Results of a phase Ib study of olaparib with concomitant radiotherapy in soft-tissue sarcoma: a French sarcoma group study

被引:2
作者
Sargos, P. [1 ]
Sunyach, M. P. [2 ]
Ducassou, A. [3 ]
Llacer, C. [4 ]
Dinart, D. [5 ,6 ]
Michot, A. [7 ,8 ]
Valentin, T. [9 ]
Firmin, N. [10 ,11 ]
Blay, J. Y. [12 ,13 ]
Gillon, P. [1 ]
Bellera, C. [5 ,6 ]
Italiano, A. [14 ]
机构
[1] Inst Bergonie, Dept Radiotherapy, Bordeaux, France
[2] Leon Berard Canc Ctr, Dept Radiotherapy, Lyon, France
[3] Inst Univ Canc Toulouse Oncopole, Inst Claudius Regaud, Dept Radiotherapy, Toulouse, France
[4] Inst Canc Montpellier, Dept Radiotherapy, Montpellier, France
[5] Univ Bordeaux, Bordeaux Populat Hlth Res Ctr, Epicene Team, Inserm,UMR 1219, Bordeaux, France
[6] Inst Bergonie, Comprehens Canc Ctr, Clin & Epidemiol Res Unit, INSERM CIC1401, Bordeaux, France
[7] Univ Bordeaux, Fac Med, Bordeaux, France
[8] Inst Bergonie, Reg Comprehens Canc Ctr Bordeaux, Dept Oncol Surg, Bordeaux, France
[9] Inst Univ Canc Toulouse Oncopole, Inst Claudius Regaud, Dept Surg Oncol, INSERM Oncogenesis Sarcoma CRCT19, Toulouse, France
[10] Inst Canc Montpellier, Dept Med Oncol, Montpellier, France
[11] Montpellier Univ, Montpellier INSERM U1194, IRCM, Montpellier, France
[12] Unicanc, Ctr Leon Berard, Dept Med, Lyon, France
[13] Univ Lyon 1, Lyon, France
[14] Inst Bergonie, Dept Med, Bordeaux, France
关键词
sarcoma; radiation therapy; olaparib; PARP; RADIATION-THERAPY; COMBINATION; INHIBITION; CISPLATIN;
D O I
10.1016/j.annonc.2025.01.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Radiotherapy is essential for locoregional control in resectable soft-tissue sarcoma and remains a key strategy for unresectable soft-tissue sarcoma. Poly-ADP-ribose polymerase inhibitors, such as olaparib, may enhance Patients and methods: This multicenter phase Ib trial evaluated the combination of olaparib and radiotherapy in softtissue sarcoma of the limbs or trunk wall. Olaparib was administered twice daily at doses of 25, 50, 100, or 150 mg during the dose-escalation phase. Radiotherapy consisted of 50 Gy (25 fractions) for resectable tumors or 59.4 Gy (33 fractions) for unresectable tumors. Radiotherapy was exclusively preoperative for operable patients. Primary objectives were to determine the maximum tolerated dose and recommended phase II dose. Dose escalation was conducted using the time-to-event continual reassessment method. Histological response was assessed in surgical cases, and RECIST 1.1 criteria were applied for non-surgical cases. Results: Between October 2016 and April 2021, 41 patients were recruited across five French centers. The recommended phase II dose was identified as 100 mg olaparib twice daily. For operable patients, a favorable histological response was observed in 33% of patients, with a local relapse-free survival rate of 90.5% at 1 year. In contrast, among patients with inoperable tumors, the median progression-free survival was 7.7 months (95% confidence interval 2.6-28.4 months), with partial responses achieved in 20% of cases and stable disease in 60%. Grade 3 radiation dermatitis was the most frequent adverse event (34.1%), and two patients experienced grade 5 toxicity (4.8%). Conclusion: The combination of olaparib and radiotherapy is feasible for soft-tissue sarcoma patients but requires stringent selection, avoiding patients with tumors involving critical vascular structures or those at high surgical risk, to minimize severe complications. Further randomized trials are warranted to validate efficacy and safety compared with radiotherapy alone.
引用
收藏
页码:592 / 600
页数:9
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