Tumor-infiltrating lymphocyte transfusion in a patient with treatment refractory triple negative breast cancer

被引:1
作者
Jacover, Arielle [1 ]
Zarbiv, Yonaton [1 ,2 ,3 ]
Haran, Tal Kiedar [4 ]
Klein, Shira [3 ]
Breuer, Shani [1 ,2 ]
Durst, Ronen [2 ,5 ]
Avni, Batia [2 ]
Grisariu, Sigal [2 ]
Stepensky, Polina [2 ,6 ]
Lotem, Michal [1 ,2 ,3 ]
Maimon, Ofra [1 ,2 ]
Yablonski-Peretz, Tamar [1 ,2 ]
机构
[1] Hadassah Med Ctr, Sharett Inst Oncol, Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Fac Med, Jerusalem, Israel
[3] Hadassah Canc Res Inst, Hadassah Med Ctr, Jerusalem, Israel
[4] Hadassah Med Ctr, Dept Pathol, Jerusalem, Israel
[5] Hadassah Med Ctr, Dept Cardiol, Jerusalem, Israel
[6] Hadassah Med Ctr, Dept Bone Marrow Transplant, Jerusalem, Israel
关键词
adoptive cell therapy; triple negative breast cancer; tumor infiltrating lymphocyte; CHEMOTHERAPY; BLOCKADE; THERAPY;
D O I
10.1002/cnr2.1894
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Triple negative breast cancer (TNBC) is an aggressive form of breast cancer that is treated with chemotherapy. Recently, programmed death 1 (PD1) inhibition, as well as antibody-drug conjugates, have been added to the available treatment regimen, yet metastatic disease is fatal. Adoptive cell therapy (ACT) using tumor infiltrating lymphocytes (TILs) has been well described in melanoma, but less data is available on other solid malignancies. Case: Herein, we present a case of a 31-year-old patient diagnosed with Breast Cancer gene 1 (BRCA1) positive, TNBC. The patient's disease rapidly progressed while under standard treatment protocols. As a result, additional genetic testing of the tumor was carried out and revealed loss of BRCA1 heterozygosity, a double Tumor Protein 53 (TP53) mutation, and MYC amplification. Due to resistance to conventional therapy, an experimental approach was attempted using tumor-infiltrating lymphocytes in November 2021 at Hadassah University Medical Center. While receiving this treatment, the patient exhibited a reported subjective clinical improvement including a month spent out of the hospital. However, the final result, presumably due to Interleukin 2 (IL-2) toxicity, was the patient's passing. Conclusion: This case is unique and peculiar regarding the treatment modality chosen, due to the extremely refractory disease the patient suffered from. After standard therapies rapidly failed, adoptive cell therapy was attempted with the infusion of TILs. This treatment has been shown effective in melanoma, however, there is an extreme paucity of data on other solid tumors, including TNBC. Although the patient ultimately demised presumably due to treatment side effects, brief clinical benefit was apparent. Further studies are warranted.
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