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Pediatric Blood and Cancer

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Institución detectada Período Navegá Descargá Solicitá
No detectada desde ene. 2004 / hasta dic. 2023 Wiley Online Library

Información

Tipo de recurso:

revistas

ISSN impreso

1545-5009

ISSN electrónico

1545-5017

País de edición

Estados Unidos

Cobertura temática

Tabla de contenidos

Characterizing adolescents with heavy menstrual bleeding and generalized joint hypermobility

Nicole E. Kendel; Fareeda W. Haamid; Myra Christian‐Rancy; Sarah H. O'BrienORCID

<jats:title>Abstract</jats:title><jats:p>Patients with generalized joint hypermobility (JHM) may experience excessive bruising/bleeding, with heavy menstrual bleeding (HMB) commonly reported. We performed a retrospective review of 30 adolescents seen in a Young Women's Hematology Clinic with both HMB and JHM. We found that (1) a significant delay (mean 36 months, range 5–72) occurred between menarche and referral to specialty care, (2) HMB had moderate to severe impact on school and physical activities in 60% of patients, and (3) most patients (68%) required escalation of their initial therapy. We suggest providers consider JHM as a risk factor for a more complex clinical course.</jats:p>

Palabras clave: Oncology; Hematology; Pediatrics, Perinatology and Child Health.

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Recalcitrant transient abnormal myelopoiesis in neonatal Down syndrome

Sophie TimmisORCID; Angus Hodder; Niteesh Bharadwaj; Sarah Inglott; Jane Chalker; Danny Cheng; Sneha Tandon; Jack BartramORCID

Palabras clave: Oncology; Hematology; Pediatrics, Perinatology and Child Health.

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A sensitive and inexpensive high‐resolution melting‐based testing algorithm for diagnosis of transient abnormal myelopoiesis and myeloid leukemia of Down syndrome

Ricardo Camargo; Agenor de Castro Moreira dos Santos; Bruna Cândido GuidoORCID; Larissa Lemos Mendanha Cavalcante; Anna Carolina Silva Dias; Robéria Mendonça de Pontes; Felipe Magalhães Furtado; Cristiane Feitosa SalvianoORCID; Valdenize Tiziani; José Carlos Martins Córdoba; Isis Maria Quezado Magalhães

Palabras clave: Oncology; Hematology; Pediatrics, Perinatology and Child Health.

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Rhabdomyosarcoma with isolated lung metastases: A report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group

Juan C. VasquezORCID; Leo Y. Luo; Susan M. HinikerORCID; Daniel S. RheeORCID; Roshni Dasgupta; Sonja Chen; Brenda J. Weigel; Wei Xue; Rajkumar Venkatramani; Carola A. Arndt

Palabras clave: Oncology; Hematology; Pediatrics, Perinatology and Child Health.

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The role of neoadjuvant chemotherapy in the management of metastatic central nervous system germinoma: A meta‐analysis

Mohammad H. Abu‐ArjaORCID; Margaret S. Shatara; M. Fatih Okcu; Susan L. McGovern; Jack M. Su; Mohamed S. AbdelbakiORCID

Palabras clave: Oncology; Hematology; Pediatrics, Perinatology and Child Health.

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Adjuvant chemotherapy does not improve outcome in children with ovarian immature teratoma: A comparative analysis of clinical trial data from the Malignant Germ Cell International Consortium

Ana Glenda Santarosa VieiraORCID; Vidya PuthenpuraORCID; Mark Krailo; Negar Fallahazad; Mark F. H. Brougham; Matthew J. MurrayORCID; A. Lindsay FrazierORCID; Luiz Fernando Lopes; Farzana PashankarORCID

<jats:title>Abstract</jats:title><jats:sec><jats:title>Background/objectives</jats:title><jats:p>Surgery is the mainstay of therapy for children with ovarian immature teratoma (IT), whereas adults receive adjuvant chemotherapy, except those with stage‐I, grade‐1 disease. In Brazil, children with metastatic ovarian IT received postoperative chemotherapy. This practice variation allowed evaluation of the value of chemotherapy, by comparison of Brazilian patients with those in the United States and United Kingdom.</jats:p></jats:sec><jats:sec><jats:title>Design/methods</jats:title><jats:p>From the Malignant Germ Cell International Consortium data commons, data on ovarian IT patients from two recently added Brazilian trials (TCG‐99/TCG‐2008) were compared with data from US/UK (INT‐0106/GC‐2) trials. Primary outcome measure was event‐free (EFS) and overall survival (OS).</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Forty‐two Brazilian patients were included (stage I: 27, stage II: 4, stage III: 8, stage IV: 3). Twenty‐nine patients had surgery alone, whereas 13 patients received postoperative chemotherapy. The EFS and OS for entire cohort was 0.80 (95% CI: 0.64–0.89) and 0.97 (0.84–0.99). There was no difference in relapse risk based on stage, grade, or receipt of chemotherapy. Comparing the Brazilian cohort with 98 patients in US/UK cohort (stage I: 59, stage II: 12, stage III: 27), there was no difference in EFS and OS across all stages, despite 87% of stage II–IV Brazilian patients receiving postoperative chemotherapy compared with only 13% of US/UK patients. The EFS and OS for Brazilian compared with US/UK cohort was stage I: 88% versus 98% (<jats:italic>p</jats:italic> = .05), stage II–IV EFS: 67% versus 79% (<jats:italic>p</jats:italic> = .32), stage II–IV OS: 93% versus 97% (<jats:italic>p</jats:italic> = .44); amongst grade‐3 patients, there was no difference in EFS or OS.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Addition of postoperative chemotherapy did not improve outcome in children with ovarian IT, even at higher grade or stage, compared with surgery alone.</jats:p></jats:sec>

Palabras clave: Oncology; Hematology; Pediatrics, Perinatology and Child Health.

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