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Table 2 The characteristics of patients with ROS1 rearrangement

From: Comparison of detection methods and follow-up study on the tyrosine kinase inhibitors therapy in non-small cell lung cancer patients with ROS1 fusion rearrangement

Cases No.

Smokinga

Staging/Gradingb

IHC resultc

H-score

FISH result

Direct sequencing

Histopathology predominant pattern

Staining Pattern

Another gene aberranced

1

N

II B/

Score 5/Grade 2

3+/90 %

260

Fusion positive

SLC34A2-E4; ROS1-E32/SLC34A2-E4; ROS1-E34

Acinar

Cytoplasmic; membrane

ALK\EGFR\KRAS(−)

2

N

I A/Score 3/Grade 2/

2+/65 %

150

Fusion positive

CD74-E6; ROS1-E34

Acinar

Cytoplasmic; focal granular

ALK\EGFR\KRAS(−)

3

P

IV/−/−

2+/70 %

160

Fusion positive

CD74-E6; ROS1-E34

Invasive mucinous adenocarcinoma

Mucinous staining

ALK\EGFR\KRAS(−)

4

N

I A/Score 5/Grade 2

2+/90 %

200

Fusion positive

TPM3-E8; ROS1-E35

Papillary and acinar

Cytoplasmic; focal granular

ALK\EGFR\KRAS(−)

5

N

I A/Socre 5/Grade 3

2+/90 %

200

Fusion positive

SLC34A2-E14del; ROS1-E32/SLC34A2-E14del; ROS1-E34

Papillary and micropapillary

Cytoplasmic; focal granular

ALK\EGFR\KRAS(−)

6

N

IV/ Socre4/Grade 2

3+/85 %

250

Fusion positive

CD74-E6; ROS-E34

Acinar

Cytoplasmic; granular

ALK\EGFR\KRAS(−)

7e

N

IV/−/−

2+/70 %

160

Fusion positive

Invasive adenocarcinoma with acinar pattern

Cytoplasmic; focal granular

ALK\EGFR\KRAS(−)

8

S

I A/Score 5/Grade 3

3+/90 %

250

Fusion positive

Papillary and micropapillary

Cytoplasmic; focal granular

ALK\EGFR\KRAS(−)

9

S

I B/Socre 3/Grade 2

2+/80 %

180

Fusion positive

Acinar and lepidic

Cytoplasmic; focal granular

ALK\EGFR\KRAS(−)

10

N

I B/Score 3/Grade 1

2+/80 %

180

Fusion positive

Lepidic

Cytoplasmic; focal granular

ALK\EGFR\KRAS(−)

  1. a N, non-smoker; S, smoker; P, previous smoker
  2. bTNM staging, SICA grading and WHO grading
  3. cIHC results were containing intensity and extent scores
  4. dALK rearrangement, EGFR and KRAS mutation have been also investigated at the sme time. The cases harboring ROS1 rearrangement were exclusive to ALK rearrangement, EGFR and KRAS mutation
  5. ecases 7 was biopsy sample