Solid malignancies during the first year of life: A 20-year review at Red Cross War Memorial Children?s Hospital, Cape Town, South Africa

被引:1
作者
Jacquier, N. [1 ,2 ]
English, N. [1 ,2 ]
Davidson, A. [3 ,4 ]
Cox, S. G. [1 ,2 ]
机构
[1] Univ Cape Town, Dept Paediat Surg, Red Cross War Mem Childrens Hosp, Cape Town, South Africa
[2] Univ Cape Town, Fac Hlth Sci, Cape Town, South Africa
[3] Univ Cape Town, Haematol Oncol Serv, Red Cross War Mem Childrens Hosp, Fac Hlth Sci, Cape Town, South Africa
[4] Univ Cape Town, Dept Paediat & Child Hlth, Fac Hlth Sci, Cape Town, South Africa
来源
SAMJ SOUTH AFRICAN MEDICAL JOURNAL | 2022年 / 112卷 / 06期
关键词
CHILDHOOD-CANCER; SURGICAL COMPLICATIONS; NEONATAL TUMORS; CLASSIFICATION; EPIDEMIOLOGY; DIAGNOSIS; UPDATE;
D O I
10.7196/SAMJ.2022.v112i6.15823
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Among paediatric tumours, two groups stand out: neonatal and infantile tumours, which respectively represent 2% and 10% of paediatric tumours. The distribution of tumours in these age groups is different from that in older children. Objectives. Descriptive analysis of a cohort of patients treated for a solid malignancy at Red Cross War Memorial Children's Hospital (RCWMCH), Cape Town, South Africa. Methods. A 20-year retrospective case series review of patients aged <1 year at diagnosis was performed on data extracted from the RCWMCH oncology database. Results. Of 243 cases extracted from the database, 198 were solid tumours, of which 122 (61.1%) were included in the analysis; the 76 excluded were benign or of eye, bone or central nervous system origin and therefore did not meet the inclusion criteria. There were 38 renal malignancies (31.2%), 30 neuroblastomas (24.6%), 25 soft-tissue sarcomas (20.5%), 17 germ cell tumours/gonadal tumours (13.9%) and 12 liver tumours (9.8%). Of the patients, 119 (97.5%) had surgery, 91 (74.6%) had chemotherapy and 10 (8.2%) had radiotherapy. Tumour group 5-year survival was 78.5% for neuroblastic tumours, 79.0% for nephroblastomas, 81.5% for hepatoblastomas, 62.5% and 54.2% for rhabdomyosarcoma and non-rhabdomyosarcoma soft-tissue sarcomas, respectively, and 79.5% for malignant extracranial and extragonadal germ cell tumours. For the entire cohort, the mean follow-up was 46 months, with an estimated 5-year overall survival of 74.6%. Mortality was 21.5% and loss to follow-up 6.6%. Conclusion. The distribution of tumours differs slightly from the literature, with a predominance of renal tumours over neuroblastomas. The overall mortality rate of 21.5%, the surgical complication rate of 10.9% and the 5-year overall survival of 74.6% correspond with the literature, supporting the view that a paediatric hospital in a middle-income country can achieve results similar to those in higher-income countries when international protocols are applied by a dedicated multidisciplinary team.
引用
收藏
页码:418 / 425
页数:8
相关论文
共 33 条
[1]   Neonates with cancer and causes of death; lessons from 615 cases in the SEER databases [J].
Alfaar, Ahmad S. ;
Hassan, Waleed M. ;
Bakry, Mohamed Sabry ;
Qaddoumi, Ibrahim .
CANCER MEDICINE, 2017, 6 (07) :1817-1826
[2]   Editorial [J].
Bhattacharya, Sujit .
JOURNAL OF SCIENTOMETRIC RESEARCH, 2012, 1 (01) :1-2
[3]  
BIRCH JM, 1992, BRIT J CANCER, V66, pS2
[4]   REVISIONS OF THE INTERNATIONAL CRITERIA FOR NEUROBLASTOMA DIAGNOSIS, STAGING, AND RESPONSE TO TREATMENT [J].
BRODEUR, GM ;
PRITCHARD, J ;
BERTHOLD, F ;
CARLSEN, NLT ;
CASTEL, V ;
CASTLEBERRY, RP ;
DEBERNARDI, B ;
EVANS, AE ;
FAVROT, M ;
HEDBORG, F ;
KANEKO, M ;
KEMSHEAD, J ;
LAMPERT, F ;
LEE, REJ ;
LOOK, AT ;
PEARSON, ADJ ;
PHILIP, T ;
ROALD, B ;
SAWADA, T ;
SEEGER, RC ;
TSUCHIDA, Y ;
VOUTE, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (08) :1466-1477
[5]   Neonatal solid tumors [J].
Chandrasekaran, Aravindan .
PEDIATRICS AND NEONATOLOGY, 2018, 59 (01) :65-70
[6]   The Clavien-Dindo Classification of Surgical Complications Five-Year Experience [J].
Clavien, Pierre A. ;
Barkun, Jeffrey ;
de Oliveira, Michelle L. ;
Vauthey, Jean Nicolas ;
Dindo, Daniel ;
Schulick, Richard D. ;
de Santibanes, Eduardo ;
Pekolj, Juan ;
Slankamenac, Ksenija ;
Bassi, Claudio ;
Graf, Rolf ;
Vonlanthen, Rene ;
Padbury, Robert ;
Cameron, John L. ;
Makuuchi, Masatoshi .
ANNALS OF SURGERY, 2009, 250 (02) :187-196
[7]   A Single Center Experience in 266 Patients of Infantile Malignancies [J].
Das, Umesh ;
Appaji, L. ;
Kumari, B. S. Aruna ;
Lakshmaiah, K. C. ;
Padma, M. ;
Kavitha, S. ;
Sathyanarayanan, Vishwanath .
PEDIATRIC HEMATOLOGY AND ONCOLOGY, 2014, 31 (06) :489-497
[8]  
Dasgupta R, 2016, SEMIN PEDIATR SURG, V25, P284, DOI 10.1053/j.sempedsurg.2016.09.012
[9]   Rhabdomyosarcoma [J].
Dasgupta, Roshni ;
Fuchs, Joerg ;
Rodeberg, David .
SEMINARS IN PEDIATRIC SURGERY, 2016, 25 (05) :276-283
[10]   Malignant solid tumors in neonates: a study of 71 cases [J].
de Bouyn-Icher, C. ;
Minard-Colin, V. ;
Isapof, A. ;
Quang, D. -A. Khuong ;
Redon, I. ;
Hartmann, O. .
ARCHIVES DE PEDIATRIE, 2006, 13 (12) :1486-1494