Pathologic complete response in patients with localized soft tissue sarcoma treated with neoadjuvant therapy and its correlation with clinical outcomes: A systematic review

被引:1
作者
Boulouta, A. [1 ]
Kyriazoglou, A. [1 ]
Kotsantis, I. [1 ]
Economopoulou, P. [1 ]
Anastasiou, M. [1 ]
Pantazopoulos, A. [1 ]
Kyrkasiadou, M. [1 ]
Moutafi, M. [1 ]
Gavrielatou, N. [1 ]
Zazas, E. [1 ]
Caglar, C. [1 ]
Nixon, I. [2 ]
Tolia, M. [3 ]
Kavourakis, G. [1 ]
Psyrri, A. [1 ]
机构
[1] Attikon Univ Hosp, Dept Internal Med 2, Oncol Unit, Athens, Greece
[2] Beatson West Scotland Canc Ctr, Dept Clin Oncol, Glasgow, Scotland
[3] Univ Crete, Fac Med, Sch Hlth Sci, Dept Radiotherapy, Iraklion, Greece
关键词
Soft tissue sarcoma; Neoadjuvant treatment; Preoperative treatment; Pathologic complete response; PHASE-I TRIAL; HIGH-RISK; HIGH-GRADE; REGIONAL HYPERTHERMIA; RADIATION-THERAPY; PLUS SORAFENIB; OPEN-LABEL; BODY-WALL; CHEMOTHERAPY; SURVIVAL;
D O I
10.1016/j.ctrv.2024.102820
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Soft tissue sarcomas (STS), comprising approximately 1% of adult solid malignancies, are primarily treated with surgery, with the choice of perioperative treatment being a challenging and highly individualized decision. Clinical trials assessing neoadjuvant modalities in STS predominantly use clinical outcomes or radiologic response as endpoints, with pathologic complete response (pCR) not being employed as a designated study endpoint. Our systematic review aimed to assess the rates of pCR in clinical trials of different neoadjuvant modalities for STS and its correlation with patient clinical outcomes. 23 phase I, II and III studies were included, from which data regarding rates of pCR with each treatment, as well as correlation of pCR with clinical outcomes were retrieved. In 16 trials that assessed pCR, the percentage of patients who achieved a pCR ranged from 8 to 58%. Most of these trials did not aim to establish an association between pCR and clinical outcomes. However, among those that did investigate this correlation, a positive association was identified between pCR and both 5year disease-specific survival (DSS) and 5-year overall survival (OS). While pCR serves as a crucial marker guiding treatment decisions in other neoplasms like triple negative breast cancer and urothelial cancer, it is not yet used in a similar setting for STS. Our findings indicate variability in patients achieving pCR across different neoadjuvant treatments for STS and a possible positive correlation with patient outcomes. Consequently, we propose considering pCR as a surrogate endpoint in future prospective trials for STS.
引用
收藏
页数:6
相关论文
共 42 条
[1]   The Epidemiology of Sarcoma [J].
Burningham, Zachary ;
Hashibe, Mia ;
Spector, Logan ;
Schiffman, Joshua D. .
CLINICAL SARCOMA RESEARCH, 2012, 2
[2]   Phase I Trial of Neoadjuvant Conformal Radiotherapy Plus Sorafenib for Patients with Locally Advanced Soft Tissue Sarcoma of the Extremity [J].
Canter, Robert J. ;
Borys, Dariusz ;
Olusanya, Abimbola ;
Li, Chin-Shang ;
Lee, Li-Yuan ;
Boutin, Robert D. ;
Christensen, Scott D. ;
Tamurian, Robert M. ;
Monjazeb, Arta M. .
ANNALS OF SURGICAL ONCOLOGY, 2014, 21 (05) :1616-1623
[3]   Radiographic and Histologic Response to Neoadjuvant Radiotherapy in Patients With Soft Tissue Sarcoma [J].
Canter, Robert J. ;
Martinez, Steve R. ;
Tamurian, Robert M. ;
Wilton, Maaya ;
Li, Chin-Shang ;
Ryu, Janice ;
Mak, Walter ;
Monsky, Wayne L. ;
Borys, Dariusz .
ANNALS OF SURGICAL ONCOLOGY, 2010, 17 (10) :2578-2584
[4]   Pathological and radiological response following neoadjuvant treatments in primary localized resectable myxofibrosarcoma and undifferentiated pleomorphic sarcoma of the extremities and trunk wall [J].
Danieli, Maria ;
Barretta, Francesco ;
Radaelli, Stefano ;
Fiore, Marco ;
Sangalli, Claudia ;
Barisella, Marta ;
Palassini, Elena ;
Miceli, Rosalba ;
Frezza, Anna Maria ;
Callegaro, Dario ;
Collini, Paola ;
Casali, Paolo Giovanni ;
Stacchiotti, Silvia ;
Gronchi, Alessandro .
CANCER, 2023, 129 (21) :3417-3429
[5]   A randomised, open-label, phase II study of neo/adjuvant doxorubicin and ifosfamide versus gemcitabine and docetaxel in patients with localised, high-risk, soft tissue sarcoma [J].
Davis, Elizabeth J. ;
Chugh, Rashmi ;
Zhao, Lili ;
Lucas, David R. ;
Biermann, J. Sybil ;
Zalupski, Mark M. ;
Feng, Mary ;
Wong, Sandra L. ;
Jacobson, Jon ;
Zyczynski, Laurie ;
Reinke, Denise ;
Metko, Gino ;
Baker, Laurence H. ;
Schuetze, Scott M. .
EUROPEAN JOURNAL OF CANCER, 2015, 51 (13) :1794-1802
[6]   Evaluation of Neoadjuvant Therapy and Histopathologic Response in Primary, High-Grade Retroperitoneal Sarcomas Using the Sarcoma Nomogram [J].
Donahue, Timothy R. ;
Kattan, Michael W. ;
Nelson, Scott D. ;
Tap, William D. ;
Eilber, Frederick R. ;
Eilber, Fritz C. .
CANCER, 2010, 116 (16) :3883-3891
[7]   Treatment-induced pathologic necrosis: A predictor of local recurrence and survival in patients receiving neoadjuvant therapy for high-grade extremity soft tissue sarcomas [J].
Eilber, FC ;
Rosen, G ;
Eckardt, J ;
Forscher, C ;
Nelson, SD ;
Selch, M ;
Dorey, F ;
Eilber, FR .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (13) :3203-3209
[8]   Burden and centralised treatment in Europe of rare tumours: results of RARECAREnet-a population-based study [J].
Gatta, Gemma ;
Capocaccia, Riccardo ;
Botta, Laura ;
Mallone, Sandra ;
De Angelis, Roberta ;
Ardanaz, Eva ;
Comber, Harry ;
Dimitrova, Nadya ;
Leinonen, Maarit K. ;
Siesling, Sabine ;
van der Zwan, Jan M. ;
Van Eycken, Liesbet ;
Visser, Otto ;
Zakelj, Maja P. ;
Anderson, Lesley A. ;
Bella, Francesca ;
Innos, Kaire ;
Otter, Renee ;
Stiller, Charles A. ;
Trama, Annalisa .
LANCET ONCOLOGY, 2017, 18 (08) :1022-1039
[9]   A randomised phase II study on neo-adjuvant chemotherapy for 'high-risk' adult soft-tissue sarcoma [J].
Gortzak, E ;
Azzarelli, A ;
Buesa, J ;
Bramwell, VHC ;
van Coevorden, F ;
van Geel, AN ;
Ezzat, A ;
Santoro, A ;
Oosterhuis, JW ;
van Glabbeke, M ;
Kirkpatrick, A ;
Verweij, J .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (09) :1096-1103
[10]   Soft tissue and visceral sarcomas: ESMO-EURACAN-GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Gronchi, A. ;
Miah, A. B. ;
DeiTos, A. P. ;
Abecassis, N. ;
Bajpai, J. ;
Bauer, S. ;
Biagini, R. ;
Bielack, S. ;
Blay, J. Y. ;
Bolle, S. ;
Bonvalot, S. ;
Boukovinas, I ;
Bovee, J. V. M. G. ;
Boye, K. ;
Brennan, B. ;
Brodowicz, T. ;
Buonadonna, A. ;
De Alava, E. ;
Del Muro, X. G. ;
Dufresne, A. ;
Eriksson, M. ;
Fagioli, F. ;
Fedenko, A. ;
Ferraresi, V ;
Ferrari, A. ;
Frezza, A. M. ;
Gasperoni, S. ;
Gelderblom, H. ;
Gouin, F. ;
Grignani, G. ;
Haas, R. ;
Hassan, A. B. ;
Hecker-Nolting, S. ;
Hindi, N. ;
Hohenberger, P. ;
Joensuu, H. ;
Jones, R. L. ;
Jungels, C. ;
Jutte, P. ;
Kager, L. ;
Kasper, B. ;
Kawai, A. ;
Kopeckova, K. ;
Krakorova, D. A. ;
Le Cesne, A. ;
LeGrange, F. ;
Legius, E. ;
Leithner, A. ;
Lopez-Pousa, A. ;
Martin-Broto, J. .
ANNALS OF ONCOLOGY, 2021, 32 (11) :1348-1365