2020
DOI: 10.1016/j.ijrobp.2020.09.020
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Patterns of Disease Progression after Carboplatin/Etoposide + Atezolizumab in Extensive-Stage Small-Cell Lung Cancer (ES-SCLC)

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Cited by 23 publications
(17 citation statements)
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“… 18 , 19 With the report that the most dominant pattern of SCLC progression was at initial thoracic sites of the disease, it is also likely that tRT provides treatment consolidation to residual tumor cells that might have escaped the antitumor effect of systemic therapy. 3 , 29 Alternatively, improved OS with tRT may be accounted for by the fact that patients who received tRT had numerically lower proportion (but not statistically significant, p = 0.06) of M1c disease (American Joint Committee on Cancer TNM eighth edition M-status) than those who did not receive such treatment as found in our Supplementary Table 1 .…”
Section: Discussionmentioning
confidence: 71%
“… 18 , 19 With the report that the most dominant pattern of SCLC progression was at initial thoracic sites of the disease, it is also likely that tRT provides treatment consolidation to residual tumor cells that might have escaped the antitumor effect of systemic therapy. 3 , 29 Alternatively, improved OS with tRT may be accounted for by the fact that patients who received tRT had numerically lower proportion (but not statistically significant, p = 0.06) of M1c disease (American Joint Committee on Cancer TNM eighth edition M-status) than those who did not receive such treatment as found in our Supplementary Table 1 .…”
Section: Discussionmentioning
confidence: 71%
“…The percentage of enrolled patients who received PCI in the IMpower133 and KEYNOTE-604 was 11 and 13%, respectively, whilst in the CASPIAN trial, PCI was allowed only in the control arm after completion of CT, and 8% of patients in this arm received it ( 4 6 ). Noteworthy, in the IMpower133 trial, time to intracranial progression was longer in patients receiving CT + atezolizumab vs. CT only (20.2 vs. 10.5 months, respectively), even though they did not receive PCI (16.7 vs. 9.8 months, respectively) ( 34 ). This evidence further questioned the role of PCI in the era of chemoimmunotherapy.…”
Section: Brain Metastases In the Chemoimmunotherapy Eramentioning
confidence: 99%
“…The CASPIAN trial allowed PCI in the chemotherapy alone arm but only 8% (21 patients) received it (47) and although PCI was permitted in both arms of the IM-Power 133 trial, only 11% (22 patients) in each arm received it (45). The IM-Power 133 study showed that atezolizumab significantly delayed the time to intracranial progression (20.2 months versus 10.5 months, P=0.046) compared with placebo (48). Similarly, in the setting of AJCC stage III non-small cell lung cancer (NSCLC), the PACIFIC trial showed that the addition of adjuvant durvalumab reduced the incidence of BM from 11.8% to 6.3% (49).…”
Section: Pci In Es-sclcmentioning
confidence: 99%