Oncology

CIMAvax Success Rate: What Do the Studies Say?

Relatives who search for the CIMAvax success rate or “Cuban cancer vaccine reviews” really want to know one thing: does it work? The soundest answer comes from published studies that compare patients who received the vaccine with patients who did not.

  • 6 min read
  • 3 sources
  • Updated 7 November 2026
A doctor filling in a medical history form for a patient asking about CIMAvax

The right source

CIMAvax success rate: why do we look at studies?

Every patient’s experience matters, but the strength of a treatment is best shown by comparative studies.

Two people with the same disease can have very different courses. That is why the effect of a treatment is shown by studies that compare patients who received the vaccine with patients who did not, under the same conditions.

Below we summarise what these studies found for CIMAvax-EGF and Vaxira. All the figures come from papers published in international peer-reviewed journals.

In brief

What are CIMAvax-EGF and Vaxira?

CIMAvax-EGF and Vaxira (racotumomab) are therapeutic cancer vaccines developed at the Center of Molecular Immunology (CIM) in Havana. In Cuba they are licensed for advanced (stage IIIB/IV) non-small cell lung cancer, as maintenance treatment after first-line chemotherapy or radiotherapy. CIMAvax-EGF has been licensed in Cuba since 12 June 2008 and Vaxira since 7 January 2013; Vaxira is also licensed in Argentina.

These vaccines are used in patients who have been diagnosed with cancer: they activate the immune system against the tumour and aim to keep the disease under control for longer after first-line treatment. CIMAvax-EGF aims to lower the EGF signal that feeds tumour growth; Vaxira builds an immune response against NeuGcGM3, a structure on tumour cells. CIMAher (nimotuzumab), from the same centre, is an antibody treatment given by infusion.

A doctor reviewing the reports in an oncology file
The oncologist who reviews your file assesses whether the vaccine suits you and how much benefit you may expect.

CIMAvax-EGF

What did the CIMAvax-EGF phase III trial find?

The trial was published in Clinical Cancer Research in 2016. It enrolled 405 patients with stage IIIB/IV non-small cell lung cancer who, after first-line chemotherapy, received either the vaccine or best supportive care.

  1. 01

    Longer survival in those who completed the programme

    In patients who received at least four doses, median survival was 12.43 against 9.43 months, a statistically significant difference.

  2. 02

    The vaccine group was ahead overall too

    When all patients were assessed together, median survival was 10.83 months in the vaccine group and 8.86 months in the comparison group.

  3. 03

    14.66 months with a high EGF level

    In patients with a high EGF level in the blood at the start, median survival reached 14.66 months. This finding sheds light on who may benefit most from the vaccine.

  4. 04

    Mild side effects

    Reported side effects were mostly mild: pain at the injection site, fever, vomiting and headache. It was also well tolerated in long-term use.

A later review reported, in long-term follow-up, two-year survival of 37% against 20% and five-year survival of 23% against 0% in vaccinated patients compared with the comparison group.

Vaxira

What did the Vaxira studies find?

A randomised, placebo-controlled phase II/III trial of Vaxira, published in Clinical Cancer Research in 2014, included 176 patients. Median survival was 8.23 months in the vaccine group and 6.80 months with placebo; progression-free survival was measured at 5.33 against 3.90 months.

In a later phase III trial, Vaxira was compared with a standard chemotherapy as maintenance treatment, and the researchers reported that the vaccine did not fall behind the chemotherapy. Being given by injection, with mostly mild side effects, makes long maintenance treatment easier for patients.

Who is it for?

Who are these vaccines considered for?

The vaccines were developed for patients in a particular situation. These are the main points the oncologist looks at in the assessment.

  1. 01

    A clear diagnosis and stage

    The pathology report and current staging imaging are the basis of the assessment. The more complete the file, the faster the opinion arrives.

  2. 02

    First-line treatment completed

    The vaccines are used as maintenance treatment after first-line chemotherapy or radiotherapy.

  3. 03

    Molecular test results

    EGFR, ALK, ROS1 and PD-L1 results help the oncologist make the best plan; if a targeted option exists, the plan is shaped accordingly.

  4. 04

    General condition and other illnesses

    For patients who can manage daily activities and whose other illnesses are under control, a long programme and travel are easier to plan.

Next step

What does this mean for you?

The oncologist who reviews your file assesses whether the vaccine suits you and how much benefit you may expect. We prepare your file, translate it and send it to the licensed oncologist in Cuba. The opinion reaches you in writing, and we are with you at every step.

If you are wondering about cost, see Cuba lung cancer vaccine cost; for access from outside Cuba, see CIMAvax-EGF from the USA, Canada and abroad. The whole process is laid out in the treatment journey, step by step. When you are ready, you can fill in the application form.

Frequently asked questions

Most asked questions about the Cuban cancer vaccine studies

Does the Cuban cancer vaccine work?

In published studies, patients who received the vaccine as planned had longer survival and a longer time without progression. The oncologist who reviews your file assesses how much benefit you may expect.

What is the aim of the Cuban cancer vaccine?

To activate the immune system against the tumour, keep the disease under control for longer after first-line treatment and extend survival.

Do patients on the Cuban cancer vaccine have side effects?

Reported side effects are mostly mild: pain at the injection site, fever, vomiting and headache. Administration and follow-up take place under the supervision of the oncology team.

How many doses are given?

With CIMAvax-EGF, a few induction doses are followed by monthly maintenance doses, and treatment continues for months while the benefit lasts and the patient tolerates it. The oncologist sets your own plan.

What is the CIMAvax success rate?

Studies measure success by survival. In the CIMAvax-EGF phase III trial, patients who had at least 4 doses reached a median survival of 12.43 months, against 9.43 months in the comparison group, and those with a high EGF level at the start 14.66 months. With Vaxira, median survival was 8.23 months (placebo 6.80) and time without progression 5.33 months (placebo 3.90).

How can I reach it from abroad?

Your file goes to the oncologist in Cuba; if you are found suitable, treatment starts in Cuba and the doctor plans the continuation. We explain more in CIMAvax-EGF from the USA, Canada and abroad.

Sources

What this article is based on

  1. CIMAvax-EGF phase III trial — PubMed
  2. U.S. CIMAvax combination trial — ClinicalTrials.gov
  3. Racotumomab/Vaxira phase II trial — PubMed

Prepared by the Cuba Health Assist medical content team · Last updated: · Editorial and medical content policy

Diagnosis and treatment decisions are made by the specialist who reviews your file.

Start with your file

Start the review with your medical file

Send your documents through the secure application area. We prepare your file, send it to the oncologist in Cuba and explain the next steps to you. For general information, see our page on the Cuban cancer vaccine.

This article is general information. It is not a diagnosis, personal treatment advice or a decision on suitability. If you have an urgent symptom, contact local emergency care right away. Medical disclaimer