Outcome and prognostic variables in childhood rhabdomyosarcoma (RMS) with emphasis on impact of FOXO1 fusions in non-metastatic RMS: experience from a tertiary cancer centre in India

被引:1
作者
Ramanathan, Subramaniam [1 ]
Sisodiya, Sneha [2 ]
Shetty, Omshree [3 ,4 ]
Prasad, Maya [4 ,5 ]
Parambil, Badira C. [4 ,5 ]
Shah, Sneha [4 ,6 ]
Ramadwar, Mukta [4 ,7 ]
Khanna, Nehal [4 ,8 ]
Laskar, Siddhartha [4 ,8 ]
Qureshi, Sajid [4 ,9 ]
Vora, Tushar [10 ]
Chinnaswamy, Girish [4 ,5 ]
机构
[1] Royal Victoria Infirm, Great North Childrens Hosp, Dept Paediat Oncol, Newcastle Upon Tyne NE1 8SG, England
[2] Lokmanya Tilak Municipal Gen Hosp & Med Coll, Dept Pathol, Mumbai 400022, India
[3] Tata Mem Hosp, Dept Pathol, Div Mol Pathol, Mumbai 400012, India
[4] Homi Bhabha Natl Inst, Mumbai 400094, India
[5] Tata Mem Hosp, Dept Pediat Oncol, Mumbai 400012, India
[6] Tata Mem Hosp, Dept Nucl Med, Mumbai 400012, India
[7] Tata Mem Hosp, Dept Pathol, Mumbai 400012, India
[8] Tata Mem Hosp, Dept Radiat Oncol, Mumbai 400012, India
[9] Tata Mem Hosp, Dept Pediat Surg, Mumbai 400012, India
[10] SickKids Hosp, Dept Pediat Oncol, Toronto, ON M5G 1X8, Canada
来源
ECANCERMEDICALSCIENCE | 2023年 / 17卷
关键词
rhabdomyosarcoma; FOXO1; fusions; paediatric soft tissue sarcomas; LMIC; India; PEDIATRIC RHABDOMYOSARCOMA; ALVEOLAR RHABDOMYOSARCOMA;
D O I
10.3332/ecancer.2023.1539
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
While factors influencing outcomes of rhabdomyosarcoma (RMS) in developed countries have evolved from clinical characteristics to molecular profiles, similar data from devel-oping countries are scarce. This is a single-centre analysis of outcomes in treated cases of RMS, with emphasis on prevalence, risk-migration and prognostic impact of Forkhead Box O1 (FOXO1) in non-metastatic RMS. All children with histopathologically proven RMS, treated between January 2013 and December 2018 were included. Intergroup Rhabdomyosarcoma Study-4 risk stratification was used, with treatment based on a mul-timodality-regimen with chemotherapy (Vincristine/Ifosfamide/Etoposide and Vincris-tine/Actinomycin-D/Cyclophosphamide) and appropriate local therapy. Formalin-fixed paraffin-embedded tissues were tested using Reverse Transcriptase-Polymerase Chain Reaction for FOXO1-fusions (PAX3(P3F); PAX7(P7F)). A total of 221 children (Cohort-1) were included, of which 182 patients had non-metastatic disease (Cohort-2). Thirty-six (16%), 146 (66%), 39 (18%) patients were low-risk (LR), intermediate-risk (IR) and high -risk, respectively. FOXO1-fusion status was available in 140 patients with localised RMS (Cohort 3). P3F and P7F were detected in 25/49 (51%) and 14/85 (16.5%) of alveolar and embryonal variants, respectively. The 5-year-event-free survival (EFS)/overall survival (OS) of Cohorts 1, 2 and 3 was 48.5%/55.5%, 54.6%/62.6% and 55.1%/63.7%, respec-tively. Amongst the localised RMS, presence of nodal metastases and primary tumour size > 10 cms were adverse prognostic factorvs (p < 0.05). On incorporating fusion-status in risk-stratification, 6/29 (21%) patients migrated from LR (A/B) to IR. All patients who re-categorised as LR (FOXO1 negative) had a 5-year EFS/OS of 80.81%/90.91%. FOXO1-negative tumours had a better 5-year relapse-free survival (58.92% versus 44.63%; p = 0.296) with a near-significant correlation in favourable-site tumours (75.10% versus 45.83%; p = 0.063). While FOXO1-fusions have superior prognostic utility compared to histology alone in localised, favourable-site RMS, traditional prognostic factors (tumour size and nodal metastases) impacted outcome the most in this subset. Strengthening of early referral systems in community and timely local interven-tion can help in improving outcome in resource-constrained countries.
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页数:19
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