Table 1.

Characteristics and responses of initial patients with measurable disease (n = 10)

PatientAge/
sex
HistologyPrior therapiesSites of diseaseTotal DCs given*Anti-Id responsesClinical response, time to progressionCurrent status, subsequent therapies, months since DC vaccine
T cellAb
D1 59/F FM Chl, ChlVB Paracardiac, mediastinal 69 × 106 − CR, 44 months RD after CHOP, rituximab, XRT, fludarabine, repeat DC vaccine, 94 mos 
D2 44/F FM Chl, CVP Peri-aortic, para-iliac 22 × 106 − PR, 12 months NED after Id-KLH/SAF,1-153 fludarabine, 83 mos 
D3 34/F F/DSC CVP, fludarabine BM 14 × 106  Cleared BM PCR signal NED 79 mos after DC vaccine without subsequent therapies  
D4 45/M FSC CVP, fludarabine Cervical, axillary, peri-aortic, iliac, inguinal 16 × 106 − PD at 10 mos NED after MINE, rituximab, 69 mos  
D5 50/F FM CVP, fludarabine Peri-aortic, BM 23 × 106 − PD at 7 mos NED after Id-KLH/SAF,1-153 rituximab, 65 mos 
D6 47/M FSC Chl, CHOP Peri-aortic, spleen, mesenteric 22 × 106 − PD at 12 mos RD after Id-KLH/SAF,1-153 rituximab, XRT, 63 mos 
D7 43/F FSC CHOP Axillary, mesenteric 27 × 106 − PD at 9 mos MRD after rituximab, 58 mos  
D8 40/M FSC CVP, XRT, CEP, fludarabine Axillary, peri-aortic 10 × 106  PD at 5 mos NED after Id-KLH/SAF,1-153 57 mos 
D9 43/F FSC Chl, Id-KLH/SAF Axillary, iliac, peri-aortic 13 × 106 − − CR, 57 mos PD at single site 57 mos after DC vaccine  
D10 51/F FM CVP, fludarabine, CHOP Axillary, spleen 12 × 106 − − PD at 7 mos NED after Id-KLH/SAF,1-153 tositumomab, 47 mos 
PatientAge/
sex
HistologyPrior therapiesSites of diseaseTotal DCs given*Anti-Id responsesClinical response, time to progressionCurrent status, subsequent therapies, months since DC vaccine
T cellAb
D1 59/F FM Chl, ChlVB Paracardiac, mediastinal 69 × 106 − CR, 44 months RD after CHOP, rituximab, XRT, fludarabine, repeat DC vaccine, 94 mos 
D2 44/F FM Chl, CVP Peri-aortic, para-iliac 22 × 106 − PR, 12 months NED after Id-KLH/SAF,1-153 fludarabine, 83 mos 
D3 34/F F/DSC CVP, fludarabine BM 14 × 106  Cleared BM PCR signal NED 79 mos after DC vaccine without subsequent therapies  
D4 45/M FSC CVP, fludarabine Cervical, axillary, peri-aortic, iliac, inguinal 16 × 106 − PD at 10 mos NED after MINE, rituximab, 69 mos  
D5 50/F FM CVP, fludarabine Peri-aortic, BM 23 × 106 − PD at 7 mos NED after Id-KLH/SAF,1-153 rituximab, 65 mos 
D6 47/M FSC Chl, CHOP Peri-aortic, spleen, mesenteric 22 × 106 − PD at 12 mos RD after Id-KLH/SAF,1-153 rituximab, XRT, 63 mos 
D7 43/F FSC CHOP Axillary, mesenteric 27 × 106 − PD at 9 mos MRD after rituximab, 58 mos  
D8 40/M FSC CVP, XRT, CEP, fludarabine Axillary, peri-aortic 10 × 106  PD at 5 mos NED after Id-KLH/SAF,1-153 57 mos 
D9 43/F FSC Chl, Id-KLH/SAF Axillary, iliac, peri-aortic 13 × 106 − − CR, 57 mos PD at single site 57 mos after DC vaccine  
D10 51/F FM CVP, fludarabine, CHOP Axillary, spleen 12 × 106 − − PD at 7 mos NED after Id-KLH/SAF,1-153 tositumomab, 47 mos 

FSC indicates follicular small cleaved cell; FM, follicular mixed small cleaved and large cell; F/DSC, follicular and diffuse small cleaved cell; Chl, chlorambucil; ChlVB, chlorambucil, vincristine, and bleomycin; CVP, cyclophosphamide, vincristine, and prednisone; CHOP, cyclophosphamide, adriamycin, vincristine, and prednisone; CEP, cyclophosphamide, etoposide, and prednisone; Id-KLH/SAF, Id protein coupled to KLH plus Syntex adjuvant formulation; XRT, radiation therapy; MINE, mesna, ifosfamide, mitoxantrone, etoposide; PD, progressive disease; NED, no clinical evidence of disease; MRD, minimum residual disease; RD, residual disease; Ab, antibody; BM, bone marrow.

*

Total number of DCs infused over the course of 4 vaccinations.

Previously reported in original pilot study.22 

IgM, but not IgG anti-Id antibodies detectable in serum.

F1-153

Revaccinated with Id-KLH plus SAF adjuvant. See Table 3.

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