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Pediatric Hematology/Oncology

Pediatric Hematology/Oncology

Clinical discussions on pediatric blood disorders, childhood cancers, and specialized treatment protocols.

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Do you recommend continuous antibiotic prophylaxis for patients on complement inhibitors such as eculizumab?

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3 Answers

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Neurology · Christiana Care

This is an extremely important and timely question. There simply isn’t enough data or firm guidelines on this leading to different practices. The reality is that there have been a number of meningococcal breakthrough infections in those vaccinated against meningococcal disease. Complement therapies ...

Does "preoperative rupture" always necessitate whole abdomen RT for Wilms' tumor?

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Radiation Oncology · Northwestern University Feinberg School of Medicine

This is controversial. Theoretical arguments aside, our committee (COG) feels strongly that for any preoperative rupture, whole abdomen RT is required.

What is the role of PD-1 inhibitors in relapsed B-cell ALL?

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Pediatric Hematology/Oncology · The University of Texas MD Anderson Cancer Center

The role of PD-1 inhibitors in pedi is currently being explored in relapsed B-ALL in the study AALL1821. No interim results have been posted.Primary samples from pediatric patients with relapsed B-ALL were shown to demonstrate marked up-regulation of PD-1 on T-cells, and up-regulation of PD-L1 on th...

How would you approach cytopenias 5 weeks after initial dosing in a young patient with MDS treated with Azacitadine as a bridge to transplant?

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Medical Oncology · University of Maryland Cancer Center

Bridging with HMA to transplant in MDS patients is a common practice although it did not show improved outcomes. You will definitely have to r/o other potential causes of pancytopenia (i.e., infections, etc). I would repeat a BM A/Bx to make sure that blasts are not increasing (< 20% and preferably ...

What would your next line treatment be for a patient previously treated with repeat resection, craniospinal irradiation, and initial cisplatin/vincristine/CCNU with medulloblastoma?

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Pediatric Hematology/Oncology · C. S. Mott Children’s Hospital, University of Michigan

As you will agree, this is an extremely unfortunate situation. I am assuming this patient has progressed either while on therapy or soon after completion? Depending on his age, a potential option is to enroll him on any available clinical trials. PBTC58 study uses intrathecal omburtumab along with c...

How do you work up a young patient with increasing ferritin and normal TSAT without infectious, inflammatory, or liver disorders?

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Hematology · Georgetown University School of Medicine

This is a tough one. If the ferritin is increasing and the TSAT is normal and there is no evidence of hemochromatosis, the ONLY possible explanation is some underlying morbidity, inflammatory, rheumatologic, malignant, or infectious is present. In pediatrics, HLH (hemophagocytic lymphohistiocytosi...

What is the choice of treatment for a teenager with low risk neuroblastoma s/p resection?

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Pediatric Hematology/Oncology · Vanderbilt University Medical Center

According to the Revised Neuroblastoma Risk Classification (Irwin et al., PMID 34319759), age is not a factor in determining whether someone is low risk. So if this child has been determined to have low-risk neuroblastoma, they have/had an L1 tumor, either without MYCN amplification, or with MYCN am...

How do you integrate surgery in treatment of recurrent tenosynovial giant cell tumors (TGCT) when using Pexidartinib?

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Medical Oncology · Dana-Farber Cancer Institute

This is an interesting question, but one that has little (if any) data to guide management. With recurrent TGCT, the patient presumably already had surgery. It is possible that a good response to pexidartinib may reduce the morbidity of a repeat surgery but the risk of additional recurrence would re...

Which chemo regimen, if any, would you use as adjuvant treatment in a young patient with primary malignant thyroid teratoma?

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Medical Oncology · Testicular Cancer Commons

There is no evidence base to guide you here. The term "malignant teratoma" is not particularly helpful here and does not distinguish between benign teratoma, somatic transformation, or active germ cell malignancies. If classic markers AFP and HCG are significantly elevated, that would favor a malign...

What is the treatment of choice for mixed phenotype ALL?

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Pediatric Hematology/Oncology · The University of Texas MD Anderson Cancer Center

These are difficult to treat. The limited available data suggest that an ALL–like regimen followed by HSCT may be recommended. If no response is achieved, you could try a myeloid-like strategy. For T/Myeloid, combining asparaginase with AML therapy (FA + PEG or Capizzi II) could be an option. The sp...