Skip to main content

Table 2 Summary of major antibody–drug conjugates in R/R DLBCLs and NHLs

From: The progress of novel strategies on immune-based therapy in relapsed or refractory diffuse large B-cell lymphoma

Medicine name

Targets

Study

Patients

Treatment

Responses

Lonca

CD19

Phase II LOTIS-2 trial (NCT03589469)

R/R DLBCL (NOS), HGBCL, PMBCL

Monotherapy

ORR/CRR: 48.3% (70/145)/24.1% (35/145)

Median DOR/PFS/OS: 10.3/4.9/9.9 mo

Phase II LOTIS-3 trial (NCT03684694)

Advanced DLBCL

Lonca plus ibrutinib

ORR/CRR in total: 57.1% (20/35)/34.3% (12/35)

ORR/CRR in GCB: 76.9% (10/13)/46.2% (6/13)

ORR/CRR in non-GCB: 45.5% (10/22)/27.3% (6/22)

Median DOR: 5.49 mo (NR in both GCB and non-GCB)

SAR3419

CD19

Phase II (NCT01472887)

R/R DLBCL

Monotherapy

ORR/CRR in total: 43.9% (18/41)/14.6% (6/41)

ORR/CRR in refractory to last regimen: 26.7% (4/15)/6.7% (1/15)

ORR/CRR in relapsed DLBCL: 53.8% (14/26)/19.2% (5/26)

ORR/CRR in primary refractory: 21.4% (3/14)/7.1% (1/14)

median DOR/PFS/OS: 4.7/4.4/9.2 mo

BV

CD30

Phase II (NCT01421667)

DLBCL, other B-cell NHL

Monotherapy

ORR/CRR in total DLBCL: 44% (21/44)/17% (8/48)

ORR/CRR in refractory DLBCL: 44% (17/39)/15% (6/39)

ORR/CRR in relapsed DLBCL: 38% (3/8)/25% (2/8)

ORR/CRR in other B-cell NHL: 26% (5/19) 16% (3/19)

Phase I (NCT02086604)

R/R DLBCL

BV plus Len

ORR/CRR in CD30+/GCB, 87.5% (7/8)/50% (4/8)

ORR/CRR in CD30−/GCB, 25% (3/12)/17% (2/12)

ORR/CRR in CD30+/non-GCB, 57% (4/7)29% (2/7)

ORR/CRR in CD30−/non-GCB, 70% (7/10)/50% (5/10)

median PFS/ OS in total, 10.2/14.3 mo

Phase III (NCT04404283)

R/R DLBCL

BV plus R2

Clinical trials ongoing

Pina

CD22

Phase II ROMULUS trial (NCT01691898)

R/R DLBCL

R/R FL

R-Pina

ORR/CRR in R/R DLBCL, 60% (25/42)/26% (11/42)

ORR/CRR in R/R FL, 62% (13/21)/5% (1/21)

Median DOR/PFS/OS of R/R DLBCL, 6.2/5.4/16.5 mo

Median DOR/PFS/OS of R/R FL, 6.5/12.7/NR mo

Pola

CD79b

Phase II ROMULUS trial (NCT01691898)

R/R DLBCL

R/R FL

R-Pola

ORR/CRR in R/R DLBCL, 54% (21/39)/21% (8/39)

ORR/CRR in R/R FL, 70% (14/20)/45% (9/20)

Median DOR/PFS/OS of R/R DLBCL, 13.4/5.6/20.1 mo

Median DOR/PFS/OS of R/R FL, 9.4/15.3/NR mo

Phase II DCDS4501A trial

(NCT02257567)

R/R DLBCL

R/R FL

Pola-BR vs. BR

Best responses (INV)

ORR, 70% (28/40) vs. 32.5% (13/40)

CRR, 57.5% (23/40) vs. 20% (8/40)

Median DOR/PFS/OS: 10.3 VS. 4.1 mo/7.6 vs. 2.0 mo/12.4 vs. 4.7 mo

Phase Ib/II (NCT02600897)

R/R DLBCL

Pola-R-Len

Best responses (INV)

ORR/CRR, 74% (36/49)/35% (17/49)

Median DOR/PFS/OS, 8.1/6.3/10.9 mo

Phase Ib/II (NCT02611323)

R/R DLBCL

Pola-Ven-R

Best responses (INV)

ORR/CRR, 65% (31/48)/38% (18/48)

Median DOR/PFS/OS, 5.8/4.4/11.1 mon

Phase III POLARGO trial

(NCT04182204)

R/R DLBCL

Pola-R-GemOx vs. R-GemOx

Clinical trials ongoing

  1. R/R relapsed/refractory, DLBCL diffuse large B-cell lymphoma, NHL non-Hodgkin lymphoma, Lonca loncastuximab tesirine, SAR3419 coltuximab ravtansine, BV brentuximab vedotin, Pina pinatuzumab vedotin, Pola polatuzumab vedotin, NOS not otherwise specified, HGBCL high-grade B-cell lymphoma, PMBCL primary mediastinal large B-cell lymphoma, FL follicular lymphoma, Len lenalidomide, R2 rituximab + lenalidomide, Ven venetoclax, GemOx rituximab, gemcitabine, and oxaliplatin, GCB germinal center B-cell, ORR overall response rate, CRR complete response rate, mDOR median duration of response, mOS median overall survival, mPFS median progression-free survival, NR not reached, INV investigator, mo months