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World J Gastroenterol. Aug 7, 2013; 19(29): 4651-4670
Published online Aug 7, 2013. doi: 10.3748/wjg.v19.i29.4651
Published online Aug 7, 2013. doi: 10.3748/wjg.v19.i29.4651
Table 5 Anti-p53 auto-antibody and sero-conversion in colorectal cancer
Ref. | Patients, method | Follow-up | Findings |
Müller et al[123] | 303 patients, 197 colon, 46 rectal | Median 6 mo | All cancers: 3.6% (11/303) sero(-)→ (+); 3.6% (11/303) sero(+)→ (-); Total 7.2% (22/303) sero-conversion. |
Colon cancer: 3% (4/137) sero(-)→ (+); 3.6% (5/137) sero(+)→ (-); Total 6.6% (9/137) sero-conversion. | |||
Rectal cancer: 6.5% (2/31) sero(-)→ (+); 3.2% (2/31) sero(+)→ (-); Total 12.9% (4/31) sero-conversion | |||
Lechpammer et al[88] | Immunoblot 32 , ELISA (Oncogene, Research Products, Cambridge, United States) | Up to 20 wk; 8 patients-48 wk | Non-significant decrease at 4 wk (pre-first cycle chemo) and significant decrease at 12 wk post-surgery |
Significant decreases during chemotherapy and 2 patients with anti-p53 increase at 12 wk (during chemotherapy) developed recurrence | |||
8 patients with extended follow-up: 7/8 had decreased anti-p53 with no recurrence. 1/8 anti-p53 decrease post-surgery/chemotherapy but increased at 12 wk corresponding with liver metastases. Anti-p53 fluctuates in response to tumour load but does not disappear. Anti-p53 levels reflects tumour load even during chemotherapy | |||
Takeda et al[174] | 30 CUR A, 5 CUR B, 5 CUR C, anti-p53 EIA, Pharmacell | Median 26 mo (13-144) | CUR A (n = 30): 28/30 sero(+)→(-) in 6 mo; 2 no sero-conversion: 1 recurrence |
CUR B (n = 5): 2 sero(+)→(-) no recurrence. 3 no sero-conversion, 2 had metastases | |||
CUR C: No sero-conversion | |||
Correlation between post-operative negative conversion and operative curability | |||
Takeda et al[98] | 17 mucosal/submucosal, ELISA (anti-p53 EIA, Pharmacell, France) | Up to 2 years | 94%, 16/17 sero(+)→(-) within 3 wk post-surgery |
No recurrences as early stage tumours and hence not able to comment on anti-p53 and recurrence rates | |||
Polge et al[128] | 10, ELISA (Dianova, Hamburg, Germany) | Up to 6 mo | 8 followed-up: 5/8 remained sero(+) post-operatively. All developed metastases |
3/8 decreased anti-p53 titres. No metastases or recurrence. | |||
Anti-p53 titres decreased within 1 mo of surgery/chemotherapy but no sero-conversion to anti-p53(-) | |||
Angelopoulou et al[81] | 6, “In house” immunofluorometric assay | Up to 17 mo | Anti p53 decreases with surgery/chemotherapy but persists at low levels |
Anti-p53 increases with recurrence | |||
Anti-p53 reflects tumour load more sensitively than CEA (n = 5) and in non-CEA producing tumour (n = 1) | |||
Hammel et al[175] | 12, “In house” ELISA | Up to 20 mo | Anti-p53 in 5/8 patients decrease by > 25% within 1 mo. |
At 1 year, 3 with normal anti-p53 levels and 3 with substantial decrease in anti-p53 remain disease-free | |||
2 patients with post-operative increased anti-p53: 1 developed recurrence and 1 developed metastases | |||
Anti-p53 decreased again following surgery in both patients. CEA and CA19-9 were normal in both cases |
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Citation: Suppiah A, Greenman J. Clinical utility of anti-
p53 auto-antibody: Systematic review and focus on colorectal cancer. World J Gastroenterol 2013; 19(29): 4651-4670 - URL: https://www.wjgnet.com/1007-9327/full/v19/i29/4651.htm
- DOI: https://dx.doi.org/10.3748/wjg.v19.i29.4651