Table 2.

Development of GVHD after HCT and clinical response


ID no.

Previous therapies

GVHD grade

GVHD site

GVHD, d

CSA stop, d

GVHD treatment

CEA before transplantation/at GVHD onset or d + 100, ng/mL

CEA expression by tumor cells*

Clinical response

HLA-A*0201
GVHD involvement           
   1   De Gramont, Tomudex, FOLFOX, CPT-11, MMC   II   GI   49   150   PDN   110/160   ND   SD  NEG  
   2   5FU-VP 16, liver surgery, FOLFOX   III   GI   110   94   CSA + PDN   2/6  ND   MR   NEG  
   4   FOLFIRI, FOLFOX   II   Skin, GI, liver   41   180   PDN   8/9   ND   None   NEG  
   8   FOLFOX, FOLFIRI, De Gramont, MMC   IV   GI, liver   88   86   CSA + PDN, infiximab   2/3   +++   SD  POS  
   10   FOLFOX, liver surgery   III   Skin, GI   121   110   CSA + PDN, infliximab   56/480   ++   None   NEG  
   11   FOLFOX, liver surgery, FOLFIRI   II   GI, liver   210   140   CSA   607/61   +++   PR   POS  
   12   FOLFOX, surgery, FOLFIRI   III   Skin, GI   120   100   PDN + CSA   18/36   +++   None   POS  
   15   FOLFIRI, CPT-11, 5FU, MMC, cetuximab   II   Skin, GI   51   NA   PDN   2112/1800   ND   None   NEG  
No GVHD involvement           
   3   FOLFOX, liver surgery   0   NA   NA   91   NA   90/100   ND   None   POS  
   5   FOLFOX   0   NA   NA   118   NA   8/9   ++   SD  NEG  
   6   FOLFIRI, FOLFIRI   0   NA   NA   85   NA   365/780   ND   None   NEG  
   7   FOLFIRI, FOLFOX   0   NA   NA   NA   NA   90/170   ND   None   POS  
   9   FOLFOX   0   NA   NA   90   NA   1/2   ++   None   POS  
   13   FOLFOX, FOLFIRI, liver criosurgery, MMC   0   NA   NA   88   NA   370/ND   ND   None   NEG  
   14
 
FOLFOX, FOLFIRI, De Gramont
 
0
 
NA
 
NA
 
NA
 
NA
 
2380/ND
 
ND
 
None
 
NEG
 

ID no.

Previous therapies

GVHD grade

GVHD site

GVHD, d

CSA stop, d

GVHD treatment

CEA before transplantation/at GVHD onset or d + 100, ng/mL

CEA expression by tumor cells*

Clinical response

HLA-A*0201
GVHD involvement           
   1   De Gramont, Tomudex, FOLFOX, CPT-11, MMC   II   GI   49   150   PDN   110/160   ND   SD  NEG  
   2   5FU-VP 16, liver surgery, FOLFOX   III   GI   110   94   CSA + PDN   2/6  ND   MR   NEG  
   4   FOLFIRI, FOLFOX   II   Skin, GI, liver   41   180   PDN   8/9   ND   None   NEG  
   8   FOLFOX, FOLFIRI, De Gramont, MMC   IV   GI, liver   88   86   CSA + PDN, infiximab   2/3   +++   SD  POS  
   10   FOLFOX, liver surgery   III   Skin, GI   121   110   CSA + PDN, infliximab   56/480   ++   None   NEG  
   11   FOLFOX, liver surgery, FOLFIRI   II   GI, liver   210   140   CSA   607/61   +++   PR   POS  
   12   FOLFOX, surgery, FOLFIRI   III   Skin, GI   120   100   PDN + CSA   18/36   +++   None   POS  
   15   FOLFIRI, CPT-11, 5FU, MMC, cetuximab   II   Skin, GI   51   NA   PDN   2112/1800   ND   None   NEG  
No GVHD involvement           
   3   FOLFOX, liver surgery   0   NA   NA   91   NA   90/100   ND   None   POS  
   5   FOLFOX   0   NA   NA   118   NA   8/9   ++   SD  NEG  
   6   FOLFIRI, FOLFIRI   0   NA   NA   85   NA   365/780   ND   None   NEG  
   7   FOLFIRI, FOLFOX   0   NA   NA   NA   NA   90/170   ND   None   POS  
   9   FOLFOX   0   NA   NA   90   NA   1/2   ++   None   POS  
   13   FOLFOX, FOLFIRI, liver criosurgery, MMC   0   NA   NA   88   NA   370/ND   ND   None   NEG  
   14
 
FOLFOX, FOLFIRI, De Gramont
 
0
 
NA
 
NA
 
NA
 
NA
 
2380/ND
 
ND
 
None
 
NEG
 

De Gramont indicates 400 mg/m2 fluorouracil, 600 mg/m2 fluorouracil, and 200 mg/m2 leucovorin; Tomudex, 4 mg/m2; FOLFOX, 100 mg/m2 oxaliplatin, 400 mg/m2 fluorouracil, 600 mg/m2 fluorouracil, and 200 mg/m2 leucovorin; CPT-11, 100 mg/m2 Irinotecan; MMC, 10 mg/m2 mytomicin-C; 5FU/VP16, 500 mg/m2 fluorouracil, 200 mg/m2 leucovorin, and 100 mg/m2 VP 16; FOLFIRI, 180 mg/m2 irinotecan, 400 mg/m2 fluorouracil, 600 mg/m2 fluorouracil, and 200 mg/m2 leucovorin; cetuximab, 400 mg/m2 on day 1, 250 mg/m2 on days 8, 14, 21; PDN, prednisone; ND, not determined; and NA, not applicable.

*

CEA expression on tumor biopsies as detected by immunohistochemistry. ++ indicates moderately reactive; +++, strongly reactive tumor cells (“Patients, materials, and methods”)

SDs that lasted more than 90 days were considered as relevant clinical responses; short lasting stable disease were excluded

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