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. Author manuscript; available in PMC: 2019 Feb 11.
Published in final edited form as: Sci Transl Med. 2013 Oct 23;5(208):208ra147. doi: 10.1126/scitranslmed.3006941

Table 1.

Patient demographics, treatment received, and clinical outcome. M, male; F, female; PR, partial response; SD, stable disease; PD, progressive disease.

Patient Age (years)/
sex
Tumor
site*
Tumor
mesothelin
expression
No. of
previous
therapies
No. of SS1P
cycles
received
Overall
tumor
response
Delayed tumor
response§
Post-study
chemotherapy
Response to
post-study
chemotherapy
Overall
survival
(months)
2 50/M Peritoneum 100%, 3+ 2 2 PR (−44%) Yes (7 months) 18.2+
3 56/F Pleura 100%, 3+ 2 6 PR (−74%) 17.1+
4 67/F Pleura 100%, 3+ 3 2 SD Yes PR (−55%) 14
5 51/M Peritoneum 100%, 3+ 4 4 PR (−70%) 14.5+
6 43/M Pleura 100%, 3+ 4 2 SD 8.8
7 48/F Pleura 90%, 3+ 2 2 PD 6.2
8 60/M Pleura 100%, 2+ 6 2 PD 5.7
9 52/F Pleura 70%, 2+ 5 2 PD Yes (4 months) Yes 85% decrease in tumor FDG uptake** 10.6+
10 62/M Pleura 30%, 2+ 2 2 PD 4.2
11 65/M Pleura 50%, 3+ 1 2 SD Yes No 7.3
*

All patients had epithelial-type mesothelioma.

Mesothelin expression was determined by immunohistochemistry and presented as percentage of positive cells, and the degree of staining intensity (absent; 1+, mild; 2+, moderate; or 3+, strong) is shown.

For patients with tumor response, the percent decrease in the sum of target lesions is shown.

§

Months from study initiation to the time when response was first observed.

Patient 8 had progressive disease due to new brain metastasis but had a 10% reduction in target lesions.

Patient 9 had initial progressive disease but, at 4 months, had a 25% reduction in size of one of the target lesions and a marked decrease in metabolic activity by PET.

**

Patient 9 had an 85% reduction in tumor SULpeak/cm3 compared to baseline PET scan and stable disease by CT scan on post-study chemotherapy.