Prognostic impact of pre-referral tumor resection in unilateral Wilms tumor: A single-institute experience from a lower middle-income country

被引:2
作者
Khan, Muhammad Saghir [1 ]
Maaz, Ata Ur Rehman [2 ]
Qazi, Abid Quddus [3 ]
Aslam, Sophia [4 ]
Riaz, Shazia [5 ,6 ]
Malik, Ayesha Saeed [7 ]
Shaheen, Najma [8 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Pediat, Al Madinah Al Munawarrah, Saudi Arabia
[2] Sidra Med, Child Hlth, Div Hematol Oncol, Doha, Qatar
[3] Al Jalila Childrens Specialty Hosp Dubai, Dubai, U Arab Emirates
[4] Pediat Oncol Royal Victoria Infirm, Newcastle Upon Tyne, England
[5] Childrens Hosp, Dept Pediat Hematol Oncol, Lahore, Pakistan
[6] Inst Child Hlth Lahore, Lahore, Pakistan
[7] King Edward Med Univ, Dept Pediat, Lahore, Pakistan
[8] Shaukat Khanum Canc Hosp & Res Ctr, Dept Pediat Oncol, Lahore, Pakistan
关键词
education; low-resource settings; nephrectomy; pre-referral tumor resection; Wilms tumor; CHILDHOOD-CANCER; MANAGEMENT; CHILDREN; SURVIVAL;
D O I
10.1002/pbc.30760
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The objectives of this study were to evaluate the prognostic impact of pre-referral surgical resection of Wilms tumor (WT) performed at non-oncology centers, and to strategize an improved care plan for this very curable pediatric tumor.Methods: In this study conducted in a large pediatric cancer center in Pakistan, we retrospectively reviewed the electronic medical records (EMR) of 149 patients with unilateral WT from September 2008 to August 2017. Based on treatment approach, patients were categorized into two groups: (i) pre-referral tumor resection (PTR: n = 75), and (ii) post-neoadjuvant chemo nephrectomy (PCN: n = 74).Results: The proportion of metastatic disease in PTR and PCN groups was 33.3% and 35.1%, respectively. In the PTR subset, median time to admission after PTR was 5 weeks (mean 11, SEM 2.8, range: 2-202) weeks, with 53.3% (n = 40) presenting more than 4 weeks after PTR. Twenty patients had no cross-sectional imaging prior to PTR and underwent surgery after abdominal ultrasound only. On baseline imaging at our center, 58.7% (n = 44) of the PTR group had radiologically evaluable disease (four metastases only, 19 local residual tumor only, 21 both localized tumor and visible metastases). Disease staging was uncertain in 23 patients because of no or inadequate histology specimens and/or lymph node sampling in patients with no evaluable disease. Statistically significant differences were recorded for the two subsets regarding tumor volume, extent and nodularity, renal vein and renal sinus involvement, lymph node status, tumor rupture and histopathologic features, and tumor stage, with a 10-year event-free survival (EFS) for PCN and PTR of 74.3% and 50.7%, respectively (p < .001). In the PTR group, EFS for those presenting within 4 weeks and later was 91.4% versus 15.0%, respectively (p < .0001).Conclusion: Suboptimal pre-referral surgical intervention results in poor survival outcomes in unilateral WT. Our findings highlight the need for a comprehensive action plan for educating healthcare professionals engaged in WT diagnosis and referral process. PCN in a multidisciplinary team approach can reduce surgical morbidity and seems to be a better strategy to improve the survival rates in low-resource settings.
引用
收藏
页数:12
相关论文
共 32 条
[1]   Wilms tumour treatment in Sudan: A 10-year single-centre experience [J].
Abdalla, Mohammed ;
Hameed, Somaya .
CANCER REPORTS, 2022, 5 (11)
[2]   Childhood cancer burden: a review of global estimates [J].
Bhakta, Nickhill ;
Force, Lisa M. ;
Allemani, Claudia ;
Atun, Rifat ;
Bray, Freddie ;
Coleman, Michel P. ;
Steliarova-Foucher, Eva ;
Frazier, A. Lindsay ;
Robison, Leslie L. ;
Rodriguez-Galindo, Carlos ;
Fitzmaurice, Christina .
LANCET ONCOLOGY, 2019, 20 (01) :E42-E53
[3]   Many faces of Wilms Tumor: Recent advances and future directions [J].
Bhutani, Namita ;
Kajal, Pradeep ;
Sharma, Urvashi .
ANNALS OF MEDICINE AND SURGERY, 2021, 64
[4]   Working Together to Build a Better Future for Children With Cancer in Africa [J].
Chitsike, Inam ;
Paintsil, Vivian ;
Sung, Lillian ;
Njuguna, Festus ;
Mavinkurve-Groothuis, Annelies ;
Kouya, Francine ;
Hesseling, Peter ;
Kaspers, Gertjan ;
Afungchwi, Glenn M. ;
Ilbawi, Andre ;
Renner, Lorna ;
Pritchard-Jones, Kathy ;
Hessissen, Laila ;
Molyneux, Elizabeth ;
Chagaluka, George ;
Israels, Trijn .
JCO GLOBAL ONCOLOGY, 2020, 6 :1076-1078
[5]   Factors contributing to delayed childhood cancer care in low- and middle-income countries: A systematic review protocol [J].
Cotache-Condor, Cesia ;
Grimm, Andie ;
Williamson, Jahsarah ;
Kantety, Vinootna ;
Landrum, Kelsey ;
Schroeder, Kristin ;
Staton, Catherine A. ;
Majaliwa, Esther ;
Rice, Henry E. ;
Smith, Emily R. .
PEDIATRIC BLOOD & CANCER, 2022, 69 (05)
[6]   Advances in Wilms Tumor Treatment and Biology: Progress Through International Collaboration [J].
Dome, Jeffrey S. ;
Graf, Norbert ;
Geller, James I. ;
Fernandez, Conrad V. ;
Mullen, Elizabeth A. ;
Spreafico, Filippo ;
Van den Heuvel-Eibrink, Marry ;
Pritchard-Jones, Kathy .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (27) :2999-U94
[7]  
Dome Jeffrey S, 2014, Am Soc Clin Oncol Educ Book, P215, DOI 10.14694/EdBook_AM.2014.34.215
[8]   Management and outcome of pediatric metastatic Wilms' tumor at the National Cancer Institute, Egypt [J].
Elayadi, Moatasem ;
Magdy, Sarah ;
Khalil, Ehab ;
Zekri, Wael .
JOURNAL OF THE EGYPTIAN NATIONAL CANCER INSTITUTE, 2020, 32 (01)
[9]   Wilms' Tumor-Lessons and Outcomes-A 25-Year Single Center UK Experience [J].
Fawkner-Corbett, David W. ;
Howell, Lisa ;
Pizer, Barry L. ;
Dominici, Carlo ;
McDowell, Heather P. ;
Losty, Paul D. .
PEDIATRIC HEMATOLOGY AND ONCOLOGY, 2014, 31 (05) :400-408
[10]   Clinical trials to improve childhood cancer care and survival in sub-Saharan Africa [J].
Israels, Trijn ;
Kambugu, Joyce ;
Kouya, Francine ;
El-Mallawany, Nader Kim ;
Hesseling, Peter B. ;
Kaspers, Gertjan J. L. ;
Eden, Tim ;
Renner, Lorna ;
Molyneux, Elizabeth M. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2013, 10 (10) :599-604