Unfortunately, joint pain while on immunotherapy is fairly common. The degree to which the patient suffers is almost the only variable. Some of us are managed fairly well with things like ibuprofen and stubbornness. Others are debilitated to the point that treatments must be delayed and other medications like steroids and immune modulators like Remicaid are required. If you search this blog under 'immunotherapy side effects', you will find zillions of articles on joint pain and immunotherapy.
Now, there's this:
Rheumatic immune-related adverse events secondary to anti-programmed death-1 antibodies and preliminary analysis on the impact of corticosteroids on anti-tumour response: A case series. Mitchell, Lau, Khoo, et al. Eur J Cancer. 2018 Nov 12
Rheumatic immune-related
adverse events (irAEs) occur in approximately 10-20% of
anti-programmed death 1 (anti-PD1)-treated cancer patients. There are
limited data on the natural history, optimal treatment and long-term
oncological outcomes of patients with rheumatic irAEs.
The objective of the study was
to describe the spectrum and natural history of rheumatic irAEs and
the potential impact of rheumatic irAEs and immunomodulators on
anti-PD1 tumour efficacy.
Cancer patients with
pre-existing rheumatic disease before anti-PD1 therapy or de novo
rheumatic irAEs on anti-PD1 therapy were retrospectively reviewed
across three sites. Patient demographics, treatment history, anti-PD1
irAEs, and anti-PD1 responses were evaluated. Relationships between
the development or pre-existence of rheumatic irAE, use of
immunomodulatory agents and outcomes were evaluated.
This multicenter case series
describes 36 cancer patients who had rheumatic disease before
anti-PD1 therapy (n = 12) or developed de novo rheumatic
irAEs (n = 24). Thirty-four of the 36 patients sustained
rheumatic irAEs (median time to rheumatic irAE: 14.5 weeks),
including 24 de novo (18 inflammatory arthritis, three myositis, two
polymyalgia rheumatica, one fasciitis) and 10 flares in 12
patients with pre-existing rheumatic disease. Corticosteroids were
used in 30 of 36 patients (median duration: 10 months), and
disease-modifying antirheumatic drugs were used in 14 of 36
patients (median duration: 5.5 months). The objective response rate
to anti-PD1 therapy was 69% (n = 25/36) overall and 81%
(n = 21/26) in the melanoma subgroup.
Rheumatic irAEs are often
chronic and require prolonged immunomodulatory therapy. Prospective
studies are required to define optimal management of rheumatic irAEs
that maintain long-term anticancer outcomes.
So yes, there may be the need to continue treatment for joint pain and arthralgias after completing immunotherapy. However, these response rates look pretty good!!! Pros and cons - the life of a melanoma rattie. Hang tough out there! - c
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