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Processing-independent quantitation of chromogranin A in plasma from patients with neuroendocrine tumors and small-cell lung carcinomas.

The human chromogranin A (CgA) protein, a member of the granin family, is an acidic 439 amino acid protein with a sequence containing several mono--and dibasic cleavage sites. CgA is normally found in endocrine cells and neurons and is a promising tumor marker because most neuroendocrine tumors, including silent tumors without secretion of known hormones, express and release CgA (1-4).

Processing of neuroendocrine tumor proteins is often heterogeneous and attenuated (5, 6); therefore an analytical principle has been developed to improve the diagnosis of neuroendocrine tumors. Processing-independent-analysis (PIA), which measures an epitope even when the epitope is hidden in precursors and processing intermediates, quantifies the entire translation product of a given protein system irrespective of the degree of posttranslational processing (7). PIA was first applied to progastrin and procholecystokinin (7-9), and recent reports illustrate its diagnostic advantages (5, 6,10-14).

The purpose of this study was to develop a PIA for human CgA in plasma and to evaluate the diagnostic accuracy of measurement of the entire CgA translation product (total CgA) with the CgA PIA (index test) to differentiate between patients with gastrointestinal tumors, small-cell lung carcinoma (SCLC), or pheochromocytoma and healthy individuals. In addition we investigated whether the CgA plasma concentrations correlate with the tumor burden.

Materials and Methods


The specificity of the assays (antisera) is described by indicating the N--or C-terminal amino acid of the hapten as recognized by the antiserum. Thus, "CgA (340[right arrow]) assay 'indicates that the antiserum employed in this assay binds an epitope that starts at amino acid number 340 of CgA and includes amino acid residues located in the C-terminal direction.


Index test: development of a PIA for human CgA. An amino acid sequence of 6-8 amino acid residues is selected for immunization. It should not undergo posttranslational modifications, and it must be located between suitable (tryptic) cleavage sites. The sample to be assayed is preincubated with trypsin. In addition to exposing the epitope, the endoproteolytic cleavage ensures that equal-sized fragments with lengths similar to the assay calibrator are released so that proprotein and final products are quantitated with equimolar potency (5, 7, 9,11). The CgA(340-348) sequence neighbors suitable tryptic cleavage sites, i.e., trypsination will release the CgA fragment [Leu.sup.340]-[Lys.sup.355]. Trypsin treatment (described below) and subsequent quantification by the CgA(340[right arrow]) assay thus provide an estimate of the total CgA mRNA translation product, i.e., total CgA. Furthermore the CgA (340-348) sequence does not undergo posttranslational modifications.

Sequence-specific CgA (340-348) RIA. We previously developed an RIA specific for the N-terminus of the sequence CgA(340-348) [CgA(340[right arrow])], adjacent to a dibasic site ([Lys.sup.338][Arg.sup.339]) in the midportion of hCgA (using antibody 95058) (15). The interassay CVs of replicate samples for the CgA(340[right arrow]) assay were 21% at 15 pmol/L and 18% at 62 pmol/L.

Sequence-specific RIAs for CgA(1-9) and CgA(250-301) amide. We previously developed an RIA specific for the N-terminus of human CgA [using antibody 94188 (CgA(1[right arrow])] (15). The CgA([left arrow]301) assay (using antibody 871w-1) is specific for the amidated C-terminus of pancreastatin (16). The antiserum reacted fully with the synthetic peptides hCgA(273-301) amide and hCgA(250-301)amide.


Blood samples were collected as previously described (15). All plasma samples were analyzed with the CgA(1[right arrow]), CgA([left arrow]301 amide), and CgA(340[right arrow]) assays. Furthermore, the samples were analyzed with the index test, i.e., treated with trypsin, as described below, and subsequently analyzed with the CgA(340[right arrow]) assay.


For trypsin cleavage, equal volumes of plasma and 0.1 mol/L sodium phosphate buffer (pH 7.5) containing 2.0 g trypsin/L were incubated at room temperature for 30 min. For enzymatic cleavage of column fractions a trypsin concentration of 0.2 g/L was used. The enzymatic reaction was terminated by boiling for 10 min. Parallel control experiments were performed by omission of trypsin from the sodium phosphate buffer.


Plasma samples from carcinoid tumor patients (150-200 [micro]L) were applied to a Superose 12 HR column. Chromatography was performed as described previously (15). The column was calibrated with synthetic hCgA(250-301 amide) and an hCgA (340-372) fragment purified from a midget carcinoid tumor. The identity of the fragment was established by mass spectrometry analysis. The fractions were analyzed, before and after tryptic cleavage, with the CgA(340[right arrow]) assay.


For tumor patients histopathological analysis was performed as a routine test for diagnosis and classification. Biopsy material, surgical or coarse-needle biopsy specimens, was fixed in formalin and paraffin-embedded. The tumors were immunostained with a panel of antibodies to general neuroendocrine markers (e.g., CgA and synaptophysin) as well as specific hormones. The microscopy report included a general morphological description; immunohistochemical profile; mitotic rate; vascular, perineural, or lymphatic invasion; infiltration of surrounding tissues; lymph node status; and distant metastases (17-20).

For 24,14, 8, and 8 of the patients the reference test was performed at the Departments of Pathology, at Hillerod Hospital, Rigshospitalet, Herlev Hospital, and other Danish hospitals, respectively. The test was performed by trained technicians and read by medical specialists in pathology (n = 10). The readers of the reference test had access to the clinical information on the patients, but not to index test results.


Plasma samples from tumor patients. Included in this study were 27 patients with gastrointestinal neuroendocrine tumors, 6 patients with pheochromocytoma, and 21 patients with SCLC recruited consecutively upon referral for treatment of the tumors/carcinomas at the Departments of Surgical Gastroenterology and Urology, Rigshopitalet; the Department of Endocrinology, Herlev Hospital; and the Department of Internal Medicine, Hillerod Hospital. Inclusion criteria for all patients were an established histopathological diagnosis (reference standard) made from biopsy material or tumor tissue. Exclusion criteria were initiated chemotherapy or concurrent diseases (Fig. 1, gate 1 criteria). For the patients with gastrointestinal neuroendocrine tumors the reference test was performed between May 1994 and October 1997, and the patients were recruited and the plasma samples for the index tests were collected at median (range) 2 (0.25-24) months after the reference test was performed. The patients did not receive chemotherapy in the time interval between the 2 tests, and for all these patients it was shown by computer tomography and/or ultrasonography that tumor tissue was present at the time of plasma sample collection.


For the 6 pheochromocytoma patients the reference test was performed between August 1995 and September 1996. In these patients the plasma samples used for index tests were drawn shortly before surgery and reference testing.

The reference tests on the 21 SCLC patients were made between May 1991 and November 1992, and the plasma samples for index tests were collected shortly after the reference test was performed. No treatment (chemotherapy or operation) took place between the 2 tests.

The patient characteristics (age, sex, and severity of disease) are shown in Table 1.

The study was approved by the local ethics committee and informed consent was obtained from all patients (KF01-393/95, KF01-352/96, KF01-290/97, KF01-014/98).

Plasma samples from healthy controls. To establish reference intervals for the CgA(340[right arrow]) and CgA(340[right arrow]) posttryptic assays, we obtained plasma samples after 15-min rest from 88 healthy nonfasting control individuals. These controls were volunteers recruited from hospital staff. Only persons who reported being healthy (i.e., feeling well, without known diseases, and not taking any medications) were included (Fig. 1, gate 2 criteria). Control age and sex are shown in Table 1.

The CgA response to a mixed meal was studied in 8 healthy volunteers (4 men and 4 women; age range, 23-50 years) after an overnight fast. Consecutive postprandial blood samples were drawn 5-180 min after ingestion of the meal and analyzed with the 4 CgA assays.

For all patients and controls the index tests were performed at the Department of Clinical Biochemistry, Rigshospitalet, between January 1999 and July 2002. The index test was carried out by 2 trained technicians and read by the same technicians and a medical specialist in clinical biochemistry. The readers of the index test knew whether the plasma samples were from healthy persons or from tumor patients and also knew the result of the reference standard. Clinical information (symptoms, scan/operation results, and medication) on the patients was made available to the medical specialist after the index test had been performed.


Kruskal-Wallis ANOVA, Mann-Whitney U-test (2-tailed), and Wilcoxon rank sum test were performed with GraphPad Prism 4 for Windows; version 4.03, GraphPad Software Inc. For calculating reference values and performing the Kolmogorov-Smirnov test of normality we used SP55 for Windows v.12.0, SP55 Inc. The 0.95 confidence intervals (CIs) of the 2.5th and 97.5th percentiles were calculated according to Tietz et al. (21). We performed the exact binomial test to calculate 95% CIs for diagnostic sensitivity. Differences in diagnostic sensitivities in subgroups of patients were tested for significance with Fishers exact test. The exact binomial test and Fishers exact test (2-tailed) were performed using R Version 2.3.1 (22).



Trypsin treatment of plasma increased the median CgA(340[right arrow]) immunoreactivity 9-fold in controls and 6- to 16-fold in patients with neuroendocrine tumors and SCLC (Table 2 and Fig. 2). However, a large variation in the increase of CgA(340[right arrow]) immunoreactivity was found within the tumor groups, with up to 500-fold increases found in some patients.


Size-exclusion chromatography profiles of plasma samples from patients with midget carcinoid tumors showed that the majority of the CgA(340[right arrow]) immunoreactivity eluted from a Sepharose HR 12 column with coefficients of distribution (Kds) of 0.6-0.7. After trypsin treatment of the chromatography fractions, the majority of the posttryptic CgA immunoreactivity eluted in broad peaks (Kd 0.15-0.45, maximum 0.3) that comprised several high-molecular-weight forms, and only a minor fraction eluted corresponding to the peaks with Kds of 0.6-0.7 (see Fig. 1 in the Data Supplement that accompanies the online version of this article at These results indicated that the plasma samples in which trypsination markedly increased CgA(340[right arrow]) immunoreactivity contained high amounts of unprocessed or poorly processed CgA.


In agreement with a previous study (23), meal ingestion in the controls did not lead to significant changes in plasma CgA(1[right arrow]), CgA([left arrow]301), CgA(340[right arrow]), or posttryptic CgA(340[right arrow]) (Wilcoxon, P >0.05, data not shown). Consequently, reference intervals were established in a nonfasting population. The distributions of ln-transformed CgA(340[right arrow]) and ln-transformed CgA(340[right arrow]) posttryptic data were gaussian (Kolmogorov-Smirnov test of normality, P = 0.2 for both distributions). Reference intervals (central 95%) were 29-132 mol/L (95% CIs: 27-31 and 122-143) for CgA(340[right arrow]) immunoreactivity and 250-1100 pmol/L (95% CIs: 230-270 and 1020-1195 pmol/L) for CgA(340[right arrow]) post-tryptic immunoreactivity. The reference interval for the CgA(1[right arrow]) assay was 288-696 pmol/L, and for the CgA([left arrow]301) assay was 3-15 pmol/L (15).



The concentrations measured with the 4 CgA assays in the 54 plasma samples from the tumor patients and controls are shown in Table 3 and Fig. 2.

In defining the diagnostic sensitivity (the ratio of true positive to true positive plus false negative) true-positive vs true-negative designations were applied to patients with a neuroendocrine tumor diagnosis established by histopathological examination, depending on whether or not they had increased plasma CgA concentrations compared to controls. The upper limits of the reference intervals (central95%) were used as cutoffs. The diagnostic sensitivities of tumor patients are shown for the 4 CgA assays in Table 4A. In all groups the highest diagnostic sensitivities were obtained with the CgA(340[right arrow]) assay and CgA PIA. The diagnostic sensitivity obtained with the CgA(340[right arrow]) assay was 1.00 for patients with local, extensive, and very extensive gastrointestinal neuroendocrine tumors. For all other assays the diagnostic sensitivities increased with increasing tumor burden (Table 4B). However, significant differences between the diagnostic sensitivities of these groups were found only for the CgA(1[right arrow]) assay and the CgA PIA. Furthermore, significant differences between the diagnostic sensitivities obtained for limited and extensive SCLC were found only for the CgA(340[right arrow]) assay (Fishers exact test, Table 4B).

In the patients with gastrointestinal tumors a higher tumor burden was generally accompanied by higher concentrations of CgA(340[right arrow]) and total CgA immunoreactivity, as well as a lower degree of CgA processing. Kruskal-Wallis ANOVA applied on the CgA(340[right arrow]), CgA(340[right arrow]) + trypsin, and ratio [CgA(340[right arrow]) + trypsin/ CgA(340[right arrow])] results from the 3 groups of gastrointestinal tumor patients with limited (group 1), extensive (group 2), and very extensive (group 3) disease showed significant differences between the groups, P = 0.009 [CgA(340[right arrow])], P = 0.002 [CgA(340[right arrow]) + trypsin], and P = 0.002 [CgA(340[right arrow]) + trypsin/CgA(340[right arrow])], respectively. Posthoc Mann-Whitney U-test demonstrated significant differences between group 3 vs 2, 3 vs 1 and 2, and 3 vs 1 for the 3 sets of data [CgA(340[right arrow]), CgA(340[right arrow]) + trypsin, and CgA(340[right arrow]) + trypsin/CgA(340[right arrow])], whereas group 1 did not differ significantly from group 2 or from groups 2 and 3 (Table 2).

For the patients with SCLC, the concentrations measured with the CgA(340[right arrow]) assay in plasma from patients with extensive disease (group 2) were significantly higher than the concentrations measured in patients with local disease (group 1) (Mann-Whitney U-test, Table 2). The corresponding concentrations measured with the CgA PIA were borderline significantly higher (P = 0.06, Table 2).


Our results demonstrate that both the CgA(340[right arrow]) and posttryptic CgA(340[right arrow]) assays have a high diagnostic sensitivity in patients with neuroendocrine tumors or SCLC. In agreement with these results, high concentrations of unprocessed CgA were found in plasma from these patients, as corroborated by size-exclusion chromatography. These results are in accordance with reports that PIA analyses have increased the diagnostic accuracy for progastrin (6,10), probrain natriuretic peptide, and rat epidermal growth factor (11, 24). Furthermore, a PIA for procholecystokinin has recently been found to be a valuable tool for the diagnosis and monitoring of the efficiency of chemotherapy for patients with Ewing sarcomas, and the PIA proved superior to a conventional cholecystokinin RIA (14). An application of PIA for human CgA has not previously been published.

The observation that the increase in CgA(340[right arrow]) immunoreactivity after trypsination of plasma samples was significantly higher in plasma from patients with very extensive gastrointestinal neuroendocrine tumors (group 3) than in plasma from the patients with extensive (group 2) and local disease (group 1) (Table 2) is in agreement with earlier reports (5, 8) in which a lower degree of processing of progastrin was found in plasma from gastrinoma patients with metastases. A low degree of progastrin processing in gastrinomas has been previously suggested to predict a malignant clinical course (8), whether this could be the case for CgA from gastrointestinal tumors requires further study.

Furthermore, our finding that the concentrations measured with the CgA(340[right arrow]) assay and the PIA increased with the degree of tumor/carcinoma dissemination is in agreement with a previous report (25) that CgA concentrations were significantly higher in plasma from midget carcinoid tumor patients with [greater than or equal to]5 liver metastases than in those with <5 liver metastases. Plasma CgA has also been reported to be significantly higher in metastatic gastroenteropancreatic endocrine tumors than in nonmetastatic tumors (26), and higher in patients with extensive SCLC than in patients with limited disease (27). CgA plasma concentrations have also been found to correlate with tumor weight in nude mice with xenografted human deal carcinoid tumors (28). For some of the gastrointestinal neuroendocrine tumor patients with widespread, rapidly progressing disease the CgA PIA results seemed to enable better estimation of the tumor burden than the CgA(340[right arrow])assay results (results not shown). Further studies are needed to confirm this.

CgA in plasma is frequently used as a marker for neuroendocrine tumors and prostatic carcinomas. Measurements are performed with antisera raised against purified full-length CgA or large fragments from tumor patients (3, 23, 29-36), or with sequence-specific RIAs (15, 32, 37-39). Highly variable diagnostic sensitivities occur depending on tumor type and specificity of the assay employed.

With a monoclonal antibody-based RIA used for patients with SCLC, increased concentrations were measured in 53% of patients with limited and 72% with extensive disease (40). In a study using a CgA ELISA for which the antiserum was raised against a C-terminal CgA fragment purified from urine of a carcinoid tumor patient, increased concentrations were measured in 37% of patients with SCLC (27). In the present study the corresponding results using the CgA(340[right arrow]) assay were 100% (extensive disease) and 58% (limited disease), and using the CgA PIA 89% (extensive disease) and 67% (limited disease), respectively.

In a study using an antiserum raised against full-length CgA on plasma samples from 208 patients with neuroendocrine tumors, increased CgA concentrations were measured in 53% of the patients, most frequently observed in the pheochromocytoma (89%) and carcinoid tumor patients (80%) (29). In a similar study, plasma CgA was quantified with an RIA using an antiserum raised against C-terminal CgA fragments isolated from urine from a carcinoid tumor patient and a pancreastatin antiserum, respectively, and increased concentrations were measured in 99% with the CgA assay and in 46% with the pancreastatin assay (32). In a study using an antiserum raised against CgA isolated from a pheochromocytoma, plasma CgA concentrations were increased in 81% of patients with neuroendocrine tumors (1). Furthermore, with use of an immunoradiometric assay increased concentrations were found in 63% of patients with gastroenteropancreatic endocrine tumors (26).

Comparison of the diagnostic sensitivities obtained with the CgA assays referred to above and the results on the CgA(340[right arrow]) assay and the CgA PIA reported in this study shows that both are particularly potent and sensitive tools in the diagnosis of neuroendocrine tumors and SCLC. Whether one of the 2 assays is superior to the other requires analysis on a larger patient population. Both the CgA(340[right arrow]) assay and the CgA PIA results increased with the degree of metastatic disease and may thus reflect tumor burden. The diagnostic sensitivities generally increased with the degree of metastatic disease. However, for the CgA(340[right arrow]) assay the sensitivity was very high in the patients with gastrointestinal tumors, irrespective of dissemination. Further study is required to determine whether a low degree of CgA processing is a predictor of malignancy.

This study was supported by grants from the Danish Medical Research Council, the Danish Biotechnology Program for Cellular Communication, and the Danish Cancer Union.

We thank Drs. Jens Gustafsen and Ulrich Knigge, Department of Surgical Gastroenterology, and Dr. Jorgen Kvist Kristensen, Department of Urology, Rigshospitalet, University of Copenhagen; Dr. Niels Juel Christensen, Department of Endocrinology, KAS Herlev University of Copenhagen for providing the tissue and plasma samples; and Jane Lancaster and Joan Christiansen for technical assistance. Dr. Ruth Frikke-Schmidt, Department of Clinical Biochemisty, Rigshospitalet and statisticians at the Department of Biostatistics, University of Copenhagen are thanked for statistical assistance.

Received July 10, 2006; accepted December 29, 2006. Previously published online at DOI: 10.1373/clinchem.2006.076158


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[3] Nonstandard abbreviations: CgA, chromogranin A; PIA, processing-independent analysis; SCLC, small-cell lung carcinoma; Kds, coefficients of distribution; and CI, confidence interval.


[1] University Department of Clinical Biochemistry, Rigshospitalet, Copenhagen, Denmark.

[2] Department of Oncology, Storstrommens Sygehus Naestved, Denmark.

* Address correspondence to this author at: Department of Clinical Biochemistry KB, Rigshospitalet, 9 Blegdamsvej, DK-2100 Copenhagen O, Denmark. Fax 45-35-45-46-40; e-mail
Table 1. Characteristics of tumor patients and healthy controls.

 Gastrointestinal tumors Pheochromocytomas

n 27 6
Age, years 60 (57-70) (a) 42 (36-49) (a)
Female, n (%) 12 (44) 5 (83)
Severity of disease, n Local disease, (b) 3 Local disease, (a) 6
 Ext. disease, (d) 16
 Very ext. disease, (e) 8

 SCLC Healthy controls

n 21 88
Age, years 65 (57-68) (a) 41 (30-51) (a)
Female, n (%) 9 (43) 44 (50)
Severity of disease, n Local disease, (c) 12
 Ext. disease, 9

(a) Data are given as median (IQR).

(b) Disease without known liver/lymph node

(c) Disease confined to 1 hemithorax excluding
proven malignant effusion and chest wall metastases.

(d) Extensive disease: liver/lymph node metastases.

(e) Arbitrarily defined as either several large
metastases or multiple smaller metastases in the liver.

Table 2. Concentrations measured in plasma samples
from tumor patients with local and extensive disease.

Tumor CgA(340 CgA(340 CgA(340[right
 [right arrow]) [right arrow]) arrow]) +
 pmol/L trypsin trypsin/
 pmol/L CgA(3403)

GI NE tumors
 All 720 4200 7
 (n = 27) (287-2947) (1400-25 200) (4-15)
 1. Local 140a 900b 6 (c)
 (n = 3) (140-840)d (890-4200)d (5-6) (d)
 2. Extensive 335a 2255b 7 (c)
 (n = 16) (222-2012) (1390-10 860) (4-8)
 3. Very extensive 4450a 102 050b 16 (c)
 (n = 8) (2235-11 650) (20 767-276 500) (12-21)
 1. Local 380 2750 7
 (n = 6) (262-650) (1110-10 850) (3-24)
 All 300 2215 10
 (n = 21) (130-440) (1117-8535) (8-18)
 1. Local 150e 1820f 9
 (n = 12) (120-325) (1037-2278) (7-18)
2. Extensive 480e 7150f 11
 (n = 9) (245-825) (2840-10 850) (9-16)
Healthy volunteers 60 510 9
 (n = 88) (48-78) (420-660) (6-11)

Results are given as median (IQR) exceptd
where results are median (range) due to n = 3.
Gastrointestinal neuroendocrine (GI NE) tumors:

3 (a) Significantly different from: 2 (a)
(P = 0.009), 1 (a) and 2 (a) (P = 0.005),
1 (a)(P = 0.02).

3 (b) Significantly different from: 2 (b)
(P = 0.001), 1 (b) and 2 (b) (P = 0.001),
1 (b)(P = 0.01).

3 (c) Significantly different from: 2 (c)
(P = 0.001), 1 (c) and 2 (c) (P = 0.001),
1 (c)(P = 0.01).

2 (e) Significantly different
from 1 (e) (P = 0.01).

2 (f) Borderline significantly different
from 1 (f) (P = 0.06)

Table 3. Concentrations measured with the index
test (CgA PIA) and 3 sequence-specific CgA assays
in plasma samples from tumor patients with established
histopathological diagnosis (reference standard).

 Reference standard

 (n = 22)

Index test CgA(340[right arrow]) 3730 (c)
(CgA PIA) + trypsin (b) (1390-23 200) (d)
Sequence-specific CgA(1[right arrow]) 698
 CgA assays (383-2825)
 CgA([left arrow]301) 34
 CgA(340[right arrow]) 620

 Reference standard

 Other GI NE
 tumors (a)
 (n = 5)

Index test CgA(340[right arrow]) 9050
(CgA PIA) + trypsin (b) (1370-102 050)
Sequence-specific CgA(1[right arrow]) 780
 CgA assays (523-7875)
 CgA([left arrow]301) 12
 CgA(340[right arrow]) 1170

 Reference standard

 (n = 6)

Index test CgA(340[right arrow]) 2750
(CgA PIA) + trypsin (b) (1110-10 850)
Sequence-specific CgA(1[right arrow]) 840
 CgA assays (590-1503)
 CgA([left arrow]301) 15
 CgA(340[right arrow]) 380

 Reference standard

 (n = 21)

Index test CgA(340[right arrow]) 2215
(CgA PIA) + trypsin (b) (1117-8535)
Sequence-specific CgA(1[right arrow]) 610
 CgA assays (503-1025)
 CgA([left arrow]301) 16
 CgA(340[right arrow]) 300

(a) GI NE, gastrointestinal neuroendocrine.

(b) Plasma samples were incubated with trypsin
prior to CgA(3403) assay, as described in the text.

(c) All results are given in pmol/L.

(d) Results are given as median (IQR).

Table 4A. Diagnostic sensitivity obtained with the
index test (CgA PIA) and 3 sequence-specific CgA
assays for different tumor types.

 All tumors Carcinoid
 (n = 54) (n = 22)

Index test CgA(3403) 0.82 0.86
(CgA PIA) + trypsin (a) (0.69-0.91) (0.65-0.97)
 44/54 (b) 19/22
Sequence-specific CgA(1[right arrow]) 0.46 0.50
 CgA assays (0.33-0.60) (0.28-0.72)
 25/54 11/22
 CgA([left arrow]301) 0.54 0.59
 (0.40-0.67) (0.36-0.79)
 29/54 13/22
 CgA(340[right arrow]) 0.91 1.00
 (0.80-0.97) (0.85-1.00)
 49/54 22/22

 Other GI Pheochromo
 NE tumors cytoma
 (n = 5) (n = 6)

Index test CgA(3403) 0.8 0.83
(CgA PIA) + trypsin (a) (0.28-1.00) (0.36-1.00)
 4/5 5/6
Sequence-specific CgA(1[right arrow]) 0.60 0.67
 CgA assays (0.15-0.95) (0.22-0.96)
 3/5 4/6
 CgA([left arrow]301) 0.40 0.50
 (0.05-0.85) (0.12-0.88)
 2/5 3/6
 CgA(340[right arrow]) 1.00 1.00
 (0.48-1.00) (0.54-1.00)
 5/5 6/6

 (n = 21)

Index test CgA(3403) 0.76
(CgA PIA) + trypsin (a) (0.53-0.92)
Sequence-specific CgA(1[right arrow]) 0.33
 CgA assays (0.15-0.60)
 CgA([left arrow]301) 0.52
 CgA(340[right arrow]) 0.76

Table 4B. Diagnostic sensitivity obtained with the index
test (CgA PIA) and 3 sequence-specific CgA assays, related
to dissemination of disease.

 GI NE tumors (c)

 (n = 3)

Index test CgA(340[right arrow]) 0.33 (0.01-0.91)
(CgA PIA) + trypsin (a) 1/3 (b)
Sequence-specific CgA(1[right arrow]) 0.00 (0.00-0.71)
 CgA assays 0/3
 CgA([left arrow]301) 0.33 (0.01-0.91)
 CgA(340[right arrow]) 1.00 (0.29-1.00)

 GI NE tumors (c)

 (n = 16)

Index test CgA(340[right arrow]) 0.88 (0.62-0.98)
(CgA PIA) + trypsin (a) 14/16
Sequence-specific CgA(1[right arrow]) 0.38 (0.15-0.65)
 CgA assays 6/16
 CgA([left arrow]301) 0.56 (0.30-0.80)
 CgA(340[right arrow]) 1.00 (0.79-1.00)

 GI NE tumors (c)

 Very extensive
 (n = 8)

Index test CgA(340[right arrow]) 1.00 (0.63-1.00)
(CgA PIA) + trypsin (a) 8/8
Sequence-specific CgA(1[right arrow]) 1.00 (0.63-1.00)
 CgA assays 8/8
 CgA([left arrow]301) 0.63 (0.24-0.91)
 CgA(340[right arrow]) 1.00 (0.63-1.00)

 SCLC (d)

 (n = 12)

Index test CgA(340[right arrow]) 0.67 (0.35-0.90)
(CgA PIA) + trypsin (a) 8/12
Sequence-specific CgA(1[right arrow]) 0.17 (0.02-0.48)
 CgA assays 2/12
 CgA([left arrow]301) 0.42 (0.15-0.72)
 CgA(340[right arrow]) 0.58 (0.28-0.85)

 SCLC (d)

 (n = 9)

Index test CgA(340[right arrow]) 0.89 (0.52-1.00)
(CgA PIA) + trypsin (a) 8/9
Sequence-specific CgA(1[right arrow]) 0.55 (0.21-0.86)
 CgA assays 5/9
 CgA([left arrow]301) 0.67 (0.30-0.93)
 CgA(340[right arrow]) 1.00 (0.66-1.00)

(a) Plasma samples were incubated with trypsin
prior to CgA(3403) assay, as described in
the text.

(b) Results are given as diagnostic sensitivity
(95% CI) as well as the number of results above
upper reference interval limit vs the total number
of results.

(c) GI NE (gastrointestinal neuroendocrine) tumors:
The diagnostic sensitivities obtained with the CgA(13)
assay and CgA PIA were significantly different for the
local, extensive, and very extensive tumors (P = 0.002)
and (P = 0.04).

(d) SCLC: The diagnostic sensitivities obtained with
the CgA(340[right arrow]) assay were significantly
different for the local and extensive SCLC (P = 0.045).
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Title Annotation:Cancer Diagnostics
Author:Borglum, Tine; Rehfeld, Jens F.; Drivsholm, Lars B.; Hilsted, Linda
Publication:Clinical Chemistry
Date:Mar 1, 2007
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