Skip to main content
Log in

Family History of Cancer as Potential Prognostic Factor in Stage III Colorectal Cancer: a Retrospective Monoinstitutional Study

  • Brief Communication
  • Published:
Journal of Gastrointestinal Cancer Aims and scope Submit manuscript

Abstract

Background and Aims

The prognostic role of family history of cancer (FHC) in resected colorectal cancer (CRC) is controversial. The aim of the current study was to evaluate its impact in a monoinstitutional series of stage III CRC patients.

Methods

This single institution retrospective analysis is aimed at evaluating whether FHC affects overall survival (OS) and disease-free survival (DFS) in stage III CRC patients. Moreover, the role of both colorectal FHC (FHCRC, in patients with at least one relative with CRC) and FHC “burden” have been investigated; patients were classified according to FHC in FHC negative, FHC-low (one “familial cluster” among parents/children/grandparents, brothers/sisters, uncles/cousins), and FHC-high (at least two clusters of those above mentioned).

Results

From October 2000 to March 2019, 112 consecutive stage III CRC patients have been evaluated. Median age was 67 years (range 24–89); male/female ratio was 64/48. Fifty-three (47.3%) patients were FHC-negative while 59 (52.7%) patients were FHC-positive, 18 (16.1%) of whom were FHCRC-positive. Thirty-three (29.5%) patients were FHC-low, and 10 (8.9%) were FHC-high. At a median follow-up of 41.9 months, no statistically significant differences in DFS were found. FHC-positive patients had a significantly longer OS than FHC-negative (HR = 0.32 [95% CI 0.12–0.84], p = 0.0210), and a significant trend towards improved OS according to the FHC burden was found (p = 0.0255). No statistically significant differences were found in DFS and OS according to FHCRC.

Conclusion

In this retrospective analysis, FHC-positive stage III CRC patients had a significantly longer OS compared to FHC-negative. Moreover, this survival benefit seems to increase according to the FHC burden. Further prospective studies, with longer follow-up and larger sample size, are necessary to confirm FHC as prognostic factor in this setting.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Data Availability

The datasets used during the present study are available from the corresponding author upon reasonable request.

References

  1. Little J, Faivre J. Family history, metabolic gene polymorphism, diet and risk of colorectal cancer. Eur J Cancer Prev. 1999;8(Suppl 1):S61–72.

    PubMed  Google Scholar 

  2. Syngal S, Brand RE, Church JM, Giardiello FM, Hampel HL, Burt RW, et al. ACG clinical guideline: genetic testing and management of hereditary gastrointestinal cancer syndromes. Am J Gastroenterol. 2015;110(2):223–62; quiz 263. https://doi.org/10.1038/ajg.2014.435.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Schiemann U, Muller-Koch Y, Gross M, et al. Extended microsatellite analysis in microsatellite stable, MSH2 and MLH1 mutation-negative HNPCC patients: genetic reclassification and correlation with clinical features. Digestion. 2004;69(3):166–76. https://doi.org/10.1159/000078223.

  4. Cortellini A, Bersanelli M, Buti S, Gambale E, Atzori F, Zoratto F, et al. Family history of cancer as surrogate predictor for immunotherapy with anti-PD1/PD-L1 agents: preliminary report of the FAMI-L1 study. Immunotherapy. 2018;10(8):643–55. https://doi.org/10.2217/imt-2017-0167.

    Article  CAS  PubMed  Google Scholar 

  5. Cortellini A, Buti S, Bersanelli M, Giusti R, Perrone F, di Marino P, et al. Evaluating the role of FAMIly history of cancer and diagnosis of multiple neoplasms in cancer patients receiving PD-1/PD-L1 checkpoint inhibitors: the multicenter FAMI-L1 study. Oncoimmunology. 2020;9(1):1710389. https://doi.org/10.1080/2162402X.2019.1710389.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Hemminki K, Chen B. Familial risk for colorectal cancers are mainly due to heritable causes. Cancer Epidemiol Biomark Prev. 2004;13:1253–6.

    Google Scholar 

  7. Morris EJ, Penegar S, Whitehouse LE, Quirke P, Finan P, Bishop DT, et al. A retrospective observational study of the relationship between family history and survival from colorectal cancer. Br J Cancer. 2013;108(7):1502–7. https://doi.org/10.1038/bjc.2013.91.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Chong DQ, Banbury BL, Phipps AI, Hua X, Kocarnik J, Peters U, et al. Association of family history and survival in patients with colorectal cancer: a pooled analysis of eight epidemiologic studies. Cancer Med. 2018;7:2192–9.

    Article  Google Scholar 

  9. Jansson-Knodell CL, Foster NR, Sargent DJ, Limburg PJ, Thibodeau SN, Smyrk TC, et al. Family history of colorectal cancer and its impact on survival in patients with resected stage III colon cancer: results from NCCTG Trial N0147 (Alliance). J Gastrointest Oncol. 2017;8(1):1–11. https://doi.org/10.21037/jgo.2016.12.13.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Chan JA, Meyerhardt JA, Niedzwiecki D, Hollis D, Saltz LB, Mayer RJ, et al. Association of family history with cancer recurrence and survival among patients with stage III colon cancer. JAMA. 2008;299:2515–23.

    Article  CAS  Google Scholar 

  11. Shan T, Chen S, Chen X, Lin W, Li W, Ma J, et al. Association of family history of tumors with clinicopathological characteristics and prognosis of colorectal cancer. Eur J Cancer Prev. 2019;28(4):258–67. https://doi.org/10.1097/CEJ.0000000000000482.

    Article  CAS  PubMed  Google Scholar 

  12. Park Y, Park SJ, Cheon JH, Kim WH, Kim TI. Association of family history with cancer recurrence, survival, and the incidence of colorectal adenoma in patients with colorectal cancer. J Cancer Prev. 2019;24:1–10.

    Article  CAS  Google Scholar 

  13. Lee SY, Kim DW, Kang SI, Ihn MH, Oh HK, Kang SB, et al. Impact of family history on prognosis of patients with sporadic colorectal cancer. Ann Surg Oncol. 2019;26:1118–26.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Contributions

All authors contributed to the publication according to the ICMJE guidelines for the authorship. All authors read and approved the manuscript and agree to be accountable for all aspects of the research in ensuring that the accuracy or integrity of any part of the work is appropriately investigated and resolved.

Corresponding author

Correspondence to Alessandro Parisi.

Ethics declarations

Conflict of Interest

Dr. Alessio Cortellini received grants as speaker from MSD, Astra-Zeneca, and Boehringer Ingelheim and grant consultancies from BMS, Roche, Novartis, Istituto Gentili and Ipsen.

Ethical Statement

The procedures followed were in accordance with the precepts of Good Clinical Practice and the Declaration of Helsinki. The study was conducted following the rules of the local bioethical committee competent on human experimentation (Comitato etico per le province di L’Aquila e Teramo).

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Parisi, A., Cortellini, A., Venditti, O. et al. Family History of Cancer as Potential Prognostic Factor in Stage III Colorectal Cancer: a Retrospective Monoinstitutional Study. J Gastrointest Canc 51, 1094–1101 (2020). https://doi.org/10.1007/s12029-020-00452-6

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12029-020-00452-6

Keywords

Navigation