Time to surgery and pathologic complete response after neoadjuvant chemoradiation in rectal cancer: A population study on 2094 patients. (June 2017)
- Record Type:
- Journal Article
- Title:
- Time to surgery and pathologic complete response after neoadjuvant chemoradiation in rectal cancer: A population study on 2094 patients. (June 2017)
- Main Title:
- Time to surgery and pathologic complete response after neoadjuvant chemoradiation in rectal cancer: A population study on 2094 patients
- Authors:
- Macchia, Gabriella
Gambacorta, Maria Antonietta
Masciocchi, Carlotta
Chiloiro, Giuditta
Mantello, Giovanna
di Benedetto, Maika
Lupattelli, Marco
Palazzari, Elisa
Belgioia, Liliana
Bacigalupo, Almalina
Sainato, Aldo
Montrone, Sabrina
Turri, Lucia
Caroli, Angela
De Paoli, Antonino
Matrone, Fabio
Capirci, Carlo
Montesi, Giampaolo
Niespolo, Rita Marina
Osti, Mattia Falchetto
Caravatta, Luciana
Galardi, Alessandra
Genovesi, Domenico
Rosetto, Maria Elena
Boso, Caterina
Sciacero, Piera
Giaccherini, Lucia
Parisi, Salvatore
Fontana, Antonella
Filippone, Francesco Romeo
Picardi, Vincenzo
Morganti, Alessio Giuseppe
Valentini, Vincenzo
… (more) - Abstract:
- Highlights: A large population based analysis to evaluate pathologic response according to time of surgery. LARC patients were treated with modern techniques of radiotherapy and surgery. The rate of pCR increased according to time interval from 12.6% to 31.1%. The pCR increasing was 1.5% (about 0.2%/die) per each week of waiting. Lengthening the interval (>13 weeks) significantly improved the pathological response. Abstract: Background: To retrospectively evaluate the difference in terms of pathologic complete response (pCR) according to time elapsed between chemoradiation (CRT) and total mesorectal excision (TME) on a large unselected real-life dataset of locally advanced rectal cancer (LARC) patients. Methods: A multicentre retrospective cohort study of LARC patients from 21 Italian Radiotherapy Institutions was performed. Patients were stratified into 3 different time intervals from CRT. The 1st group included 300 patients who underwent TME within 6 weeks, the 2nd 1598 patients (TME within 7–12 weeks) and the 3rd 196 patients (TME within 13 or more weeks after CRT), respectively. Results: Data on 2094 LARC patients treated between 1997 and 2016 were considered suitable for analysis. Overall, 578 patients had stage II while 1516 had stage III histological proven invasive rectal adenocarcinoma. A CRT schedule of one agent ( N = 1585) or 2-drugs ( N = 509) was administered. Overall, pCR was 22.3% ( N = 468 patients). The proportion of patients achieving pCR with respectHighlights: A large population based analysis to evaluate pathologic response according to time of surgery. LARC patients were treated with modern techniques of radiotherapy and surgery. The rate of pCR increased according to time interval from 12.6% to 31.1%. The pCR increasing was 1.5% (about 0.2%/die) per each week of waiting. Lengthening the interval (>13 weeks) significantly improved the pathological response. Abstract: Background: To retrospectively evaluate the difference in terms of pathologic complete response (pCR) according to time elapsed between chemoradiation (CRT) and total mesorectal excision (TME) on a large unselected real-life dataset of locally advanced rectal cancer (LARC) patients. Methods: A multicentre retrospective cohort study of LARC patients from 21 Italian Radiotherapy Institutions was performed. Patients were stratified into 3 different time intervals from CRT. The 1st group included 300 patients who underwent TME within 6 weeks, the 2nd 1598 patients (TME within 7–12 weeks) and the 3rd 196 patients (TME within 13 or more weeks after CRT), respectively. Results: Data on 2094 LARC patients treated between 1997 and 2016 were considered suitable for analysis. Overall, 578 patients had stage II while 1516 had stage III histological proven invasive rectal adenocarcinoma. A CRT schedule of one agent ( N = 1585) or 2-drugs ( N = 509) was administered. Overall, pCR was 22.3% ( N = 468 patients). The proportion of patients achieving pCR with respect to time interval was, as follows: 12.6% (1st group), 23% (2nd group) and 31.1% (3rd group) ( p < 0.001), respectively. The pCR relative risk comparison of 2nd to 1st group was 1.8, while 3rd to 2nd group was 1.3. Moreover, between the 3rd and 1st group, a pCR relative risk of 2.4 ( p < 0.01) was noted. At univariate analysis, clinical stage III ( p < 0.001), radiotherapy dose >5040 cGy ( p = 0.002) and longer interval ( p < 0.001) were significantly correlated to pCR. The positive impact of interval ( p < 0.001) was confirmed at multivariate analysis as the only correlated factor. Conclusion: We confirmed on a population-level that lengthening the interval (>13 weeks) from CRT to surgery improves the pathological response (pCR and pathologic partial response; pPR) in comparison to historic data. Furthermore, radiotherapy dose >5040 cGy and two drugs chemotherapy correlated with pPR rate. … (more)
- Is Part Of:
- Clinical and translational radiation oncology. Volume 4(2017)
- Journal:
- Clinical and translational radiation oncology
- Issue:
- Volume 4(2017)
- Issue Display:
- Volume 4, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 4
- Issue:
- 2017
- Issue Sort Value:
- 2017-0004-2017-0000
- Page Start:
- 8
- Page End:
- 14
- Publication Date:
- 2017-06
- Subjects:
- Rectal cancer -- Time interval -- Surgery -- TME -- Chemoradiation
Cancer -- Radiotherapy -- Periodicals
Oncology -- Periodicals
Cancer -- Radiotherapy
Oncology
Radiation Oncology
Neoplasms -- radiotherapy
Translational Medical Research
Periodicals
Electronic journals
Periodicals
616.9940642 - Journal URLs:
- https://www.journals.elsevier.com/clinical-and-translational-radiation-oncology ↗
http://www.sciencedirect.com/science/journal/24056308 ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.ctro.2017.04.004 ↗
- Languages:
- English
- ISSNs:
- 2405-6308
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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