全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
ISRN Oncology  2013 

Is There a Limitation of RECIST Criteria in Prediction of Pathological Response, in Head and Neck Cancers, to Postinduction Chemotherapy?

DOI: 10.1155/2013/259154

Full-Text   Cite this paper   Add to My Lib

Abstract:

This study studied the coorelation between radiological response to induction chemotherapy and acheivement of pCR or near pCR. It was a retrospective analysis in which all patients who received NACT from 2008 till april 2012 were subjected to inclusion criteria. Coorelation analysis was performed between CR + PR and acheivement of pCR or near pCR. Twenty four patients were identified.The primary site of tumor was oral cavity in 19 patients (79.2%), maxilla in 2 patients (4.2%), laryngopharynx in 2 patients (4.2%) and oropharynx in 1 patient (4.2%). The clinical stage was stage IVA in 16 patients ( 66.7%) and IVB in 8 patients (33.3%). The overall response rates ie a combination of CR and PR was seen in 11patients (45.8%). The pCR was seen in 15 patients (62.5%) and rest had near pCR. There was no linear coorelation between radiological size decrement and tumor response. On coorelation analysis the spearman correlation coefficent was ?0.039 ( ). This suggest that presently used radiological response criterias for response assesment in head and neck cancers severly limit our ability to identify patients who would have pCR or near pCR. 1. Introduction RECIST (response evaluation criteria in solid tumors) criteria have been widely used for response assessment both in general clinical practice and clinical trials [1]. The criteria have been designed to be objective and reproducible. However, in RECIST, the focus is on unidimensional imaging and volumetric changes are not included. This lacuna was accepted in the 2009 update of RECIST (version 1.1); however, unidimensional imaging remained the standard as volumetric assessment was not considered to be standardised appropriately, and the measurements were often time-consuming and required special techniques [2]. Furthermore, RECIST criteria are easier to apply in well-defined lesions, as in metastatic nodules [3, 4]. The application of these criteria in complex, irregularly shaped tumors like head and neck cancers might be more difficult. This assumes significance in situations where response to initial therapy would dictate the next treatment protocol, especially in patients being treated with curative intent [5–7]. Prasad et al. have shown that the treatment response was graded differently based on volumetric measurement as opposed to unidimensional imaging of tumor burden in head and neck cancers [8]. Thus, reliance on RECIST criteria alone for assessing response might have an implication on the treatment algorithm in head and neck cancers. Induction chemotherapy is one of the treatment options in patients

References

[1]  J. E. Husband, L. H. Schwartz, J. Spencer et al., “Evaluation of the response to treatment of solid tumours—a consensus statement of the International Cancer Imaging Society,” British Journal of Cancer, vol. 90, no. 12, pp. 2256–2260, 2004.
[2]  E. A. Eisenhauer, P. Therasse, J. Bogaerts et al., “New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1),” European Journal of Cancer, vol. 45, no. 2, pp. 228–247, 2009.
[3]  H. Watanabe, S. Yamamoto, H. Kunitoh et al., “Tumor response to chemotherapy: the validity and reproducibility of RECIST guidelines in NSCLC patients,” Cancer Science, vol. 94, no. 11, pp. 1015–1020, 2003.
[4]  S. Khokher, M. U. Qureshi, and N. A. Chaudhry, “Comparison of WHO and RECIST criteria for evaluation of clinical response to chemotherapy in patients with advanced breast cancer,” Asian Pacific Journal of Cancer Prevention, vol. 13, no. 7, pp. 3213–3218, 2012.
[5]  J. L. Lefebvre, D. Chevalier, B. Luboinski, A. Kirkpatrick, L. Collette, and T. Sahmoud, “Larynx preservation in pyriform sinus cancer: preliminary results of a European organization for research and treatment of cancer phase III trial,” Journal of the National Cancer Institute, vol. 88, no. 13, pp. 890–899, 1996.
[6]  V. M. Patil, V. Noronha, A. Joshi et al., “Induction chemotherapy in locally advanced pharyngolaryngeal cancers with stridor: is it feasible and safe?” Chemotherapy Research and Practice, vol. 2012, Article ID 549170, 5 pages, 2012.
[7]  “Induction chemotherapy plus radiation compared with surgery plus radiation in patients with advanced laryngeal cancer. The Department of Veterans Affairs Laryngeal Cancer Study Group,” The New England Journal of Medicine, vol. 324, no. 24, pp. 1685–1690, 1991.
[8]  S. R. Prasad, K. S. Jhaveri, S. Saini, P. F. Hahn, E. F. Halpern, and J. E. Sumner, “CT tumor measurement for therapeutic response assessment: comparison of unidimensional, bidimensional, and volumetric techniques—initial observations,” Radiology, vol. 225, no. 2, pp. 416–419, 2002.
[9]  M. R. Posner, D. M. Hershock, C. R. Blajman et al., “Cisplatin and fluorouracil alone or with docetaxel in head and neck cancer,” New England Journal of Medicine, vol. 357, no. 17, pp. 1705–1715, 2007.
[10]  J. B. Vermorken, E. Remenar, C. Van Herpen et al., “Cisplatin, fluorouracil, and docetaxel in unresectable head and neck cancer,” New England Journal of Medicine, vol. 357, no. 17, pp. 1695–1704, 2007.
[11]  C. Paterson, A. G. Robertson, D. Grose, P. D. Correa, and M. Rizwanullah, “Neoadjuvant chemotherapy prior to surgery in head and neck cancer,” Clinical Oncology, vol. 24, no. 1, pp. 79–80, 2012.
[12]  T. K. Hoffmann, “Systemic therapy strategies for head-neck carcinomas: current status,” Laryngo-Rhino-Otologie, vol. 91, supplement 1, pp. S123–S143, 2012.
[13]  L. Licitra, C. Grandi, M. Guzzo et al., “Primary chemotherapy in resectable oral cavity squamous cell cancer: a randomized controlled trial,” Journal of Clinical Oncology, vol. 21, no. 2, pp. 327–333, 2003.
[14]  J. Cohen, “A power primer,” Psychological Bulletin, vol. 112, no. 1, pp. 155–159, 1992.
[15]  C. Suzuki, H. Jacobsson, T. Hatschek et al., “Radiologic measurements of tumor response to treatment: practical approaches and limitations,” Radiographics, vol. 28, no. 2, pp. 329–344, 2008.
[16]  V. A. I. Mehta and J. H. Sampson, “The limitations of imaging response criteria,” The Lancet Oncology, vol. 13, no. 11, pp. 1064–1065, 2012.
[17]  H. W. Herr, J. Sheinfeld, H. S. Puc et al., “Surgery for a post-chemotherapy residual mass in seminoma,” Journal of Urology, vol. 157, no. 3, pp. 860–862, 1997.
[18]  E. Di Cesare, G. Cerone, R. M. Enrici, V. Tombolini, P. Anselmo, and C. Masciocchi, “MRI characterization of residual mediastinal masses in Hodgkin's disease: long-term follow-up,” Magnetic Resonance Imaging, vol. 22, no. 1, pp. 31–38, 2004.
[19]  R. L. Wahl, H. Jacene, Y. Kasamon, and M. A. Lodge, “From RECIST to PERCIST: evolving considerations for PET response criteria in solid tumors,” Journal of Nuclear Medicine, vol. 50, supplement 1, pp. 122S–150S, 2009.
[20]  H. Choi, “Response evaluation of gastrointestinal stromal tumors,” Oncologist, vol. 13, supplement 2, pp. 4–7, 2008.
[21]  Y. Sato, H. Watanabe, M. Sone et al., “Tumor response evaluation criteria for HCC (hepatocellular carcinoma) treated using TACE (transcatheter arterial chemoembolization): RECIST (response evaluation criteria in solid tumors) version 1.1 and mRECIST (modified RECIST): JIVROSG-0602,” Upsala Journal of Medical Sciences, vol. 118, no. 1, pp. 16–22, 2013.
[22]  J. Desai, “Response assessment in gastrointestinal stromal tumor,” International Journal of Cancer, vol. 128, no. 6, pp. 1251–1258, 2011.
[23]  H. Choi, “Critical issues in response evaluation on computed tomography: lessons from the gastrointestinal stromal tumor model,” Current Oncology Reports, vol. 7, no. 4, pp. 307–311, 2005.

Full-Text

Contact Us

[email protected]

QQ:3279437679

WhatsApp +8615387084133