Immunotherapy for lung cancer (Part 1): Neoadjuvant and adjuvant immunotherapy

Written by: Dr Crispin Hiley
Published:
Edited by: Carlota Pano

Immunotherapy is a cancer treatment that uses medicines to stimulate your own immune system to detect and destroy cancer cells, helping to improve outcomes for people fighting lung cancer.

 

Dr Crispin Hiley is a highly renowned consultant clinical oncologist and associate professor who specialises in all the different types of lung cancer, as well as cancer immunotherapy and chemotherapy. In the first of a two-part series of articles on immunotherapy for lung cancer, Dr Hiley offers an expert insight into neoadjuvant and adjuvant immunotherapy for lung cancer.

 

 

What is neoadjuvant immunotherapy and its aim?

 

Neoadjuvant immunotherapy is a treatment given before surgery.

 

Many patients with early or locally advanced lung cancer are treated with surgery. For a long time, early or locally advanced lung cancer that had spread to the lymph nodes, as well as large cancers (for example, bigger than four centimetres), would be treated with surgery followed by chemotherapy. Adjuvant chemotherapy, as this is known, is given once all the cancer has been removed surgically to reduce the risk of any cancer coming back.

 

More recently, some clinical trials have studied the use of other agents - including immunotherapy - either before surgery (for neoadjuvant therapy) or after surgery (for adjuvant therapy).

 

With neoadjuvant immunotherapy, the CheckMate 816 trial study showed that there was significant benefit in giving some patients chemotherapy and immunotherapy before surgery. During the clinical trial, the patients received three cycles (or three courses) of chemotherapy and nivolumab, and then underwent surgery. Following surgery, the Checkmate 816 study showed that there was significant benefit in the reduction of the risk of cancer recurrence. Treatment worked very well for some patients, and when the tumour was examined under a microscope after it was removed during surgery, it was very difficult to find any active cancer left following neoadjuvant treatment and surgery.

 

Patients with a very good response to neoadjuvant treatment have had very good long-term outcomes from all of these trials of neoadjuvant chemotherapy and immunotherapy, so far. The use of neoadjuvant immunotherapy in combination with chemotherapy will become more prevalent over the coming years among patients where surgery is planned for their lung cancer. However, it is important to know that immunotherapy for lung cancer is mainly used for patients with no actionable mutation, such as an EGFR mutation or an ALK mutation.

 

Can you give some examples of neoadjuvant therapy and what is involved in their processes?

 

Neoadjuvant therapy for lung cancer can involve many different treatments.

 

Patients with no actionable mutation (no EGFR or ALK mutations) are now being treated with chemotherapy and immunotherapy, with three cycles of this treatment (platinum-based chemotherapy and nivolumab) prior to surgery. During the process, these patients come to hospital to have chemotherapy and immunotherapy at the start of a three-week course of treatment, which is given intravenously. The patients then return to the hospital three weeks later to receive another three-week course of treatment. Before each new cycle of treatment, the patients need to be seen by their oncologist to see if the treatment is being well-tolerated. Once three three-week courses of treatment have been finished, the patients undergo surgery. This is becoming a very common type of neoadjuvant treatment used for patients with lung cancer.

 

Despite this, other forms of neoadjuvant treatment are also used for patients with lung cancer. Some patients, for example, may be offered neoadjuvant chemoradiotherapy (chemotherapy and radiotherapy both) prior to surgery. This treatment type is mostly offered to patients who have cancers in particular positions within the lung that would be difficult to take out and thus, there is a risk that some cancer may be left behind after surgery.

 

In the future, patients with actionable mutations (for example, an EGFR mutation) may start to be offered neoadjuvant treatments, such as neoadjuvant osimertinib (an EGFR inhibitor that is given as a tablet) and chemotherapy prior to surgery. However, clinical trial results are needed to see if this is beneficial.

 

What is adjuvant immunotherapy, and how does it differ from neoadjuvant?

 

Adjuvant effectively means after surgery, whereas neoadjuvant means before surgery. Adjuvant immunotherapy is immunotherapy that is given after surgery, rather than before.

 

In some circumstances, rather than giving any type of chemotherapy and/or immunotherapy before, the patients and their team of oncologists and surgeons might think it is best to proceed straight away to a surgical operation to remove the lung cancer, and then - after the cancer has been examined by pathologists - consider the benefit of adjuvant treatment. This adjuvant treatment will take place after surgery.

 

Classically, patients have been offered adjuvant chemotherapy because it has led to a small, but significant, increase in the chances of curing lung cancer after surgery.

 

More recently, the IMpower010 and the PEARL trial studies have shown that, for some types of immunotherapies (such as, atezolizumab and pembrolizumab, respectively), there are improved outcomes for patients who receive adjuvant immunotherapy for approximately about a year after surgery. In these circumstances, patients were offered their normal adjuvant chemotherapy for approximately four cycles worth of treatment (three weekly treatments), as well as a type of immunotherapy (potentially, atezolizumab or pembrolizumab) that were taken for approximately a year afterwards. Again, these patients had to come to hospital to have their treatments, intravenously, every three weeks.

 

It is important to know that both treatments (neoadjuvant and adjuvant) are not usually given to a same patient; a patient usually has one treatment or the other. However, there are a number of clinical trials currently investigating the use of both neoadjuvant and adjuvant immunotherapy for the same patient.

 

Does adjuvant therapy have advantages over neoadjuvant immunotherapy?

 

Obviously, with adjuvant therapy, a patient can undergo surgery straight away and then have immunotherapy afterwards. The benefit of this is that, when the surgeon examines the patient’s scans before surgery, the surgeon can determine at that exact moment if there is a high chance of removing the cancer. If so, then the surgeon can proceed straight to the operation without delay.

 

This is different with neoadjuvant immunotherapy and chemotherapy, as patients have chemotherapy and immunotherapy for approximately nine weeks before having surgery. Overall, patients benefit from this approach, but there is a small number of patients, where their cancer can unfortunately grow a bit bigger despite having immunotherapy and chemotherapy neoadjuvantly. This can then complicate surgery - and even, in some circumstances, mean that surgery is not possible.

 

Overall figures from the CheckMate 816 study show that neoadjuvant chemotherapy and immunotherapy is beneficial for patients, particularly for patients with immunogenic tumours (tumours that have high levels of a marker called PDL1). Yet, there may be some patients who benefit less, potentially patients with a low PDL1 test score, where having a long period of neoadjuvant chemotherapy and immunotherapy prior to surgery means that there is a potential risk of the cancer becoming more advanced before the patients actually get to undergo surgery.

 

 

Head on over to the second part of this series of articles on immunotherapy for lung cancer to find out about consolidation therapy and the use of immunotherapy for lung cancer in the metastatic setting.

 

If you require immunotherapy treatment for lung cancer, do not hesitate to book an appointment with Dr Crispin Hiley via his Top Doctors profile today.

By Dr Crispin Hiley
Clinical oncology

Dr Crispin Hiley is a highly reputable and skilled consultant clinical oncologist who currently practises at the London-based Cromwell Hospital. He is also an associate professor in clinical oncology at University College London. 

Dr Hiley specialises in all the different kinds of lung cancer and also possesses a significant amount of expertise in chemotherapy, cancer immunotherapy, radiotherapy, proton beam therapy, as well as mesothelioma, amongst many others. He is, at present, the chief investigator or principle investigator for several academic and industry clinical trials relating specifically to lung cancer, and also leads a radiation therapy-focused research group at the University College London Cancer Institute. He has been involved in writing the RCR Lung Cancer Consensus Guidelines that establish best practice for the managment of lung cancers with radiotherapy. 

Dr Hiley is also an expert in stereotactic radiotherapy (SABR) for patients with oligometastatic cancers. These are cancers that have spread to different areas (usually less than five) where SABR in combination with other cancer treatments can be used to help control the cancer. SABR can be used to treat many different cancer types e.g. lung, breast colorectal and prostate which have become oligometastatic.

Dr Hiley graduated with honours in medicine in 2005 at the University of Manchester, before going on to undertake training across the UK and abroad, at highly established hospitals such as the MD Anderson Cancer Centre, Houston, in the USA, as well as the King's College London, but to name a few. He has, to-date, published a significantly high number of articles in some of the world's most prestigious journals, including The Lancet. He is the clinical lead and lung proton therapy lead of the University College London Hospital clinical oncology lung team, and is also the current deputy lead of clinical trials for the CRUK Lung Cancer Centre of Excellence. Dr Hiley is available for second opinions. 

View Profile

Overall assessment of their patients


  • Related procedures
  • Mouth cancer
    Prostate cancer
    Human papillomavirus (HPV)
    Human papillomavirus vaccine (HPV)
    Breast cancer
    Brain tumour
    Testicular cancer
    Thyroid cancer
    Adrenal glands cancer
    Doppler Ultrasound
    This website uses our own and third-party Cookies to compile information with the aim of improving our services, to show you advertising related to your preferences as well analysing your browsing habits. You can change your settings HERE.