Assessment of Clinical Complete Response After Chemoradiation for Rectal Cancer with Digital Rectal Examination, Endoscopy, and MRI: Selection for Organ-Saving Treatment

被引:287
作者
Maas, Monique [1 ]
Lambregts, Doenja M. J. [1 ]
Nelemans, Patty J. [2 ]
Heijnen, Luc A. [1 ,3 ]
Martens, Milou H. [1 ,3 ]
Leijtens, Jeroen W. A. [4 ]
Sosef, Meindert [5 ]
Hulsewe, Karel W. E. [6 ]
Hoff, Christiaan [7 ]
Breukink, Stephanie O. [3 ]
Stassen, Laurents [3 ]
Beets-Tan, Regina G. H. [1 ]
Beets, Geerard L. [3 ]
机构
[1] Maastricht Univ, Med Ctr, Dept Radiol, Maastricht, Netherlands
[2] Maastricht Univ, Med Ctr, Dept Epidemiol, Maastricht, Netherlands
[3] Maastricht Univ, Med Ctr, Dept Surg, Maastricht, Netherlands
[4] Laurentius Hosp Roermond, Dept Surg, Roermond, Netherlands
[5] Atrium Med Ctr, Dept Surg, Heerlen, Netherlands
[6] Orbis Med Ctr, Dept Surg, Sittard, Netherlands
[7] Leeuwarden Med Ctr, Dept Surg, Leeuwarden, Netherlands
关键词
COMPLETE PATHOLOGICAL RESPONSE; NEOADJUVANT CHEMORADIATION; PREOPERATIVE CHEMORADIOTHERAPY; NONOPERATIVE TREATMENT; RADIATION-THERAPY; WAIT; CHEMOTHERAPY; RADIOTHERAPY; METAANALYSIS; MANAGEMENT;
D O I
10.1245/s10434-015-4687-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The response to chemoradiotherapy (CRT) for rectal cancer can be assessed by clinical examination, consisting of digital rectal examination (DRE) and endoscopy, and by MRI. A high accuracy is required to select complete response (CR) for organ-preserving treatment. The aim of this study was to evaluate the value of clinical examination (endoscopy with or without biopsy and DRE), T2W-MRI, and diffusion-weighted MRI (DWI) for the detection of CR after CRT. This prospective cohort study in a university hospital recruited 50 patients who underwent clinical assessment (DRE, endoscopy with or without biopsy), T2W-MRI, and DWI at 6-8 weeks after CRT. Confidence levels were used to score the likelihood of CR. The reference standard was histopathology or recurrence-free interval of > 12 months in cases of wait-and-see approaches. Diagnostic performance was calculated by area under the receiver operator characteristics curve, with corresponding sensitivities and specificities. Strategies were assessed and compared by use of likelihood ratios. Seventeen (34 %) of 50 patients had a CR. Areas under the curve were 0.88 (0.78-1.00) for clinical assessment and 0.79 (0.66-0.92) for T2W-MRI and DWI. Combining the modalities led to a posttest probability for predicting a CR of 98 %. Conversely, when all modalities indicated residual tumor, 15 % of patients still experienced CR. Clinical assessment after CRT is the single most accurate modality for identification of CR after CRT. Addition of MRI with DWI further improves the diagnostic performance, and the combination can be recommended as the optimal strategy for a safe and accurate selection of CR after CRT.
引用
收藏
页码:3873 / 3880
页数:8
相关论文
共 29 条
[1]   Locally Advanced Rectal Cancer: MR Imaging in Prediction of Response after Preoperative Chemotherapy and Radiation Therapy [J].
Barbaro, Brunella ;
Fiorucci, Cecilia ;
Tebala, Carmen ;
Valentini, Vincenzo ;
Gambacorta, Maria Antonietta ;
Vecchio, Fabio Maria ;
Rizzo, Gianluca ;
Coco, Claudio ;
Crucitti, Antonio ;
Ratto, Carlo ;
Bonomo, Lorenzo .
RADIOLOGY, 2009, 250 (03) :730-739
[2]   MRI for assessing and predicting response to neoadjuvant treatment in rectal cancer [J].
Beets-Tan, Regina G. H. ;
Beets, Geerard L. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2014, 11 (08) :480-488
[3]   Magnetic resonance imaging for the clinical management of rectal cancer patients: recommendations from the 2012 European Society of Gastrointestinal and Abdominal Radiology (ESGAR) consensus meeting [J].
Beets-Tan, Regina G. H. ;
Lambregts, Doenja M. J. ;
Maas, Monique ;
Bipat, Shandra ;
Barbaro, Brunella ;
Caseiro-Alves, Filipe ;
Curvo-Semedo, Luis ;
Fenlon, Helen M. ;
Gollub, Marc J. ;
Gourtsoyianni, Sofia ;
Halligan, Steve ;
Hoeffel, Christine ;
Kim, Seung Ho ;
Laghi, Andrea ;
Maier, Andrea ;
Rafaelsen, Soren R. ;
Stoker, Jaap ;
Taylor, Stuart A. ;
Torkzad, Michael R. ;
Blomqvist, Lennart .
EUROPEAN RADIOLOGY, 2013, 23 (09) :2522-2531
[4]   Statistics notes - Diagnostic tests 4: likelihood ratios [J].
Deeks, JJ ;
Altman, DG .
BRITISH MEDICAL JOURNAL, 2004, 329 (7458) :168-169
[5]   Distribution of Residual Cancer Cells in the Bowel Wall After Neoadjuvant Chemoradiation in Patients With Rectal Cancer [J].
Duldulao, Marjun P. ;
Lee, Wendy ;
Streja, Leanne ;
Chu, Peiguo ;
Li, Wenyan ;
Chen, Zhenbin ;
Kim, Joseph ;
Garcia-Aguilar, Julio .
DISEASES OF THE COLON & RECTUM, 2013, 56 (02) :142-149
[6]   Radiotherapy alone in the curative treatment of rectal carcinoma [J].
Gerard, JP ;
Romestaing, P ;
Chapet, O .
LANCET ONCOLOGY, 2003, 4 (03) :158-166
[7]   Clinical examination following preoperative chemoradiation for rectal cancer is not a reliable surrogate end point [J].
Guillem, JG ;
Chessin, DB ;
Shia, J ;
Moore, HG ;
Mazumdar, M ;
Bernard, B ;
Paty, PB ;
Saltz, L ;
Minsky, BD ;
Weiser, MR ;
Temple, LKF ;
Cohen, AM ;
Wong, WD .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (15) :3475-3479
[8]   Operative versus nonoperative treatment for stage 0 distal rectal cancer following chemoradiation therapy - Long-term results [J].
Habr-Gama, A ;
Perez, RO ;
Nadalin, W ;
Sabbaga, J ;
Ribeiro, U ;
Sousa, AHSE ;
Campos, FG ;
Kiss, DR ;
Gama-Rodrigues, J .
ANNALS OF SURGERY, 2004, 240 (04) :711-717
[9]   Patterns of failure and survival for nonoperative treatment of stage c0 distal rectal cancer following neoadjuvant chemoradiation therapy [J].
Habr-Gama, Angelita ;
Perez, Rodrigo O. ;
Proscurshim, Igor ;
Campos, Fabio G. ;
Nadalin, Wladimir ;
Kiss, Desiderio ;
Gama-Rodrigues, Joaquim .
JOURNAL OF GASTROINTESTINAL SURGERY, 2006, 10 (10) :1319-1328
[10]   Local Recurrence After Complete Clinical Response and Watch and Wait in Rectal Cancer After Neoadjuvant Chemoradiation: Impact of Salvage Therapy on Local Disease Control [J].
Habr-Gama, Angelita ;
Gama-Rodrigues, Joaquim ;
Sao Juliao, Guilherme P. ;
Proscurshim, Igor ;
Sabbagh, Charles ;
Lynn, Patricio B. ;
Perez, Rodrigo O. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2014, 88 (04) :822-828