Early Results of RTOG Small-Cell Lung Cancer Trial

Publication
Article
OncologyONCOLOGY Vol 9 No 2
Volume 9
Issue 2

Survival and local control rates for limited stage small-cell lung cancer patients treated with either once-daily or twice-daily thoracic radiation plus cisplatin (Platinol) and etoposide (VePesid) are substantially better than with previously reported

Survival and local control rates for limited stage small-celllung cancer patients treated with either once-daily or twice-dailythoracic radiation plus cisplatin (Platinol) and etoposide (VePesid)are substantially better than with previously reported treatmentregimens, preliminary results of RTOG 88-15 indicate.

The 358 eligible patients were randomized to one of two arms ofthe study. In one arm, patients received thoracic irradiationonce a day to a total dose of 45 Gy in 5 weeks.

In the other arm, patients received 1.5 Gy twice daily to a totaldose of 45 Gy in 3 weeks.

All patients underwent the same chemotherapy regimen of four cyclesof cisplatin (60 mg/m² on day one of radiation treatment)and etoposide (120 mg/m² on days one, two, and three). Thisregimen was repeated at 21-day intervals.

Patients with complete response underwent prophylactic cranialirradiation (25 Gy given in 10 fractions over 2 weeks).

The median survival for patients treated twice a day with radiationwas 20.3 months, said Dr. Wally Curran, an author of the study.It was 18.6 months for patients treated once a day, he said. Thatcompares to about 14 months for patients who undergo standardtreatment. The local failure rate was 61% for patients treateddaily, and 48% for those treated twice daily.

According to Dr. Curran, 15% of patients treated daily had grade3 or worse toxicities, compared with 30% for those treated twicedaily.

"Because we observed better local control and survival rates,RTOG is continuing to pursue twice-daily treatment as a schedulefor limited stage small-cell lung cancer patients," saidDr. Curran. RTOG has two limited stage small-cell lung cancertrials open: RTOG 93-07 and RTOG 93-12.

RTOG 88-15 was an intergroup trial, coordinated by the EasternCooperative Oncology Group. RTOG contributed about one-third ofthe patients to the study.

The results of RTOG 88-15 were presented at the recent annualmeeting of the American Society for Therapeutic Radiology andOncology.

Recent Videos
With many treatments emerging in the EGFR-mutated lung cancer landscape, sequencing therapy has emerged as a key consideration for these patients.
Patients with lung cancer who achieve a complete response with neoadjuvant therapy may not experience additional benefit with adjuvant immunotherapy.
Numerous trials have displayed the evolution of EGFR inhibition alone or with chemotherapy/radiation in the EGFR-mutated lung cancer space.
Thinking about how to sequence additional agents following targeted therapy may be a key consideration in the future of lung cancer care.
Endobronchial ultrasound, robotic bronchoscopy, or other expensive procedures may exacerbate financial toxicity for patients seeking lung cancer care.
Patients with mediastinal lymph node involved-lung cancer may benefit from chemoimmunotherapy in the neoadjuvant setting.
Advancements in antibody drug conjugates, bispecific therapies, and other targeted agents may hold promise in lung cancer management.
Stressing the importance of prompt AE disclosure before they become severe can ensure that a patient can still undergo resection with curative intent.
Thomas Marron, MD, PhD, presented a session on clinical data that established standards of care for stage II and III lung cancer treatment at CFS 2025.
Decreasing the low-dose bath of proton therapy to the body may limit the impact of radiation on lymphocytes and affect tumor response.
Related Content