Musculoskeletal Manifestations of Pediatric ALL Delayed Diagnosis

News
Article

Presentation with musculoskeletal manifestations as the only symptom in pediatric B-cell acute lymphoblastic leukemia was significantly associated with diagnostic delay. However, this delay did not affect patient prognosis.

Presentation with musculoskeletal manifestations as the only symptom in pediatric B-cell acute lymphoblastic leukemia (ALL) was significantly associated with diagnostic delay, according to the results of a retrospective study published in the Journal of Pediatrics. However, this delay did not affect patient prognosis.

“Musculoskeletal manifestations appear to be associated significantly with diagnostic delay but do not affect the oncologic outcomes of ALL,” wrote study author Seungcheol Kang, MD, of the department of orthopedic surgery at the Asan Medical Center Children’s Hospital in Korea, and colleagues. “Furthermore, given that the prevalence of malignancy among children presenting with musculoskeletal pain is extremely low, we believe that intensive hematologic evaluations for leukemia may be unnecessary for children who only present with limb pain, unless they also present with leukemic symptoms.”

According to the study, patients with ALL typically present with leukemia symptoms, such as the tendency to bleed or bruise, pallor or fatigue, or fever or vulnerability to infection. However, as many as one-third of patients with ALL will present with musculoskeletal manifestations. Many of these patients are misdiagnosed or undiagnosed during their first hospital visit.

With this study, Kang and colleagues evaluated the clinical and prognostic effect of musculoskeletal manifestations. The researchers reviewed 158 children with precursor B-cell ALL with follow-up for 2 years or longer. Based on initial presenting symptoms, patients were classified as having musculoskeletal symptoms (n = 34) or not (n = 134). They examined leukemic symptoms that could indicate the presence of leukemia, and the duration of both leukemic symptom duration and any symptom duration.

Those patients with musculoskeletal manifestations had significantly longer symptom duration compared with patients with nonmusculoskeletal manifestations (42.6 vs 21.9 days; P = .006). These patients also had a shorter leukemic symptom duration (7.3 vs 21.9 days; P < .001).

The 5-year overall survival for the entire group of patients was 88.4%, with no significant difference between patients classified as having musculoskeletal manifestations and those who did not. Although longer symptom duration did not affect prognosis, longer leukemic symptom duration was association with a poorer prognosis (hazard ratio = 7.72; P = .048).

“Although further studies are needed to validate these findings, we cautiously suggest that intensive evaluations for hematologic malignancies may be unnecessary for children who complain of limb pain without any definite cause, unless they also present with accompanying leukemic symptoms,” the researchers wrote.

Recent Videos
Cytokine release syndrome was primarily low or intermediate in severity, with no grade 5 instances reported among those with diffuse large B-cell lymphoma.
Safety results from a phase 2 trial show that most toxicities with durvalumab treatment were manageable and low or intermediate in severity.
Investigators are currently evaluating mosunetuzumab in relapsed disease or comparing it with rituximab in treatment-naïve follicular lymphoma.
Compared with second-generation tyrosine kinase inhibitors, asciminib was better tolerated in patients with chronic myeloid leukemia.
Bulkiness of disease did not appear to impact PFS outcomes with ibrutinib plus venetoclax in the phase 2 CAPTIVATE study.
Greater direct access to academic oncologists may help address challenges associated with a lack of CAR T education in the community setting.
Certain bridging therapies and abundant steroid use may complicate the T-cell collection process during CAR T therapy.
Educating community practices on CAR T referral and sequencing treatment strategies may help increase CAR T utilization.
Harmonizing protocols across the health care system may bolster the feasibility of giving bispecifics to those with lymphoma in a community setting.
Establishment of an AYA Lymphoma Consortium has facilitated a process to better understand and address gaps in knowledge for this patient group.
Related Content