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. 2021 Feb 19;9(2):e002097. doi: 10.1136/jitc-2020-002097

Table 2.

Treatment outcomes

Patient # Cycles pembro # Cycles pom irAE ΔCD4+*
T cells/μL
ΔCD8+
T cells/μL
Best response Next therapy received Months from pembro initiation to last follow-up Long-term outcome
1 13 +116 +311 PR Allogeneic HSCT 13 Death
2 7 G2 hypothyroidism +132 +754 SD Trimetinib 11 Death
3 6 G2 hypothyroidism −63 −152 SD Lenalidomide +bortezomib 15 SD
4 15 −43 −37 PR R-ICE followed by allogeneic HSCT 33 CR
5 6 +52 +43 PR RIL 15 Death
6 7 12 G3 Guillain-Barre −65 −74 SD HD-MTX-Ara-C-Thiotepa 24 SD
7 22 19 G3 hepatitis +70 +517 CR Continued on pembro+pom 21 CR
8 3 −305 −1458 PD 3 Death
9 4 1 PD 4 Death
10 7 7 +94 +473 PR Daratumumab+pom 9 PR

*The change in CD4+ and CD8+ T cells is measured from baseline to the end of treatment.

Ara-C, cytarabine; CR, complete response; G, grade; HD-MTX, high-dose methotrexate; HSCT, hematopoietic stem cell transplant; irAE, immune-related adverse event; PD, progressive disease; pembro, pembrolizumab; pom, pomalidomide; PR, partial response; R-ICE, rituximab, ifosfamide, carboplatin, etoposide; RIL, rituximab, ibrutinib, lenalidomide; SD, stable disease.