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1 ssion to rapid progression despite intensive multimodal therapy.
2 pefully provide more effective, targeted and multimodal therapy.
3 hese men are the most likely to benefit from multimodal therapy.
4 ignancy with a short median survival despite multimodal therapy.
5 tor for poor outcome with current aggressive multimodal therapy.
6 rvival rates less than 40% despite intensive multimodal therapy.
7 have a high likelihood of cure with current multimodal therapy.
8 s and are likely to improve with advances in multimodal therapy.
9 in adults with rhabdomyosarcoma treated with multimodal therapy.
10 -free survival rate in patients who received multimodal therapy.
11 isease, critical for guidance of targeted or multimodal therapy.
12 x, hypopharyngeal tumors, and treatment with multimodal therapy.
13 d 7.71 weeks (95% CI, 6.71-10.14 weeks) with multimodal therapy.
14 ronous metastases, and 402 (73.0%) underwent multimodal therapy.
15 indicator of individual response to evolving multimodal therapies.
16 tients is approximately 14-16 months despite multimodal therapies.
18 riant of prostate cancer that often warrants multimodal therapy and poses a significant diagnostic ch
19 ions of survival outcomes over time with new multimodal therapies are needed for optimizing treatment
21 igh-risk patients are treated with intensive multimodal therapies but cure rates remain suboptimal.
22 gh-risk features; contemporary studies favor multimodal therapy, but high-risk disease is often under
24 apy-naive (or with prior platinum as part of multimodal therapy completed >= 4 months earlier) recurr
25 or progressed within 3-6 months of previous multimodal therapy containing platinum for locally advan
27 ring in patients with brain metastases after multimodal therapy, especially in clinical situations wi
28 rature for processes of care and outcomes of multimodal therapies for muscle-invasive urothelial carc
29 their utilization in photomedicine, that is, multimodal therapy for cancer (e.g., PDT, PTT) and antim
31 radiotherapy is becoming a key component of multimodal therapy for many stages of prostate cancer, p
34 g more effective systemic treatment into the multimodal therapy has been adopted in the CAO/ARO/AIO-0
35 but on assumptions regarding sensitivity to multimodal therapy (i.e., chemotherapy, radiation, intra
39 Children with chest wall sarcoma require multimodal therapy including chemotherapy, surgery and/o
42 of (18)F-FET PET for treatment monitoring of multimodal therapy, including checkpoint inhibitors, tar
45 f patients with oral cavity cancer requiring multimodal therapy, initiation of radiation therapy with
46 cell carcinoma (HNSCC) patients that require multimodal therapy involving chemotherapy in conjunction
50 , class III clinical trials demonstrate that multimodal therapy is important for both life quality an
53 DSRCT have not been developed, and standard multimodal therapy is insufficient, leading to a 5-year
55 oscale drug delivery vehicles can facilitate multimodal therapies of cancer by promoting tumour-selec
58 nt was defined as RP with appropriate use of multimodal therapy (optimal RP), EBRT with at least 2 ye
62 ogic features receiving guideline-concordant multimodal therapy, prostate cancer-specific mortality o
64 Patients were treated with risk-directed multimodal therapy regardless of race, ethnicity, or abi
65 nly about one third of patients treated with multimodal therapy remain disease-free, and local contro
66 dence of SNs was higher among survivors with multimodal therapy (standard risk, 9.5%; historical, 2.8
69 xclusive psychological treatment rather than multimodal therapies, substantially limiting rehabilitat
70 ) patients including 255 patients undergoing multimodal therapy (surgery with chemotherapy, radiation
72 s will all be required to accommodate PAT, a multimodal therapy that combines pharmacological and psy
73 usion: Given the considerable annual cost of multimodal therapy, the integration of (18)F-FET PET can
74 Despite the use of intensive contemporary multimodal therapy, the overall survival of patients wit
76 lthough there have been recent advances with multimodal therapy, treatment of neuroblastoma remains a
77 total of 393 consecutive patients completing multimodal therapy were studied, all with prospectively
78 ed nanoplatforms that embrace the concept of multimodal therapy, which aims to combine MHT with chemo
81 tandard isotretinoin therapy after intensive multimodal therapy would improve outcomes in high-risk n