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Case Report: Successful Immunotherapy Improved the Prognosis of the Unfavorable Subset of Cancer of Unknown Primary

Overview
Journal Front Immunol
Date 2022 Jul 11
PMID 35812375
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Abstract

Background: Cancer of unknown primary (CUP) is heterogeneous and has a wide variety of clinical presentations and a poor prognosis in most patients, with a median overall survival of only 6 months. The development of molecular profiling contributes to precision therapy, and targeted drugs and immune checkpoint inhibitors (ICIs) greatly promote individualized treatment.

Case Presentation: Here, we reported a case of an unfavorable subset of CUP who had a long time of survival after the immunotherapy-prominent comprehensive treatment. A 48-year-old man presented with back pain and a cough. A diagnostic work-up showed bone marrow, multiple bones, and lymph node metastasis. Lymph node pathology implies metastatic poorly differentiated cancer. Next-generation sequencing (NGS) showed no special targets, but the tumor proportion score (TPS) of programmed death-ligand 1 (PD-L1) was 80% and the tumor mutation burden (TMB) was 16.7 per million bases. After two cycles of pembrolizumab 200 mg D1 plus nanoparticle albumin-bound (nab)-paclitaxel 200 mg D1&8 (q3w), PET-CT and bone marrow aspiration cytology showed a complete response (CR). Subsequently, pembrolizumab alone was used for three months. The left inguinal lymph nodes showed new metastasis. After two cycles of the combination treatment of pembrolizumab and (nab)-paclitaxel, a partial response (PR) was achieved. After seven months, retroperitoneal lymph nodes showed new metastasis, and the sequential treatment with radiotherapy and pembrolizumab exhibited encouraging efficacy. To date, the patient has survived nearly 40 months with the combination therapy.

Conclusions: The ICI-prominent comprehensive treatment provided clinical benefit for the reported case of CUP. Thus, CUP patients with markers of benefiting from immunotherapy should be actively treated with immunotherapy to improve their prognosis.

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References
1.
Tanizaki J, Yonemori K, Akiyoshi K, Minami H, Ueda H, Takiguchi Y . Open-label phase II study of the efficacy of nivolumab for cancer of unknown primary. Ann Oncol. 2021; 33(2):216-226. DOI: 10.1016/j.annonc.2021.11.009. View

2.
Gatalica Z, Millis S, Vranic S, Bender R, Basu G, Voss A . Comprehensive tumor profiling identifies numerous biomarkers of drug response in cancers of unknown primary site: analysis of 1806 cases. Oncotarget. 2014; 5(23):12440-7. PMC: 4322997. DOI: 10.18632/oncotarget.2574. View

3.
Ross J, Wang K, Gay L, Otto G, White E, Iwanik K . Comprehensive Genomic Profiling of Carcinoma of Unknown Primary Site: New Routes to Targeted Therapies. JAMA Oncol. 2015; 1(1):40-49. DOI: 10.1001/jamaoncol.2014.216. View

4.
Pentheroudakis G, Golfinopoulos V, Pavlidis N . Switching benchmarks in cancer of unknown primary: from autopsy to microarray. Eur J Cancer. 2007; 43(14):2026-36. DOI: 10.1016/j.ejca.2007.06.023. View

5.
Pavlidis N, Pentheroudakis G . Cancer of unknown primary site. Lancet. 2012; 379(9824):1428-35. DOI: 10.1016/S0140-6736(11)61178-1. View