Table 1 Clinical data of donor patients

From: Establishment and characterization of new tumor xenografts and cancer cell lines from EBV-positive nasopharyngeal carcinoma

    

Clinical status

     

Case no.

Sex

Age

Histological diagnosisa

T

N

M

Overall staging

Sample typeb

Tumor recurrence

Tumor metastasis

History of chemotherapyc

History of RT treatment

23d

M

65

Non-keratinizing carcinoma

2

0

0

II

Nasopharyngectomized tissue

Yes

No

No

2D-RT (66 Gy in 33 fractions)

32

F

72

Undifferentiated carcinoma

3

2

0

III

Primary biopsy

No

No

ChemoRT then adjuvant chemotherapy

IMRT (70 Gy in 33 fractions)

38d

F

63

Moderately differentiated squamous cell carcinoma

2

0

0

II

Nasopharyngectomized tissue

Yes

No

No

2D-RT (66 Gy in 33 fractions)

43d

M

64

Poorly differentiated carcinoma

3

0

0

III

Nasopharyngectomized tissue

Yes

Yes

ChemoRT then adjuvant chemotherapy

2D-RT (66 Gy in 33 fractions)

47d

F

52

Undifferentiated carcinoma

3

0

0

III

Nasopharyngectomized tissue

Yes

No

ChemoRT alone

IMRT (70 Gy in 35 fractions)

53d

M

39

Undifferentiated carcinoma

4

1

0

IVA

Nasopharyngectomized tissue

Yes

No

ChemoRT alone

IMRT (70 Gy in 35 fractions)

76

F

57

Undifferentiated carcinoma

1

0

0

I

Primary biopsy

Yes

No

No

IMRT (66 Gy in 33 fractions)

  1. aHistopathological properties of the NPC from which PDXs and cell lines were successfully established (from the original report from pathologists in Queen Mary Hospital)
  2. bPatients with newly diagnosed NPC received either curative RT or ChemoRT with or without adjuvant chemotherapy at the time of diagnosis. When NPC recurred, patients received nasopharyngectomy. Therefore, primary biopsy was obtained before any treatment, while nasopharyngectomized tissue was recurrent tumor and collected after treatment
  3. cPatients who had ChemoRT received cisplatin 100 mg m−2 every 3 weeks for 3 cycles. For those who received adjuvant chemotherapy after ChemoRT, they received cisplatin 80 mg m−2 and 5-FU 1000 mg m−2 every 4 weeks for 3 more cycles
  4. dPatients who did not survive by 30 June 2018