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. 2017 May 24;12(5):e0177986. doi: 10.1371/journal.pone.0177986

Table 2. Characteristics of excluded studies.

Reference N Study type Age mean (range) % male Tumor locations Treatment Selection Reference standard definition tumor MRI sequences
Field strength; sequence orientation slice thickness/ gap in mm (TR/TE in ms); b values and DWI analysis method
Time point MRI Diagnostic accuracy TP FP FN TN
Chen et al., 2014 31 Pros 45 (18–68) 84 Primary site and LN of 31 nasopharynx 29 CCRT; 2 RT All patients with no prior treatment stage III/IV. Excluded if distant metastases before treatment (N = 4) or MRI artefact (N = 2) Imaging follow-up according to RECIST 1.1 and residual disease was classified by residual soft tissues or thickening of the mucous membrane of the nasopharynx with local bulges aMRI; 3.0 T; T1 fs tra, sag; T2 tra 5/1; T1C fs tra, cor
DWI; 3.0 T; 5/1 (6600/70); b 0, 800; ROI
3 days after start treatment;
20 days after start treatment; 50 days after start treatment
ADC primary
ADC LN
ADC primary
ADC LN
ADC primary
ADC LN




















Galbán et al., 2009 15 Pros Primary site (12) and LN (14) of head and neck 15 CCRT All patients for CCRT. Exclusion if claustrophobic (N = 2), metal implants (N = 2), withdrew from study (N = 3), inadequate DWI (N = 1). Histology or imaging 2 mo after end treatment and clinical outcome at 6 mo. aMRI; 3.0 T; T1; 1/0 (9.9/4.6); T2 fs 4/- (5000/120); T1C; 1/0 (9.9/4.6)
DWI; 3.0 T; 4/- (2789/59); b 0, 800; ROI
3 weeks after start treatment ADC primary
ADC LN
aMRI primary
(Δvolume %)
aMRI LN
(Δvolume %)












Kim et al., 2009 33 Pros 61 (31–78) 79 LN of 11 base of tongue; 10 tonsil; 6 larynx; 1 vallecula; 5 unknown 24 CCRT; 7 RT + immune-therapy All head/neck cancers with preoperative CCRT and with metastatic lymph nodes. Excluded if death unrelated to treatment (N = 4), claustrophobia (N = 1), withdraw (N = 1) or artefact on DWI (N = 1) Histology or 6 mo clinical/ imaging follow-up aMRI; 1.5–3.0 T; T1 tra (600/10); T1C; tra (300/4); T2 tra 5/- (4000/120) and (2000/13, 53, 80, 110);
DWI; 1.5-3T; 5/- (40000/89); b 0, 500, 1000; ROI
1 week after start treatment;
2 weeks after end treatment
ADC LN
aMRI LN
T2
volume
ADC LN
aMRI LN
T2
volume




















King et al., 2010 50 Pros 58 (45–73) 90 Primary site of 9 oral cavity/ oropharynx; 13 hypopharynx; 4 larynx; 1 maxillary sinus; 2 nasal cavity; and 21 LN of not described primary 44 CCRT; 6 RT All biopsy proven tumors with curative intent of CCRT or RT with stage III or IV. Excluded in no consent (N = 14), artefacts (N = 10) or death before definitive diagnosis (N = 4) Histology for the primary site and histology or increase in size on serial imaging follow-up >12 mo for lymph nodes; fall in ADC as local failure aMRI; 1.5 T; T1; T2; T1C.
DWI; 1.5 T; fs tra; 4/0 (2000/75); b 0, 100, 200, 300, 400, 500; ROI
6 weeks after end treatment; Primary/LN
ADC 1.4
6 0 1 13
Lell et al., 2000 39 Primary site of 21 oropharynx, oral cavity; 1 naso-pharynx; 17 hypo-pharynx, larynx CCRT Locally advanced tumor with CCRT Histology or clinical follow-up with MRI-based tumor recurrence classified as a localized expansive mass with intermediate signal on T1 and high on T2 with marked enhancement aMRI; 1.5 T; T1 tra, cor 6/0.6 (500-600/20-30); T2 tra 6/0.6 (2500-3500/30-100); T1C tra,cor 6/0.6 (500-600/20-30); IR cor 6/0.6 (1400/30) <3 mo after treatment end;
3–6 mo after treatment end
aMRI primary
aMRI primary
13
5


11
7
Matoba et al., 2014 35 Pros 66 (33–79) 86 Primary site and LN of 4 oral cavity; 9 oropharynx; 9 hypopharyx; 10 larynx; 3 supraglottic 35 CCRT All patients treated with CCRT with curative intent. Excluded if patient refuse treatment (N = 2), poor imaging quality (N = 2) or death within 3 mo after treatment (N = 1) Imaging follow-up every 6 mo with increasing mass or histology proof as indication of tumor recurrence aMRI; 1.5 T; T1 tra (630/12); T2 tra, cor (4000/90);
DWI; 1.5 T; fs tra 6/3 (4000/68); b 0, 90, 800
3 weeks after start treatment ADC primary ΔADC 0.24
ADC
ADC LN
ΔADC 0.24
ADC
aMRI primary
Δvolume
aMRI LN
Δvolume
























Mukundan et al., 2014 50 Pros 56 80 Primary site of 50 head and neck 11 OP; 26 RT; 13 OP + RT All patients with treatment without previous treatment and no significant comorbidity Histology aMRI; 1.5 T; T1 with and without fs 3-4/0-1; T2 3-4/0-1; T1C fs 3-4/0-1 12 weeks after end treatment;
24 weeks after end treatment
aMRI primary
aMRI primary




Characteristics of the 7 excluded studies are shown. See Table 1 for abbreviations.