

The current results indicated that high rates of metastases and treatment abandonment and difficulty with upfront treatment effectiveness are important contributors to the poor survival of children with pediatric sarcomas in Central America. Initiatives for early diagnosis, psychosocial support, quality improvement, and multidisciplinary care are warranted to improve outcomes. Cancer 2013. © 2012 American Cancer Society.

Ancillary