Is Concurrent Chemoradiation the Standard of Care for Locally Advanced Non-small Cell Lung Cancer? A Review of Guidelines and Evidence

被引:42
作者
O'Rourke, N. [1 ]
Macbeth, F. [2 ]
机构
[1] Gartnavel Royal Hosp, Cochrane Lung Canc Grp, Beatson Oncol Ctr, Glasgow, Lanark, Scotland
[2] Natl Inst Hlth & Clin Excellence, London, England
关键词
Concurrent chemoradiation; guidelines; NSCLC; sequential treatment; PHASE-III; SEQUENTIAL CHEMORADIOTHERAPY; ACCELERATED RADIOTHERAPY; INDUCTION CHEMOTHERAPY; THORACIC RADIOTHERAPY; STAGE-IIIA; CISPLATIN; CARCINOMA; ONCOLOGY; TRIAL;
D O I
10.1016/j.clon.2010.03.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the past 15 years, the treatment of locally advanced non-small cell lung cancer (NSCLC) has shifted from radiotherapy alone There are now schedules using induction chemotherapy, concurrent chemoradiation using either radiosensitising doses of chemotherapy or full-dose chemotherapy, consolidation chemotherapy after radiation or combinations of these options There is no consensus on the optimal chemotherapy regimen and its scheduling and the issue of radiation close and optimal fractionation equally remains unresolved This overview is in two sections First, we have evaluated a selection of international guidelines on the management of locally advanced NSCLC We assessed the methodology by which individual guidelines were produced and the levels of evidence quoted in support of the recommendations Second, we have updated the literature search of the 2004 Cochrane review on concurrent chemoradiation Trials were identified that compared sequential with concurrent chemoradiation using median survival as the primary outcome measure Two-year survival and toxicity were evaluated as secondary outcome measures. Eleven trials were identified, of which six fulfilled criteria for inclusion The median survival for concurrent treatment was 16-17 months compared with 13-15 months with sequential treatment. Treatment-related mortality was 3% for concurrent treatment and 1 7% for sequential treatment The late of grade 3 or worse oesophagitis was 19% in concurrent treatment compared with 3% for sequential treatment In conclusion, chemotherapy adds benefit to radiotherapy treatment of locally advanced NSCLC Concurrent chemoradiation is associated with significant toxicity The evidence to support concurrent chemoradiation as the standard of care is not robust, in spite of its recommendation within a number of guidelines. Further trials should be supported (C) 2010 The Royal College of Radiologists Published by Elsevier Ltd All rights reserved
引用
收藏
页码:347 / 355
页数:9
相关论文
共 38 条
[1]  
ALBERTI W, 1995, BRIT MED J, V311, P899
[2]   Concomitant radio-chemotherapy based on platin compounds in patients with locally advanced non-small cell lung cancer (NSCLC):: A meta-analysis of individual data from 1764 patients [J].
Aupérin, A ;
Le Péchoux, C ;
Pignon, JP ;
Koning, C ;
Jeremic, B ;
Clamon, G ;
Einhorn, L ;
Ball, D ;
Trovo, MG ;
Groen, HJM ;
Bonner, JA ;
Le Chevalier, T ;
Arriagada, R .
ANNALS OF ONCOLOGY, 2006, 17 (03) :473-483
[3]  
*AUSTR NAT HLTH ME, 2004, CLIN PRACT GUID PREV
[4]   Phase III study of the eastern cooperative oncology group (ECOG 2597): Induction chemotherapy followed by either standard thoracic radiotherapy or hyperfractionated accelerated radiotherapy for patients with unresectable stage IIIA and B non-small-cell lung cancer [J].
Belani, CP ;
Wang, W ;
Johnson, DH ;
Wagner, H ;
Schiller, J ;
Veeder, M ;
Mehta, M .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (16) :3760-3767
[5]   Combined chemoradiotherapy regimens of paclitaxel and carboplatin for locally advanced non-small-cell lung cancer: A randomized phase II locally advanced multi-modality protocol [J].
Belani, CP ;
Choy, H ;
Bonomi, P ;
Scott, C ;
Travis, P ;
Haluschak, J ;
Curran, WJ .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :5883-5891
[6]   Randomised trial of sequential versus concurrent chemo-radiotherapy in patients with inoperable non-small cell lung cancer (EORTC 08972-22973) [J].
Belderbos, Jose ;
Uitterhoeve, Lon ;
van Zandwijk, Nico ;
Belderbos, Huub ;
Rodrigus, Patrick ;
van de Vaart, Paul ;
Belderbos, Huub ;
Rodrigus, Patrick ;
van de Vaart, Paul ;
Price, Allan ;
van Walree, Nico ;
Legrand, Catherine ;
Dussenneh, Sonia ;
Bartelink, Harry ;
Giaccone, Giuseppe ;
Koning, Caro .
EUROPEAN JOURNAL OF CANCER, 2007, 43 (01) :114-121
[7]   A RANDOMIZED PHASE-I/II TRIAL OF HYPERFRACTIONATED RADIATION-THERAPY WITH TOTAL DOSES OF 60.0 GY TO 79.2 GY - POSSIBLE SURVIVAL BENEFIT WITH GREATER-THAN-OR-EQUAL-TO 69.6 GY IN FAVORABLE PATIENTS WITH RADIATION-THERAPY ONCOLOGY GROUP STAGE-III NON-SMALL-CELL LUNG-CARCINOMA - REPORT OF RADIATION-THERAPY ONCOLOGY GROUP 83-11 [J].
COX, JD ;
AZARNIA, N ;
BYHARDT, RW ;
SHIN, KH ;
EMAMI, B ;
PAJAK, TF .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (09) :1543-1555
[8]  
Curran WJ., 2003, Proc Am Soc Clin Oncol, V22, P621
[9]  
Dasgupta Anirban, 2006, J Cancer Res Ther, V2, P47
[10]   Accelerated regrowth of non-small-cell lung tumours after induction chemotherapy [J].
El Sharouni, SY ;
Kal, HB ;
Battermann, JJ .
BRITISH JOURNAL OF CANCER, 2003, 89 (12) :2184-2189