Determinants of tumor necrosis and its impact on outcome in patients with Localized osteosarcoma uniformly treated with a response adapted regimen without high dose Methotrexate– A retrospective institutional analysis

IF 3.4 2区 医学 Q2 Medicine Journal of Bone Oncology Pub Date : 2024-12-01 DOI:10.1016/j.jbo.2024.100651
Prabhat Gautam Roy , Shuvadeep Ganguly , Archana Sasi , Vivek Kumar , Adarsh Barwad , Asit Ranjan Mridha , Shah Alam Khan , Venkatesan Sampath Kumar , Love Kapoor , Deepam Pushpam , Sameer Bakhshi
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Abstract

Purpose

Response to neoadjuvant chemotherapy in form of tumor necrosis predicts outcome in osteosarcoma; although response-adapted treatment escalation failed to improve outcome among patients treated with high-dose methotrexate-based (HDMTx) chemotherapy. This study aimed to identify factors predicting tumor necrosis and its impact on survival among patients with non-metastatic osteosarcoma treated with a response-adapted non-HDMTx regimen.

Methods

A retrospective single-institutional study was conducted among non-metastatic osteosarcoma patients treated with neoadjuvant therapy between 2004–2019. Patients were treated uniformly with three cycles of neoadjuvant cisplatin/doxorubicin. Post-operatively, patients with favourable necrosis (≥90 %) received 3 cycles of cisplatin/doxorubicin, while patients with poor necrosis (<90 %) received escalated treatment with alternating six cycles of cisplatin/doxorubicin and ifosfamide/etoposide. Propensity score matching (PSM) analyses were conducted to ascertain independent impact of necrosis on event-free survival (EFS) and overall survival (OS).

Results

Of 594 registered osteosarcoma patients, 280 patients (median age 17 years; male 67.1 %) were included for analysis. 73 patients (26.1 %) achieved favourable necrosis. Patients with smaller tumor size (≤10 cm) (aOR = 2.28; p = 0.030), lower serum alkaline phosphatase (≤450 IU/L) (aOR = 2.10; p = 0.035), and who had surgery earlier (<115 days) (aOR = 2.28; p = 0.016) were more likely to have favourable necrosis. On 1:2 PSM analysis, patients not achieving favourable necrosis demonstrated inferior EFS (HR = 2.68; p = 0.003) and OS (HR = 3.42; p = 0.003).

Conclusions

Patients of osteosarcoma with smaller tumor, lower serum alkaline phosphatase and earlier surgery are more likely to achieve favourable necrosis. Tumor necrosis independently predicts outcome in osteosarcoma, and response-adapted treatment escalation fails to overcome the adverse impact of poor necrosis in non-HDMTx based regimen.

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局部骨肉瘤患者肿瘤坏死的决定因素及其对预后的影响,采用无高剂量甲氨蝶呤的反应适应方案进行统一治疗-回顾性机构分析
目的以肿瘤坏死形式对新辅助化疗的反应预测骨肉瘤的预后;尽管在接受高剂量基于甲氨蝶呤(HDMTx)化疗的患者中,适应反应的治疗升级未能改善预后。本研究旨在确定非转移性骨肉瘤患者接受非hdmtx治疗后肿瘤坏死的预测因素及其对生存率的影响。方法对2004-2019年接受新辅助治疗的非转移性骨肉瘤患者进行回顾性单机构研究。患者统一接受三个周期的新辅助顺铂/阿霉素治疗。术后,坏死良好的患者(≥90%)接受顺铂/阿霉素3个周期的治疗,坏死不良的患者(< 90%)接受顺铂/阿霉素与异环磷酰胺/依托泊苷交替治疗6个周期的升级治疗。进行倾向评分匹配(PSM)分析以确定坏死对无事件生存期(EFS)和总生存期(OS)的独立影响。结果在594例登记的骨肉瘤患者中,280例(中位年龄17岁;男性67.1%)纳入分析。73例(26.1%)患者实现了良好的坏死。肿瘤较小(≤10 cm)患者(aOR = 2.28;p = 0.030),血清碱性磷酸酶(≤450 IU/L)降低(aOR = 2.10;p = 0.035),较早手术(<;115天)者(aOR = 2.28;P = 0.016)更容易出现良性坏死。在1:2 PSM分析中,未达到有利坏死的患者表现为较差的EFS (HR = 2.68;p = 0.003)和OS (HR = 3.42;p = 0.003)。结论肿瘤小、血清碱性磷酸酶水平低、手术早期的骨肉瘤患者更容易出现良性坏死。肿瘤坏死是骨肉瘤预后的独立预测因素,而非hdmtx为基础的治疗方案中,适应反应的治疗升级无法克服不良坏死的不利影响。
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来源期刊
CiteScore
7.20
自引率
2.90%
发文量
50
审稿时长
34 days
期刊介绍: The Journal of Bone Oncology is a peer-reviewed international journal aimed at presenting basic, translational and clinical high-quality research related to bone and cancer. As the first journal dedicated to cancer induced bone diseases, JBO welcomes original research articles, review articles, editorials and opinion pieces. Case reports will only be considered in exceptional circumstances and only when accompanied by a comprehensive review of the subject. The areas covered by the journal include: Bone metastases (pathophysiology, epidemiology, diagnostics, clinical features, prevention, treatment) Preclinical models of metastasis Bone microenvironment in cancer (stem cell, bone cell and cancer interactions) Bone targeted therapy (pharmacology, therapeutic targets, drug development, clinical trials, side-effects, outcome research, health economics) Cancer treatment induced bone loss (epidemiology, pathophysiology, prevention and management) Bone imaging (clinical and animal, skeletal interventional radiology) Bone biomarkers (clinical and translational applications) Radiotherapy and radio-isotopes Skeletal complications Bone pain (mechanisms and management) Orthopaedic cancer surgery Primary bone tumours Clinical guidelines Multidisciplinary care Keywords: bisphosphonate, bone, breast cancer, cancer, CTIBL, denosumab, metastasis, myeloma, osteoblast, osteoclast, osteooncology, osteo-oncology, prostate cancer, skeleton, tumour.
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