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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1173531 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
6 T$ n' u3 W& m5 s: ANOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 / f# r3 r  P/ S* {
+ Author Affiliations
6 K% f8 J; |1 G) _- _9 {3 P6 j- c' w3 z9 H0 W! ~
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
* n8 c# `5 N2 C, p2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
' K+ q8 J3 h8 @: q3 q! C3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ) Z# U9 o5 }& m- M. `  o* Y
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
3 Q) i0 H2 i6 K  {  o1 M5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 9 y& q& ~( C0 v; ~; h
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan ) H& V- @* a: `! _
7Kinki University School of Medicine, Osaka 589-8511, Japan : Z: E" T7 N, ?" u% z9 R
8Izumi Municipal Hospital, Osaka 594-0071, Japan
4 A2 E1 I& c% d- [* F% z6 t# W, v9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
6 a8 ]# f' a. m. U0 \4 iCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
; [' ?1 h6 k2 E; ~( O+ cAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. # }, [, Z% I3 H& ~$ A

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
7 M+ i- r2 B* P1 r3 |' Y
1 ?$ [- l  h+ A% ^Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
7 L) b# ]+ O2 }& [; ^; [( ]1 b' H4 J3 ^" R% V
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ; d0 {9 ?# a+ {
- `2 ?' A$ M! H3 A
Published online on: Thursday, December 1, 2011 ' l- X0 I/ I& M! S9 [9 ^

+ W3 g+ i( \0 t& K8 x" p1 x: ^Doi: 10.3892/ol.2011.507
: L! i+ A+ v- Z/ K! G7 ], N* @0 R( e1 R
Pages: 405-410
7 u( k5 ^1 ?: _! L( q! H
5 n" ^% H( c. }9 N: @1 r: ?! QAbstract:- I& I6 m) A# n8 E5 |5 n5 g- V# ^& Y7 o
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
2 k* r, @" W; S/ G1 y0 TF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 4 d  t. C' c1 J2 R
+ Author Affiliations
$ h. d# }4 a: W2 \2 E0 S1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu - U6 i, T4 T- c7 T% f8 \/ ?1 j
2Department of Thoracic Surgery, Kyoto University, Kyoto 5 z. Q1 z5 ~6 v4 I7 n  f
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
5 ~) |& h8 P* Y) f6 [7 }7 Z&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp ; f( X  z$ d" G5 Y0 l, Y" {4 j
Received September 3, 2010.
* i$ r' o. a4 nRevision received November 11, 2010.
- x9 c7 ?3 _! M' V2 a0 WAccepted November 17, 2010.
6 m) r& Y' l; }6 v2 j+ g7 KAbstract
" U( o" R, Y2 o; T* }$ UBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
2 e; E4 m% z- A" L; WPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. 0 W  r6 E# |5 c( U
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. , `7 v7 K3 q2 Y! t. J
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 9 J- W% p4 K3 u6 O0 Z$ h  }
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。+ |: M6 v) N5 }$ T' U
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?
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老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy1 t+ y  W4 `. X- w' l; O
http://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC8 Z1 m3 _. H8 S$ l1 }
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑   E. [6 P0 y& F8 n0 h# x6 Y

; B: G3 Z0 f! o- ]( m+ `& s) h$ d  M从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
) b% d1 G% ]5 m9 U- l至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
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没有副作用是第一追求,效果显著是第二追求。; j  ?" K- a! C
不错。

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