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Table 1 Patient characteristicsa

From: Treatment of gastrointestinal stromal tumours in paediatric and young adult patients with sunitinib: a multicentre case series

 

Site of primary (P) and metastases (M)

Prior treatment

Morphology

Multifocal (MF)

Tumour size

Mitotic index (MI)

KIT/PDGFRA mutation status

Other clinical features of particular relevance

Patient A

P – Stomach

M – Liver

R2 surgery, imatinib

Epithelioid

MF- Yes

11.0 cm

MI >10/50 HPF

Both WT

GI bleeding, palpable tumour

Patient B

P – Stomach

M– Liver

– IP cavity

R2 surgery then imatinib after recurrence

Mixed

MF –no

3.0 cm

MI 6/50 HPF

Both WT

GI bleeding

Patient C

P – Stomach

M – Liver

– IP Cavity

R2 surgery, imatinib

Epithellioid

MF – yes

6.0 cm

MI NA

Both WT

GI bleeding

Patient D

P – Stomach

– IP cavity

R2 surgery, imatinib

Mixed

MF – yes

11.0 cm

MI 05/50 HPF

Both WT

GI bleeding

Patient E

P – Stomach

M – Omentum

Surgery, imatinib at first progression

Mixed

MF – Yes

7.0 cm

10/50 HPF

Both WT

GI bleeding from tumour

Patient F

P – Stomach

M – None

Surgery at diagnosis and recurrence

Epithelioid

MF – No

4.5 cm

MI 50//10 HPF

Both WT

Pain, nausea, vomiting, GI bleeding from tumour

Patient G

P – Stomach

M – None

Surgery

Mixed

MF – No

10.0 cm

MI 17/50 HPF

Both WT

Abdominal pain

Patient H

P – Stomach

M – Liver

– IP cavity

Imatinib

Spindle

MF-yes

NA

MI 1/20 HP

Both WT

Marked anaemia

Patient I

P – Stomach

M – Liver

Surgery, imatinib

Spindle

MF-no

3 cm

MI 20/50 HPF

Both WT

Melaena and anaemia

  1. aTo maintain patient anonymity individual data relating to age, gender, height, bodyweight, date of diagnosis, age at diagnosis and start of sunitinib therapy are summarised in the results section
  2. HPF = high powered field; GI = gastrointestinal; IP = intraperitoneal; NA = not available; R2 = macroscopic residual tumour on resection; WT = wild type