Pubfacts - Scientific Publication Data
  • Categories
  • |
  • Journals
  • |
  • Authors
  • Login
  • Categories
  • Journals

Search Our Scientific Publications & Authors

Publications
  • Publications
  • Authors
find publications by category +
Translate page:

[Multicenter clinical study on the diagnosis and treatment of childhood renal tumor].

Authors:
A A Zhang J Y Tang M Xu Y J Fang J Yan J Gao X J Yuan F Li X L Ju W Liu X J Wu L R Sun L Jiang W L Zhang J H Chu X Y Lu

Zhonghua Er Ke Za Zhi 2021 Mar;59(3):195-200

Department of Oncology Surgery, Children's Hospital of Anhui Medical University, Hefei 230022, China.

To summarize the effect of Chinese Children's Cancer Group (CCCG) Wilms tumor (WT)-2015 protocol. This was a prospective study. CCCG-WT-2015 protocol was revised on the basis of the CCCG-WT-2009 protocol. Clinical data of 288 children diagnosed with newly diagnosed kidney neoplasms in fourteen pediatric centers between September 2015 to December 2018 were summarized. The age of onset, distribution of pathological subtypes, staging, curative effect and prognostic factors of these children were analyzed. Kaplan-Meier method was used for survival curve and Log-Rank method was used for univariate analysis. Among 288 cases with kidney neoplasms, there were 261 cases of WT, including 254 cases (97.3%) with favorable histology (FH) WT and 7 cases (2.7%) with unfavorable histology WT (UFHWT). The 3 year events free survival (EFS) rate for FHWT and UFHWT were (88.9±2.1)% and (80.0±17.9)%, which were better than that in WT-2009 (81.2% and 71.7%). In the 96 cases of stage Ⅲ/Ⅳ FHWT with indications for radiotherapy, 76 cases received radiation, another 20 cases received M protocol chemotherapy (cyclophosphamide, etoposide, gentamycin, vincristine and adriamycin) instead of radiation. The 3 year EFS rate for these two groups were (84.7±4.3)% and (84.7±8.1)%(χ=0.015, =0.902). There were 22 renal clear cell sarcoma and 5 malignant rhabdoid tumor, 3 year EFS rate of them was (94.4±5.4)% and (20.0±17.9)%. Univariate analysis was performed for age, gender, pathological type, stage, whether rupture occurred during operation, whether complete remission (CR) occurred at the end of treatment and radiotherapy. Pathological types (χ=44.329,<0.01) and failure to achieve CR at the end of the treatment (χ=49.459,<0.01) were independent factor for predicting survival. Compared with CCCG-WT-2009, treatment of renal tumors in CCCG-WT-2015 study yielded good survival outcome, which can be further applied.

Download full-text PDF

Source
http://dx.doi.org/10.3760/cma.j.cn112140-20200707-00698DOI Listing
March 2021

Publication Analysis

Top Keywords

efs rate
12
year efs
8
univariate analysis
8
cases received
8
kidney neoplasms
8
cases
7
survival efs
4
events free
4
histology ufhwt
4
unfavorable histology
4
ufhwt year
4
year events
4
rate fhwt
4
free survival
4
fhwt ufhwt
4
812% 717%
4
717% cases
4
cases stage
4
stage Ⅲ/Ⅳ
4
wt-2009 812%
4

Keyword Occurance

Similar Publications

Age estimation from the biometric information of hand bones: Development of new formulas.

Authors:
Floriane Remy Bérengère Saliba-Serre Kathia Chaumoitre Laurent Martrille Loïc Lalys

Forensic Sci Int 2021 Apr 6;322:110777. Epub 2021 Apr 6.

Aix Marseille Univ, CNRS, EFS, ADES, Marseille, France.

Introduction: In the judicial context of the age estimation of living individuals, a new method was recently proposed, based on the collection of biometric information on hand bones radiographs. The aim of this study was to apply this method to a large French sample to provide new tools for age estimation MATERIALS AND METHODS: The study sample consisted of metacarpals and proximal phalanges measurements of 1003 individuals aged less than 21 years. This sample was divided into two subgroups 1-12 and 13-21 years as the age of 13 is a relevant legal threshold for most European countries. Read More

View Article and Full-Text PDF
April 2021
Similar Publications

Serotherapy-Free Regimen Improves Non-Relapse Mortality and Immune Recovery Among the Recipients of αβ TCell-Depleted Haploidentical Grafts: Retrospective Study in Childhood Leukemia.

Authors:
Larisa Shelikhova Svetlana Glushkova Ruslan Nikolaev Maria Dunaikina Zhanna Zhekhovtsova Sergey Blagov Rimma Khismatullina Dmitriy Balashov Elena Kurnikova Dmitriy Pershin Yakov Muzalevskii Alexei Kazachenok Elena Osipova Pavel Trakhtman Alexei Maschan Michael Maschan

Transplant Cell Ther 2021 Apr 14;27(4):330.e1-330.e9. Epub 2021 Jan 14.

Department of Hematopoietic Stem Cell Transplantation, Dmitriy Rogachev National Medical Center Of Pediatric Hematology, Oncology And Immunology, Moscow, Russia. Electronic address:

Depletion of αβ T cells from the graft prevents graft-versus-host disease (GVHD) and improves the outcome of hematopoietic stem cell transplantation (HSCT) from haploidentical donors. Delayed recovery of adaptive immunity remains a problem, which can be approached by adoptive T-cell transfer. In a randomized trial, we have assessed the safety and efficacy of low-dose memory (CD45RA-depleted) donor lymphocytes (mDLI) after HSCT with αβ T-cell depletion. Read More

View Article and Full-Text PDF
April 2021
Similar Publications

Profiling of somatic mutations and fusion genes in acute myeloid leukemia patients with FLT3-ITD or FLT3-TKD mutation at diagnosis reveals distinct evolutionary patterns.

Authors:
Wei Guan Lei Zhou Yan Li Erna Yang Yangyang Liu Na Lv Lin Fu Yi Ding Nan Wang Nan Fang Qian Liu Binan Wang Fuwei Li Juan Zhang Maoquan Wang Lili Wang Yu Jing Yonghui Li Li Yu

Exp Hematol Oncol 2021 Apr 9;10(1):27. Epub 2021 Apr 9.

Department of Hematology, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, 100853, China.

Background: The receptor tyrosine kinase FLT3 with internal tandem duplications within the juxtamembrane domain (FLT3-ITD) is a poor prognostic factor; however, the prognostic significance of missense mutation in the tyrosine kinase domain (FLT3-TKD) is controversial. Furthermore, the accompanying mutations and fusion genes with FLT3 mutations are unclear in acute myeloid leukemia (AML).

Methods: We investigated FLT3 mutations and their correlation with other gene mutations and gene fusions through two RNA-seq based next-generation sequencing (NGS) method and prognostic impact in 207 de novo AML patients. Read More

View Article and Full-Text PDF
April 2021
Similar Publications
© 2021 PubFacts.
  • About PubFacts
  • Privacy Policy
  • Sitemap