For patients with advanced, inoperable stage 3 lung cancer, concurrent chemotherapy and the specialised radiation treatment, proton therapy, offers improved survival compared to historical data for standard of care, according to a new study from The University of Texas MD Anderson Cancer Center.
The research, published in JAMA Oncology, reported an overall survival (OS) of 26.5 months.
In contrast, the historical OS rate with standard of care concurrent chemotherapy and traditional radiation was 16 months at the time when the study was designed.
The findings are the final results of the single institution, Phase II study and represent the longest follow-up to date of stage 3 lung cancer patients who have received proton therapy, said Joe Y. Chang, M.D., professor, Radiation Oncology and the study’s corresponding author.
“Advanced lung cancer patients with inoperable disease traditionally have been treated with concurrent chemotherapy and conventional photon radiation therapy. However, the therapy can be very difficult for patients due to associated toxicities and because many patients are also dealing with comorbidities,” explained Joe Y. Chang.
Proton therapy is an advanced type of radiation treatment that uses a beam of protons to deliver radiation directly to the tumour, destroying cancer cells while sparing healthy tissues.
Protons enter the body with a low radiation dose and stop at the tumour, matching its shape and volume or depth.
They deposit the bulk of their cancer-fighting energy right at the tumour, thereby reducing the dose to cardiopulmonary structures, which impacts the toxicity, functional status, quality of life and even survival for patients, explained Chang.
“With our study, we hypothesised that proton therapy would offer a survival benefit to patients and reduce treatment-associated toxicities, which can be very serious,” he said.
The study opened at MD Anderson in 2006; in this research, Chang and his colleague report on the study’s five-year results.
For the prospective Phase II trial, 64 patients with inoperable, Stage III non-small-cell lung cancer were enrolled.
The study’s primary endpoint was OS.
The researchers hypothesised that the median OS would increase from historical data of 16 months on standard therapy to 24 months.
Secondary endpoints included distant metastasis and local and regional recurrence rates.
Toxic effects of treatment in both the acute and late settings also were analysed.
Median follow up was 27.3 months for all patients, and 79.6 months for alive patients.
At five years, the median OS was 26.5 months, and the corresponding five-year OS was 29 percent.
Median progression-free survival was 12.9 months, with a five-year progression-free survival of 22 percent.
In sum, 39 patients experienced a relapse, with distant sites representing 62 percent of all recurrences.
Local and regional recurrence rates were low, 16 percent and 14 percent, respectively.
Among the acute and late toxic effects diagnosed in patients were: esophagitis, pneumonitis and cardiac arrhythmia.
Of note, said Chang, no patients developed the most severe, or grade five, toxicities, as seen in patients who receive standard of care.
Chang noted his study is not without limitations.
Of greatest significance: the study was designed more than a decade ago.
While the study’s survival, recurrence rates and toxic effects are still favourable when compared to rates associated with the most advanced traditional photon radiation therapy, intensity modulated radiation therapy (IMRT), technology to diagnose and stage the disease, as well all treatment modalities have significantly improved.
“When the study opened, PET imaging had just been approved for lung cancer staging. The image quality was poor and didn’t include a CT component in most facilities across the country,” said Chang. “Obviously, the technology has improved dramatically over the last decade and has made a significant impact on diagnosis and staging. Also, delivery of both the conventional intensity-modulated radiation therapy (IMRT) and proton therapy (IMPT), have improved, thereby reducing side effects for both treatment modalities.”
For example, MD Anderson proton therapy patients with advanced lung cancer now can receive IMPT.
The technique uses an intricate network of magnets to aim a narrow proton beam at a tumor and “paint” the radiation dose onto it layer by layer.
Healthy tissue surrounding the tumour is spared, and side effects are even more reduced than earlier proton delivery, said Chang.
A Phase II trial studying IMPT and concurrent chemotherapy is underway.
Chang also noted the advancements in cancer biology and immunotherapy and that both are important areas of research focus in combination with proton therapy.
Source: MD Anderson Cancer Center