成人松果体母细胞瘤:一项前瞻性研究和印度三家三级护理癌症研究所12年的经验,描述了各种独立参数和治疗策略对这种极其罕见的恶性肿瘤的进展和生存的影响。

IF 0.9 4区 医学 Q4 ONCOLOGY
Indian journal of cancer Pub Date : 2025-01-01 Epub Date: 2025-05-16 DOI:10.4103/ijc.ijc_1164_21
Abhishek Purkayastha, Neelam Sharma, Sachin Taneja, Virender Suhag, Saurabh Bobdey
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引用次数: 0

摘要

背景:松果母细胞瘤是胚胎起源的高度侵袭性恶性iv级肿瘤,预后差,占所有脑肿瘤的< 0.1%,主要影响儿童和青少年,成人极为罕见,发病率为0.1%。方法:2009年7月至2021年7月对患者进行摄入、治疗和随访。在研究期间共登记了1085例原发性脑肿瘤,包括恶性和良性的成人和儿童患者。成人松果体母细胞瘤占所有原发性脑肿瘤的10/1085例(0.9%)。所有符合条件的患者均接受手术、术后放射治疗联合化疗以及辅助化疗。采用单因素Cox回归分析确定可能的预后因素。Kaplan-Meier生存分析估计生存率。结果:中位无病生存期为63个月,中位总生存期为83个月。表现不佳(P = 0.043)、更严重的症状(P = 0.041)和残留疾病的存在(P = 0.000)被确定为无病生存降低的独立预测因素,但不影响总生存。结论:在本研究中,我们保持所有患者的术后放疗和化疗剂量不变,而不考虑手术状态,以保持生存商的一致性。尽管有局限性,这项研究可能是迄今为止印度文献中报道的最大的成人松果体母细胞瘤分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adult pineoblastoma: A prospective study and twelve-year experience from three tertiary care cancer institutes of India depicting the effect of various independent parameters and therapeutic strategy on progression and survival in this extremely rare malignancy.

Background: Pineoblastomas are highly aggressive malignant grade-IV tumors of embryonal origin with poor prognosis, accounting for < 0.1% of all brain tumors, affecting mainly the pediatric and adolescent cases but extremely rare in adults with an incidence of 0.1%-<1%. With scarce Indian and world data involving adult patients due to its rarity and lack of large prospective cohorts, this study was undertaken to determine survival outcomes in adult cases undergoing surgery, postoperative radiation therapy, and chemotherapy in terms of clinical response, prognosis, and disease progression.

Methods: Intake, treatment, and follow-up of patients were done from July 2009 to July 2021. A total of 1085 cases of primary brain tumors comprising malignant and benign adult and pediatric patients were registered over the study period. Adult pineoblastomas constituted 10/1085 (0.9%) cases of all primary brain tumors. All eligible patients underwent surgery, postoperative radiation therapy with concurrent chemotherapy, followed by adjuvant chemotherapy. Univariate Cox regression analysis was used to identify possible prognostic factors. Kaplan-Meier survival analysis was performed to estimate survival.

Results: The median disease-free survival was 63 months, and the median overall survival was 83 months. Poor performance status (P = 0.043), greater presenting symptoms (P = 0.041), and presence of residual disease (P = 0.000) were identified as independent predictors of reduced disease-free survival, without affecting overall survival.

Conclusion: We undertook this study keeping the dose of postoperative radiation therapy and chemotherapy regimens constant for all patients irrespective of surgical status to maintain uniformity in the survival quotient. Despite the limitations, this study may represent the largest analysis of adult pineoblastomas reported in Indian literature to date.

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来源期刊
Indian journal of cancer
Indian journal of cancer Medicine-Oncology
CiteScore
1.40
自引率
0.00%
发文量
67
审稿时长
>12 weeks
期刊介绍: Indian Journal of Cancer (ISSN 0019-509X), the show window of the progress of ontological sciences in India, was established in 1963. Indian Journal of Cancer is the first and only periodical serving the needs of all the specialties of oncology in India.
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