- Open Access
The value of metabolic imaging to predict tumour response after chemoradiation in locally advanced rectal cancer
© Palma et al; licensee BioMed Central Ltd. 2010
- Received: 5 September 2010
- Accepted: 15 December 2010
- Published: 15 December 2010
We aim to investigate the possibility of using 18F-positron emission tomography/computer tomography (PET-CT) to predict the histopathologic response in locally advanced rectal cancer (LARC) treated with preoperative chemoradiation (CRT).
The study included 50 patients with LARC treated with preoperative CRT. All patients were evaluated by PET-CT before and after CRT, and results were compared to histopathologic response quantified by tumour regression grade (patients with TRG 1-2 being defined as responders and patients with grade 3-5 as non-responders). Furthermore, the predictive value of metabolic imaging for pathologic complete response (ypCR) was investigated.
Responders and non-responders showed statistically significant differences according to Mandard's criteria for maximum standardized uptake value (SUVmax) before and after CRT with a specificity of 76,6% and a positive predictive value of 66,7%. Furthermore, SUVmax values after CRT were able to differentiate patients with ypCR with a sensitivity of 63% and a specificity of 74,4% (positive predictive value 41,2% and negative predictive value 87,9%); This rather low sensitivity and specificity determined that PET-CT was only able to distinguish 7 cases of ypCR from a total of 11 patients.
We conclude that 18-F PET-CT performed five to seven weeks after the end of CRT can visualise functional tumour response in LARC. In contrast, metabolic imaging with 18-F PET-CT is not able to predict patients with ypCR accurately.
- Positron Emission Tomography
- Positive Predictive Value
- Standardize Uptake Value
- Negative Predictive Value
- Regression Index
Over the past decade neoadjuvant chemo-radiotherapy (CRT) has been increasingly employed in the treatment of locally advanced rectal cancer (LARC). Clinical trials have shown a reduction in tumour size and stage, as well as a significant reduced risk of local recurrence. Tumour responses to CRT, however, vary considerably. While pathological complete response is noted in up to 30 percent of patients who undergo preoperative CRT and evidence suggests that complete response is associated with better oncologic outcomes, serious side effects and even no response - after weeks of treatment -is observed in the remaining amount of patients .
The surgical approach largely depends on a valid assessment of the preoperative extent of the tumour, particularly for distally located tumours or those that have been assessed as being nonresectable during primary staging. Regarding the further treatment, some institutions raised the question whether radical surgery should be necessary for patients with clinical complete response to CRT [2, 3]. Therefore, for the clinical practice, radiological prediction of the histopathological tumour response is quite attractive because it could enable response-guided modifications of the treatment protocol. Clinical assessment after CRT is known to be quite poor and conventional imaging modalities cannot distinguish fibrosis or scar from viable tumour cells in residual masses .
As a result, great demands are placed on imaging modalities that provide a combination of metabolic and morphologic information. Incorporation of 2-deoxy-2-[18F]fluoro-D-glucose (18-FDG) positron emission tomography (PET) scans in the management of patients with cancer has increased with the introduction of this modality into clinical practice .
After our preliminary experience with this technique dealing with staging of colorectal cancer , in the current prospective study we aim to specifically determine whether PET-CT scans could predict histopathological response in patients with LARC after treatment with preoperative CRT.
PET-CT imaging and processing
All PET-CT scans were performed by use of a dedicated Siemens Biograph 16, (Knoxville, Tennessee) with an axial field of view of 16.2 cm, a slice thickness of 3 mm, and a pixel spacing of 5.4 mm in both directions. The scanner is equipped with ultrafast detector electronics (Pico3D) and has a spatial resolution of approximately 6 mm at full-width at-half-maximum. PET imaging was done in three dimensions, requiring a proper scatter correction. CT-based attenuation correction was performed. PET images were reconstructed from the acquired list mode data, using Fourier rebinding and ordered subset expectation maximization reconstruction (three dimensional) with two iterations and eight subsets (Ordered subset expectation maximization). After a fasting period of at least 6 hours prior to FDG injection, patients received an intravenous injection of 18-FDG, with the activity normalized for the weight of the patient, followed by an injection of physiologic saline (10 ml). After an uptake period of 60 minutes, the patient was positioned on a flat tabletop, using a movable laser alignment system in a ''head-first supine'' position with the arm elevated over the head to avoid beam hardening artefacts as well as errors caused by truncation of the field of view. A PET-CT scan of the whole body was performed using an acquisition time of 2 to 4 (depending of the patient's weight) minutes per bed position. Additionally, all PET data were normalized for the blood glucose level measured shortly before 18-FDG administration (Glucocard G meter; Menarini Diagnostic, Florence).
In these calculations, Actvoi is the activity measured in the volume of interest (this is equals the voxel with highest uptake in tumour), Actadministered is the administered activity corrected for the physical decay of FDG to the start of acquisition, and BW is body weight. Dedicated software was used to calculate the SUVmax within the tumour before (SUV1) and after CRT (SUV2). Subsequently, the regression index (RI), indicating the percent reduction relative to the pre-treatment measured value, were calculated (RI = [(SUV1-SUV2)/SUV1] × 100) and correlated to the pathological tumour response. Furthermore the absolute SUV1-SUV2 difference was calculated (DSUV). If no residual metabolic activity was present on the pre-surgical PET-CT scan, the patient's tumour was classified as a metabolic complete responder, and the SUV was calculated in the same region of interest.
Pathological tumour response
For each patient, the pathological tumour response was evaluated by determining the TRG (tumour regression grade), as proposed by Mandard et al.  All tumours were prospectively classified by an experienced pathologist (JLM) who was blinded to the PET data, as follows: TRG 1, complete tumour response; TRG2, residual cancer cells scattered through fibrosis; TRG 3, an increased number of residual cancer cells, with predominant fibrosis; TRG 4, residual cancer outgrowing fibrosis; and TRG 5, no regressive changes within the tumour. Based on the TRG, the tumours were grouped into responders (TRG 1 and 2) and non-responders (TRG 3-5). Furthermore, the pathological UICC classification (ypTN), including those with complete response (ypCR), was collected from the patients' specimen pathology report.
Statistical analysis was performed using SPSS software (PASW Statistics 17.0.2). Comparison of the post-CRT SUVmax values vs. baseline was performed with the paired-samples t-test, whereas the independent-samples t-test was used to evaluate correlations between SUV, RI and DSUV values and patient's classification as responder or non-responder. Kruskal-Wallis test was employed to evaluate correlations between SUV, RI and DSUV values and the different TRG as well as the UICC ypStage. Differences were considered to be significant when the p-value was less than 0.05. The optimal cut-off value for therapy-related decrease in SUVmax was calculated by receiver-operating characteristic (ROC) analysis. Sensitivity, specificity, and positive and negative predictive values of 18F-FDG-PET-CT were calculated using standard formulas.
Patients and tumours characteristic
37 (74%) males and 13 (26%) females were included. The age of the patients ranged between 36 and 80 years (mean 60). There were 35 (70%) patients with good to moderate and 15 (30%) with poor differentiated adenocarcinoma. 6 (12%) patients revealed mucinous components. In 31 (62%) patients capecitabine was used as chemotherapy combined with radiotherapy, in further 19 (38%) patients oxaliplatine was added according to hospital guidelines. Treatment plan was followed by all 50 patients. Tumour location ranged between 0 and 11 centimetres (cm) from the anal verge (mean 6 cm).
Total mesorectal excision was performed in 48 patients (96%). There was 1 patient (2%) with high anterior resection (partial mesorectal excision) and another with local resection after complete response. 15 of 50 (30%) patients were submitted to abdomino-perineal resection (APR) surgery and 33 (66%) to low anterior resection (LAR). In 9 of 33 (27%) patients submitted to LAR, a permanent colostomy was left. In all other cases with LAR, protective ileostomy was indicated for three months. Timing between CRT and surgery ranged between 45-103 days (mean 59).
Histopathological results: according to preoperative clinical UICC-Stage and tumor regression grade (TRG).
Stage n (%)
Histopathological results: according to UICC stage before and after CRT.
Stage n (%)
The pre-treatment (SUV1) values ranged from 4,85 to 34,56 (mean 13,67). After completion of neoadjuvant CRT, the glucose uptake (SUV2) values ranged from 2,36 to 15,85 (mean 5,73) (p < 0.001). DSUV and the regression index (RI) mean and SD values were 7,9 (6,2 SD) and 53,2 (23,3 SD), respectively. DSUV assumed negative value (SUV2 higher than SUV1) in 1 patient (2%). The median time between the end of CRT and the restaging PET and between PET and surgery was 42+6,3 and 17+10,7 days, respectively.
18F-FDG-PET/CT findings and pathological response
Tumor 18F-FDG uptake before (SUV1) and after neoadjuvant CRT (SUV2) according to UICC and Mandard's criteria (Kruskal-Wallis test).
ROC analysis of 18F-FDG-PET findings for responders according to Mandard criteria (TRG1-2) and specifically to complete pathological response (ypCR).
T test for ypCR vs. no ypCR
Complete Pathologic Response
T test for responders (TRG 1-2) vs. non-responders (TRG 3-5)
18F-FDG-PET/CT findings and ypCR
The SUV1 values were lower in the ypCR group than in the no-ypCR group (11,28 SD 4,02 vs.14,34 SD 6,54,(p = 0,149), on the contrary the RI values were higher comparing the same groups (59,10 SD 16,88 vs. 51,64 SD 24,82) (table 5). The SUV2 was significantly different in ypCR group vs. no-ypCR patients (Figure 3). ROC analysis identified a 4,07 (SUV2) as the cut-off value to predict ypCR (AUC = 0,748, p = 0.001); relative specificity and negative predictive value (NPV) were 74,4% and 87,9, respectively; whereas sensibility and positive predictive value (PPV) were 63% and 41,2, respectively; total accuracy was 72% (Table 4).
Positron emission tomography using fluoro-deoxy-glucose has demonstrated added value in the clinical management of patients with colorectal cancer . This includes primary staging, detection of recurrence, prediction of individual prognosis, therapy response, and evaluation of treatment response as assessed in this investigation .
The interest in FDG-PET to assess tumour response to CRT began in the early 1990 s. Rectal cancer is a disease model of particular interest, not only for its high incidence, but also because an accurate and non-invasive method to evaluate response to preoperative CRT could lead to patients' selection for minimally invasive surgical approaches or even selection of candidates for additional chemotherapy and observation without any kind of surgery [2, 3].
Experts at the Memorial Sloan-Kettering Cancer Center reported a pioneer prospective assessment of LARC response to preoperative CRT using FDG-PET in 2000 . Today, literature is mixed in regard to the ability of 18-FDG-PET to predict response to neaodjuvant treatment in patients with rectal cancer. The majority of studies have reported post-treatment SUV to be lower than pre-treatment scans, but posttreatment SUV was not found to correlate with pCR. Furthermore, combining PET and CT with fusing of function and morphologic data has increased the sensitivity and specificity in restaging of various malignant tumours including LARC after CRT.
Recently, de Geus-Oei analysed in an outstanding review the difficulty in comparing the outcome of different studies because of the use of several methods to analyse i.e. visual FDG-PET response, SUVmax, SUVmean, SUV ratio or even TLG (change in total lesion glycolysis) and that even at different intervals after CRT, varying from 12 days up to 7 weeks. It is interesting to note that all analysed papers found a significant relation of the investigated FDG-PET parameter to semiquantitative histological response [10–15]. Referring to response criteria, predictive values of FDG-PET response (negative predictive value) ranged between 83 to 100%; predictive values of FDG-PET non-response (positive predictive value) varied from 77 to 100%. The authors addressed that the more rigorous criteria of treatment response were defined the worse results were obtained [10–15].
Our results using SUVmax and performing the analysis 5 to 7 weeks after completion of CRT are in accordance with those found in literature . We noticed a statistically significant difference between responders and non-responders according to Mandard's criteria for SUV 1 and SUV2 with a specificity of 76,6% and a PPV of 66,7%. Furthermore, SUV2 values were able to differentiate patients with complete pathologic response with a sensitivity of 63% and a specificity of 74,4% (PPV 41,2% and NPV 87,9%); This rather low sensitivity and specificity determined that PET-CT was only able to distinguish 7 patients with confirmed pCR from a total of 11 (4 cases were false negative). In addition to that, further 10 patients were false positive for pCR upon PET-CT.
While there are substantial data regarding the relationship between pCR and improved oncologic outcome, the prognostic significance of responders without pCR has not been extensively evaluated . In our investigation, sampling the histopathological results according to the UICC (TNM) and Mandard's criteria appear to be in accordance with daily practice in hospitals. Whether Mandard's 1 and 2 classes belong both unequivocally to the responders is still a matter of discussion, on the contrary pCR seems to represent one of the most important prognostic factors leading to a more conservative surgical therapy and even to a wait and see non-resection policy in some series [2, 3]. It should be also underlined that several publications have focussed on the prognostic value of metabolic response assessed by PET, independent of the final pathology report [17–19].
Time interval between the end of CRT and surgery and time interval between the end of CRT and posttreatment PET-CT scan are two variables not previously investigated that could affect the ability of PET scans to predict response to CRT. Cascini  and Janssen , have described the increased predictive value of FDG-PET when performed at an earlier and perhaps more relevant clinical stage, i.e.12 and 14 days (respectively) after CRT.
Our results are similar to those obtained using only PET for preoperative staging. Thus, the anatomical information obtained from the CT in a PET-CT scan does not seem to improve the detection rate of residual disease in our investigation. A drawback of post-CRT 18F-FDG PET is the radiation-induced inflammation that can accumulate approximately 25% of FDG update. On the other hand, direct effect of radiation may induce tumour cell dormancy ("stunning") that mimics response. Whether the different chemotherapeutical drugs used and combined with radiotherapy differentially affect the metabolism of the FDG at the tumour site is still unknown .
Our data are in accordance with literature that showed that PET-CT performed 5 to 7 weeks after completion of CRT can visualise functional tumour response in patients treated with neoadjuvant CRT. In contrast, metabolic imaging with FDG-PET is not able to predict pathologic complete response in LARC accurately.
Our investigation identified PET-CT scan response as a complementary diagnostic and prognostic method in patients with locally advanced rectal cancer treated with neoadjuvant chemoradiotherapy. On the contrary, our results indicate that due to the rather low sensitivity and specificity, it does not seem possible to select patients upon metabolic imaging by means of 18F-FDG PET-CT to whom radical surgery after neoadjuvant CRT could be avoided.
Preliminary data of this work were presented by RCM and awarded at the 2009 Annual Meeting of the Spanish Society of Coloproctology (AECP) held in Barcelona. Founded by the Fundación Investigación Mutua Madrileña. We are indebted to M. Expósito Ruiz for statistical support. and to J-L Marín Aznar for pathologic analysis.
- Glynne-Jones R, Dunst J, Sebag-Montefiore D: The integration of oral capecitabine into chemoradiation regimens for locally advanced rectal cancer: how successful have we been? Ann Oncol 2006, 17: 361-371. 10.1093/annonc/mdj052View ArticlePubMedGoogle Scholar
- Habr-Gama A, Perez RO: Non-operative management of rectal cancer after neoadjuvant chemoradiation. Br J Surg 2009, 96: 127-127. 10.1002/bjs.6470View ArticleGoogle Scholar
- Neuman HB, Elkin EB, Guillem JG, Paty PB, Weiser MR, Wong WD, Temple LK: Treatment for patients with rectal cancer and a clinical complete response to neoadjuvant therapy: A decision analysis. Dis Colon Rectum 2009, 52: 863-871.View ArticlePubMedGoogle Scholar
- Kim SH, Lee JM, Hong SH, Kim GH, Lee JY, Han JK, Choi BI: Locally advanced rectal cancer: Added value of diffusion-weighted MR imaging in the evaluation of tumor response to neoadjuvant chemo- and radiation therapy. Radiology 2009, 253: 116-125. 10.1148/radiol.2532090027View ArticlePubMedGoogle Scholar
- Ruhlmann J, Schomburg A, Bender H: Fluorodeoxyglucose whole-body positron emission tomography in colorectal cancer patients studied in routine daily practice. Dis Colon Rectum 1998, 40: 1195-1204.View ArticleGoogle Scholar
- Llamas-Elvira JM, Rodríguez-Fernández A, Gutiérrez-Sáinz J, Gomez-Rio M, Bellón-Guardia M, Ramos-Font C, Rebollo-Aguirre AC, Cabello-García D, Ferrón Orihuela A: Fluorine-18 fluorodeoxyglucose PET in the preoperative staging of colorectal cancer. Eur J Nucl Med Mol Imaging 2007, 34: 859-867. 10.1007/s00259-006-0274-4View ArticlePubMedGoogle Scholar
- Mandard AN, Dalibar DF, Mandard JC: Pathological assessment of tumor regression after preoperative chemotherapy of oesophageal carcinoma: clinico-pathological correlations. Cancer 1994, 73: 2680-2686. 10.1002/1097-0142(19940601)73:11<2680::AID-CNCR2820731105>3.0.CO;2-CView ArticlePubMedGoogle Scholar
- de Geus-Oei LF, Vriens D, van Laarhoven HWM, van der Graaf WTA, Oyen WJG: Monitoring and predicting response to therapy with 18F-FDG PET in colorectal cancer: a systematic review. J Nucl Med 2009, 50: 43-54. 10.2967/jnumed.108.057224View ArticleGoogle Scholar
- Guillem JG, Puig-La Calle J Jr, Akhurst T, Tickoo S, Ruo L, Minsky BD, Gollub MJ, Klimstra DS, Mazumdar M, Paty PB, Macapinlac H, Yeung H, Saltz L, Finn RD, Erdi Y, Humm J, Cohen AM, Larson S: Prospective assessment of primary rectal cancer response to preoperative radiation and chemotherapy using 18-fluorodeoxyglucose positron emission tomography. Dis Colon Rectum 2000, 43: 18-24. 10.1007/BF02237238View ArticlePubMedGoogle Scholar
- Calvo FA, Domper M, Matute R, Martínez-Lázaro R, Arranz JA, Desco M, Alvarez E, Carreras JL: 18F-FDG positron emission tomography staging and restaging in rectal cancer treated with preoperative chemoradiation. Int J Radiat Oncol Biol Phys 2004, 58: 528-535. 10.1016/j.ijrobp.2003.09.058View ArticlePubMedGoogle Scholar
- Denecke T, Rau B, Hoffmann KT, Hildebrandt B, Ruf J, Gutberlet M, Hünerbein M, Felix R, Wust P, Amthauer M: Comparison of CT, MRI and FDG-PET in response prediction of patients with locally advanced rectal cancer after multimodal preoperative therapy: is there a benefit in using functional imaging? Eur Radiol 2005, 15: 1658-1666. 10.1007/s00330-005-2658-4View ArticlePubMedGoogle Scholar
- Capirci C, Rampin L, Erba PA, Galeotti F, Crepaldi G, Banti E, Gava M, Fanti S, Mariani G, Muzzio PC, Rubello D: Sequential FDG-PET/CT reliably predicts response of locally advanced rectal cancer to neo-adjuvant chemo-radiation therapy. Eur J Nucl Med Mol Imaging 2007, 34: 1583-1593. 10.1007/s00259-007-0426-1View ArticlePubMedGoogle Scholar
- Melton GB, Lavely WC, Jacene HA, Schulick RD, Choti MA, Wahl RL, Gearhart S: Efficacy of preoperative combined 18-fluorodeoxyglucose positron emission tomography and computed tomography for assessing primary rectal cancer response to neoadjuvant therapy. J Gastrointest Surg 2007, 11: 961-969. 10.1007/s11605-007-0170-7View ArticlePubMedGoogle Scholar
- Kristiansen C, Loft A, Berthelsen AK, Graff J, Lindebjerg J, Bisgaard C, Jakobsen A: PET/CT and histopathologic response to preoperative chemoradiation therapy in locally advanced rectal cancer. Dis Colon Rectum 2008, 51: 21-25. 10.1007/s10350-007-9095-1View ArticlePubMedGoogle Scholar
- Konski A, Li T, Sigurdson E, Cohen SJ, Small W Jr, Spies S, Yu JQ, Wahl A, Stryker S, Meropol NJ: Use of molecular imaging to predict clinical outcome in patients with rectal cancer after preoperative chemotherapy and radiation. Int J Radiat Oncol Biol Phys 2009, 74: 55-59. 10.1016/j.ijrobp.2008.07.050PubMed CentralView ArticlePubMedGoogle Scholar
- de Campos-Lobato LF, Stocchi L, da Luz Moreira A, Kalady MF, Geisler D, Dietz D, Lavery IC, Remzi FH, Fazio VW: Downstaging without complete pathologic response after neoadjuvant treatment improves cancer outcomes for cIII but not cII rectal cancers. Ann Surg Oncol 2010, 17: 1758-1766. 10.1245/s10434-010-0924-4View ArticlePubMedGoogle Scholar
- Capirci C, Rubello D, Chierichetti F, Crepaldi G, Fanti S, Mandoliti G, Salviato S, Boni G, Rampin L, Polico C, Mariani G: Long-term prognostic value of 18FFDG PET in patients with locally advanced rectal cancer previously treated with neoadjuvant radiochemotherapy. AJR 2006, 187: 202-208. 10.2214/AJR.05.0902View ArticleGoogle Scholar
- Guillem JG, Moore HG, Akhurst T, Klimstra DS, Ruo L, Mazumdar M, Minsky BD, Saltz L, Wong WD, Larson S: Sequential preoperative fluorodeoxyglucose-positron emission tomography assessment of response to preoperative chemoradiation: a means for determining long-term outcomes of rectal cancer. J Am Coll Surg 2004, 199: 1-7. 10.1016/j.jamcollsurg.2004.02.024View ArticlePubMedGoogle Scholar
- Nakagawa K, Yamashita H, Nakamura N, Igaki H, Tago M, Hosoi Y, Momose T, Ohtomo K, Muto T, Nagawa H: Preoperative radiation response evaluated by 18-fluorodeoxyglucose positron emission tomography predicts survival in locally advanced rectal cancer. Dis Colon Rectum 2008, 51: 1055-1060. 10.1007/s10350-008-9243-2View ArticlePubMedGoogle Scholar
- Cascini GL, Avallone A, Delrio P, Guida C, Tatangelo F, Marone P, Aloj L, De Martinis F, Comella P, Parisi V, Lastoria S: 18F-FDG PET is an early predictor of pathologic tumor response to preoperative radiochemotherapy in locally advanced rectal cancer. J Nucl Med 2006, 47: 1241-1248.PubMedGoogle Scholar
- Janssen MH, Ollers MC, Riedl RG, van der Bogaard J, Buijsen J, van Stiphout RGPM, Aerts HJWL, Lambin P, Lammering G: Accurate prediction of pathological rectal tumor response after two weeks of preoperative radiochemotherapy using 18F-Fuorodeoxyglucose-positron emission tomography-computed tomography imaging. Int J Radiation Oncology 2010, 77: 392-399. 10.1016/j.ijrobp.2009.04.030View ArticleGoogle Scholar
- Akhurst T, Kates TJ, Mazumdar M, Yeung H, Riedel ER, Burt BM, Blumgart L, Jarnagin W, Larson SM, Fong Y: Recent chemotherapy reduces the sensitivity of 18F-fluorodeoxyglucose positron emission tomography in the detection of colorectal metastates. J Clin Oncol 2005, 23: 8713-8716. 10.1200/JCO.2005.04.4222View ArticlePubMedGoogle Scholar
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