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Recently, labeling of the SLN or nodes for tumor staging and locoregional surgical clearance has been developed or its development has started

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The sentinel lymph node (SLN) is defined as the first regional lymph node to receive lymphatic fluid from a malignant tumor. Therefore, this node is a ªsentinelº for second metastatic lymph node sta- tions and for labeling regional tumor spread. (For editorials and overviews see: Veronesi et al. 1997;

Dixon 1998; della Rovere and Bird 1998.) This node is useful for locoregional tumor staging and for sub- sequent individual related further surgical strate- gies. In some ways, this has been a logical develop- ment after the more or less successful use of lymph- angiography by many radiologists in the 1970s. This older method has been used to detect cancer metas- tases or infiltration of lymph nodes, for example in cases of prostate or bladder cancer as well as in Hodgkin or non-Hodgkin lymphomas.

The lymphangiographic signs indicating tumor infiltration were filling defects or distorted archi- tecture within the lymph nodes and interruption of lymphatic vessels. Pathologic lymphangiography findings in regional or distant node groups were utilized to assess lymphatic tumor spread.

Recently, labeling of the SLN or nodes for tumor staging and locoregional surgical clearance has been developed or its development has started.

This means that the detection of the first node or nodes of a particular tumor may be involved in the lymphogenic spread of the primary, and if this is so more extensive regional lymphadenectomy can follow. When the SLN is negative on pathohis- tological examination extensive lymphadenectomy can be avoided.

This staging procedure has been developed for the following tumor categories: breast cancer (al- ready used in many clinics, but in others still in development); malignant melanomas (already well developed); lung tumors; gastrointestinal tumors and head and neck tumors (discussion and prelim- inary approaches in progress). In addition, new approaches for tumors of the pelvis (cervix, penis, bladder, prostate, etc.) are also under discussion, as is node labeling of neuroendocrine tumors.

Lymphatic mapping techniques have several ob- jectives, but no generally accepted and practiced uniform concept is universally available.

So far, three strategies for detection of sentinel nodes have been proposed:

· Labeling of the sentinel node(s) with a dye, such as ªpatent blue,º to identify draining lymph ves- sels and the position(s) of the first regional lymph node(s), which are then surgically re- moved and examined by the techniques of histol- ogy, immunohistochemistry (IHC) and/or the polymerase chain reaction (PCR) (Min et al.

1998);

· Labeling of the sentinel node(s) by99mTc-colloid scintigraphy;

· Sophisticated nuclear medicine and radiological methods:

± Increased glucose metabolism using [F- 18]FDG-PET (fluor-18-fluorodeoxy-d-glucose positron emission tomography) to localize in- creased metabolism in regional small (<1 cm) lymph nodes (Adler et al. 1997).

± New development of radioimmunolabeling or peptide labeling with surface or cytoplasmic markers (e.g., extracellular domain of Her2/

Neu oncoprotein (p185) or EGFR; CEA, gas- trin, somatostatin receptors) (Schauer et al.

1990, 1992; Marx et al. 1990; Borg et al.

1991). No systematic investigations on these lines have so far been published, and these markers can only be used when an initial as- piration biopsy has identified the tumor as positive specifically for these.

± Tissue-specific magnetic resonance imaging (MRI) contrast agents for the reticuloen- dothelial system, such as superparamagnetic iron oxide nanoparticles (Sinerem or AMI 227), which are presently being investigated in clinical trials for detection of lymph node metastasis (Weissleder et al. 1990 a,b, 1994) (see also chapter 19).

Chapter 1

Definition of the Sentinel Lymph Node 1

and Basic Principles of Detection

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Such investigations of SLNs can helpto detect me- tastatic infiltration while it is still in situ before gamma probe imaging analysis.

With these methods, neoplastic infiltration of the lymph nodes can even be detected in palpatory negative sentinel basins. It seems to be clear from the start that these new techniques must be mea- sured in terms of their false-negative rates.

The main questions connected with the signifi- cance of localization of a SLN are:

· Can a SLN be defined so as to have significance for primaries with different localizations?

· How is it possible to label the node preopera- tively without influencing the primary tumor, especially by the opening of veins that can be caused by increased local pressure or necrosis, for example after the injection of contrast me- dia, which can induce hematogenous metastatic spread?

· Is biopsy of sentinel node(s) efficient in detect- ing occult metastases and does it have the po- tential for selecting patients who may benefit from sentinel node dissection alone?

· Is investigation of the sentinel node really sig- nificant in avoidance, for instance, of extended axilla revision in breast cancer patients (levels I and II) in sentinel node-negative cases?

· What is the best method of SLN detection and investigation?

· What are the consequences of positive or nega- tive results of investigation of the sentinel node?

· Does SLN investigation, with avoidance for in- stance of axilla revision in negative cases, have to be included in the matters discussed with the patient and listed in the informed consent pro- vided by the patient?

References

Adler LP, Faulhaber PF, Schnur Kc, Al-Kasi NL, Shenk RR (1997) Axillary lymph node metastases: screening with (F-18)2-deoxy-2-fluoro-d-glucose (FDG) PET. Radiology 203:323, 327

Borg A, BaldetorpB, Fernæ M, Killander D, Olsson H, Si- gurdson H (1991) ErbB2 amplification in breast cancer with high rate of proliferation. Oncogene 6:137±143 Borgstein PJ, Pijpers R, Comans EF, van-Diest PJ, Boom RP,

Meijer S (1998) Sentinel lymph node biopsy in breast cancer: guidelines and pitfalls of lymphoscintigraphy and gamma probe detection. J AM Coll Surg 186:275±

Dixon M (1998) Sentinel node biopsy in breast cancer. BMJ283 317:295±296

Marx D, Schauer A, Reiche C, May A, Ummenhofer L, Reles A, Rauschecker HF, Sauer R, Schumacher M (1990) c- erbB2-expression in correlation to other biological para- meters of breast cancer. J Cancer Res Clin Oncol 116:15±

Min CJ, Tafra L, Verbanac KM (1998) Identification of20 superior markers for polymerase chain reaction detec- tion of breast cancer metastases in sentinel lymph nodes.

Cancer Res 15(58):4581±4584

Rovere G della, Bird PA (1998) Sentinel lymph node in breast cancer. Lancet 352:421±422

Schauer A, Marx D, Ummenhofer L, Rauschecker H, Gatze- meier W, Sauer R, Schumacher M, Sauerbrei W (1990) Die Multicenter Studie ¹Kleines Mammacarcinom. Vor- låufige Ergebnisse ± Neue Aspekteª. Dtsch Ørzteblatt 87:3628±3638

Veronesi U, Paganelli G, Galimberti V, Viale G, Zurrida ST, Bodeni N, Costa A, Chicco C, Geraghty JG, Luine A, Sac- chini V, Veronesi P (1997) Sentinel node biopsy to avoid axillary dissection in breast cancer with clinically nega- tive lymph nodes. Lancet 349:1864±1867

Weissleder R, Elizondo G, Wittenberg J, Rabito CA, Bengele HH, Josephson L (1990 a) Ultrasmall superparamagnetic iron oxide: characterization of a new class of contrast agents for MR imaging. Radiology 175:489±493

Weissleder R, Elizondo G, Wittenberg J, Lee AS, Josephson L, Brady TJ (1990 b) Ultrasmall superparamagnetic iron oxide: an i.v. contrast agent for assessing lymph nodes with MR imaging. Radiology 175:494±498

Weissleder R, Heautot JF, Schaffer BK, Nossiff N, Papisov M, Bogdanov AJ, Brady T (1994) MR lymphography study of a high efficiency lymphography agent. Radiol- ogy 191:225±230

Chapter 1 Definition of the Sentinel Lymph Node and Basic Principles of Detection 4

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