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Rtog 1308

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RTOG 1308: Phase III Randomized Trial Comparing Overall Survival After Photon Versus

Proton Chemoradiotherapy for Inoperable Stage II-IIIB NSCLC (Non-Small Cell Lung Cancer)
The RTOG 1308 clinical trial was set in place to improve the mean survival for patients
affected by non-small cell lung cancer in both patient groups treated with photons and proton
therapy. This trial is currently being held through the NRG. One of the main factors for this trial
being that the prescribed dose would be 70 Gy based on previous clinical trials and their results
to help lower toxicities to various organs at risk (OAR) and increase the average survival time
for patients.1 Other secondary objectives include evaluating pulmonary function, quality of life,
and cost effectiveness.2 Patients receive concurrent chemotherapy while radiation treatments are
ongoing. Patients eligible for this clinical trial must be diagnosed with stage II-IIIB NSCLC.
Patients also had to be considered ineligible for surgery and could not have received prior
radiotherapy or chemotherapy. Following stratification, patients are randomized into two
different study arms.1 It is hypothesized that the patients in the proton arm will show less severe
symptoms at the 6-month follow-up.

There are little treatment options available for patients who are affected by NSCLC, thus
this study also aims to explore the potential benefits of radiation therapy at these dose levels. As
proton centers are not available at every clinical site, with promising results this could encourage
the use of photon therapy as a form of treatment for NSCLC.2 The concurrent chemotherapy
regimen will be determined by the physician prior to the start of radiation treatments. Some of
the technical factors involving the treatment planning include only using energies of 6-10 MeV
with a total dose of 70 Gy delivered over 35 fractions.1 Proton plans are permitted to use energies
that lead to adequate tissue penetration. Simulation requires motion management in some form.
This can include utilizing a 4D CT scan or other respiratory gating options.1 The target volumes
must include a: GTV, IGTV, CTV, ITV and a PTV. Primary planning objectives regarding tumor
volume coverage is for 95% of the PTV to receive a minimum of 95% of the prescribed dose.1 If
this criterion is not able to be met, there are slight variations acceptable. The following OAR
must be delineated in the treatment plan: Spinal canal, lungs- GTV, bilateral lungs, esophagus,
brachial plexi, heart, liver, and bilateral kidneys.1 There is currently no published data on the trial
as it is still ongoing. The projected completion date is in December 2024.
References:

1. NRG. RTOG 1308: Phase III Randomized Trial Comparing Overall Survival After
Photon Versus Proton Chemoradiotherapy for Inoperable Stage II-IIIB NSCLC. National
Library of Medicine.
2. NIH. History of Changes for Study: NCT01993810 Comparing Photon Therapy to Proton
Therapy to Treat Patients with Lung Cancer. History of changes for study:
NCT01993810. Accessed July 18, 2023.
https://classic.clinicaltrials.gov/ct2/history/NCT01993810?V_13=View#StudyPageTop.

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