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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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1308650 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 Type5 O4 a  f/ N% Z
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 7 ?. L" h1 \- o
+ Author Affiliations
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9 w# r6 t: h$ u  }# t  x) p1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
  g! c5 C  y- P6 j% D: m2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 u! P* s( O9 u: I  V3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
, ~9 X- b" f# q4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan + |6 T2 Z* @) q" O- [8 N$ j' [
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 5 x6 ]3 `5 H/ W4 y* y+ f; ^1 \+ n
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 5 t/ ~6 B0 _# ^4 ]
7Kinki University School of Medicine, Osaka 589-8511, Japan : F6 ^- c/ d2 H' K5 C; v
8Izumi Municipal Hospital, Osaka 594-0071, Japan ( \; J. W6 a% \. Y/ ^- a; i! e
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
% _+ C6 j: a' M* g1 [4 VCorrespondence 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
+ s7 l- l! h* O5 E& nAbstractBackground: 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. 1 Q! V; V7 d* q3 }

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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 # l. s2 k! l) z6 }

, z  }: _1 u, q! tAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ' }' G, J) w# y5 Z% F: I$ R

/ x$ B/ D* H! X) P8 s7 k# `) MAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
3 t4 K; [* s: S3 P1 y# f3 _) V) \: ]
2 ~6 E# j' M: PPublished online on: Thursday, December 1, 2011
6 m( `8 O; p9 h% x
# ?% N/ [1 T% d" o6 m& nDoi: 10.3892/ol.2011.507
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Pages: 405-410 9 F' m9 J6 G7 z. H! o# X' S, M
7 V$ h# W; `+ k* S9 n6 j
Abstract:
% ]* o1 A9 O' D# c) W5 Z! AS-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.8 K3 {; x6 Z& m& V0 O: Q
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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 population8 T' T, G/ ^: B2 z5 s/ V- n7 h
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
" u5 ~. D8 {) A; r+ Author Affiliations
$ S: K8 |! L1 F, R1 ^3 d8 T1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
/ ]: s5 k' H1 B& \3 y* J! Y2Department of Thoracic Surgery, Kyoto University, Kyoto
" S! k* y& \, v- f8 p* i5 F3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 4 m1 n, o) V; L! e6 U
&#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
9 D5 e$ l- H8 h! z" B0 p/ |2 RReceived September 3, 2010.
' I; m: Z9 F: h3 e' URevision received November 11, 2010.
; u+ C. f1 Q! G! X' C' ZAccepted November 17, 2010. 7 s1 T3 g! {1 e8 O
Abstract
' u; D* O4 T0 }Background: 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. ; ~. T; c' l) r8 {$ p
Patients 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. " T8 Z0 F8 q7 |- l; s6 C( V& t
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.
+ {: P# Y& L2 x; H8 fConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. + Y- G$ P) d% O/ r
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。
; N, ^, i% V" j3 g9 d$ T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?. ]3 F1 O; K: M% F9 y& f( o
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 Chemotherapy3 l8 S! d9 p  y, _
http://clinicaltrials.gov/ct2/show/NCT01523587
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- u4 O% {5 d+ L# jBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC, P  A6 q! n" R+ Z* T  \
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
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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。
$ e3 |+ m; }8 R( ?; d5 T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
老马 发表于 2012-4-29 20:53 9 G  F( |3 M5 a. t0 \
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。0 d% G/ S5 R) K' u5 `7 ~3 f
至今为止,未出 ...

' v; j0 R9 |$ X0 c没有副作用是第一追求,效果显著是第二追求。# J5 t3 J: p3 ~3 H  C
不错。

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