Table 1.

Baseline features, major outcomes, and events after first-line therapy in 862 patients participating in the PETAL trial

All patientsDLBCL PMBCLFL grade 3 Other aNHL ALK+ ALCLALK- PTCL§ No aNHL 
Number of patients 862 (100.0) 623 (72.3) 42 (4.9) 54 (6.3) 43 (5.0) 21 (2.4) 55 (6.4) 24 (2.7) 
Baseline features at study inclusion 
Age, y (range) 60 (18-80) 62 (18-80) 35 (18-80) 58 (29-80) 61 (28-76) 33 (19-66) 65 (26-79) 62 (21-79) 
International Prognostic Index risk group       
Low 329 (38.3) 228 (36.7) 25 (59.5) 26 (48.2) 9 (20.9) 16 (76.2) 18 (32.7) 7 (31.8) 
Low-intermediate 224 (26.1) 163 (26.3) 9 (21.4) 14 (25.9) 10 (23.3) 5 (23.8) 15 (27.3) 8 (36.4) 
High-intermediate 180 (21.0) 130 (20.9) 5 (11.9) 10 (18.5) 17 (39.5) 0 (0.0) 15 (27.3) 3 (13.6) 
High 125 (14.6) 100 (16.1) 3 (7.2) 4 (7.4) 7 (16.3) 0 (0.0) 7 (12.7) 4 (18.2) 
Major outcomes       
Survival rate at 5 y after iPET evaluation#       
Progression-free survival 66.9 (63.8-70.0) 67.5 (63.8-71.2) 90.4 (81.4-99.4) 79.4 (68.6-90.2) 67.4 (53.5-81.3) 75.9 (57.5-94.3) 32.3 (19.8-44.8) 53.6 (33.4-73.8) 
OS 75.6 (72.7-78.5) 75.8 (72.5-79.1) 97.6 (92.9-102.3) 88.6 (80.0-97.2) 76.7 (64.2-89.2) 90.5 (78.0-103.0) 39.8 (26.9-52.7) 70.0 (51.4-88.6) 
Survival rate at 10 y after iPET evaluation#       
Progression-free survival 57.0 (53.5-60.5) 58.1 (54.0-62.2) 84.9 (73.7-96.1) 61.5 (47.0-76.0) 56.3 (40.8-71.8) 75.9 (57.5-94.3) 21.7 (9.5-33.9) 32.5 (11.9-53.1) 
OS 66.0 (62.7-69.3) 65.5 (61.4-69.6) 92.0 (83.4-100.6) 79.4 (67.8-91.0) 68.1 (53.6-82.6) 90.5 (78.0-103.0) 26.0 (12.9-39.1) 65.3 (45.7-84.9) 
Events after first-line therapy 
Progression or relapse 240 (27.8) 158 (25.4) 4 (9.5) 16 (29.6) 14 (32.6) 5 (23.8) 31 (56.4) 12 (50.0) 
Time to first relapse, y (range) 0.8 (0.0-14.1) 0.8 (0.0-14.1) 0.3 (0.2-2.5) 3.0 (0.6-12.2) 0.8 (0.2-7.7) 0.2 (0.1-2.2) 0.5 (0.0-8.3) 1.6 (0.3-9.5) 
Type of salvage therapy∗∗       
Supportive care alone 16 (6.7) 12 (7.6) 0 (0.0) 1 (6.3) 0 (0.0) 1 (20.0) 1 (3.2) 1 (8.3) 
Chemotherapy, immunotherapy, and/or radiotherapy 127 (52.9) 79 (50.0) 1 (25.0) 8 (50.0) 9 (64.3) 1 (20.0) 20 (64.5) 9 (75.0) 
Auto-SCT 69 (28.7) 53 (33.5) 0 (0.0) 5 (31.3) 3 (21.4) 1 (20.0) 6 (19.4) 1 (8.3) 
Auto-SCT 28 (11.7) 14 (8.9) 3 (75.0) 2 (12.5) 2 (14.3) 2 (40.0) 4 (12.9) 1 (8.3) 
Survival rate at 5 y after first relapse††       
Progression-free survival 25.3 (19.6-31.0) 27.6 (20.3-34.9) ≤25.0‡‡ (−17.5 to 67.5) 34.3 (9.4-59.2) 21.4 (−0.2 to 43.0) 20.0 (−15.1 to 55.1) 6.5 (−2.1 to 15.1) 38.1 (9.3-66.9) 
OS 33.5 (27.4-39.6) 33.1 (25.5-40.7) 75.0 (32.5-117.5) 48.1 (23.0-73.2) 35.7 (10.6-60.8) 60.0 (17.1-102.9) 9.7 (−0.7 to 20.1) 54.7 (24.5-84.9) 
Second primary malignancies and deaths      
Second primary malignancy 100 (11.6) 72 (11.6) 3 (7.1) 6 (11.1) 6 (14.0) 2 (9.5) 7 (12.7) 4 (16.7) 
Time to second primary malignancy, y (range) 4.7 (0.3-13.3) 4.9 (0.3-13.3) 9.1 (4.9-9.6) 2.9 (0.4-4.0) 5.0 (3.0-8.3) 3.7 (2.8-4.5) 3.7 (1.5-8.1) 3.0 (2.3-11.3) 
Death 286 (33.2) 206 (33.1) 3 (7.1) 12 (22.2) 15 (34.9) 3 (14.3) 39 (70.9) 8 (33.3) 
All patientsDLBCL PMBCLFL grade 3 Other aNHL ALK+ ALCLALK- PTCL§ No aNHL 
Number of patients 862 (100.0) 623 (72.3) 42 (4.9) 54 (6.3) 43 (5.0) 21 (2.4) 55 (6.4) 24 (2.7) 
Baseline features at study inclusion 
Age, y (range) 60 (18-80) 62 (18-80) 35 (18-80) 58 (29-80) 61 (28-76) 33 (19-66) 65 (26-79) 62 (21-79) 
International Prognostic Index risk group       
Low 329 (38.3) 228 (36.7) 25 (59.5) 26 (48.2) 9 (20.9) 16 (76.2) 18 (32.7) 7 (31.8) 
Low-intermediate 224 (26.1) 163 (26.3) 9 (21.4) 14 (25.9) 10 (23.3) 5 (23.8) 15 (27.3) 8 (36.4) 
High-intermediate 180 (21.0) 130 (20.9) 5 (11.9) 10 (18.5) 17 (39.5) 0 (0.0) 15 (27.3) 3 (13.6) 
High 125 (14.6) 100 (16.1) 3 (7.2) 4 (7.4) 7 (16.3) 0 (0.0) 7 (12.7) 4 (18.2) 
Major outcomes       
Survival rate at 5 y after iPET evaluation#       
Progression-free survival 66.9 (63.8-70.0) 67.5 (63.8-71.2) 90.4 (81.4-99.4) 79.4 (68.6-90.2) 67.4 (53.5-81.3) 75.9 (57.5-94.3) 32.3 (19.8-44.8) 53.6 (33.4-73.8) 
OS 75.6 (72.7-78.5) 75.8 (72.5-79.1) 97.6 (92.9-102.3) 88.6 (80.0-97.2) 76.7 (64.2-89.2) 90.5 (78.0-103.0) 39.8 (26.9-52.7) 70.0 (51.4-88.6) 
Survival rate at 10 y after iPET evaluation#       
Progression-free survival 57.0 (53.5-60.5) 58.1 (54.0-62.2) 84.9 (73.7-96.1) 61.5 (47.0-76.0) 56.3 (40.8-71.8) 75.9 (57.5-94.3) 21.7 (9.5-33.9) 32.5 (11.9-53.1) 
OS 66.0 (62.7-69.3) 65.5 (61.4-69.6) 92.0 (83.4-100.6) 79.4 (67.8-91.0) 68.1 (53.6-82.6) 90.5 (78.0-103.0) 26.0 (12.9-39.1) 65.3 (45.7-84.9) 
Events after first-line therapy 
Progression or relapse 240 (27.8) 158 (25.4) 4 (9.5) 16 (29.6) 14 (32.6) 5 (23.8) 31 (56.4) 12 (50.0) 
Time to first relapse, y (range) 0.8 (0.0-14.1) 0.8 (0.0-14.1) 0.3 (0.2-2.5) 3.0 (0.6-12.2) 0.8 (0.2-7.7) 0.2 (0.1-2.2) 0.5 (0.0-8.3) 1.6 (0.3-9.5) 
Type of salvage therapy∗∗       
Supportive care alone 16 (6.7) 12 (7.6) 0 (0.0) 1 (6.3) 0 (0.0) 1 (20.0) 1 (3.2) 1 (8.3) 
Chemotherapy, immunotherapy, and/or radiotherapy 127 (52.9) 79 (50.0) 1 (25.0) 8 (50.0) 9 (64.3) 1 (20.0) 20 (64.5) 9 (75.0) 
Auto-SCT 69 (28.7) 53 (33.5) 0 (0.0) 5 (31.3) 3 (21.4) 1 (20.0) 6 (19.4) 1 (8.3) 
Auto-SCT 28 (11.7) 14 (8.9) 3 (75.0) 2 (12.5) 2 (14.3) 2 (40.0) 4 (12.9) 1 (8.3) 
Survival rate at 5 y after first relapse††       
Progression-free survival 25.3 (19.6-31.0) 27.6 (20.3-34.9) ≤25.0‡‡ (−17.5 to 67.5) 34.3 (9.4-59.2) 21.4 (−0.2 to 43.0) 20.0 (−15.1 to 55.1) 6.5 (−2.1 to 15.1) 38.1 (9.3-66.9) 
OS 33.5 (27.4-39.6) 33.1 (25.5-40.7) 75.0 (32.5-117.5) 48.1 (23.0-73.2) 35.7 (10.6-60.8) 60.0 (17.1-102.9) 9.7 (−0.7 to 20.1) 54.7 (24.5-84.9) 
Second primary malignancies and deaths      
Second primary malignancy 100 (11.6) 72 (11.6) 3 (7.1) 6 (11.1) 6 (14.0) 2 (9.5) 7 (12.7) 4 (16.7) 
Time to second primary malignancy, y (range) 4.7 (0.3-13.3) 4.9 (0.3-13.3) 9.1 (4.9-9.6) 2.9 (0.4-4.0) 5.0 (3.0-8.3) 3.7 (2.8-4.5) 3.7 (1.5-8.1) 3.0 (2.3-11.3) 
Death 286 (33.2) 206 (33.1) 3 (7.1) 12 (22.2) 15 (34.9) 3 (14.3) 39 (70.9) 8 (33.3) 

Numbers are given as n (%) unless otherwise noted.

aNHL, aggressive non-Hodgkin lymphoma; FL, follicular lymphoma; PMBCL, primary mediastinal B-cell lymphoma; PTCL, peripheral T-cell lymphoma.

Including 574 DLBCL and 49 DLBCL combined with FL (n = 43), marginal zone lymphoma (n = 5), or lymphoid granulomatosis grade 2 (n = 1). Because DLBCL alone and DLBCL combined with an indolent lymphoma had similar relapse rates, progression-free survival, and OS (supplemental Figure 1), the 2 groups were combined.

Including 25 FL grade 3a, 17 FL grade 3b, and 12 FL grade 3 combined with grade 1 or 2. Because the 3 groups had similar relapse rates, progression-free survival, and OS (supplemental Figure 1), they were combined.

Including 4 B-cell lymphomas with features intermediate between DLBCL and Burkitt lymphoma, 3 B-cell lymphomas with features intermediate between DLBCL and Hodgkin lymphoma, 2 plasmablastic lymphomas, and 34 unclassified large B-cell lymphomas.

§

Including 13 ALK ALCL, 18 angioimmunoblastic T-cell lymphomas, 20 PTCL not otherwise specified, and 4 unclassified PTCL. Because the 4 groups had similar relapse rates, progression-free survival, and OS (supplemental Figure 1), they were combined.

Including 10 FL grade 1 or 2, 7 marginal zone lymphomas, 1 unclassified indolent B-cell lymphoma, 2 mantle cell lymphomas, 2 Burkitt lymphomas, 1 Hodgkin lymphoma, and 1 breast cancer.

Percentages refer to patients with documented data only.

#

Kaplan-Meier estimate of the percentage of patients surviving after 5 or 10 years, respectively (95% CI). After undergoing first-line immunochemotherapy as specified in the study protocol, 23 patients received consolidating radiotherapy. This was counted as a treatment-failure event in the event-free survival analysis but not in the progression-free survival or OS analyses (Figure 3).

∗∗

The type of salvage therapy was defined on the basis of the entire disease course (up to 7 lines of salvage therapy), including (1) supportive care alone; (2) chemotherapy, immunotherapy, and/or radiotherapy with or without supportive care, but without transplantation; (3) high-dose chemotherapy with auto-SCT with or without chemotherapy, immunotherapy, radiotherapy, or supportive care, but without allogeneic transplantation; and (4) allogeneic transplantation with or without autologous transplantation, chemotherapy, immunotherapy, radiotherapy, or supportive care.

††

Kaplan-Meier estimate of the percentage of patients surviving after 5 years (95% CI).

‡‡

Indicated time point not yet reached, that is, estimate for an earlier time point.

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