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RNA/DNA Based Detection of Minimal Residual Head and Neck Cancer

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Book cover Micrometastasis

Part of the book series: Cancer Metastasis - Biology and Treatment ((CMBT,volume 5))

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Abstract

The prognosis of head and neck cancer is largely determined by the radicality of treatment: residual tumour cells will grow out and develop in manifest local recurrences, regional recurrences and distant metastases. Classical diagnostic methods such as radiology and histopathology have limited sensitivities, and only by molecular techniques minimal residual cancer or disseminated tumour cells can be detected. In tissue samples containing the normal tissue counterpart of a tumour only (pre)cancer cell-specific markers can be exploited, whereas in other samples tissue-specific markers can be used. Currently, there are two main methodologies in use, one based on antigen-antibody interaction, and the other based on amplified nucleic acids. The most commonly used nucleic acid markers are mutations or alterations in tumour DNA (tumour-specific markers) or differentially expressed mRNA (tissue-specific markers). The limits of detection of these molecular assays can reach levels of a single tumour cell in a background of 2 107 normal cells. The assays are, however, often complex, demand a large experience and are usually laborious. Nevertheless, the data collected with these assays enable the elucidation of unexplained clinical phenomena. Further technical developments might allow implementation in clinical practice once the relevance has been assessed in large prognostic trials with long-term follow-up. In this chapter a number of the molecular assays used for (pre)cancer cell detection in head and neck cancer patients will be presented.

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References

  1. Boring CC, Squires TS, Tong T. Cancer statistics. CA Cancer J Clin. 1992;42:19–38.

    PubMed  CAS  Google Scholar 

  2. Howaldt HP, Kainz, M. Projektbericht des Zentralregisters der Deutsch-Österreichisch-Schweizerischen Arbeiteitskreises für Tumoren im Kiefer-und Gesichtsbereich, 1992.

    Google Scholar 

  3. Franceschi D, Gupta R, Spiro RH, Shah JP. Improved survival in the treatment of squamous carcinoma of the oral tongue. Am J Surgery. 1993;166:360–5.

    CAS  Google Scholar 

  4. Zarbo RJ, Crissman JD. The surgical pathology of head and neck cancer. Seminars in Oncology. 1988;15:10–19.

    PubMed  CAS  Google Scholar 

  5. Alvi A, Johnson JT. Development of distant metastasis after treatment of advanced-stage head and neck cancer. Head & Neck. 1997;19:500–5.

    Article  CAS  Google Scholar 

  6. Vikram B. Changing patterns of failure in advanced head and neck cancer. Arch Otolaryngol. 1984;110:564–5.

    PubMed  CAS  Google Scholar 

  7. Hannahs KJ, Hooper JA, Sigler A. Nursing care of the head and neck cancer patient. In: Suen JY, Myers EN (eds) Cancer of the Head and Neck. Churchill Livingstone, New York, 1981, p. 839.

    Google Scholar 

  8. Callery CD, Spiro RH, Strong EW. Changing trends in the management of squamous carcinoma of the tongue. Am J Surgery. 1984;148:449–54.

    Article  CAS  Google Scholar 

  9. Crile G. Excision of cancer of the head and neck — with special reference to the plan of dissection based on one hundred and thirty-two operations. J Am Med Ass. 1906;47:1780–7.

    Google Scholar 

  10. Brizel DM, Albers ME, Fisher SR, Scher RL, Richtsmeier WJ, Hars V et al. Hyperfractionated irradiation with or without concurrent chemotherapy for locally advanced head and neck. New Engl J Med. 1998;338:1798–804.

    Article  PubMed  CAS  Google Scholar 

  11. McGuirt WF, Johnson JT, Myers EN, Rothfield R, Wagner R. Floor of mouth carcinoma. The management of the clinically negative neck. Arch Otolaryngol Head & Neck Surg. 1995;121:278–82.

    Google Scholar 

  12. Petruzzelli GJ, Benefield J, Yong S. Mechanism of lymph node metastases: current concepts. Otolaryngology. Clin North Am. 1998;31:585–99.

    CAS  Google Scholar 

  13. Tupchong L, Scott CB, Blitzer PH, Marcial VA, Lowry LD, Jacobs JR et al. Randomized study of preoperative versus postoperative radiation therapy in advanced head and neck carcinoma: long-term follow-up of RTOG study 73–03. Int. J Rad Oncol. 1991;20:21–8.

    CAS  Google Scholar 

  14. Vokes EE, Weichselbaum RR, Lippman SM, Hong KW. Medical Progress; Head and Neck Cancer. New Engl J Med. 1993;328:184–94.

    Article  PubMed  CAS  Google Scholar 

  15. Harrison LB, Lee HJ, Pfister DG, Kraus DH, White C, Raben A et al. Long term results of primary radiotherapy with/without neck dissection for squamous cell cancer of the base of tongue. Head & Neck. 1998;20:668–73.

    CAS  Google Scholar 

  16. Fisher B, Fisher ER. Barrier function of lymph node to tumour cells and erythrocytes; I Normal nodes; II Effect of X-Ray/inflammation/sensitization and tumour growth. Cancer. 1967;20:1907–19.

    PubMed  CAS  Google Scholar 

  17. Jones AS, Roland NJ, Field JK, Phillips DE. The level of cervical lymph node metastases: their prognostic relevance and relationship with head and neck squamous carcinoma primary sites. Clin Otolaryngol. 1994;19:63–9.

    PubMed  CAS  Google Scholar 

  18. Snow GB, Annyas AA, Van Slooten EA, Bartelink H, Hart AAM. Prognostic factors of neck node metastasis. Clin Otolaryngol. 1982;7:185–92.

    PubMed  CAS  Google Scholar 

  19. Leemans ChR, Tiwari R, Nauta JJ, Van der Waal I, Snow GB. Regional lymph node involvement and its significance in the development of distant metastases in head and neck carcinoma. Cancer. 1993;71:452–6.

    PubMed  CAS  Google Scholar 

  20. Violaris NS, O’Neil D, Helliwell TR, Caslin AW, Roland NJ, Jones AS. Soft tissue cervical metastases of squamous carcinoma of the head and neck. Clin Otolaryngol. 1993;19:394–9.

    Google Scholar 

  21. Lindberg R. Distribution of cervical lymph node metastases from squamous cell carcinoma of the upper respiratory and digestive tracts. Cancer. 1972;29:1446–9.

    PubMed  CAS  Google Scholar 

  22. Shah JP, Candela FC, Poddar AK. The patterns of cervical lymph node metastases from squamous carcinoma of the oral cavity. Cancer. 1990;66:109–13.

    PubMed  CAS  Google Scholar 

  23. Shah JP. Patterns of cervical lymph node metastasis from squamous carcinomas of the upper aerodigestive tract. Am J Surgery. 1990;160:405–9.

    CAS  Google Scholar 

  24. Candela FC, Kothari K, Shah JP. Patterns of cervical node metastases from squamous carcinoma of the oropharynx and hypopharynx. Head & Neck. 1990;12:197–203.

    CAS  Google Scholar 

  25. Candela FC, Shah J, Jaques DP, Shah JP. Patterns of cervical node metastases from squamous carcinoma of the larynx. Arch Otolaryngol Head & Neck Surg. 1990;4:432–5.

    Google Scholar 

  26. Bataini JP, Bernier J, Brugere J, Jaulerry Ch, Picco Ch, Brunin F. Natural history of neck disease in patients with squamous cell carcinoma of oropharynx and pharyngolarynx. Radiother Oncol. 1985;3:245–55.

    PubMed  CAS  Google Scholar 

  27. Lindberg RD. Distribution of cervical lymph node metastases from squamous cell carcinoma of the upper respiratory and digestive tracts. Cancer. 1972;29:1446–9.

    PubMed  CAS  Google Scholar 

  28. Kinsey DL, James AG, Bonta JA. A study of metastatic carcinoma of the neck. Ann Surg. 1985;147: 366–74.

    Google Scholar 

  29. Byers RM, Wolf PF, Ballantyne AJ. Rationale for elective modified neck dissection. Head & Neck. Surg. 1988;3:160–7.

    Google Scholar 

  30. Byers RM, Weber RS, Andrews T, McGill D, Kare R, Wolf P. Frequency and therapeutic implications of’ skip metastases’ in the neck from squamous carcinoma of the oral tongue. Head & Neck. 1997;19:14–19.

    Article  CAS  Google Scholar 

  31. Dennington ML, Carter DR, Meijers AD. Distant metastases in head and neck carcinoma. Laryngoscope. 1980;90:196–201.

    PubMed  CAS  Google Scholar 

  32. Nishijima W, Takooda S, Tokita N, Takayama S, Sakura M. Analyses of distant metastases in squamous cell carcinoma of the head and neck and lesions above the clavicle at autopsy. Arch Otolaryngol Head & Neck. Surgery. 1993;119:65–8.

    CAS  Google Scholar 

  33. Zbären P, Lehmann W. Frequency and sites of distant metastases in head and neck squamous cell carcinoma. An analysis of 101 cases at autopsy. Arch Otolaryng Head & Neck Surg. 1987;113:762–4.

    Google Scholar 

  34. Spiro RH. The management of neck nodes in head and neck cancer: a surgeon’s view. Bulletin NY Acad Med. 1985;61:629–37.

    CAS  Google Scholar 

  35. Vernham GA, Crowther JA. Head and neck carcinoma — stage at presentation. Clin Otolaryngol. 1994;19:120–4.

    PubMed  CAS  Google Scholar 

  36. Cooper JS, Pajak TF, Rubin P, Tupchong L, Brady LW, Leibel SA et al. Second malignancies in patients who have head and neck cancer: incidence, effect on survival and implications based on the RTOG experience. Int J Radiat Oncol. 1989; 17:449–56.

    CAS  Google Scholar 

  37. Licciardello JT, Spitz MR, Hong WK. Multiple primary cancer in patients with cancer of the head and neck: second cancer of the head and neck, esophagus, and lung. Int J Radiat Oncol. 1989;17:467–76.

    CAS  Google Scholar 

  38. Schaart LH, Ozsahin M, Zhang GN, Touboul E, De-Vataire F, Andolenko P et al. Synchronous and metachronous head and neck carcinomas. Cancer. 1994;74:1933–8.

    Google Scholar 

  39. Warren S, Gates O. Multiple primary malignant tumours: a survey of the literature and a statistical study. Am J Cancer. 1932;16:1358–414.

    Google Scholar 

  40. Hong WK, Lippman SM, Itri LM, Karp DD, Lee JS, Byers RM et al. Prevention of second primary tumours with isotretinoin in squamous-cell carcinoma of the head and neck. New Engl J Med. 1990;323:795–801.

    Article  PubMed  CAS  Google Scholar 

  41. Bedi GC, Westra WH, Gabrielson E, Koch W, Sidransky D. Multiple head and neck tumours: evidence for a common clonal origin. Cancer Res. 1996;56:2484–7.

    PubMed  CAS  Google Scholar 

  42. Leong PP, Rezai B, Koch WM, Reed A, Eisele D, Lee DJ et al. Distinguishing second primary tumours from lung metastases in patients with head and neck squamous cell carcinoma. J Natl Cancer Inst. 1998;90:972–7.

    Article  PubMed  CAS  Google Scholar 

  43. Slaughter DP, Southwick HW, Smejkal W. Field cancerisation in oral stratified squamous epithelium: clinical implication of multicentric orgin. Cancer. 1953;6:963–8.

    PubMed  CAS  Google Scholar 

  44. Cloos J, Braakhuis BJM, Steen I, Copper MP, de Vries N, Nauta JJP, Snow GB. Increased mutagen sensitivity in head-and-neck squamous-cell carcinoma patients, particularly those with multiple primary tumours. Int J Cancer. 1994;56:816–19.

    PubMed  CAS  Google Scholar 

  45. Cloos J, Spitz MR, Schantz SP, Hsu TC, Zhang Z, Tobi H et al. Genetic susceptibility to head and neck squamous cell carcinoma. J Natl Cancer Inst. 1996;88:530–5.

    PubMed  CAS  Google Scholar 

  46. Cloos J, Nieuwenhuis EJC, Boomsma DI, Kuik DJ, van der Sterre MLT, Arwert F et al. Inherited susceptibility to bleomycin-induced chromatid breaks in cultured peripheral blood lymphocytes. J Natl Cancer Inst. 1999;91:1125–30.

    Article  PubMed  CAS  Google Scholar 

  47. Van Zandwijk N, Dalesio O, Pastorino U, De Vries N, Van Tinteren, H. EUROSCAN, a randomized trial of vitamin A and N-acetylcysteine in patients with head and neck cancer or lung cancer. J Natl Cancer Inst. 2000;92:977–86.

    PubMed  Google Scholar 

  48. Lee JJ, Hong WK, Hittelman WN, Mao L, Lotan R, Shin DM et al. Predicting cancer development in oral leukoplakia: Ten years of translational research. Clin Cancer Res. 2000;6:1702–10.

    PubMed  CAS  Google Scholar 

  49. Fearon ER, Vogelstein B. A genetic model for colorectal tumourigenesis. Cell. 1990;61:759–67.

    Article  PubMed  CAS  Google Scholar 

  50. Cairns P, Sidransky D. Molecular methods for the diagnosis of cancer. Biochem Biophys Acta. 1999;1423:C11–18.

    PubMed  CAS  Google Scholar 

  51. Sidransky D. Nucleic acid-based methods for the detection of cancer. Science. 1997;278:1054–9.

    Article  PubMed  CAS  ADS  Google Scholar 

  52. Weber JL, May PE. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am J Hum Genet. 1989;44:388–96.

    PubMed  CAS  Google Scholar 

  53. Califano J, van der Riet P, Westra W, Nawroz H, Clayman G, Piantadosi S et al. Genetic progression model for head and neck cancer: implications for field cancerization. Cancer Res. 1996;56:2488–92.

    PubMed  CAS  Google Scholar 

  54. Hollstein M, Sidransky D, Vogelstein, B, Harris CC. P53 mutations in human cancers. Science. 1991;253:49–53.

    PubMed  CAS  ADS  Google Scholar 

  55. Greenblatt MS, Bennett WP, Hollstein M, Harris CC. Mutations in the p53 tumour suppressor gene: clues to cancer etiology and molecular pathogenesis. Cancer Res. 1994;54:4855–78.

    PubMed  CAS  Google Scholar 

  56. Van Houten VMM, Snijders PJF, Van den Brekel MWM, Meijer CJML, Van Leeuwen B, Smeele LE et al. Biological evidence that human papillomaviruses are etiologically involved in a subgroup of head and neck squamous cell carcinomas. Int J Cancer. 2001;93:232–5.

    PubMed  Google Scholar 

  57. Sidransky D, Von Eschenbach A, Tsai YC, Jones P, Summerhayes I, Marshall F et al. Identification of p53 gene mutations in bladder cancers and urine samples. Science. 1991;252:706–9.

    PubMed  CAS  ADS  Google Scholar 

  58. Steiner G, Schoenberg MP, Linn JF, Mao L, Sidransky D. Detection of bladder cancer recurrence by microsatellite analysis of urine. Nature Med. 1997;3:621–4.

    PubMed  CAS  Google Scholar 

  59. Brennan JA, Mao L, Hruban RH, Boyle JO, Eby YJ, Koch WM et al. Molecular assessment of histopathological staging in squamous-cell carcinoma of the head and neck. N Engl J Med. 1995;332:429–35.

    PubMed  CAS  Google Scholar 

  60. Takeda S, Ichii S, Nakamura Y. Detection of K-ras mutation in sputum by mutant-allele-specific amplification (MASA). Hum Mutation. 1993;2:112–17.

    CAS  Google Scholar 

  61. Landegren U, Kaiser R, Sanders J, Hood L. A ligase-mediated gene detection technique. Science. 1988;241:1077–80.

    PubMed  CAS  ADS  Google Scholar 

  62. Somers VA, Moerkerk PT, Murtagh JJ. Jr, Thunnessen FB. A rapid, reliable method for detection of known point mutations: POINT-EXACCT. Nucl Acids Res. 1994;22:4840–1.

    PubMed  CAS  Google Scholar 

  63. Kahn SM, Jiang W, Culbertson TA, Weinstein IB, Williams GM, Tomita N et al. Rapid and sensitive non-radioactive detection of mutant K-ras genes via enriched PCR amplification. Oncogene. 1991;6:1079–83.

    PubMed  CAS  Google Scholar 

  64. Levi S, Urbanoispizua A, Gill R, Thomas DM, Gilbertson J, Foster C et al. Multiple K-ras codon-12 mutations in cholangiocarcinomas demonstrated with a sensitive polymerase chain-reaction technique. Cancer Res. 1991;51:3497–502.

    PubMed  CAS  Google Scholar 

  65. Behn M, Qun S, Pankow W, Havemann K, Schuermann M. Frequent detection of RAS and p53 mutations in brush cytology samples from lung cancer patients by a restriction fragment length polymorphism-based ‘Enriched PCR’ technique. Clin Cancer Res. 1998;4:361–71.

    PubMed  CAS  Google Scholar 

  66. Ward R, Hawkins N, O’Grady R, Sheehan C, O’Connor T, Impey H et al. Restriction endonuclease-mediated selective polymerase chain reaction — a novel assay for the detection of K-ras mutations in clinical samples. Am J Pathol. 1998;153:373–9.

    PubMed  CAS  Google Scholar 

  67. Vogelstein B, Kinzler KW. Digital PCR. Proc Natl Acad Sci USA. 1999;96:9236–41.

    Article  PubMed  CAS  ADS  Google Scholar 

  68. Ahrendt SA, Halachmi S, Chow JT, Wu L, Halachmi N, Yang SC et al. Rapid p53 sequence analysis in primary lung cancer using an oligonucleotide probe array. Proc Natl Acad Sci USA. 1999;96:7382–7.

    Article  PubMed  CAS  ADS  Google Scholar 

  69. Fu DJ, Tang K, Braun A, Reuter D, Darnhoferdemar B, Little DP et al. Sequencing exons 5 to 8 of the p53 gene by MALDI-TOF mass spectrometry. Nature Biotech. 1998;16:381–4.

    CAS  Google Scholar 

  70. Williams C, Ponten F, Moberg C, Soderkvist P, Uhlen M, Ponten J et al. A high frequency of sequence alterations is due to formalin fixation of archival specimens. Am J Pathol. 1999;155:1467–71.

    PubMed  CAS  Google Scholar 

  71. Brennan JA, Sidransky D. Molecular staging of head and neck squamous carcinoma. Cancer Metast Rev. 1996;15:3–10.

    Article  CAS  Google Scholar 

  72. Sakai E, Tsuchida, N. Most human squamous cell carcinomas in the oral cavity contain mutated p53 tumour-suppressor genes. Oncogene. 1992;7:927–33.

    PubMed  CAS  Google Scholar 

  73. Burns JE, McFarlane R, Clark LJ, Mitchell R, Robertson G, Soutar D et al. Maintenance of identical p53 mutations throughout progression of squamous cell carcinomas of the tongue. Eur J Cancer Part B, Oral Oncology. 1994;30B:335–7.

    CAS  Google Scholar 

  74. Tjebbes GWA, Van der Straat FGJL, Tilanus MGJ, Hordijk GJ, Slootweg PJ. P53 tumour suppressor gene as a clonal marker in head and neck squamous cell carcinoma: p53 mutations in primary tumour and matched lymph node metastases. Oral Oncology. 1999;35:384–9.

    Article  PubMed  CAS  Google Scholar 

  75. Zariwala M, Schmid S, Pfaltz M, Ohgaki H, Kleihues P, Schafer R. P53 gene mutations in oropharyngeal carcinomas: a comparison of solitary and multiple primary tumours and lymph-node metastases. Int J Cancer. 1994;56:807–11.

    PubMed  CAS  Google Scholar 

  76. Ahomadegbe JC, Barrois M, Fogel S, Le Bihan ML, Douc-Rasy S, Duvillard P et al. High incidence of p53 alterations (mutation, deletion, overexpression) in head and neck primary tumours and metastases, absence of correlation with clinical outcome. Frequent protein overexpression in normal epithelium and in early non-invasive lesions. Oncogene. 1995;10:1217–27.

    PubMed  CAS  Google Scholar 

  77. Kropveld A, Van Mansfeld AD, Nabben N, Hordijk GJ, Slootweg PJ. Discordance of p53 status in matched primary tumours and metastases in head and neck squamous cell carcinoma patients. Eur J Cancer Part B, Oral Oncology. 1996;32B:388–93.

    CAS  Google Scholar 

  78. Tabor MP, Van Houten VMM, Kummer JA, Vosjan MJWD, Vlasblom R, Snow GB, Leemans ChR et al. Discordance of genetic alterations between primary head and neck tumours and corresponding metastases associated with mutational status of the TP53 gene. Genes Chrom Cancer. 2001;33:168–77.

    Google Scholar 

  79. Kropveld A, Rozemuller EH, Leppers FGJ, Scheidel KC, de Weger RA, Koole R et al. Sequencing analysis of RNA and DNA of exons 1 through 11 shows p53 gene alterations to be present in almost 100% of head and neck squamous cell cancers. Lab Invest. 1999;79:347–53.

    PubMed  CAS  Google Scholar 

  80. Van Houten V, Denkers F, Van Dijk M, Van den Brekel M, Brakenhoff, R. Labeling efficiency of oligonucleotides by T4 polynucleotide kinase depends on 5′-nucleotide. Anal Biochem. 1998;265:386–9.

    PubMed  Google Scholar 

  81. Van Houten VMM, Tabor MP, Van den Brekel MWM, Denkers F, Wishaupt RGA, Kummer JA et al. Molecular assays for the diagnosis of minimal residual head and neck cancer: methods, reliability, pitfalls and solutions. Clin Cancer Res. 2000;6:3803–16.

    PubMed  Google Scholar 

  82. Nawroz H, Koch W, Anker P, Stroun M, Sidransky D. Microsatellite alterations in serum DNA of head and neck cancer patients. Nature Med. 1996;2:1035–7.

    PubMed  CAS  Google Scholar 

  83. Jahr S, Hentze H, Englisch S, Hardt D, Fackelmayer FO, Hesch RD, Knippers R. DNA fragments in the blood plasma of cancer patients: quantitations and evidence for their origin from apoptotic and necrotic cells. Cancer Res. 2001;61:1659–65.

    PubMed  CAS  Google Scholar 

  84. Tindall KR, Kunkel TA. Fidelity of DNA synthesis by the Thermus aquaticus DNA polymerase. Biochemistry. 1988;27:6008–13.

    Article  PubMed  CAS  Google Scholar 

  85. Saiki RK, Gelfand DH, Stoffel S, Scharf SJ, Higuchi R, Horn GT et al. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science. 1988;239:487–91.

    PubMed  CAS  ADS  Google Scholar 

  86. Nees M, Homann N, Discher H, Andl T, Enders C, Herold-Mende C et al. Expression of mutated p53 occurs in tumour-distant epithelia of head and neck cancer patients: a possible molecular basis for the development of multiple tumours. Cancer Res. 1993;53:4189–96.

    PubMed  CAS  Google Scholar 

  87. Cruz IB, Snijders PJF, Meijer CJLM, Braakhuis BJM, Snow GB, Walboomers JMM et al. P53 expression above the basal cell layer in oral mucosa is an early event of malignant transformation and has predictive value for developing oral squamous cell carcinoma. J Pathol. 1998;184:360–8.

    Article  PubMed  CAS  Google Scholar 

  88. Knudson AG Jr. Mutation and cancer: statistical study of retinoblastoma. Proc Natl Acad Sci USA. 1971;68:820–3.

    PubMed  ADS  Google Scholar 

  89. Boland CR, Thibodeau SN, Hamilton SR, Sidransky D, Eshleman JR, Burt RW et al. National Cancer Institute Workshop on Microsatellite Instability for Cancer Detection and Familial Predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res. 1998;58:5248–57.

    PubMed  CAS  Google Scholar 

  90. Aaltonen LA, Peltomaki P, Leach FS, Sistonen P, Pylkkanen L, Mecklin JP et al. Clues to the pathogenesis of familial colorectal cancer. Science. 1993;260:812–16.

    PubMed  CAS  ADS  Google Scholar 

  91. Vogelstein B. Lessons from hereditary colorectal cancer. Cell. 1996;87:159–70.

    PubMed  Google Scholar 

  92. Tabor MP, Brakenhoff RH, Van Houten VMM, Kummer JA, Snel MHJ, Snijders PJF et al. Persistence of genetically altered fields in head and neck cancer patients: biological and clinical implications. Clin Cancer Res. 2001;7:1523–32.

    PubMed  CAS  Google Scholar 

  93. Braakhuis BJM, Tabor MP, Leemans ChR, Van der Waal I, Snow GB, Brakenhoff, RH. Second primary tumours and field cancerization in oral and oropharyngeal cancer: molecular techniques provide new insights and definitions. Head & Neck. 2002;24:198–206.

    Article  Google Scholar 

  94. Ashworth TA. A case of cancer in which cells similar to those in the tumours were seen in the blood after death. Australian Med J. 1869;14:146.

    Google Scholar 

  95. Lindemann F, Schlimok G, Dirschedl P, Witte J, Riethmüller G. Prognostic significance of micrometastatic tumour cells in bone marrow of colorectal cancer. Lancet. 1992;340:685–9.

    Article  PubMed  CAS  Google Scholar 

  96. Pantel K, Izbicki J, Passlick B, Angstwurm M, Häussinger K, Thetter O et al. Frequency and prognostic significance of isolated tumour cells in bone marrow of patients with non-small-cell lung cancer without overt metastases. Lancet. 1996;347:649–53.

    Article  PubMed  CAS  Google Scholar 

  97. Braun S, Pantel K, Muller P, Janni W, Hepp F, Kentenich CRM et al. Cytokeratin-positive cells in the bone marrow and survival of patients with stage I, II, or III breast cancer. New Engl J Med. 2000;342:525–33.

    Article  PubMed  CAS  Google Scholar 

  98. Wollenberg B, Ollesch A, Maag K, Funke I, Wilmes E. Mikrometastasen im knock-enmark von patienten mit karzinomen des kopf-hals-bereiches. Laryngo Rhino Otol. 1994;73:88–93.

    Article  CAS  Google Scholar 

  99. Gath H, Brakenhoff RH. Minimal residual disease in head and neck cancer. Cancer Metas Rev. 1999;18:109–26.

    CAS  Google Scholar 

  100. Brakenhoff, RH, Stroomer JGW, Ten Brink C, De Bree R, Weima SM, Snow GB et al. Sensitive detection of squamous cells in bone marrow and blood of head and neck cancer patients by E48 reverse transcriptase polymerase chain reaction. Clin Cancer Res. 1999;5:725–32.

    PubMed  CAS  Google Scholar 

  101. Nieuwenhuis EJC, Castelijns JA, Pijpers R, Van den Brekel MWM, Brakenhoff RH, Van der Waal I et al. Wait and see policy for the N0 neck in early stage oral and oropharyngeal SCC using ultrasound guided cytology: is there a role for identification of the sentinel node. Head & Neck.. 2002;24:282–9.

    Article  Google Scholar 

  102. Nieuwenhuis EJC, Jaspers EHJ, Castelijns JA, Bakker B, Wishaupt RGA, Denkers F, Leemans ChR, Snow GB, Brakenhoff RH. Quantitative molecular detection of minimal residual head and neck cancer in lymph node aspirates. Clin Cancer Res. 2003;9:755–61.

    PubMed  CAS  Google Scholar 

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Brakenhoff, R.H. (2003). RNA/DNA Based Detection of Minimal Residual Head and Neck Cancer. In: Pantel, K. (eds) Micrometastasis. Cancer Metastasis - Biology and Treatment, vol 5. Springer, Dordrecht. https://doi.org/10.1007/0-306-48355-6_2

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