How Children’s National Specializes in Treatment for Sarcoma Patients

Sixteen-year-old Alexx thought the swelling in her leg was attributed to a cheerleading injury, but an MRI revealed osteosarcoma.

“Anytime someone is diagnosed with cancer, it’s a serious condition.” says Jeffrey Dome, MD, PhD, Division Chief of Hematology and Oncology at Children’s National Health System.

“Osteosarcoma is the most common bone cancer that we see in children and teenagers and the problem is that it starts in the bone, but it has the potential to spread…then we worry it can be life-threatening.”

Dr. Dome worked with a team of specialists to ensure Alexx’s treatment was successful and her 16th birthday was sweeter because she also celebrated beating cancer.

Most pediatricians see sarcoma once or twice in the span of their entire career. Our team of sarcoma specialists has the expertise to improve outcomes for young patients with these tumors.

Pediatric soft tissue sarcomas, which can arise in bone, muscle, and connective tissues anywhere in the body, account for just 7 percent of all childhood tumors. Because these tumors can be aggressive, prompt diagnosis and treatment by an experienced multidisciplinary team is needed to provide the best chance for cure and functional recovery.

“If there is a suspected diagnosis of sarcoma, we prefer referral as early as possible,” says Dr. Dome. “If the tumor turns out not to be a sarcoma, families are happy to hear that, but if it is sarcoma, at least we have planned everything from the beginning.”

Children’s National has advanced imaging equipment available for diagnosis, staging, treatment, and follow-up for all bone and soft tissue sarcomas in children, adolescents, and young adults. In addition, the Children’s National sarcoma program is one of the few in the United States where patients can see a pediatric oncologist, orthopaedic oncologist, biologist, and physical therapist in one comprehensive visit.

“Prior to each clinic, individual cases are reviewed by the multidisciplinary team,” says AeRang Kim, MD, PhD, pediatric oncologist at Children’s National. “Then, the patient has access to this team of experts where diagnosis, planning, and treatment can occur with the patient and family.”

Part of Alexx’s team was nurse practitioner Katarina Steacy, NP, NP-C, who was not only familiar with her treatment plan, but also was a point of contact to the family.

“The entire team; the doctor, the nurse practitioner, the nurse coordinator, the social worker, really try to forge a relationship with them from the get-go so that they have hope that we know they can get through this,” says Steacy. “For Alexx, her grandmother and I forged a close relationship and she knew that she could email me or call me with any question or concern throughout her treatment.”

Treatment typically consists of multimodal therapy, which may include chemotherapy, surgery, radiation, and rehabilitation. Patients also have access to the most novel therapies available. As one of the select institutions in the Children’s Oncology Group (COG) consortium, Children’s National has access to COG Phase I and II trials.

“The feat to a successful outcome is having great psychosocial support. It’s not enough to deliver the medicine or the chemotherapy, we also have to support the family and the child,” says Dr. Dome. “For us, just having patients survive the cancer is not enough. We want patients to survive with a good quality of life and full functionality.”

 

Joey's Story

Joey's Story

When Joey was 10-years-old, he was sent to Children's National and diagnosed with leukemia. Today, Joey is 16-years-old and cancer-free. He is enjoying his junior year of high school and playing baseball.

Read More of Joey's Story