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 Table 3. Anti mesothelin CAR-T cell US clinical trials in mesothelioma

 NCT ID  Phase Product  Target patient population  Outcomes                      Reference

 CAR-T +/- chemotherapy conditioning
 NCT01355965 1  Autologous mesothelin re-directed T cells  18 patients with DPM.  4 Patients treated with anaphylaxis, off-target   [70,71]
                                      toxicity
 NCT02159716  1  Lentiviral transduced CART-mesothelioma cells   15 patients with DPM, ovarian ca, pancreatic ductal ca.  Cells well tolerated, expanded in blood, limited   [72]
                                      clinical activity
 NCT03054298 1  Lentiviral transduced fully human CART-mesothelioma cells   Up to 15 patients with mesothelin-expressing refractory  Study Ongoing
 DPM, lung cancer, and ovarian ca.
 NCT04577326 1  M28z1XXPD1DNR: CAR T-cell with cell-intrinsic PD-1 blockade   7 patients with DPM.  Study Ongoing  [73]
 NCT01583686  1  Anti-mesothelin CAR transduced peripheral blood lymphocytes +  15 patients with mesothelin expressing metastatic   Study Terminated for poor accrual
 aldesleukin (IL-2)   disease.
 NCT03608618  1  MCY-M11: mesothelin targeting CAR-T- Intraperitoneal   14 patients with ovarian Ca, primary peritoneal or   Following the treatment of 11 patients with initial   [74]
 fallopian tube ca, and peritoneal mesothelioma.  feasibility and safety reported, study terminated-
                                      sponsor priority.

 NCT05568680 1  SynKIR-110:   42 patients with ovarian Ca, primary peritoneal Ca,   Study Ongoing
 T-cell transduced with mesothelin KIR-CAR  ovarian or fallopian tube Ca, mesotheliomas,
 cholangiocarcinoma
 NCT05451849 1/2  TC-510   115 patients with advanced mesothelin-expressing   Study Ongoing
 T cell expressing both a mesothelin-CD3ε subunit and PD-1:CD28  tumors including DPM
 switch receptor

 CAR-T + Immune Checkpoint Inhibition
 NCT02414269 1/2  CD28-costimulated mesothelin CAR with the Icaspase-9 safety   113 patients with mesothelin expressing malignant   19 DPM patients: 2 complete metabolic response  [75]
 gene (IcasM28z) + pembrolizumab (mesothelioma cohort only)  pleural disease.  on PET, 5 partial response, 4 stable disease.
                                      Study Ongoing.
 NCT03907852  1/2  Gavocabtagene autoleucel (autologous anti-mesothelin TCR   175 patients with advanced mesothelin-expressing   Tumor regression in first 5 patients treated.   [76]
 fusion construct [TRuC]) with and without nivolumab or   cancers
 ipilimumab/nivolumab                 Study ongoing.

 CA: Cancer; CAR: chimeric antigen receptor; DPM: diffuse pleural mesothelioma.



 patients in the trial had BAP1 alterations). In this unselected population, olaparib had limited activity, with one (4%) partial response. In this small sample,

 germline BAP1 mutations were associated with decreased OS compared to wild type (4.6 vs. 9.6 months, respectively, P = 0.004).



 Base excision repair (BER) is a coordinated cellular process by which damaged DNA base pairs can be excised and repaired ; inhibition of this pathway in a
                                                     [94]
 tumor with DNA damage repair deficiencies, such as BAP1 loss, could lead to synthetic lethality. A recent phase 1 trial examined the safety and activity of
 TCR102, a BER pathway inhibitor, in combination with chemotherapy for the treatment of multiple advanced solid tumors . In the DPM cohort, 14 patients
                                                    [87]
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