Immuno-oncology is a way to treat cancer by using the body’s immune system. BiTE (bispecific T-cell engager) technology is a targeted immuno-oncology platform that binds a patient’s own T cells to cancer cells. Because BiTE technology is flexible, it is easy to make molecules that attack tumor-specific antigens, which makes immuno-oncotherapy possible. Blinatumomab was the first standard BiTE molecule to be approved. It targets CD19 surface antigens on B cells and is mostly unaffected by genetic changes or escape mechanisms inside cells. More BiTE molecules are being made to treat other blood cancers (like multiple myeloma, acute myeloid leukaemia, and B-cell chłoniak nieziarniczy) and solid tumours (like prostate cancer, glioblastoma, stomach cancer, and small-cell lung cancer). BiTE molecules that have a longer half-life than the standard ones are also being made. With BiTE technology, advances in immuno-oncology could make it easier to treat both blood and solid tumours and make them more effective when used with other treatments.
Czym jest terapia BiTe?
Immuno-oncology therapies are scientifically proven ways to treat different types of solid and nowotwory krwi. Hematologic cancers are a good fit for treatments that target the immune system because cancerous blood cells move around with immune cells. Several immunoterapia trwają prace nad lekami na raka.
Monoclonal antibody checkpoint inhibitors that stop the binding of checkpoint proteins (like PD-1 and CTLA-4) are useful against many types of cancer. They work well and are safe for many solid tumours, especially when they target PD-1. Non-small-cell lung, kidney, and bladder cancers have all been treated successfully with these drugs. But many people don’t react to checkpoint inhibitors or get sick again after taking them. Except for non-Hodgkin chłoniak, most results on hematologic cancers have been disappointing, especially for myeloma and leukaemia, where the overall response rate in approved indications ranges from 12.0% to 48.5%.8-15.
Other immuno-oncology treatments, on the other hand, have a higher success rate. Chimeric antigen-receptor (CAR) T-cell therapies change a patient’s T cells to attack a specific cellular antigen, such as CD19 in the treatment of B-cell malignancies and B-cell maturation antigen (BCMA) in the treatment of szpiczak mnogi (MM). CAR T-cell treatments have shown promise in treating hematologic cancers. They haven’t been as effective in treating solid tumours, but there have been some good results with nerwiak niedojrzały, human epidermal growth factor receptor tumours, and non-small-cell lung cancer. The genetic modification and in vitro multiplication of T cells take a long and complicated manufacturing process. This is a downside of this therapy because it makes it harder for patients to get this treatment quickly and in large numbers. The fact that lymphodepletion through chemotherapy preparation must be done first as a requirement for improved effectiveness is also a drawback.
Terapie BiTE (bispecyficzny czynnik angażujący komórki T) łączą własne komórki T pacjenta z antygenami eksprymowanymi przez guz. To włącza cytotoksyczną zdolność własnych komórek T pacjenta do zabijania raka bez zmiany genów komórek T lub konieczności ich wzrostu lub manipulowania nimi poza organizmem. Cząsteczki BiTE mogą być stosowane samodzielnie jako leki lub w połączeniu z innymi metodami leczenia, aby zwiększyć ich skuteczność.
Mechanizm działania BiTe
BiTE molecules are antibody constructs with two binding domains. One recognises tumor-expressed antigens (such as BCMA, CD19, or -like protein [DLL3]), and the other, CD3, recognises T cells (Fig. 1). Two single-chain variable fragment (scFv) regions from monoclonal antibodies are connected by a flexible peptide linker to make the binding domains. The first scFv binding region can be changed to target any surface antigen, so it can be used right away to treat a wide range of tumours and can be used again later. The second scFv binding region always binds to CD3, which is a part of the T-cell receptor complex that never changes. When a BiTE molecule interacts with both a cytotoxic T cell and a tumour cell, the T cells begin to multiply. This increases the amount of effector cells and makes BiTE therapy more effective. Then, the death of cancer cells is started. BiTE molecules can get any T cells to do this because they don’t need co-stimulation or the usual processes of the major histocompatibility complex.
Blinatumomab is the first and only BiTE therapy that has been approved. It targets the CD19 receptor on both normal and cancerous B cells. It is a highly potent molecule with cytotoxic effects seen at low exposures (10–100 pg/mL)26. In its presence, T cells can perform serial-target lysis, quickly binding to and killing many cells. This is how BiTE therapies work, and it can be seen in other BiTE molecules that are still in research. In ostra białaczka limfoblastyczna (ALL), blinatumomab has been shown to be effective and safe. In 2014, the US Food and Drug Administration gave it fast approval, and in 2017, it got full approval for relapsed or refractory (R/R) B-cell precursor (BCP) ALL. In 2018, accelerated approval was given to blinatumomab for treating BCP-ALL with minimum residual disease (MRD). This was the first approval for this use. In November 2015, the European Medicines Agency also gave it a green light for BCP-ALL with a Philadelphia chromosome (Ph) that is negative and R/R. Blinatumomab is approved for R/R BCP-ALL in adults and children in 57 countries, including Japan, all countries in the European Union, Canada, and Australia.
Blinatumomab w leczeniu pacjentów z BCP-ALL
Blinatumomab zmienił sposób leczenia BCP-ALL. W porównaniu ze standardową chemioterapią (SOC), zwiększyła ona całkowity czas przeżycia (OS) i zmniejszyła liczbę niektórych działań niepożądanych (AE). Kilka ważnych badań, w tym badania z randomizacją, wykazało, że blinatumomab jest bezpieczny i działa na BCP-ALL zarówno u dorosłych, jak iu dzieci. Terapia limfocytami T CARistnieją tylko dane z 2 badań jednoramiennych (identyfikatory clinicaltrials.gov NCT01626495 i NCT01029366), w których leczono 25 dzieci (w wieku 5–22 lat) i 5 dorosłych (w wieku 26–60 lat) z R/R BCP-ALL i ALL z komórek T. Ale wyniki są obiecujące (całkowita odpowiedź [CR] u 90%, trwała remisja z 6-miesięcznym przeżyciem wolnym od zdarzeń u 67% i całkowity czas przeżycia [OS] 78% [mediana okresu obserwacji, 7 miesięcy; zakres, 1–24 miesiące]).
W badaniu TOWER (randomizowane, otwarte badanie fazy 3, oceniające skuteczność przeciwciała BiTE Blinatumomab w porównaniu ze standardową chemioterapią u dorosłych pacjentów z nawrotową/oporną na leczenie białaczką prekursorową B; identyfikator kliniczny.gov NCT02013167) porównywało wpływ monoterapii blinatumomabem na chemioterapię SOC u intensywnie wcześniej leczonych osób dorosłych z Ph-ujemnym, R/R BCP- WSZYSTKO. Ponieważ ludzie żyli dłużej, badanie przerwano wcześniej. AE w grupie blinatumomabu były takie same jak we wcześniejszych badaniach, a wskaźniki AE skorygowane o ekspozycję blinatumomabu były niższe niż SOC.34 Blinatumomab działa również u osób z Ph-dodatnim, R/R BCP-ALL oraz u dzieci z Ph-ujemnym, R/R BCP-ALL.
30% to 50% of people with BCP-ALL in complete hematologic remission show persistent MRD. In the single-arm, phase 2 BLAST study (A Confirmatory Multicenter, Single-Arm Study to Assess the Efficacy, Safety, and Tolerability of the BiTE Antibody Blinatumomab in Adult Patients With MRD of B-Precursor Acute Lymphoblastic Leukaemia; clinicaltrials.gov identifier NCT01207388), blinatumomab was tested on patients with BCP-ALL in first or later complete After blinatumomab treatment, 78% of patients who were MRD positive became MRD negative. The 5-year OS study showed a median OS of 36.5 months, and more than half of those who had a complete MRD response after the first cycle of blinatumomab were still alive at 5 years, which suggests that the treatment might be able to cure some patients. AEs were seen that were linked to zespół uwalniania cytokin (CRS).31 Other studies, like NCT03023878 and NCT03340766, are still looking at blinatumomab in first-line settings and in combination with other treatments.
CD19-targeted treatments have been linked to failure because of the loss of CD19 antigen after treatment. The failure rates for blinatumomab range from 8% to 35%, and for Terapie CAR z limfocytami T., they range from 39% to 65%.36-40 We don’t fully understand what causes therapy to fail, but one possibility is immunoediting, in which antigen loss is caused by a T-cell-dependent process called immunoselection, which lets tumour cells get away.41 Lineage switch and epitope loss under therapy pressure have also been suggested as ways for tumours to escape treatment. However, a recent study on epitope loss found that some CD19 isoforms that help CAR T-cells escape were already present at the time of diagnosis. This suggests that combining treatments might be helpful. Another thing that can cause immunotherapy to fail is called “inhibitory T-cell signalling.” In this case, the blocking programmed death ligand-1 (PD-L1) is interesting because it is more common in B-cell ALL cells from patients who don’t respond to blinatumomab and can make CD3 BiTE molecules less effective.43 By making a CD28/PD-L1 BiTE that triggers the CD28 co-stimulatory signal instead of the inhibitory signaling pathway that is usually seen when a T cell binds to a PD-L1-expressing cancer cell, this inhibition could be turned off.43 Dual-targeted CAR T cells are also being looked into as a way to make up for the loss of tumour antigens. This can be done by modifying each T cell with 2 CAR molecules and 2 different binding domains (dual-signaling CAR) or by putting 2 different binding domains on 1 CAR molecule at the same time (TanCAR).
Zdarzenia niepożądane związane z BiTE i jego postępowaniem
W badaniach klinicznych blinatumomabu najczęstszymi zdarzeniami niepożądanymi były gorączka, mała liczba białych krwinek i mała liczba płytek krwi. Niektóre z najważniejszych zagrożeń to CRS, neurotoksyczność i błędy lekowe. Neurotoksyczność może również wystąpić w przypadku leczenia komórkami T CAR specyficznymi dla CD19, ale może nie być spowodowana CD19. Wyniki trwającego nadal badania fazy 1/1b dotyczącego docelowych wartości CD20/CD3 wykazały, że zdarzenia niepożądane ośrodkowego układu nerwowego stopnia 3. lub wyższego występowały rzadko (3% wszystkich zdarzeń niepożądanych stopnia 3.). W większości przypadków reakcja blinatumomabu na CRS jest łagodna, ale w rzadkich przypadkach może być ciężka, a nawet zagrażać życiu. Reakcje zapalne można złagodzić za pomocą kortykosteroidów. Aby zmniejszyć ryzyko CRS, najlepiej podać wlew prednizonu lub deksametazonu przed pierwszą dawką blinatumomabu i powoli zwiększać dawkę. To zastosowanie kortykosteroidów przed innymi cząsteczkami BiTE dało powód do stosowania deksametazonu jako premedykacji przy stosowaniu innych cząsteczek BiTE. Nie jest jednak jasne, czy efekt ten można zastosować do całej platformy BiTE, a rozważane są inne sposoby radzenia sobie z CRS. Interleukina 6 jest cytokiną, która powoduje CRS i jest wysoka u osób, które ją mają. Tocilizumab, który blokuje receptor interleukiny-6, był stosowany w leczeniu CRS, który jest bardzo zły po leczeniu komórkami T CAR.49 W szpitalu inhibitory czynnika martwicy nowotworów były również stosowane w leczeniu CRS.
