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Effect of induction immunochemotherapy before concurrent chemoradiotherapy on outcomes in limited-stage small cell lung cancer.
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e20158
Background:
Immunotherapy, chemotherapy, and radiotherapy all play significant roles in the management of small cell lung cancer (SCLC). Combining radiotherapy with chemotherapy followed by immunotherapy shows promise for limited-stage SCLC (LS-SCLC), offering good tolerability and survival benefits. However, there is limited data on whether immunotherapy combined with chemotherapy for LS-SCLC can be performed before chemoradiotherapy. Therefore, we investigated the safety and effectiveness of induction immunochemotherapy followed by concurrent chemoradiotherapy (CCRT) for LS-SCLC.
Methods:
A retrospective analysis was conducted on 138 patients with LS-SCLC who received chemoradiotherapy between January 2019 and December 2024. This study included 34 patients receiving induction immunochemotherapy and 104 patients receiving induction chemotherapy. All patients underwent 2-4 cycles of induction therapy before CCRT. Clinical outcomes, including survival and toxicity, were compared between groups. Imaging assessments were performed before and 1 month after CCRT. The evaluations included the tumor response to induction therapy, treatment-related adverse events, complications during and after CCRT, tumor response after CCRT, progression-free survival (PFS), and overall survival (OS). Follow-up data were collected through regular check-ups or inpatient records.
Results:
Compared to the induction chemotherapy group, the objective response rate (ORR) of tumors after induction treatment in the induction immunochemotherapy group was 67.6% (23/34) versus 45.2% (47/104) (P = 0.023). After CCRT, the ORR in two groups was 79.4% (27/34) versus 60.6% (63/104) (P = 0.045). The median follow-up time was 25.3 months for the induction immunochemotherapy group and 28.2 months for the induction chemotherapy group. The median progression-free survival (PFS) for two groups was 21.3 months versus 13.1 months (P = 0.015), and the median overall survival (OS) was not reached versus 41.7 months (P = 0.039). Treatment-related toxicities of grade 1-2 were 64.7% versus 54.8% (P = 0.311), and grade 3-4 toxicities were 41.2% versus 41.3% (P = 0.986). No grade 5 treatment-related toxicities were observed.
Conclusions:
Induction immunochemotherapy followed by CCRT for patients with LS-SCLC is effective and safe with a high ORR, PFS and OS rate, as well as a tolerable toxicity profile. Larger, randomized controlled trials are required to confirm our findings.
Characteristics
Induction immunochemotherapy (n=34)
Induction chemotherapy (n=104)
Best response to induction therapy-n(%)
CR/PR
23 (67.6)
47 (45.2)
SD
10 (29.4)
52 (51.0)
PD
1 (2.9)
4 (3.8)
Best response to CCRT-n(%)
CR/PR
27 (79.4)
63 (60.6)
SD
6 (17.6)
34 (32.7)
PD
1 (2.9)
7 (6.7)
The median progression-free survival-months
21.3
13.1
The median overall survival-months
NR
41.7
American Society of Clinical Oncology (ASCO)
Title: Effect of induction immunochemotherapy before concurrent chemoradiotherapy on outcomes in limited-stage small cell lung cancer.
Description:
e20158
Background:
Immunotherapy, chemotherapy, and radiotherapy all play significant roles in the management of small cell lung cancer (SCLC).
Combining radiotherapy with chemotherapy followed by immunotherapy shows promise for limited-stage SCLC (LS-SCLC), offering good tolerability and survival benefits.
However, there is limited data on whether immunotherapy combined with chemotherapy for LS-SCLC can be performed before chemoradiotherapy.
Therefore, we investigated the safety and effectiveness of induction immunochemotherapy followed by concurrent chemoradiotherapy (CCRT) for LS-SCLC.
Methods:
A retrospective analysis was conducted on 138 patients with LS-SCLC who received chemoradiotherapy between January 2019 and December 2024.
This study included 34 patients receiving induction immunochemotherapy and 104 patients receiving induction chemotherapy.
All patients underwent 2-4 cycles of induction therapy before CCRT.
Clinical outcomes, including survival and toxicity, were compared between groups.
Imaging assessments were performed before and 1 month after CCRT.
The evaluations included the tumor response to induction therapy, treatment-related adverse events, complications during and after CCRT, tumor response after CCRT, progression-free survival (PFS), and overall survival (OS).
Follow-up data were collected through regular check-ups or inpatient records.
Results:
Compared to the induction chemotherapy group, the objective response rate (ORR) of tumors after induction treatment in the induction immunochemotherapy group was 67.
6% (23/34) versus 45.
2% (47/104) (P = 0.
023).
After CCRT, the ORR in two groups was 79.
4% (27/34) versus 60.
6% (63/104) (P = 0.
045).
The median follow-up time was 25.
3 months for the induction immunochemotherapy group and 28.
2 months for the induction chemotherapy group.
The median progression-free survival (PFS) for two groups was 21.
3 months versus 13.
1 months (P = 0.
015), and the median overall survival (OS) was not reached versus 41.
7 months (P = 0.
039).
Treatment-related toxicities of grade 1-2 were 64.
7% versus 54.
8% (P = 0.
311), and grade 3-4 toxicities were 41.
2% versus 41.
3% (P = 0.
986).
No grade 5 treatment-related toxicities were observed.
Conclusions:
Induction immunochemotherapy followed by CCRT for patients with LS-SCLC is effective and safe with a high ORR, PFS and OS rate, as well as a tolerable toxicity profile.
Larger, randomized controlled trials are required to confirm our findings.
Characteristics
Induction immunochemotherapy (n=34)
Induction chemotherapy (n=104)
Best response to induction therapy-n(%)
CR/PR
23 (67.
6)
47 (45.
2)
SD
10 (29.
4)
52 (51.
0)
PD
1 (2.
9)
4 (3.
8)
Best response to CCRT-n(%)
CR/PR
27 (79.
4)
63 (60.
6)
SD
6 (17.
6)
34 (32.
7)
PD
1 (2.
9)
7 (6.
7)
The median progression-free survival-months
21.
3
13.
1
The median overall survival-months
NR
41.
7.
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